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<h3>Job Description</h3>
Job DescriptionABOUT STRM.BIO STRM.BIO (pronounced “storm bio”) is a VC-backed biotech startup building a new kind of gene therapy delivery platform based on naturally occurring extracellular vesicles (EVs). We're leveraging the unique biology of EVs to unlock targeted, scalable, and low-immunogenicity genentic medicines that target the bone marrow. We’re a small, fast-moving team based at The Engine in Cambridge, MA. We believe in simplicity, integrity, and keeping people at the center of everything we do. We’re here to do great science and build a company we’re proud of. THE OPPORTUNITY We’re looking for a Senior Scientist to help lead and grow our research engine. You’ll work shoulder-to-shoulder with the VP of R&amp;D and Director of Research to drive key programs forward and manage external collaborations. This is a hands-on, highly cross-functional role ideal for someone who’s ready to lead and execute in equal measure. This is a full-time, on-site role. WHAT YOU’LL DO (Key Responsibilities)&nbsp;
<ul>
<li>Lead day-to-day scientific execution across internal teams and CRO/academic partners</li>
<li>Own program timelines and technical plans; troubleshoot and drive decisions to keep progress on track</li>
<li>Design, run, and refine experiments, hands-on and alongside junior team members</li>
<li>Coordinate with collaborators, ensure data integrity, and maintain clean documentation across projects</li>
<li>Contribute to company strategy through project planning, milestone tracking, and resource scoping</li>
<li>Present internally and externally, including pitch decks, grant applications, and scientific meetings</li>
<li>Stay sharp on emerging EV, gene therapy, and CAR-T technologies to shape R&amp;D direction</li>
<li>Pitch in on lab ops, team culture, and whatever else it takes to get the job done</li>
</ul>
WHAT YOU BRING (Required Qualifications)
<ul>
<li>Ph.D. + 5 years’ postdoc or industry experience in gene therapy/genetic medicines, CAR-T, or related areas</li>
<li>Deep expertise in in vivo gene delivery platforms (viral vectors, LNPs, EVs)</li>
<li>Strong bench skills in molecular/cell biology, including flow cytometry, qPCR, Western, microscopy, NGS</li>
<li>Experience developing ex vivo and in vivo CAR-T or other T-cell based therapies</li>
<li>Solid working knowledge of genome editing tools (CRISPR, Cre-lox, etc.)</li>
<li>Experience managing external partners (CROs, academic labs)</li>
<li>Comfortable navigating ambiguity, shifting priorities, and high ownership environments</li>
<li>Excellent communicator, highly organized, strong attention to detail</li>
<li>Bonus: experience with startup ops, grant writing, or early product development</li>
</ul>
KEY POSITION DETAILS
<ul>
<li>100% on-site in Cambridge, MA</li>
<li>Full time with competitive compensation
<ul>
<li>The salary range for this position is $140,000 to $160,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. &nbsp;</li>
</ul>
</li>
</ul>
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TgpBmxlWvO

Senior Scientist

<h3>Job Description</h3>
Job Description&nbsp;Work closely with Scientists to evaluate antibodies, proteins, small molecules, and drugs by in vitro cell-based assays including cytotoxicity assays, flow cytometry, functional assays, and molecular biology assays, including ELISA, WB, ect.&nbsp; Job will involve maintaining cell lines, setting up and developing in vitro assays, working closely with in vivo team to supply cells and then receive ex vivo samples and analyzing assays with harvested blood serum/tissue, and maintaining a lab notebook.&nbsp; &nbsp;
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YmFHsmtNfV

