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<h3>Job Description</h3>
Job DescriptionSenior Micro Injection Molding EngineerAbout the Role
At Parallel Fluidics, we are building the infrastructure to power the next generation of life science tools. We seek a skilled Micro Injection Molding Engineer to lead and optimize our microinjection molding processes for producing cutting-edge microfluidic devices and precision components. This role involves a hands-on approach to developing, scaling, and improving molding operations while collaborating with a multidisciplinary team in a fast-paced startup environment.
Key Responsibilities
<ul>
<li>
Process Development:
<ul>
<li>
Design and optimize microinjection molding processes for manufacturing high-precision microfluidic devices.
</li>
<li>
Develop and implement protocols for material selection, tooling, and part production to ensure consistent quality.
</li>
</ul>
</li>
<li>
Tooling and Equipment:
<ul>
<li>
Oversee the design, testing, and fabrication of molds, including micro-scale tooling.
</li>
<li>
Collaborate with external vendors and in-house teams for mold fabrication and modifications.
</li>
<li>
Program and operate molding machines, ensuring they meet production specifications.
</li>
</ul>
</li>
<li>
Quality and Troubleshooting:
<ul>
<li>
Conduct root cause analysis for defects and implement corrective actions.
</li>
<li>
Utilize metrology tools to inspect molded components for precision and compliance with specifications.
</li>
<li>
Maintain detailed documentation of production parameters and performance metrics.
</li>
</ul>
</li>
<li>
Collaboration:
<ul>
<li>
Work closely with engineering and manufacturing teams to align processes with company goals.
</li>
<li>
Provide technical expertise to support customer inquiries and product development efforts.
</li>
</ul>
</li>
<li>
Innovation and Continuous Improvement:
<ul>
<li>
Stay updated on advancements in injection molding technologies and materials.
</li>
<li>
Drive innovations in process efficiency, cycle time reduction, and sustainability.
</li>
</ul>
</li>
</ul>
Qualifications
Required:
<ul>
<li>
Bachelor’s degree in Mechanical Engineering, Materials Science, or related field.
</li>
<li>
3+ years of experience in injection molding, with a focus on microinjection processes.
</li>
<li>
Proficiency in CAD/CAM software (e.g., SolidWorks, Autodesk Fusion, Hypermill).
</li>
<li>
Deep understanding of thermoplastics and other materials used in microfluidic manufacturing.
</li>
<li>
Proven track record of effectively manufacturing micro-scale components.
</li>
<li>
Excellent written and verbal communication skills.
</li>
</ul>
Preferred:
<ul>
<li>
Experience working in cleanroom environments.
</li>
<li>
Familiarity with automation systems and robotics for molding operations.
</li>
<li>
Knowledge of advanced inspection systems for micro-scale manufacturing.
</li>
<li>
Experience in early-stage startups or innovative product development settings.
</li>
</ul>
What We Offer
<ul>
<li>
A collaborative and dynamic work environment where your contributions directly impact our success.
</li>
<li>
Opportunities to work on cutting-edge technologies in life sciences and microfluidics.
</li>
<li>
Comprehensive benefits, including health, dental, vision, and life insurance coverage.
</li>
<li>
Equity options to share in the company’s growth and success.
</li>
</ul>
We value diversity and inclusion, welcoming individuals from all backgrounds, experiences, and perspectives. If you are passionate about innovation and precision manufacturing, apply today to help shape the future of microfluidics.

Senior Micro Injection Molding Engineer

<h3>Job Description</h3>
Job Description
Job Description
<ul>
<li>Install and service Building Automation and Control Systems</li>
<li>Perform end-to-end system checks, startup, and commissioning</li>
<li>Troubleshoot and repair DDC, HVAC, and lighting control systems</li>
<li>Read and interpret control drawings, electrical and mechanical plans</li>
<li>Work with low-voltage wiring, sensors, actuators, and control panels</li>
<li>Coordinate with contractors and internal teams on site</li>
<li>Provide preventive maintenance and customer training</li>
<li>Maintain accurate records of work, time, materials, and costs</li>
<li>Travel locally as needed, including occasional overtime or weekends</li>
</ul>
 
