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<h3>Job Description</h3>
Job Description
Are you ready to join a team that's pioneering the future of medicine? We are seeking a highly motivated and skilled Quality Control (QC) Analyst to focus on Environmental Monitoring (EM) within our state-of-the-art Good Manufacturing Practice (GMP) laboratories.
In this critical role, you'll be responsible for executing the routine and specialized sampling necessary to ensure the highest standards of environmental control for our groundbreaking technology. If you thrive in a fast-paced, collaborative environment and have a passion for microbiological quality assurance, this is your opportunity to make a direct impact on transforming human health.
salary: $40 - $43 per hour shift: First work hours: 10 AM - 8 PM education: Bachelors 
Responsibilities
What You'll Do: Core Responsibilities
<ul>
<li>Execute comprehensive Environmental Monitoring (EM) activities, including routine, in-process, and Environmental Monitoring Performance Qualification (EMPQ) sampling.</li>
<li>Perform essential utility sampling, including Water for Injection (WFI) and Compressed Gas sampling.</li>
<li>Maintain and calibrate laboratory equipment; perform general laboratory housekeeping and supply inventory.</li>
</ul>
What You'll Need: Required Qualifications
<ul>
<li>Education: A Bachelor's Degree in a Science, Technology, Engineering, or Math (STEM) discipline.</li>
<li>Experience: At least 3+ years of hands-on experience in a GMP Quality Control laboratory setting, with a strong focus on microbiology.</li>
</ul>
 Skills
<ul>
<li>Quality Control</li>
 Qualifications
<li>Years of experience: 0 years</li>
<li>Experience level: Experienced</li>
 Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. 
</ul>

Quality Control Microbiology Associate

<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>
&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. &nbsp;
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Principal Scientist/Associate Director, Translational Sciences

<h3>Job Description</h3>
Job DescriptionSenior Product Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a Senior Product Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing new platform technologies for environmental protection and implementing at our customers around the world. A master’s or doctorate in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science, or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop functional materials, test methods, and implementation solutions for the environmental protection of automotive and consumer electronics.</li>
<li>Maintain project plans, timelines, and deliverables related to product launch strategy.</li>
<li>Communicate technical advances and project strategy to a global team of technical and sales personnel.</li>
<li>Work autonomously on open-ended projects, from new coating development to novel application techniques.</li>
<li>Expand actnano’s IP portfolio by innovating on coatings and application technology.</li>
<li>Serve as the subject matter expert on coatings and participate in developing customer implementation strategies.</li>
<li>Collaborate with cross-functional teams and maintain project plans, timelines, and deliverables for product launches.</li>
<li>Mentor technicians and co-ops on conducting experiments for coating development.</li>
<li>International and domestic travel is required.</li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $115,000 – $125,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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Senior Product Development Engineer / Scientist

<h3>Job Description</h3>
Job DescriptionThe Role: Title: Senior/Principal Scientist, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated and independent Senior/ Principal Scientist in immunology/cancer pharmacology with a track record of scientific excellence in immunology or oncology, to join our team in Greater Boston, MA USA. As a key project team member, you will be focused on delivering all aspects of in vitro, in vivo, and ex-vivo pharmacology support. You will bring your theoretical and practical expertise to establish assay systems and deliver datasets that will have direct impact on the drug discovery process and pipeline. The Company: It’s not often that 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, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the 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. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Work with in-house data scientists and or CRO to identify new targets for new project initiation. </li>
<li>Design and conduct POC study for target validation. </li>
<li>Assist discovery project leaders to set up goals and objectives for the achievement of project milestones. </li>
<li>Support cross-functional teams and work collaboratively with project leaders to ensure the timely generation and dissemination of critical program data.</li>
<li>Stay up to date with relevant technical and intellectual scientific expertise in Immune-oncology and Pharmacology and have a genuine passion for this field of research.</li>
<li>Prepare and deliver clear and accurate scientific presentations for internal and external use.</li>
</ul>
 Essential Qualifications: &nbsp;
<ul>
<li>Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>9+ years of relevant post-PhD experience in industry.</li>
<li>Demonstrated scientific capability as evidenced by high-quality independent research and high impact peer-reviewed scientific publications, presentations, projects as a leading contributor. </li>
<li>Comprehensive knowledge of immunology, autoimmunity and cancer biology.</li>
<li>Extensive hand-on experiences in the initiation and leading drug discovery projects in the industry setting.</li>
<li>Strong track record of success in leading projects achieving discovery/development milestones.</li>
<li>Work independently, assess and report data in a clear and concise manner, with a clear understanding of its implications within the overall context of drug discovery.</li>
<li>Strong interpersonal and collaboration skills together with evidence of delivery in a team-oriented, collaborative environment.</li>
<li>Excellent communication and presentation skills: impactful oral and written communication.</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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MHqXmhrqEx