Research Associate I/II/III

<h3>Job Description</h3>
Job DescriptionRepertoire Immune Medicines is a biotechnology company working to unlock and direct the remarkable power of the human immune system to treat cancer and autoimmune disease. The company&nbsp;was&nbsp;founded on the belief that&nbsp;understanding&nbsp;the repertoire of T cell receptor (TCR)-antigen&nbsp;immune synapses&nbsp;that maintain health and drive disease represents one of the greatest opportunities for innovation in medical science. Repertoire scientists created and developed the DECODETM&nbsp;platform, which allows in-depth characterization of TCR-antigen pairs, and the ability to&nbsp;deploy this information in the form of&nbsp;novel targeted immune medicines&nbsp;to fundamentally reprogram the immune system to kill tumors or induce immune homeostasis. From its sites in Cambridge, Massachusetts and Zurich, Switzerland, Repertoire’s team is advancing a pipeline of DECODE-enabled immune medicines. For cancer, we are developing a pipeline of TCR bispecifics molecules for treatment of multiple cancer types. Repertoire is progressing through IND-enabling studies with its lead development candidate and is planning to initiate a Phase 1/2 clinical trial in multiple cancer indications.&nbsp; In addition, we are developing a pipeline of mRNA tolerizing vaccines for treatment of autoimmune diseases. Repertoire was founded&nbsp;in 2019 by Flagship Pioneering and&nbsp;is supported by a strong investor base.&nbsp; The company entered into a collaboration and license agreement with Genentech in April of 2025 to discover and develop innovative T cell-targeted immune medicines for an autoimmune indication.&nbsp; In addition, Repertoire entered a strategic partnership in April of 2024 with Bristol Myers Squibb to develop tolerizing vaccines for up to three autoimmune diseases.&nbsp; Principal Scientist/Associate Director, Translational Sciences (Oncology) We are seeking a highly motivated and experienced Principal Scientist/Associate Director in Translational Sciences that will be responsible for developing, implementing, and executing cross-functional activities to bridge preclinical and clinical development programs, across multiple therapeutic areas and drug modalities. A successful candidate will have a deep knowledge and focus on protein therapeutics, immune-oncology drug development, and genomic capabilities.&nbsp; Reporting to the Vice President, Project Lead and Head of Translational Medicine, this accomplished professional will have deep expertise in biomarkers in oncology to lead the design, implementation, and oversight of biomarker strategies for Phase I clinical trials in solid tumors. The ideal candidate will have a strong background in circulating tumor DNA (ctDNA), genomic profiling, and immune/DNA-based assays, as well as hands-on experience managing biomarker vendors and ensuring high-quality execution of exploratory biomarker analyses. Key Responsibilities 
<ul>
<li>Design and execute translational biomarker strategies to support mechanism-of-action, PK/PD, dose predictions, and patient stratification in Phase I/II first-in-human oncology trials.</li>
<li>Integrate preclinical and clinical data to generate hypotheses and guide data-driven decision-making in early development.</li>
<li>Lead development and implementation of exploratory and translational biomarkers, including immune profiling, ctDNA, and genomic assays, with a strong understanding of solid tumor biology.</li>
<li>Evaluate and oversee protein biomarker assays relevant to therapeutic response and resistance.</li>
<li>Manage external vendors and CROs for biomarker assay development, sample testing, and data delivery; ensure high-quality execution and troubleshooting as needed.</li>
<li>Oversee sample logistics (tumor tissue, liquid biopsies) to ensure integrity and timely analysis.</li>
<li>Partner closely with Clinical Development and Discovery Research teams to ensure translational plans align with clinical objectives and regulatory strategies.</li>
<li>Work closely with leadership to develop, manage, and deliver translational research timelines, budgets, metrics, and milestones.</li>
<li>Demonstrate a strong work ethic and ability to work well in team environment.</li>
<li>Communicate key findings and recommendations to senior leadership.</li>
</ul>
 Qualifications 
<ul>
<li>PhD, MD, or equivalent in cancer biology, oncology, immunology, molecular biology, or related field.</li>
<li>8+ years of biotech/pharma experience in translational sciences or biomarker research, ideally in a biotech or pharmaceutical environment.</li>
<li>Deep understanding of solid tumor biology, immune biomarkers, and ctDNA/genomic analysis, along with hands-on experience managing biomarker execution in early-phase clinical trials.</li>
<li>Strong understanding of drug development for protein therapeutics and immune-oncology mechanisms.</li>
<li>Demonstrated experience supporting Phase I/II first-in-patient clinical studies.</li>
<li>Experience incorporating ctDNA endpoints into Phase I/II oncology clinical trials, including exploratory biomarker strategies and regulatory considerations.</li>
<li>Experience transferring and overseeing assays at CROs or central labs.</li>
<li>Working knowledge of pharmacokinetics (PK) and anti-drug antibody (ADA) assessments for protein therapeutics, and ability to integrate PK/ADA findings with biomarker and clinical data to guide early development decisions.</li>
<li>Hands-on or oversight experience with circulating tumor DNA (ctDNA), including use in solid tumor clinical trials for patient stratification and treatment response monitoring.</li>
<li>Entrepreneurial mindset, excellent communication skills, and passion for advancing new therapies for patients.</li>
</ul>
The base salary for this role ranges from $150,000 to $215,000&nbsp;and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future. &nbsp;Repertoire is committed towards social responsibility and developing an inclusive culture.&nbsp; Much as the power of the immune system lies in the diversity of T and B cells, our work requires the creativity and ingenuity of a diverse workforce.&nbsp; We believe in actively pursuing equity in all facets of the work experience at Repertoire.&nbsp; We will continue to educate ourselves about the inequities and barriers present in our society and take action as a company where we can make a difference. Repertoire is proud to be an Equal Opportunity Employer. Recruitment &amp; Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto.
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Sc8SLX5mN7

