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<h3>Job Description</h3>
Job DescriptionSalary: $1,634 to $1,814/week commensurate with experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Easton, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

Project Geotechnical Engineer - Easton

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
Support regulatory approval of biologics drug substances by authoring Chemistry, Manufacturing, and Controls (CMC) filing content and by leading cross-functional CMC teams throughout Phase 1, Phase 2, and Phase 3 development&nbsp;
Responsibilities:
<ul>
<li>Author sections of regulatory documents, including INDs and BLAs, based on relevant source documentation.</li>
<li>Partner with subject matter experts in various process development functions to ensure technical information is accurately transcribed into regulatory documents.</li>
<li>Lead CMC teams in the development of robust control strategies and presentation of Control Strategy Reviews (CSRs)</li>
<li>Drive alignment with key business stakeholders including Product Development Directors, Development Sciences, and Quality Assurance and escalate issues to senior management when appropriate</li>
<li>Contribute on program acceleration and increased efficiency initiatives.</li>
</ul>
Qualifications 
<ul>
<li>BS or equivalent education in Biology, Biochemistry, Engineering or related discipline and 8+ years of experience in the biopharmaceutical industry; MS and 6+ years experience; PhD and 3+ years experience.</li>
<li>Demonstrated knowledge of biologics manufacturing processes, including cell culture and purification operations, and knowledge of process development.</li>
<li>Demonstrated knowledge of Good Documentation Practices (GDP) and technical writing.</li>
<li>Demonstrated knowledge of scientific and regulatory requirements for biopharmaceutical products.</li>
<li>High proficiency with Microsoft Word and Excel.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, II CMC Sciences Biologics Development and Launch (BDL) -Remote Role

<h3>Job Description</h3>
Job Description
Overview

Now Hiring: Research and Development Specialist (Culinary) Location: Lowell, MA
Pay Range: $22-$25/hr. *based on experience*
Schedule: Monday-Friday 9am-5pm *occasional weekends*
Benefits &amp; Perks:
<ul>
<li>401(K)</li>
<li>Dental Insurance. </li>
<li>Employee Assistance Program.</li>
<li>Health, Life and Vision Insurance. </li>
<li>PTO</li>
<li>Tuition Reimbursement</li>
</ul>
 Who We Are: PGI Foods, Inc, is a food manufacturer with an extensive line of versatile soups, sauces and value-added specialty food items, our foodservice division offers restaurants and grocery stores many delicious ways to please their customers. 
We are looking for an Research and Development Specialist to support our organization. 
COME GROW WITH US!
We're looking for talented individuals who share our passion for food and are ready to contribute to our continued success. We offer a collaborative and supportive environment where you can develop your skills and advance your career.
WHO WE ARE
We're a dynamic and growing food manufacturer specializing in an extensive line of soups, sauces, and specialty food items. Our passion lies in providing restaurants and grocery stores with delicious, high-quality products that help them delight their customers.

OUR MISSION
To produce quality, culinary-driven products and to be a valued supplier and business partner to our customers.
HOW THIS ROLE SUPPORTS OUR MISSION
The Research &amp; Development Specialist plays a crucial role in the development and commercialization of new products. Working closely with the Director of R&amp;D, the culinary team, and production staff, this position ensures seamless product transitions into production. This role encompasses a broad range of responsibilities, from assisting in product formulation and testing to facilitating regulatory compliance.
WHAT YOU’LL DO
<ul>
<li>Assist in developing new product formulas and procedures</li>
<li>Prepare samples as directed </li>
<li>Record the product attributes such as: pH, consistency, water activity.</li>
<li>Manage daily production reviews and record taste panel results. </li>
<li>Assist with trade shows and customer presentations. </li>
<li>Maintain and manage sample inventory and record keeping on all development samples.</li>
<li>Assist in requisitioning and recording usage of raw materials/ingredients as needed.</li>
<li>Maintain a neat, sanitized and organized test kitchen.</li>
</ul>
WHAT WE’RE LOOKING FOR 
We’re looking for someone who shares our passion for great food and our commitment to doing things the right way. At PGI Foods, we value teamwork, integrity, and a spirit of continuous improvement. If you do too..
and have the following qualifications:
REQUIRED QUALIFICATIONS
<ul>
<li>Being able to follow instructions</li>
<li>Basic understanding of food science and technical application</li>
<li>Excellent verbal and written communication skills with the ability to collaborate effectively across all levels of the organization</li>
<li>Strong attention to detail</li>
<li>Impeccable time management skills</li>
<li>Proficiency in Microsoft Office application</li>
</ul>