Senior/ Principal Scientist, Immunology and Pharmacology

<h3>Job Description</h3>
Job DescriptionProduct Development Engineer/Scientist About actnanoWe are a dynamic materials technology company in Malden, MA. With a strong global technical team, we develop and manufacture coatings that protect printed circuit boards in electronics, allowing them to function in water-laden environments. We work with the biggest brands in the consumer electronics and automotive industries to increase product reliability and improve product performance in wet and humid conditions. Not only do we provide a portfolio of coatings, but we also work closely with our customers to help solve some of their most difficult problems through rapid innovation and ingenuity. About this RoleWe are seeking a roduct Development Engineer/Scientist to join our talented and diverse technical team in Malden, MA. This position will focus on developing novel coatings platforms from lab-to-scale to address customer needs. A bachelor’s degree or higher in Mechanical, Chemical or Electrical Engineering, Chemistry, Materials Science,or associated technical field is required. Fluency in Mandarin, Spanish, or German preferred but not required. Candidate must be legally allowed to work in the US. Key Responsibilities
<ul>
<li>Develop novel coating platforms, test metrics, and design experiments by working in a lab-based environment with minimal day-to-day guidance.</li>
<li>Develop hypotheses and conduct experiments to improve understanding and performance of actnano’s coating technology by coordinating with various team members.</li>
<li>Communicate technical advances internally with other members of the company and interact with external vendors, independent testing laboratories, and customers to explain and troubleshoot application of the technology.</li>
<li>Support scaling of coating from lab or pilot scale to a manufacturing environment.</li>
<li>Collaborate with sales or technical service to address customer requests.</li>
<li>Expand actnano’s coating portfolio by innovating on current coating technology and developing new coating platforms.</li>
<li>Some international and domestic travel required. </li>
</ul>
This position is based in Malden, MA, accessible via the Orange Line. The salary range for this position is $75,000 – $90,000 per year, which reflects the base pay the Company reasonably and in good faith expects to pay at the time of this posting. &nbsp;
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I3Y9Z3UrYH