Principal Scientist/Associate Director, Translational Sciences

<h3>Job Description</h3>
Job DescriptionJob Description: Senior Computational Biologist Department: Data Science, PIRC Reports to: Director of AI in Drug Development Job Summary: We are seeking a highly motivated and skilled Senior Computational Biologist to join our dynamic data science team. This individual will apply advanced OMICS-oriented analytical methods, statistical modeling, and ML/AI to accelerate discovery and decision-making in support of PIRC’s expanding research programs. The ideal candidate will leverage their deep expertise in computational biology, deep learning, and data-driven drug discovery to develop state-of-art solutions. This role involves close, cross-functional collaboration with Immunology, Translational Science, and Biologics teams to build sophisticated algorithms and predictive models that drive our pipeline. The Company: It’s not often you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology and oncology, with one approved product and a diversifying pipeline. We believe in the potential to improve both health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese-American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung.&nbsp; This role will be in the PharmaEssentia Innovation Research Center (PIRC), the US R&amp;D center for PharmaEssentia. As PIRC is essentially in startup mode with the full backing of PharmaEssentia HQ, this is an exciting time for PIRC and the Data Scientist will have great influence in developing and growing PIRC from the ground floor up. Key Responsibilities
<ul>
<li>Lead multi-omics data analysis across diverse datasets, including genomics, bulk and single-cell transcriptomics, proteomics, metabolomics and pathway analysis, to address critical questions in target identification, prioritization, and translational science</li>
<li>Design and implement novel computational modules and frameworks to enable seamless integration and interpretation of multi-omics data, driving insights for R&amp;D</li>
<li>Develop and apply machine learning and AI algorithms to uncover patterns and generate predictions from complex biological datasets, and accelerate target discovery and validation efforts</li>
<li>Enhance internal cross-disciplinary collaboration with project teams to align computational strategies with project goals and ensure robust biological interpretation of data</li>
<li>Establish best practices for data management, quality control, and reproducibility in bioinformatics pipelines, and create intuitive visualizations and detail-oriented reports to communicate findings with stakeholders, enabling data-driven decision-making&nbsp;</li>
<li>Continuously evaluate and adopt cutting-edge computational tools, algorithms and technologies to stay at the forefront of the field and enhance data analysis capabilities</li>
<li>Contribute to the strategic planning of computational/AI initiatives, influencing the direction of research programs and technological investments</li>
<li>Contribute to scientific publications, conference presentations, showcasing advancements in bioinformatics and AI, and their impact on drug discovery and translational research</li>
</ul>
 Qualifications
<ul>
<li>Ph.D. in Bioinformatics, Computational Biology, Computer Science or relevant quantitative discipline</li>
<li>At least 3-years work experience in combining bioinformatics/computational biology analysis and cutting-edge computational approaches (including ML/AI) for project support in cross-functional biotech or pharma setting.&nbsp;</li>
<li>Expertise in multi-omics data analysis and result interpretation (genomics, transcriptomics and scRNASeq are must, spatial omics and image are plus)</li>
<li>Proficiency in Python and R, familiarity with database management</li>
<li>A strong understanding of the drug discovery and development, including target identification, lead optimization, translational research, and early clinical development</li>
<li>Experience in a therapeutic area relevant to oncology and immunology</li>
<li>Working knowledge of traditional machine learning algorithms, Deep learning frameworks and LLM, and their applications in drug discovery</li>
</ul>
 EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Qxw3iqJodz