PREFERRED QUALIFICATIONS
<ul>
<li>Associate’s degree in culinary arts or food science preferred</li>
<li>2+ years of related experience in a foodservice and/or manufacturing environment</li>
<li>Strong culinary background and skills</li>
</ul>
PGI Foods is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. PGI Foods strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, sex (including pregnancy), age, national origin or ancestry, ethnicity, religion, creed, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, training, promotion, discipline, compensation, benefits, and termination of employment.

Research and Development Culinary Specialist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Biologics Discovery Sciences group at AbbVie is seeking a highly skilled and self-motivated scientist to join a dynamic team supporting Discovery Biotherapeutics. This position will impact projects through engineering, production, and characterization of multispecific biopharmaceutical products. The ideal candidate should have extensive experience with biologics and multispecifics production platforms, analytical characterization (e.g., SEC, MS), and a proven track record implementing multispecific engineering and production strategies to advance early- and late-stage discovery programs. The ideal candidate will also have people and project management experience. The applicant should be an enthusiastic, creative scientist who will make tangible contributions to the continuous improvement and innovation within the organization.
Key Responsibilities:
<ul>
<li>Responsible for design, engineering and production of multispecific biologics to support all Abbvie therapeutic areas</li>
<li>Evaluate and integrate state-of-the-art technology to improve therapeutic production platforms, and demonstrate creative “out-of-the-box” thinking to solve difficult problems</li>
<li>Supervise 1-2 scientists, evaluate team performance, and is accountable for the effective performance of team</li>
<li>Serve as a Multispecifics Engineering representative for cross-functional teams, and contribute scientific insights into multiple projects across various therapeutic areas; recognized expert in multispecifics design and production</li>
<li>Serve as the Biologics lead on projects to coordinate activities and transitions from hit generation through candidate nomination</li>
<li>Identify and solve technical problems independently, conceive and implement innovative process research ideas</li>
<li>Ensure consistency and quality of technical reports</li>
<li>Provide project update, analysis and advice to cross-functional teams and senior management</li>
<li>Present original work internally across departments and at internal and external scientific conferences; may author or co-author peer-reviewed scientific papers or patents</li>
</ul>
Qualifications 
Qualifications:
<ul>
<li>PhD, MS, or BS degree in Biochemistry, Biochemical engineering or related disciplines with typically 4+ (PhD), 10+ (BS) or 12+ years of experience</li>
<li>Extensive experience in multispecific biologics engineering and knowledge of biologic pipeline progression from exploratory through candidate nomination</li>
<li>Extensive experience with protein, biologics, fragments, and multi-specifics design, expression and purification</li>
<li>Experience managing direct reports and providing performance evaluations and development opportunities</li>
<li>Program management experience preferred</li>
<li>Experience with CRO coordination</li>
<li>Ability to explore and develop new approaches to further advance innovative purification and screening technologies for multispecifics</li>
<li>Sound scientific understanding of current state of protein expression/separation/analytical technologies</li>
<li>Experience with in vitro analytical techniques for protein characterization (e.g. SEC, MS, DSF); experience with developability screening for multispecifics preferred</li>
<li>Strong molecular biology skills (e.g. molecular cloning)</li>
<li>Experience with sequence analysis tools (Vector NTI, Geneious, Genedata)</li>
<li>Excellent organizational skills and the ability to manage multiple projects simultaneously</li>
<li>Team player with the ability to operate in a fast-paced multi-disciplinary environment</li>
<li>Adapt to rapid changes in project priorities and timelines</li>
<li>Recognized in the scientific community through a sustained record of peer-reviewed publications and patents preferred</li>
<li>Candidate must be a goal-oriented team player with excellent verbal and written communication skills and strong can-do attitude</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of the team to enable high performance.</li>
<li>Learns fast, grasps the “essence” and can change the course quickly where indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​
​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive programs.&nbsp;​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II, Multispecific Engineering