Background Profile
<ul>
<li>510 years of experience in building automation, controls, or related fields</li>
<li>Knowledge of BAS/BMS/DDC/HVAC systems</li>
<li>Strong troubleshooting and analytical skills</li>
<li>Familiarity with Ethernet, RS485, BACnet, and LON networks</li>
<li>Experience with Windows OS, Microsoft Office, and basic networking</li>
<li>Able to work independently and communicate clearly with customers</li>
<li>Valid drivers license and ability to get security clearance (no criminal record or DUI)</li>
<li>Experience with platforms like Siemens Talon, Smart 2, AX, N4, or PPCL is a plus</li>
<li>Bilingual in English/Spanish is a plus</li>
<li>Relevant certifications (e.g., Tridium AX, N4) are a plus</li>
</ul>
 
Education
<ul>
<li>High school diploma plus a 4-year vocational program or equivalent work experience</li>
<li>Associates or Bachelors degree in a related field preferred</li>
<li>Professional certifications are a bonus</li>
</ul>

BAS/Controls Specialist

<h3>Job Description</h3>
Job DescriptionSalary: 
The Electronic Technician performs standard testing processes on a variety of equipment, then records and analyzes results. This position requires the ability to thoroughly understand schematics and the ability to troubleshoot electronic PCBs to the component level. This position requires knowledge of industry specific tests and testing equipment including multimeters, power supplies, spectrum analyzers and oscilloscopes. This role requires a person who can work independently as well as work in a team environment with the lead technician and production manager.
The role will require following approved test procedures, recording specific test data and ensuring all necessary documents are recorded as required. This is a full-time position based at GSSIs Nashua, NH headquarters.
Primary Responsibilities:
<ul>
<li>Perform testing and any necessary troubleshooting of electronic assemblies, working with peers in test and assembly positions as well as other departments as required.</li>
<li>Diagnose and isolate malfunctions to the component level. Identify necessary rework and coordinate rework efforts with assembly personnel.</li>
<li>Communicate on a regular basis with the Production Manager, Quality Manger as well as Manufacturing Engineering to ensure products, processes and procedures are improved when necessary.</li>
<li>Load firmware &amp; software and confirm performance of software-controlled electronics as well as test fixtures.</li>
<li>Maintain test equipment and fixtures used for final and inprocess testing</li>
<li>Setsup and conducts final test of complete units under operational conditions to determine final acceptance status. On rare occasions this may include outdoor testing as required.</li>
<li>Record test procedures and results, numerical and graphical data, and make recommendations for changes in product or test method</li>
<li>Crosstrain with other technicians to ensure ability to test all products required by the Production Manager</li>
<li>Validate performance on new designs</li>
<li>Ensure that end product meets specific standards by inspecting products and processes, conducting tests, or collecting data</li>
<li>Troubleshoot and assist in preparation of test procedures and deliver test results</li>
<li>Work from schedules, specifications, test procedures, manuals, schematics, wiring diagrams, sketches, engineering change orders, complex computer programs and manufacturing procedures</li>
<li>Other related duties as assigned by the Production Manager</li>
</ul>
Requirements:
<ul>
<li>Associate or bachelor's degree preferred or equivalent experience (minimum 3 years' experience)</li>
<li>Communicate in a positive and friendly manner and able to articulate precise written and verbal details</li>
<li>Must be a highly motivated team player with an ability to organize and prioritize multiple tasks</li>
</ul>
Physical Demands:
 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to talk, hear, and use fine motor skills. The employee is frequently required to stand, walk, sit and reach. The employee is required to bend, kneel, squat, and lift. The employee must occasionally lift or carry a maximum of 45 lbs.