Senior Computational Biologist

<h3>Job Description</h3>
Job Description
Senior Research Technician (Full-time)
DynamiCure Biotechnology is a clinical stage biopharmaceutical company located in Waltham MA, established to pioneer the next generation of therapies in the oncology and autoimmune space. Driven by science and passionate about advancing patient care, we are translating potentially revolutionizing new insights on immuno-normalization into a pipeline of innovative antibody candidates with first-in-class and best-in-class potential. DynamiCure is guided by empathy for the patients we serve, dedication, collaboration and transparency.
We are currently looking for a Senior Research Technician to support our R&amp;D team. Candidates should be reliable self-starters who embrace a high level of ownership over their work, a can-do attitude, and a collaborative, team-centered approach to support our efforts to accelerate biological discovery and the development of new therapeutics.
As a Key Contributor You Will work closely with the In Vivo Pharmacologist to support lab operations and you will further develop your research career. 
Reports to (title): In Vivo Pharmacologist
Number of direct/indirect reports: N/A
Travel expectations (in %): N/A
Key Responsibilities and Activities
<ul>
<li>Provide animals with fresh and adequate food and water daily</li>
<li>Perform scheduled health observations and assessments, communicating any animal anomalies observed</li>
<li>Change and clean animal cages as scheduled</li>
<li>Assist with animal intake, evaluation and treatment</li>
<li>Complete and maintain all applicable logs and check sheets, as required</li>
<li>Comply with Standard Operating procedures </li>
<li>Monitor facility conditions (including temperature and humidity data) and maintain all applicable logs and check sheets for same, reporting any facilities issue</li>
<li>Operate &amp; maintain cage washers and other equipment, as instructed</li>
<li>Clean and sanitize animal facility following established protocols and schedules</li>
<li>Process bio-hazard waste streams</li>
<li>Create a foundation for your future success and contributions in animal studies </li>
<li>Other projects/duties as assigned for the overall benefit of the organization</li>
</ul>
Required Education, Experience, Skills and Competencies
<ul>
<li>Associates or bachelor’s degree in medical technology, biology, chemistry or related field and 2-4 years’ lab experience; or equivalent combination of education and experience</li>
</ul>
<ul>
<li>BS/MS in Biology, Pharmacology, Animal Science or related field is preferred</li>
<li>Good understanding of laboratory information systems and automated laboratory equipment</li>
<li>Be a reliable team player that shows a willingness to learn </li>
<li>Ability to establish and maintain cooperative working relationships with co-workers and other stakeholders</li>
</ul>
<ul>
<li>Ability to adjust to workload changes and prioritize competing demands</li>
<li>Team player, show up, reliable and dependable </li>
<li>Ability to balance the big picture and fine technical details</li>
<li>Outstanding organizational, critical thinking, and problem-solving skills</li>
<li>Excellent written and verbal and communication skills</li>
</ul>
Why Work for DynamiCure
Around the Office:
<ul>
<li>Flexible scheduling</li>
<li>Casual dress code</li>
<li>Unlimited drinks &amp; snacks</li>
</ul>
Benefits:
<ul>
<li>20 days Paid Time Off</li>
<li>10 paid holidays plus Winter Break</li>
<li>Paid Family Leave</li>
<li>Full benefits package including:
<ul>
<li>Medical </li>
<li>Dental</li>
<li>Vision</li>
<li>HSA Account with Company contribution</li>
<li>401(K) with up to 5% match</li>
<li>Company paid life and AD&amp;D insurance</li>
<li>Supplemental life &amp; AD&amp;D insurance</li>
<li>Company paid short- and long-term disability insurance</li>
<li>Employee Assistance Program</li>
</ul>
</li>
</ul>
Employee Programs:
<ul>
<li>Employee Referral Program</li>
<li>Employee Assistance Program</li>
</ul>
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, creed, national origin, ancestry, sex, age, handicap or disability, marital status, sexual orientation, gender identity or expression, pregnancy or pregnancy-related condition, genetic information, veteran status, immigration or citizenship status, military obligations, status as a domestic violence victim or a victim of sexual assault or stalking, participation in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law.
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v2D8Yf7UtH