<h3>Job Description</h3>
Job DescriptionSalary: $1,615 - $1,793/week based on experience and qualifications 
We are currently accepting applications for an immediate opening for a full time Project Geotechnical Engineer in Boylston, Massachusetts. S. W. Cole Engineering team is an established employee owned firm with a history of over 45 years of success and stable growth serving clients throughout New England. This position involves planning, coordinating and leading project work and engineering assignments. Will also evaluate field and laboratory testing, and perform field services. 
 
The Project Geotechnical Engineer independently evaluates and selects procedures based on specific project needs; manages and executes all aspects of projects by planning, preparing proposals, budgets, scopes, schedules, and assigning necessary tasks to staff involved with the project(s); analyzes, interprets and evaluates data from field and laboratory findings; communicating effectively and consistently with teammates, design professionals and contractors; accurately reviews project billing, and tracks time spent on projects consistently; safely operates and handling of company testing equipment and vehicles in accordance with company policies/safety policies; performs and/or coordinates field services (i.e. subgrade observations, pile driving observations, installation of geotechnical instrumentation, etc.); interacts during project work with staff, general public, clients, contractors, and others, attends project meetings and maintains specific client relationships; regularly attends professional meetings and business and industry events; and practices confidentiality according to company policy.
 
Job Requirements
<ul>
<li>B.S. Civil Engineering required, with emphasis in Geotechnical Engineering, or Engineering Geology preferred.</li>
<li>Familiarity with geology and site conditions in New England.</li>
<li>Registered Professional Engineer (P.E.) in Massachusetts and/or Rhode Island, or, holds F.E./E.I.T. and ability to obtain P.E. within 1 year, required.</li>
<li>Minimum of 4 years of related engineering and project management experience, or demonstrated ability to perform the essential functions required of Project Geotechnical Engineer.</li>
<li>Risk management training.</li>
<li> Valid drivers license, active auto insurance, and reliable transportation.</li>
<li>Experience with and in-depth knowledge of computer software including Microsoft Office, SharePoint, MathCAD, geotechnical analysis programs, and able to learn new programs.</li>
<li> Understand and apply advanced, industry related math skills.</li>
<li>Ability to meet deadlines.</li>
<li>Ability to direct and organize activities.</li>
<li> Broad knowledge of civil engineering principles and practices.</li>
<li>Skilled in collecting, analyzing, and organizing complex data.</li>
<li>Ability to maintain records of materials, supplies, time, and work performed.</li>
<li> Ability to communicate effectively in both verbal and written form.</li>
<li>Has an established network of industry contacts and clients in New England and regularly participates in related trade events.</li>
<li> Regularly spend long hours sitting/standing and using office equipment..</li>
<li>Occasionally conducts field and/or laboratory testing on soil, aggregate and rock samples and equipment, requiring lifting, carrying and bending with up to 100 pounds.</li>
<li>Driving for long periods of time and more frequent shorter trips.</li>
<li>Close, distant, and peripheral vision.</li>
<li>Ability to communicate effectively in both written and oral form.</li>
<li>Ability to remember and understand verbal and written instructions.</li>
<li>Ability to reason logically and make decisions.</li>
<li>Applicants must be legally authorized to work in the United States for any employer. We are not able to sponsor employment Visas at this time. </li>
</ul>
To be considered for this position please fill out the application, and upload a resume and a cover letter. The cover letter should demonstrate your writing skills and summarize how your experience and qualifications make you a good candidate for this position.
 