Electronic Technician

<h3>Job Description</h3>
Job Description
IMMEDIATE START - APPLY TODAY - START TOMORROW &nbsp;Job Title: Machine Operator - 2nd shift&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;MON-FRI 2pm-10:30pm
Location: Attleboro, MA
Pay Range: $20/hr
Responsibilities
<ul>
<li>As our Machine Operator you are to package paint and related products by operating, setting up, adjusting, and performing QC checks while tending to machines/hand fills to package paint in a safe, consistent, and efficient manner, according to specifications</li>
<li>Inspect and examine products for quality, packaging accuracy, conformance to specifications, and external defects</li>
<li>Change over equipment, adjust equipment, or otherwise adjust machines to improve equipment performance and quality</li>
<li>Set and adjust speed, temperature, product flow, and positions and tolerances of equipment</li>
<li>Examine job orders to determine details such as quantities to be filled, production times, stock specifications, BOM’s, and SKU sequences</li>
<li>Monitor filling equipment to maintain specified operating levels and to detect malfunctions, making adjustments as necessary</li>
<li>Operate equipment at most efficient speed to ensure proper quality and output</li>
<li>Responsibility for the equipment performance, efficient changeovers, operation, and preventative maintenance</li>
</ul>
If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of:Manpower, Experis, Talent Solutions, and Jefferson Wells
ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands –&nbsp;Manpower, Experis, Talent Solutions, and Jefferson Wells&nbsp;– creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

Machine Operator - 2nd Shift

<h3>Job Description</h3>
Job Description
The company is a leading manufacturing partner to OEMs and product manufacturers across a variety of markets. With a skilled workforce of over 800, 11 manufacturing facilities across the Northeast, 750,000 sq. ft. of manufacturing space, and a full suite of in-house metal manufacturing and value-added capabilities, we are an integral and trust supply chain partner to many. But we didn't get here over night. The company&nbsp;values each team member and understands each person plays a critical part in our on-going success. We offer medical, dental, vision, employer paid Short Term Disability, employer paid life insurance, Paid Time Off, Holidays, 401k with a match and more.
Successfully perform tasks as assigned as the Electrical-Mechanical Maintenance Technician in Aluminum Extrusion Manufacturing Operations. Must work independently on all facets of the Electrical, Industrial and PLC Technician responsibilities. Responsible for analyzing, troubleshooting, maintaining production machines and improving equipment reliability. Participate in preventative and predictive maintenance practices. Effectively communicate with co-workers and Team Leaders, including continuous improvement activities. This is a 1st shift position, Monday through Friday (7:00am – 3:00pm) with overtime as needed. Primary Responsibilities:
<ul>
<li>Independently troubleshoot, repair and rebuild all types of complex electrical/electronic, hydraulic, and pneumatically controlled production equipment, with proficiency and versatility.</li>
<li>Install and troubleshoot AC and DC circuits and equipment. (24vdc, 120/208/480vac)</li>
<li>PLC programming, troubleshooting and networking.</li>
<li>Installation, programming and troubleshooting of AC drives.</li>
<li>Installation, programming and troubleshooting of HMI panels.</li>
<li>Plan work for proper operational sequences, minimize interference, and delay of production.</li>
<li>Perform preventive maintenance as directed by equipment schedule.</li>
<li>Rebuild electrical mechanical devices.</li>
<li>Work with Engineering to design, select, modify, and/or adapt equipment or procedures to specific project requirements.</li>
<li>Test, Calibrate, and repair electronic, mechanical, electromechanical, and electronic measuring, recording, and indicating instruments and equipment for conformance to establish standards, and assist in formulating calibrating standards.</li>
<li>Maintain work records (work orders, PM's, Materials and parts) on Maintenance system.</li>
</ul>
This job description is designed to broadly cover the activities and responsibilities required of the employee to be successful in the role. It is not designed to contain a specific list of all job duties. Other duties, responsibilities and activities may be changed or be assigned at any time based on business need with or without notice. Requirements:
<ul>
<li>The qualified candidate must meet one of the following sets of educational and experience requirements: Bachelor’s degree in electrical engineering, Industrial Engineering, or a related field. Advanced degree or certifications in Programmable Logic Controls (PLC) systems a plus. With 3-years’ experience troubleshooting, repairing and rebuilding electrical, PLC and hydraulic machinery. Or a minimum of 7 years of industrial experience in a skilled trade with an electrical discipline with experience with Programmable Logic Controls (PLC) with no formal post-secondary education.</li>
<li>Must have own trade tools.</li>
<li>Demonstrate the ability to install, repair, troubleshoot and maintain machinery and equipment.</li>
<li>Formal electronic training on AC/DC circuits. Formal PLC training- advanced PLC function, communications, working knowledge of mechanical systems, and instrumentation &amp; controls experience.</li>
<li>Should work well with others, have good verbal, written communication &amp; interpersonal skills.</li>
<li>Working knowledge and use of safe work practices.</li>
<li>Read, write and speak English</li>
<li>Follow manufacturing/equipment specifications</li>
<li>Demonstrate mechanical skills techniques</li>
<li>Perform basic math calculations</li>
<li>Use blueprints and schematics, knowledge of controls, hydraulic and electrical schematics</li>
<li>Use a computer</li>
<li>Use/understand measuring devices/tolerances</li>
<li>Use various hand, power tools and machine tools such as drills, lathes, millers etc.</li>
<li>Learn and apply quality standards of workmanship/product</li>
<li>Must demonstrate strong work ethic and commitment to hours of operation. An example includes strict adherence to attendance expectations.</li>
<li>Must work effectively, both independently as well as within a team, as appropriate.</li>
<li>Must demonstrate respect for organizational policies and procedures, including but not limited to Safety and Quality.</li>
<li>Must demonstrate respect for others through effective communication with peers, team leaders, and managers.</li>
</ul>
Company DescriptionUnited Employment Group, Inc. is a search and placement firm specializing in Concrete Products and Construction, Metals, Refrigeration, Engineering/Surveying and Plastic Industries. 
<h3>Company Description</h3>
United Employment Group, Inc. is a search and placement firm specializing in Concrete Products and Construction, Metals, Refrigeration, Engineering/Surveying and Plastic Industries.