Product Development Engineer / Scientist

<h3>Job Description</h3>
Job Description
Scientist II/ Senior Scientist – Viral Vector / Discovery &nbsp;
(Hybrid – Greater Boston, on-site lab work required)&nbsp; NOTE: Applicants must be legally authorized to work in the United States on a permanent basis. At this time, the Company does not provide, and will not provide in the future, sponsorship for employment visas.
Why Work With Us?&nbsp;
At Candel, our people drive our mission to transform cancer care. We value curiosity, collaboration, and bold science in a supportive environment where everyone has visibility and impact. You’ll join a team that embraces creativity, trusts its people, and fosters growth through coaching and open discussion. This is the place to bring your ideas forward, dig deep into data, and see your work make a real difference for patients.&nbsp;
Our Science: Advancing Cancer Immunotherapies&nbsp;
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies designed to stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs, advancing novel treatments through discovery, IND-enabling studies, and into clinical development. With positive Phase 3 results for our lead candidate and multiple pipeline programs on the horizon, it’s an exciting time to join us. Learn more: <a href="http://www.candeltx.com&amp;nbsp" target="_blank">www.candeltx.com&amp;nbsp</a>;
Position Summary&nbsp;
This is a highly visible, hands-on role reporting directly to the VP of Research. As Scientist II /Senior Scientist, (We will determine final title and level based on your experience and background.) you’ll balance bench work and strategic contributions to advance novel viral vectors into IND-enabling studies and first-in-human trials. You’ll gain full-spectrum exposure across discovery, development, regulatory, and clinical programs, while contributing to the future of Candel’s viral immunotherapy platform.&nbsp;
We’re looking for a scientist who thrives in a fast-paced biotech with a “can-do” mindset — someone versatile enough to design experiments at the bench, analyze data, and present insights across functions. If you’re inquisitive, data-driven, and energized by the chance to innovate while still being hands-on, this role offers both the challenge and growth you’re seeking.&nbsp;
What You Will Do&nbsp;
<ul>
<li>
Support scientific strategy and execution for viral immunotherapy programs from discovery through IND-enabling studies.&nbsp;
</li>
</ul>
<ul>
<li>
Design and optimize viral vectors (e.g., HSV) for therapeutic applications, including genome engineering and payload design.&nbsp;
</li>
</ul>
<ul>
<li>
Oversee and perform in vitro and ex vivo assays to evaluate vector potency, transduction efficiency, and immunological activity.&nbsp;
</li>
</ul>
<ul>
<li>
Collaborate closely with cross-functional teams including CMC and Regulatory to ensure seamless program progression.&nbsp;
</li>
</ul>
<ul>
<li>
Guide the development and transfer of analytical and process development methods to the CMC team.&nbsp;
</li>
</ul>
<ul>
<li>
Mentor and manage junior scientists and research associates; foster a culture of scientific rigor, innovation, and collaboration.&nbsp;
</li>
</ul>
<ul>
<li>
Contribute to regulatory documentation, including IND-enabling study design and data interpretation.&nbsp;
</li>
</ul>
<ul>
<li>
Stay current with scientific literature and emerging technologies in viral vector design, immunotherapy, and oncology.&nbsp;
</li>
</ul>
What You Will Bring&nbsp;
<ul>
<li>
Ph.D. in Virology, Molecular Biology, Immunology, or related field with 3–5+ years biotech industry experience&nbsp;
</li>
</ul>
<ul>
<li>
Extensive hands-on experience with viral vector systems, including design, production, purification, and characterization; HSV experience a plus&nbsp;
</li>
</ul>
<ul>
<li>
Strong background in mammalian cell culture, transduction assays, and molecular biology techniques (qPCR, ELISA, flow cytometry)&nbsp;
</li>
</ul>
<ul>
<li>
Demonstrated experience developing and implementing platform-based approaches in cell and gene therapy (e.g., scalable vector design, modular assays, standardized workflows)&nbsp;
</li>
</ul>
<ul>
<li>
Familiarity with IND-enabling studies, GLP/GMP environments, and regulatory expectations for gene therapy products&nbsp;
</li>
</ul>
<ul>
<li>
Comfort running your own bench work while also contributing strategically&nbsp;
</li>
</ul>
<ul>
<li>
Proven ability to thrive in a lean, entrepreneurial environment without big-pharma infrastructure&nbsp;
</li>
</ul>
<ul>
<li>
Curious, data-driven mindset — eager to ask questions, revisit data, and generate new insights&nbsp;
</li>
</ul>
<ul>
<li>
Excellent written and verbal communication skills with confidence to present across levels and functions&nbsp;
</li>
</ul>
<ul>
<li>
Must be legally authorized to work in the United States. Sponsorship is not available; U.S. citizenship or permanent residency is required&nbsp;
</li>
</ul>
Preferred Attributes&nbsp;
<ul>
<li>
Desire to grow into leadership, with experience mentoring or guiding junior staff&nbsp;
</li>
</ul>
Work Environment&nbsp;
This is a hybrid role based in Greater Boston, with significant on-site lab work (bench and data analysis). Expect to be onsite most of the week to fully engage with research, team collaboration, and laboratory execution.&nbsp;
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tfgqQ3Hl92

Scientist II / Senior Scientist - - Viral Vector / Discovery

<h3>Job Description</h3>
Job Description
Elevate Quality &amp; Safety: Quality Control Microbiology Associate I 
 
Are you a highly motivated microbiologist ready to be the frontline defender of quality for groundbreaking clinical and commercial manufacturing?
We are seeking a meticulous and experienced Quality Control Microbiology Associate I to join our team. In this critical role, your expertise in environmental and utility monitoring will directly ensure the safety, compliance, and integrity of our entire manufacturing operation. If you thrive on precise execution, love troubleshooting, and are ready to contribute to a Bold, Relentless, and Collaborative culture, this is your next career challenge!
 