S.W.COLE has Great Benefits!!
 
Our team members are offered a benefits package that, depending on eligibility, includes:
<ul>
<li>Medical, dental and vision insurance</li>
<li>Health Reimbursement Arrangement (HRA) and Health Savings Account (HSA) with employer match</li>
<li>8 paid holidays and paid time off (PTO) accrued each week</li>
<li>Paid short and long termdisabilityand basic life insurance</li>
<li>401k with employer match and profit sharing</li>
<li>Voluntary life insurance</li>
<li>Critical Illness and Accident protection plans</li>
<li>Mobile phone stipend</li>
<li>Tuition reimbursement</li>
<li>Safety toe shoe program and an allowance to use at our company clothing store</li>
</ul>
We have three options for travelling between our office and job sites for field based team members 1) Use your own suitable vehicle and we compensate you for your time and mileage. 2) Use one of our company trucks. 3) Join our Company Vehicle Program, which includes an allotment for personal use.
 
S. W. Cole Engineering, Inc. is an Equal Opportunity Employer/Veterans/Disabled.

Project Geotechnical Engineer - Boylston

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
The work schedule and hours for this position are Wednesday through Saturday, 4:00pm to 2:30am.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Scientist, Quality Control (2nd shift, Wed-Sat, 4pm-2:30am)