Senior Research Technician

<h3>Job Description</h3>
Job Description
WHDH-TV in Boston, MA is looking for an accurate weather forecaster for our newscasts. Must be able to generate creative, animated weather graphics. Must have an AMS Seal and a minimum of 3-5 years experience. WHDH-TV is an Equal Opportunity Employer. This position requires candidate to work 100% in Boston office.
The expected salary range for this position is $105,000 to $125,000 annually. The final offer will be determined by a variety of factors, including but not limited to the candidate's experience, knowledge and skills.

Meteorologist - Weekend Mornings-FT

<h3>Job Description</h3>
Job DescriptionSummary: PerkinElmers purpose is to enable scientists, researchers, and clinicians to address their most critical challenges across science and healthcare. With a mission focused on innovating for a healthier world, we deliver unique solutions to serve the diagnostics, life sciences, food and environmental markets. PerkinElmer is seeking an Associate Lab Computing Analyst. Responsibilities: Implements, monitors and provides technical support of customer laboratory IT environments, typically integrated with instrumentation Implements customer specified benchtop computing design and processes Administers and assures connectivity of customers Windows based platform Maintains and supports the operating system, desktop hardware and peripherals, enterprise print strategy, management tools, application packaging, desktop tool development, software distribution, and core desktop applications Manage On-boarding, retirement and relocation of equipment Implements Windows based security, including but not limited to: user / group permissions, file / folder permissions, group policies, local security policies, etc. Analyzes, identifies, and implements enhancements, upgrades and/or solutions to improve the overall support of the desktop platform in a timely manner Ensures adherence to clients corporate policies through periodic reporting and compliance programs Acts as the technical support contact for field service engineers, repairing and troubleshooting client instrument and information technology issues Follow documented procedures, policies, troubleshooting and best practices Create and maintain a physical inventory of lab equipment, PCs, software and any other information pertinent to the environment Submit weekly Engineer reports to the team lead by COB on the last business day of the week Acts as Liaison for software/hardware related inquiries Escalates IT issues that are not resolved PKI Lab IT analysts Participates in client team meetings Escalates delivery concerns to the team lead Basic Qualifications: Associate degree in Computer Science or technology industry experience OR 1+ year of relevant technical experience including (but not limited to); Windows technologies including Microsoft Office, networking, remote computing and backup systems Excellent customer service skills complimented by an ability to listen to and interpret client requests. Ability to troubleshoot complex technology issues. Strong verbal and written communication skills. Ability to identify, track and complete tasks for multiple projects under prescribed timeframes Service Now Windows 11 upgrade Group policy Active directory Windows 11 upgrade