The Mission: What You'll Be Doing
You will be responsible for the routine monitoring and control of our critical manufacturing environment and utilities:
<ul>
<li>Routine &amp; Critical Sampling: Conduct routine Environmental Monitoring (EM), including In-Process and EMPQ's, WFI Sampling, and Compressed Gas Sampling across clinical and commercial operations.</li>
<li>Compliance &amp; Documentation: Write, revise, and strictly follow SOPs, protocols, and reports. You will support quality systems records such as deviations, change controls, and CAPAs.</li>
<li>Data Integrity: Ensure meticulous data entry, review, and trending using LIMS (Laboratory Information Management System).</li>
<li>Lab Operations &amp; Collaboration: Maintain lab equipment, perform housekeeping tasks, and collaborate with internal and external labs for sample coordination and testing.</li>
<li>Troubleshooting: Actively troubleshoot equipment and test methods and participate in audits and continuous improvement initiatives.</li>
</ul>
 
What You'll Need to Bring
Education: Bachelor's Degree (Master's Degrees will not be considered).
Technical Skills: Proficiency with Microsoft Office Programs and electronic databases (LIMS, SAP, eQMS).
Experience: 3+ years of experience in a GMP QC laboratory setting, specifically focusing on microbiology.
Instrumentation: Hands-on experience with particle counters, viable air samplers, and gas equipment.
Core Knowledge: Knowledge of GMP, microbiology, aseptic techniques, and general laboratory instrumentation.
Regulatory: Familiarity with relevant FDA, EU, ICH guidelines, and regulations.
Communication: Strong written and oral communication skills and organizational abilities.
Environment: Ability to work effectively in a fast-paced, cross-functional matrix environment.
Export to Sheets
 
Compensation &amp; Culture
<ul>
<li>Pay: Competitive rate of $43.00/hour (with shift differential, potentially $49.45/hour).</li>
<li>Culture: Join a high-growth, transformational company that values curiosity, boldness, and collaboration.</li>
</ul>
 
If you are ready to apply your microbiology expertise where it matters most, ensuring product safety from the ground up, apply today!
 FOR MORE IMMEDIATE CONSIDERATION, email a current resume to <a href="mailto:iris.levy@randstadusa.com" target="_blank">iris.levy@randstadusa.com</a>
Company DescriptionRandstad Staffing. We provide outsourcing, staffing, consulting, and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration, and sales and marketing. We can’t wait to tell you all about it! 
<h3>Company Description</h3>
Randstad Staffing. We provide outsourcing, staffing, consulting, and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration, and sales and marketing. \r\n\r\nWe can’t wait to tell you all about it!

Quality Control Microbiology Associate I

<h3>Job Description</h3>
Job Description
We’re seeking a Senior Dam Safety Engineer with deep expertise in geotechnical engineering and dam safety evaluations. This leadership role is ideal for someone with FERC Part 12 Independent Consultant approval—or the experience to qualify—and a passion for risk-based analysis and infrastructure resilience.
You’ll play a pivotal role in guiding project teams, mentoring junior staff, and shaping the future of our dam safety services. This is your opportunity to work on meaningful, high-impact projects in clean energy and environmental restoration. Ready to make a difference? Let’s build something lasting—together!
**Remote work options available for highly qualified candidates
 