PLC Technician

<h3>Job Description</h3>
Job Description Description:
GENTEX AT A GLANCE:
At Gentex Corporation, we've created an environment where great ideas and great people can thrive. Leveraging a history that spans over 130 years, Gentex is a global leader in personal protection and situational awareness solutions for defense forces, emergency responders, and industrial personnel operating in high performance environments. Join our multinational team of exceptional and dedicated employees around the world and work on challenging and rewarding projects, grow your skills, and advance your career all while making a positive difference in the lives of our customers. Together, you and Gentex can build a career that's uniquely yours.
 
MINIMUM QUALIFICATIONS:
<ul>
<li>H.S. Diploma or equivalent (BA or BS preferred)</li>
<li>10 + years of previous manufacturing experience, including supervisory experience</li>
<li>Previous experience coaching or mentoring employees on skills and techniques for best practice.</li>
<li>Experience with Quality, Lean Manufacturing, and continuous improvement preferred.</li>
<li>Previous experience scheduling and planning preferred.</li>
<li>Prior J-STD / IPC610 experience preferred</li>
<li>Analytical problem solving and root cause analysis skills required.</li>
<li>Proficiency with MS Office to include Word, Excel, Power Point, and Outlook.</li>
</ul>
ABOUT THE JOB!
The Production Supervisor is responsible for overseeing daily activities of an assigned manufacturing area. This includes the general quality of work, planning and training of employees, as well as performance evaluations and discipline. This position will communicate assignments effectively so that daily production schedules are achieved.
 