Lab Computing Analyst

<h3>Job Description</h3>
Job DescriptionSalary: $100,000 - $120,000 
TreeFrog Therapeutics is an innovative, international biotechnology company aiming to bring cell therapies to millions of patients using our C-STEM encapsulation technology, enabling large-scale amplification of iPS and differentiated cell products for patients. Using our C-STEM format, TreeFrog is currently developing multiple cell therapy programs for disease indications including Parkinsons disease and acute liver failure. TreeFrog has also entered into a collaboration with Vertex Pharmaceuticals to incorporate C-STEM in the production of iPS-derived islets for type 1 diabetes. Our US team is newly located in our own, renovated space in Cambridgeport Labs and supports a combination of internal R&amp;D programs as well as collaborations with external partners.Find out more at our website: <a href="https://treefrog.fr" target="_blank">https://treefrog.fr</a>
 
Description of Position
We are seeking a highly motivated and detail-oriented laboratory scientist to support iPS expansion and differentiation activities at TreeFrog. This position will support internal research activities and external collaborations to grow and differentiate iPS cells within the C-STEM platform. The successful candidate will be a collaborative laboratory scientist with a passion for stem cell differentiation and a track record of hPSC differentiation and characterization experience. This position will work in collaboration with scientists across multiple teams and report directly to the cell differentiation group lead at TreeFrog, US.
 
Job Responsibilities :
<ul>
<li>Culture and differentiation of iPS in multiple 2D and 3D formats</li>
<li>Encapsulation and expansion of iPS cells in TreeFrogs C-STEM capsule technology</li>
<li>Testing and optimizing differentiation methods within the C-STEM platform</li>
<li>Routine analysis of differentiated cell products including
<ul>
<li>Flow cytometry</li>
<li>2D cytochemistry</li>
<li>3D immunocytochemistry</li>
<li>Protein analysis (ELISA, western blot, etc.)</li>
<li>RNA analysis (Real Time RT-PCR, RNAseq)</li>
</ul>
</li>
</ul>
<ul>
<li>Support method development efforts involving the C-STEM platform</li>
<li>Routine laboratory maintenance</li>
<li>Diligent record keeping and thorough electronic lab notebook practices</li>
</ul>
 
Required Skills
<ul>
<li>B.S. or equivalent in Biology or a related field</li>
<li>Previous stem cell culture and differentiation experience (industry preferred)</li>
<li>Excellent tissue culture technique and ability to maintain large number of cultures at once</li>
<li>Experience in differentiation protocol optimization and development</li>
<li>Flow cytometry sample preparation and data analysis</li>
<li>Self-motivated, independent laboratory scientist</li>
<li>Ability to work in a larger research team and communicate effectively with other team members</li>
<li>Ability to work limited weekend hours</li>
</ul>
 
TreeFrog is an Equal Opportunity Employer. We comply with all applicable national, state, and local laws governing nondiscrimination in employment, as well as the employment eligibility verification requirements of the Immigration and Nationality Act.
 All applicants must be authorized to work in the United States.