 
Key Responsibilities
<ul>
<li>Lead and coordinate design teams for FERC and state-regulated dam safety projects</li>
<li>Conduct dam safety evaluations, including FERC Part 12 inspections</li>
<li>Design earthen embankments and perform geotechnical assessments for dams and civil works</li>
<li>Develop and analyze geotechnical monitoring and testing programs</li>
<li>Review construction sequencing, design plans/specs, and permitting documents</li>
<li>Represent the firm in technical discussions with regulators, clients, and public forums</li>
<li>Author and review technical reports and project documentation</li>
<li>Mentor engineers in technical execution and career development</li>
<li>Support proposal writing, cost estimating, and project scheduling</li>
</ul>
Qualifications
<ul>
<li>B.S. in Civil or Geotechnical Engineering (M.S. preferred)</li>
<li>Licensed Professional Engineer (PE) with willingness to maintain multi-state registrations</li>
<li>FERC Part 12 Independent Consultant approval or eligibility</li>
<li>Comprehensive Assessments expert</li>
<li>Strong communication skills and attention to detail</li>
<li>Experience with risk-based analysis preferred</li>
<li>15+ years of experience in:
<ul>
<li>Dam safety evaluations and geotechnical design</li>
<li>Project management and client engagement</li>
<li>Earthquake response analysis for embankments</li>
<li>Proposal development and team mentoring</li>
<li>Familiarity with federal/state dam safety standards</li>
</ul>
</li>
<li>Some travel required to project sites</li>
</ul>
Benefits
We offer a competitive and comprehensive benefits package, including:
<ul>
<li>Medical, dental, and vision insurance</li>
<li>Generous vacation, comp time, and flexible holidays</li>
<li>Paid sick leave and extended medical leave account</li>
<li>Educational assistance and professional development support</li>
<li>Parental leave and Dependent Care FSA</li>
<li>Short and long-term disability coverage, Life Insurance</li>
<li>401K and profit-sharing program</li>
<li>Relocation provided and supported</li>
</ul>

Senior Geotechnical Dam Safety Engineer - PE

<h3>Job Description</h3>
Job Description
Adecco staffing is recruiting for Assemblers in Devens! We have openings on 1st shift. These are 10 hour, 4 day work weeks. This position is temp to hire. SCHEDULE: Monday-Thursday, 5:00AM-3:30PM
PAY RANGE: $19-20 per hr
Job Summary:
As an Assembly Operator I, you will be instrumental in the success of our products being at or above our customers' requirements and standards. Accordingly, you will be responsible for product movement, monitoring and identifying quality issues to achieve required quality standards.
Job Duties:
· Maintain the tools used to create products.
· Keep a clean and well-maintained workspace.
· Maintain a helpful and collaborative culture through communication and a strong work ethic.
· Cross train as required within the Value Stream
· Carry out any other activities to support the business as required
 Requirements:
· Awareness of cGMP requirements.
· Can use personal initiative to work collaboratively as one team with a “can do” approach.
· Be delivery focused with strong attention to detail and an ability to work under pressure.
 INTERESTED? If so, please apply directly to this posting!
 Pay Details: $19.00 to $20.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://uat.adecco.com/en-us/candidate-privacy" target="_blank">https://uat.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Clean Room Assembler

<h3>Job Description</h3>
Job Description
Cell Biologist needs 3+ years for MS - 5+ years for BS. Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.
Cell Biologist requires:
<ul>
<li>Proficiency in gene editing and cell line development, including optimization of protocols, familiarity with flow-based sorting.</li>
<li>Hands-on experience with cell delivery methods of gene editing tools.</li>
<li>Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.</li>
<li> Strong organizational skills and diligent record keeping.</li>
<li>Experience in pancreatic islet directed differentiation is highly desirable</li>
<li>Hands-on experience in transitioning research-grade processes to GMP-grade is highly desirable.</li>
<li>Mandatory weekend cell culture responsibilities on rotation basis.</li>
</ul>
Cell Biologist duties:
<ul>
<li>Enabling and advancing iPSC gene editing, cell line development and evaluation of differentiated cells.</li>
<li>Routine iPSC cell culture, passaging and media making.</li>
<li>Optimize workflows for iPSC CRISPR based gene-editing, gRNA screening and delivery.</li>
<li>Optimize and perform assays for on-/off-target analysis via PCR and NGS workflows.</li>
<li>Generate clonal gene edited iPSC lines and characterize via flow cytometry, ddPCR, dPCR and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets performing drug substance assessments such as cell counts, viability, metabolite assessments.</li>
<li>Assist scientists in the team to evaluate and design mitigation strategies to ensure genomic stability of the iPSC lines and drug substance.</li>
<li>Collaborate cross-functionally to support transfer of R&amp;D assays to GMP.</li>
<li>Maintain accurate and detailed records of all experiments, synthesize results, prepare reports and present in meetings.</li>
<li>Contribute to SOP development.</li>
<li>Work seamlessly in executing workplans and meeting deadlines.</li>
</ul>

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