RESPONSIBILITIES:
<ul>
<li>Oversee assigned production lines, equipment, and manufacturing personnel assigned area. </li>
<li>Ensure that all personnel are trained in accordance with department work instructions, company SOPs and safety practices.</li>
<li>Accurately document and address employee disciplinary issues and conduct personnel performance appraisals.</li>
<li>Bring disciplinary issues to the attention of the department manager and HR when appropriate. </li>
<li>Coordinate the manufacturing team to meet the daily production requirements.</li>
<li>Ensure all members of assigned personnel are crossed trained in accordance with their capabilities.</li>
<li>Establish an effective organizational structure capable of handling the complexity and challenges of manufacturing within the value stream.</li>
<li>Meet personal and manufacturing goals set by the Production Manager.</li>
<li>Support team as required in order to achieve daily, monthly, and annual production requirements.</li>
<li>Work with and support Manufacturing Engineering during New Product Introduction efforts.</li>
<li>Work with Manufacturing Engineering in order to solve technical issues as they arise on the production floor.</li>
<li>Initiate requests to Manufacturing Engineering, IT, and Facilities for repairs or improvements.</li>
<li>Maintain a clean and organized department ensuring that safety and 6S best practices are in place at all times.</li>
<li>Ensure line leads are updating communication boards daily for their respective work cells.</li>
<li>Ensure that continuous improvement in the areas of lean, visual aids, and product flow are occurring regularly within each assigned work cell.</li>
<li>Maintain company Quality Management System (QMS) standards and requirements as defined.</li>
<li>Perform all functions per Manufacturing Work Instructions, Routers and verbal instruction. Conduct routine audits to ensure the integrity of the process controls in place.</li>
<li>Ensure that all production documentation and records are completed, are accurate, and are stored as defined.</li>
<li>Schedule flexibility to support critical deadlines may be required.</li>
</ul>
 
TO APPLY:
Visit: <a href="https://gentexcorp.com/careers/" target="_blank">https://gentexcorp.com/careers/</a>
 
LOCATION:
Gentex's Manchester facility is located in southern New Hampshire. Manchester is the largest convention, sports, entertainment, and arts &amp; cultural destination in New Hampshire. There is so much to do, see and experience in Manchester including major concerts and ECHL Hockey, AA minor league baseball, live performances at the historic Palace Theatre or exhibits at our renowned museums. Located in the heart of New England, Manchester is also conveniently located within an hour's drive of Boston, an hour from the Atlantic Ocean and less than two hours from New Hampshire's scenic White Mountains, Lake Winnipesaukee and the many other well-known vacation destinations in Maine, Vermont and Massachusetts.
 
 
Gentex Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard for any applicable state or federal protected class. Gentex is an E-Verify Participant. Pre-employment drug/alcohol/background screening is required.
Requirements:
 
 
PI0876aa38a13f-25405-36930769

Production Supervisor

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The QC Scientist - Critical Reagents is responsible for overseeing all reference standards and other critical reagents in line with internal SOPs and ICH guidelines. This individual will work collaboratively with QC Operations, Analytical Development, and Quality Assurance in support of clinical pipeline and commercial products. This position requires strong leadership skills, statistical and technical knowledge, and a commitment to quality and compliance
ESSENTIAL JOB FUNCTIONS 
<ul>
<li>Oversee the Critical Reagents and Materials function. </li>
<li>Oversee the day-to-day operations of the GC QC Technical Services group. </li>
<li>Provided operational oversight for critical reagent and materials management across the quality organization. </li>
<li>Develop and maintain robust systems for the qualification, monitoring, tracking and storage of critical reagents and materials. </li>
<li>Collaborate with cross-functional groups to ensure the continued supply of qualified reagents and materials. </li>
<li>Act as the primary point of contact for the monitoring, tracking, and storage of critical reagents and materials. </li>
<li>Manage inventory, strategic planning, and lifecycle management of reference standards and critical materials.</li>
<li>Represent Quality Control on project teams and in meetings as required.</li>
<li>Authors and reviews standard operating procedures, protocols, and reports as required.</li>
<li>Manages the implementation/maintenance/continuous improvement of Quality Systems as required. </li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS or MS in Life Sciences or Engineering
Essential
ON-THE-JOB EXPERIENCE

8+ years of pharma/biotech industry experience
Essential
Well versed in cGMP/ICH/FDA/EU regulations and guidelines 
Essential
Large molecule, gene or cell therapy experience is required. 
Essential
Expertise in reference standards programs, including ICH regulations and quality control methods. 
Essential
Strong background in biostatistics for evaluation comparability and qualification of new reference standards and control reagents. 
Desired
Experience in Quality Control within the biological pharmaceutical industry. 
Desired
Proficiency in writing SOPs, qualifications protocols, and reports. 
Essential
Familiarity with statistical software (JMP).
Essential
SKILLS / ABILITIES