Senior Research Associate

<h3>Job Description</h3>
Job Description
Job Title: Lab Technician II Location: Braintree, MA, 02184
Pay rate: $20 - $30 an hour
Contract Duration: 6-month contract - temp to perm
Client: Integra LifeSciences Corporation Job ID: IGRAJP00001661
We offer medical, dental, vision, and 401(k) benefits.
My apologies if your profile doesn't suit this job. This is a blast email.
Description:
<ul>
<li>ISO 13485 exp preferred, along with ISO 7 and 8 cleanroom</li>
<li>ISO 5 is even better</li>
</ul>
Must Have:
<ul>
<li>Environmental Monitoring</li>
<li>Water Monitor &amp; Collecting</li>
<li>Microsoft Office experience - Advanced/Proficient</li>
</ul>
Exp with Bioburden testing is great
Responsibilities:
<ul>
<li>Responsible for performing Microbiological testing such as Bioburden, Endotoxin, Growth promotion testing, TOC &amp; Conductivity testing, sending samples for Microbial ID testing and other micro testing.</li>
<li>Perform Environmental monitoring of clean rooms including Viables and Non-viables testing and responsible of water samples collection and testing.</li>
<li>Working knowledge of aseptic techniques and provides database support, generates reports, and analyzes the data as needed.</li>
<li>Inspection and testing of raw materials, in-process, and final product testing.</li>
<li>Assist in trending environmental monitoring data. Report and investigate any monitoring excursions.</li>
<li>Monitors equipment and instrumentation used daily to ensure proper operation and calibration.</li>
<li>Maintains a working inventory of all components, materials and solutions as needed.</li>
<li>Develops and revises SOPs &amp; Forms</li>
<li>Responsible for identifying and alerting supervisor of issues on instruments and/or test executions; makes initial recommendations for possible solutions and/or corrective actions.</li>
<li>Assist in Out of Specification (OOS) Investigations, Non-conformances, and Corrective Action/Preventive Actions (CAPAs).</li>
<li>Assists in the writing and updating of Microbiological test procedures, protocol, logbooks, and checklists.</li>
<li>Assist as needed in test method validation, investigation studies or other product development studies.</li>
<li>Assist in preparing for and participating in FDA audits, customer audits, etc.</li>
<li>All other duties as assigned</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Microbiology, Biology, or a relevant scientific discipline.</li>
<li>A minimum of 2-4 years’ experience in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other cGMP-regulated product environment.</li>
<li>Familiarity with the application of FDA and/or ISO quality standards in a government-regulated industry. Quality Certification (e.g., CQE, CQA, Six Sigma) preferred.</li>
<li>Proficient computer competence, including experience with databases and Microsoft Office software to create reports, spreadsheets, analyze data, and prepare presentations.</li>
<li>Experience with performing Microbiological assays in cGMP cGMP-compliant lab and understanding of aseptic techniques.</li>
<li>Working knowledge of standard laboratory practices and safety.</li>
<li>Ability to follow instructions precisely, recognize deviations, and recommend corrective action.</li>
<li>Experience working in ISO Class 7 &amp; 8 cleanrooms.</li>
</ul>
Company DescriptionTechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. We serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. We also have national recruiting 
<h3>Company Description</h3>
TechLink Systems is a national provider of staffing services with offices all over the USA as well as development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified minority business that has been awarded 2017 TAPFIN Premier Partner, 2016 Manpower Excellence Award, 2016 TAPFIN Elite Partner, are a Known Tier Supplier for Agile 1, and have been ranked as a Top Women and Minority Owned Company since 2004 by several businesses including Philadelphia Business Journal, Diversity Business, Inc 5000, Inc 500, San Francisco Business Times, Diversity2000, and Los Angeles Business Journal. \r\n\r\nWe serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and project outsourcing needs of clients nationwide. Striving to create personal relationships with clients, TechLink Systems becomes a virtual extension of clients’ own in-house capabilities to help achieve new levels of growth, productivity, and competitiveness. \r\n\r\nWe also have national recruiting