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The PDS&amp;T Analytical Development team is seeking an analytical project lead to develop a comprehensive analytical strategy for mAbs, ADCs, bi-specifics, fusion proteins, AAVs etc. This position calls for a strategic thinker with a robust technical background in analytics, coupled with the ability to lead cross-functional teams, manage intricate projects, and communicate effectively with stakeholders.
<ul>
<li>Represent Analytical Development in AbbVie's CMC teams, providing support for both early and late-stage assets. Serve as the key contact for stakeholders, ensuring balanced expectations between PDST and Analytical fields.</li>
<li>Formulate and convey analytical strategies to Analytical PDS&amp;T functions and CMC business partners, guiding experimental execution for product analytical control strategies, method development/validation/transfer, and studies on release, stability, comparability, and extended characterization of biologics.</li>
<li>Manage a team by providing guidance and support to achieve goals. Foster a positive environment, encourage development, address performance issues, and promote collaboration and communication.</li>
<li>Lead analytical sub-teams, translating development goals into practical analytical tasks, and providing expert advice to peers and senior management.</li>
<li>Design and implement work packages essential for achieving development and commercial objectives.</li>
<li>Proficient in utilizing a broad range of analytical techniques to support DS process development, characterization, validation studies, product liability assessments, and analysis of impurities and variants.</li>
<li>Analyze and identify data trends in key analytical release and stability assays, showcasing scientific excellence in the analytical characterization of biologics.</li>
<li>Draft and review Module 3 content for both early and late-stage programs as needed.</li>
<li>Mentor peers in project management and the creation of analytical strategies.</li>
<li>Communicate project strategy, key issues, and risks to relevant teams, escalating risks and promoting resolution within and across functional areas.</li>
</ul>
Qualifications 
• &nbsp;&nbsp;&nbsp; BS or equivalent education and extensive, typically 14+ years of experience; MS or equivalent education with typically 12+ years of experience; PhD with typically 6+ years of experience in area or scientific area of discipline.
<ul>
<li>Experience in managing and leading analytical development activities for biologic compounds, such as mAbs, bispecifics, antibody-drug conjugates, and/or fusion proteins, along with a strong understanding of CMC analytical and regulatory requirements.</li>
<li>Proficient in protein HPLC (e.g., SEC, IEX, RPLC), capillary electrophoresis (CE, icIEF), and other separation techniques for protein analysis. Experience in mass spectrometry (intact/reduced LCMS, peptide mapping) and ELISA is a good plus.</li>
<li>Familiarity with industry USP/ICH guidance for the development, qualification, and validation of analytical methods.</li>
<li>Hands-on experience in authoring, reviewing, submitting, and responding to regulatory requests related to IND, IMPD, BLA/MAA. Skilled in technical writing, including drafting method validation protocols/reports and comparability protocols/reports.</li>
<li>Ability to work effectively across functions, anticipating and addressing overall program development needs.</li>
<li>Open to collaborative efforts, valuing diverse perspectives and managing relationships effectively to enhance decision-making.</li>
<li>A self-motivated, meticulous individual who thrives in a fast-paced team environment.</li>
<li>Exhibits creative and innovative thinking to tackle complex challenges and advocates for new technologies to fulfill project objectives.</li>
<li>Quickly comprehends and adapts to new situations, demonstrating agility when necessary.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Principal Research Scientist I - Analytical Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Background of Biologics Drug Product Development
The Biologics Drug Product Development (BIO DPD) team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content.
We are looking for a highly motivated person to support Developability assessments for candidate molecules across a range of modalities. The candidate will support early-stage assessment of candidates coming out of the Discovery pipeline. In this role, the candidate will be part of a global team and will work closely with scientists from multiple functional areas, including Discovery, Analytical, and Process R&amp;D.
Your Responsibilities:
<ul>
<li>Characterization of Oligonucleotides (siRNA, mRNA), monoclonal antibodies, Antibody-Conjugates (various payloads), novel multi-specifics, and gene therapies via LCMS and physiochemical assessments</li>
<li>Employ modern LC-MS instruments and techniques to understand degradation pathways and gain insight into therapeutic biologic molecules and assess their quality</li>
<li>Experience evaluating the stability (chemical &amp; physical) of biologics against solution conditions (pH, ionic strength, temperature, light, etc.) using standard analytical approaches</li>
<li>Compilation and assessment of analytical data regarding function and stability of molecules to support candidate screening in a high throughput manner. Elucidation of structure and impurity/variant characterization of protein and oligonucleotide-based drug materials.</li>
<li>Ability to build and manage strategic alignments with key stakeholders, revise and improve business workflows, manage project timelines and resources.&nbsp; Contribute to development of CMC development path for assigned discovery projects together with clients from various discovery and development functions with an emphasis on collaboration, quality and with a sense of urgency.</li>
<li>Operate in a matrix team environment, aligning across and executing shared departmental and divisional strategies.&nbsp; Additionally, the candidate has communication skills, confidence and experience to influence strategic outcomes with stakeholders and matrix teams as needed.</li>
<li>Data review, documentation and preparation of technical memos and reports.</li>
<li>Mentor junior staff on troubleshooting equipment and experimental problems</li>
<li>Provision of scientific expertise and engagement in cross-functional teams within AbbVie. Takes initiative to develop independent research ideas and pursues scientific questions that may arise during candidate selection/ nomination screening studies.&nbsp; Presents data at&nbsp;internal and external professional conferences and prepares manuscripts for publication in peer reviewed journals or patent applications.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree with 12+ years’ experience, Masters with 10+ years’ experience, or a PhD with 4+ years experience with a degree in chemistry, chemical engineering, (structural) biology or related field</li>