Excellent analytical and problem-solving skills 
Essential
Must possess excellent communication and organizational skills 
Essential
Cross functional collaboration ability to work well with diverse groups 
Essential
Ability to manage multiple activities with challenging timelines 
Essential
Proficient in using Microsoft applications (MS Word, MS Excel, MS PowerPoint) 
Essential
Effective oral and written communication skills 
Essential
Confident, independent, self-starter, proactive, and results-oriented with high performance and compliance standards 
Essential
Exhibits highest integrity and committed to ethics and compliance standards 
Essential
Open and transparent in sharing data and information 
Essential
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock</li>
<li>Occasionally exposed to extremely loud noise levels</li>
</ul>
Movement
<ul>
<li>Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 25 pounds</li>
<li>Occasionally lift and/or move up to 50 pounds</li>
</ul>
Vision
<ul>
<li>Frequently utilize close vision and the ability to adjust focus Communication</li>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

QC Scientist - Critical Reagents

<h3>Job Description</h3>
Job DescriptionTop Job Located in South Natick, MA Salary: $20-$22/hour Our client, a family owned and operated manufacturing company, is looking for a Manufacturing Associate to join their team! The ideal candidate is someone who thrives in a fast-paced environment and is skilled at problem-solving. While specific equipment experience isn't required, patience and a strong ability to tackle challenges are essential. Schedule: Monday - Friday (Can be flexible after training) Pay: $20.00 - $22.00 per hour Responsibilities of the Manufacturing Associate: 
<ul>
<li>Manufacture medical grade stainless steel tubing using machinery including draw blocks, draw benches and straighteners</li>
<li>Set up straightener machines </li>
<li>Set up centerless grinding machines </li>
<li>Manage multiple machines and monitor the production runs </li>
<li>Complete all required paperwork </li>
<li>Measure (using micrometers), inspect and count product </li>
</ul>
 Qualifications, Skills and Experience of the Manufacturing Associate: 
<ul>
<li>Experience working in a manufacturing environment (preferred)</li>
<li>Excellent attention to detail </li>
<li>Dexterity/hand skills (must be ok with getting dirty)</li>
<li>Basic familiarity with computers (scanning barcodes/look up records)</li>
<li>Ability to problem solve </li>
<li>Lift up to 50 pounds unassisted </li>
</ul>
 #3368ST Express Office: Waltham-Framingham 326 Washington Street Annex Second Floor Wellesley Hills, MA 02481

Manufacturing Associate

<h3>Job Description</h3>
Job Description
Job Title: Test Technician 1st shift&nbsp;
Location: Franklin MA
Pay Range: $26.10/hr
SUMMARY: Technical background. Performs technical functions supporting manufacturing and/or engineering activities. Conducts functional testing and analysis of products to ensure operation and reliability. Runs diagnostic procedures and basic troubleshooting from design, test, and checkout, to modification, fabrication and assembly tasks in the production of products . ACCOUNTABILITIES: • Analyzes and troubleshoots failures using diagnostic software and test • Obtains working knowledge of test equipment set up and use • Participates in continuous improvement in processes, quality and productivity • Identifies more complex failures and escalates to higher technical levels • Identifies defective materials, highlights failure trends and maintains test logs • Transfer daily status information to other shift personnel
SKILLS: • Ability to move a fully loaded board rack on wheels • Ability to safely reach and remove a board from a 3 tier board storage rack • Ability to influence others to achieve results; mentoring/coaching skills • Proficient technical aptitude; ability to describe subsystems at a functional level
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About ManpowerGroup, Parent Company of:Manpower, Experis, Talent Solutions, and Jefferson Wells
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Production Associate - Test Technician 1st Shift