Laboratory Technician (Med Device/Pharma) AO2025

<h3>Job Description</h3>
Job DescriptionCompany Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.
Job Description 
Apply today for a rewarding career with opportunities for growth!!&nbsp;&nbsp; &nbsp;Must live a commutable distance to Derry, New Hampshire.&nbsp; PFAS experience preferred but not required.
We are looking for to fill full-time year round position.&nbsp; Mon-Fri&nbsp; &nbsp;8:00am- 4:30pm&nbsp; &nbsp; Compensation is $21-23/hour (DOE) plus benefits
The Analyst I prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP’s.
Responsibilities include, but are not limited to, the following:
<ul>
<li>Demonstrates and promotes the company vision</li>
<li>Regular attendance and punctuality</li>
<li>Applies GMP/GLP in all areas of responsibility, as appropriate</li>
<li>Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include:
<ul>
<li>Preparation of samples using standard techniques</li>
<li>Performing chemical analysis using standard techniques</li>
<li>Calculating data</li>
<li>Recording and reporting data and any unusual test occurrences to the supervisor</li>
<li>Performing routine instrument maintenance</li>
</ul>
</li>
<li>Responsible for performing job functions in compliance with Eurofins’ EHS and QA standards</li>
<li>Responsible for general housekeeping in his/her work area</li>
<li>Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems.</li>
<li>Works under close supervision using routine and standard methods</li>
<li>Aliquots and weighs samples</li>
<li>Washes glassware</li>
<li>Conducts all activities in a safe and efficient manner</li>
<li>Performs other duties as assigned&nbsp;</li>
</ul>
The ideal candidate would possess:
Reading, writing and speaking skills&nbsp;
Problem solving skills&nbsp;
Team participation and meeting management skills&nbsp;
Time management and organization skills
<ul>
<li>Ability to use calculator/mathematical formulas and concepts</li>
<li>Ability to complete work within time and quality constraints</li>
<li>Can work independently following written or verbal instructions</li>
<li>Cooperate and coordinate both orally and in writing</li>
<li>Able to follow and learn appropriate protocols in one or more of the following disciplines:
<ul>
<li>Organic preparation</li>
<li>Metals preparation and analysis</li>
<li>Gas Chromatography</li>
<li>Gas Chromatography/Mass Spectrometry</li>
<li>Radio Chemistry</li>
<li>Wet Chemistry</li>
<li>High Resolution preparation and analysis</li>
<li>Low Resolution preparation and analysis</li>
</ul>
</li>
</ul>
Qualifications 
Basic Minimum&nbsp;Qualifications (BMQ):&nbsp;
<ul>
<li>A minimum of an Associate of Science degree in Chemistry or equivalent experience</li>
<li>Experience in an environmental lab is a plus</li>
<li>At least 1-2 year’s preparation, analytical experience, or combination, at company or equivalent experience elsewhere preferred</li>
<li>Some previous PFAS experience&nbsp; preferred</li>
<li>Experience with LC/MS-MS operation and general maintenance preferred</li>
<li>Demonstrated effective communication skills and relate well to people in direct communication</li>
<li>Consciousness of and a positive attitude toward quality, service and safety procedures</li>
<li>Sound reasoning, good judgment and decision making</li>
<li>Strong organization and problem solving skills</li>
<li>Detail oriented, ability to handle multiple tasks simultaneously and able to coordinate multiple priorities</li>
<li>Versatility, flexibility in dealing with people</li>
<li>Ability to synthesize and retain information</li>
<li>Computer skills, experience with LIMs software a plus</li>
<li>Ability to perform basic math skills including multiplication, division and algebra</li>
<li>Work independently</li>
<li>Work within time constraints</li>
<li>Must be able to lift up to 25 lbs frequently, and up to 50 lbs occasionally&nbsp;</li>
<li>Willingness to put in overtime hours, as necessary to meet work needs</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English.</li>
<li>Final candidate will be given pre-employment background check and drug screen</li>
<li>Perform other duties as assigned</li>
</ul>
Disclaimer:
This position description is written as a guideline to inform employees of what is generally expected of them at each job level.&nbsp; The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment.&nbsp; Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole.
 Additional Information 
Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work.&nbsp; We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options.
We support your development!&nbsp;Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.
We embrace diversity!&nbsp;Eurofins network of companies believe in strength and innovation through diversity, being an&nbsp;Equal Opportunity Employer.&nbsp;We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.
Sustainability matters to us!&nbsp;We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!
Find out more in our career page: <a href="https://careers.eurofins.com/" target="_blank">https://careers.eurofins.com/</a>
Company description:&nbsp;Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years.
We do not offer Visa Sponsorship for this role.
Eurofins is a&nbsp;M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

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