<li>At least 4 years of experience in comprehensive LCMS characterization of oligonucleotides and therapeutic antibodies in an industry setting are beneficial</li>
<li>Experience with characterization of genetic medicines, including AAVs and LNPs, is highly desired</li>
<li>Deep understanding of biologics characterization by LC/ESI-HR-MS (e.g. peptide Mapping, intact mass analysis) and insights into the causes of protein degradation</li>
<li>Knowledge of functional excipient degradation pathways is a plus</li>
<li>Experience in determination of PTM and chemical modifications and their influence on the molecule’s function and structure</li>
<li>Additional robotics expertise and protein analytical experience (e.g. SEC, IEX, HIC, CE) is beneficial&nbsp;</li>
<li>Highly motivated, self-driven and results-oriented person with excellent communication and presentation skills</li>
<li>High degree of flexibility in adapting to different projects and people; embraces the ideas of others, nurtures innovation and manages innovation to reality</li>
<li>Excellent team player with the ability to build strong networks with peers</li>
</ul>
Key AbbVie Competencies:
<ul>
<li>Builds strong relationships with peers and cross functionally with partners outside of teams to enable higher performance.</li>
<li>Learns fast, grasps the "essence" and can change course quickly where indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</li>
</ul>
Level and compensation will be commensurate with experience. 
An equal opportunity employer.&nbsp;AbbVie welcomes and encourages diversity in our workforce.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>This is an on-site opportunity located at AbbVie Bioresearch Center (ABC) in Worcester, MA.&nbsp;</li>
<li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​</li>
<li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li>
<li>This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​</li>
<li>This job is eligible to participate in our long-term incentive&nbsp;programs​</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist II, Biologics Drug Product Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
A Scientist II position is available within the Biologics Process Development Department at the Antibody Drug Conjugate Center of Excellence in Waltham, MA. The group is responsible for developing and supporting cell culture and purification manufacturing processes for early and late phase clinical programs. We strive for speedy delivery of quality processes that are high yield, amenable to efficient manufacturing operations, robust and provide desirable product quality attributes. The group interacts closely with other development groups, along with Manufacturing and Discovery. The selected candidate will be involved in process development, process characterization, tech transfer, and scale-up. We are seeking for an enthusiastic, creative scientist that can work independently and as part of a dynamic team environment.
Key Responsibilities:
<ul>
<li>Develop recovery and purification process that utilizes clarification, chromatography, and membrane filtration technologies for monoclonal antibodies, bispecifics, and antibody drug conjugates (ADC).</li>
<li>Proactively seek opportunities to come up with innovative solutions to cater challenging business problems through creative solutions.</li>
<li>Design and execute process development and characterization activities, impurity and viral clearance studies.</li>
<li>Build experimentally verified fit for purpose mathematical models for downstream purification processes.</li>
<li>Provide deeper understanding of process performance using appropriate experimental and modeling tools.</li>
<li>Highly independent and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.</li>
<li>Work collaboratively and cross-functionally with colleagues in other functional areas (Analytical Development, Discovery, Manufacturing and Quality).</li>
<li>Conceive, investigate and execute scientific research and development to significantly improve platform processes and workflows, develop new methods, build technical expertise and intellectual property, and deepen scientific understanding.</li>
<li>Proactively seek out new information and opportunities to advance our technologies and pipeline.&nbsp; Critically evaluate relevant scientific, regulatory and business advances and integrate this knowledge.</li>
<li>A primary author of publications, presentations, regulatory documents and/or primary inventor of patents.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, and GMP compliance.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s Degree or equivalent education with typically 8 years of experience, or Master’s Degree or equivalent education with typically 5 years of experience.</li>
<li>Education background in chemical engineering, biomedical engineering, biochemistry, biochemical engineering, or biotechnology is preferred.</li>
<li>Experience in areas of purification process development is preferred.</li>
<li>Demonstrate excellent communication skills and specifically illustrate strong oral and written technical communications.</li>
<li>Seamlessly present research outcomes to multifunctional teams</li>
<li>Demonstrated problem-solving skills and capability to overcome complex issues.</li>
<li>Demonstrated success in coordinating and executing important projects to achieve business goals.</li>
<li>Must have a “results-oriented” work ethic and a positive “can-do” attitude with a strong sense of urgency and self-motivated desire to achieve.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Scientist II, Process Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
Purpose:
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.
Responsibilities:
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for the department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Qualifications 
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>2+ years of related work experience in a GMP and Quality Control environment (with knowledge of/experience with techniques such as Infrared (IR), FTIR, UV-vis, SoloVPE, Truscan)</li>
<li>Maintains their certifications as needed for assigned job tasks.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:&nbsp;​​
​​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company believes in&nbsp;good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and we may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the future.​​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision&nbsp;insurance and 401(k) to eligible employees.​​
</li>
<li>
This job is eligible to participate in our short-term incentive programs.&nbsp;​​
</li>
</ul>
​​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and determinable.&nbsp;The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

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