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The QC Scientist Analytical Method Validation is key role within our Quality Control Technical Services (QCTS) department. The individual in this role will work collaboratively with the analytical development team, quality control, and quality assurance to transfer and validate next generation analytical procedures for the testing of viral vectors, cell banks and gene therapy products in support of Genezen's services and commercial products in compliance with company policies and procedures and regulatory guidelines.
ESSENTIAL JOB FUNCTIONS 
<ul>
<li>Works under guidance of QC Manger responsible for optimization, qualification, transfer and validation of analytical methods associated with cGMP production</li>
<li>Writes protocols and reports related to QC Method transfer, qualification, feasibility and validation</li>
<li>May assist in writing protocols or participate in instrument qualifications</li>
<li>Perform statistical analyses of data generated during method validation studies, qualification and critical material qualification</li>
<li>Support monitoring of analytical method performance, including assessment</li>
<li>of analytical method system suitability requirements</li>
<li>Assist with data trending and aid in compilation of trend reports</li>
<li>Support cGMP operations, including generation of documentation in support of change controls and corrective actions/preventative actions, deviations, out-of-specification (OOS) results, and other investigations or assay troubleshooting</li>
<li>Present to cross-functional teams and effectively communicate critical analytical issues and solutions</li>
<li>Subject matter expertise in product quality attribute methods relevant to gene therapeutic product (e.g. cell function characterization assays, HPLC, PCR / qPCR, ELISA, Potency Assay, SDS-PAGE and western blot) and/or viral vector manufacturing</li>
<li>Familiar with FDA and EMA guidance documents relevant to gene therapy</li>
<li>Working knowledge of quality systems requirements</li>
<li>Ability to work in a fast-paced, collaborative environment, working with minimal direction and able to manage workload based on changing priorities</li>
<li>Demonstrated leadership skills and the ability to collaborate with and effectively influence others</li>
<li>Establish, revise, review and maintain procedures (including protocol and technical report)</li>
<li>Assure that laboratory procedures are current and facilitate updates as required</li>
<li>As applicable perform routine/non-routine testing of in-process, final product in accordance with Standard Operating Procedures (e.g., Q-PCR, Potency Assay, Western Blot, Refractometry, ELISA, etc.) as needed</li>
<li>Complete documentation in accordance with current Good Manufacturing Practices (cGMP)</li>
<li>Maintain QC lab and related systems to ensure compliance with industry standards</li>
<li>Identify, lead, and/or support continuous improvements to current processes/procedures accordingly for increased compliance and efficiency</li>
<li>Troubleshoot equipment and analytical testing methods</li>
<li>Training of other QC Analysts within the department</li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS or MS in Chemistry/Biochemistry or other related Life Sciences
Essential
ON-THE-JOB EXPERIENCE

Minimum 6 years of analytical laboratory experience in GLP/cGMP environment ideally associated with analytical method validation and transfer.
Essential
Prior experience with analytical method validations, analytical data trending/statistical analysis
Essential
Understanding of QC instrument qualification is preferred.
Desired
Thorough understanding of industry testing requirements/standards
Desired
Preferred experience with performing cell based bioassays using mammalian cell-lines (such as HELA, HEK-293, Huh-7 etc.) along with QC instrument qualification is essential.
Essential
Thorough understanding of industry testing requirements/standards related to gene/cell therapy products.
Essential
Familiar with ICH, FDA and EMA guidance documents relevant to gene/cell therapy
Desired
Working knowledge of quality systems requirements
Desired
SKILLS / ABILITIES

Computer/software literacy (MS Word, Excel, JMP, Minitab, and LIMS etc.)
Essential
Ability to thrive in a quickly changing, CDMO environment where flexibility and teamwork is essential
Essential
Ability to work in a fast-paced, collaborative environment, working with minimal direction and able to manage workload based on changing priorities
Essential
Proven demonstration of technical writing skills such as protocol, reports, procedures etc.
Essential
Effective project management and presentation skills
Desired
Good/effective communication and organizational skills with the ability to work well with others and independently
Desired
Ability to work collaboratively with cross functional departments
Desired
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock</li>
<li>Occasionally exposed to extremely loud noise levels</li>
</ul>
Movement
<ul>
<li>Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 25 pounds</li>
<li>Occasionally lift and/or move up to 50 pounds</li>
</ul>
Vision
<ul>
<li>Frequently utilize close vision and the ability to adjust focus Communication</li>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

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