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Biotech Manufacturing Associate Jobs in Bothell, WA

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Biotech Manufacturing Associate information

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$13

$23

$37

How much do biotech manufacturing associate jobs pay per hour?

As of Jun 23, 2026, the average hourly pay for biotech manufacturing associate in Bothell, WA is $23.69, according to ZipRecruiter salary data. Most workers in this role earn between $18.56 and $26.49 per hour, depending on experience, location, and employer.

What are Biotech Manufacturing Associates?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by Biotech Manufacturing Associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the role of a manufacturing associate?

A Biotech Manufacturing Associate is responsible for performing tasks related to the production of biopharmaceutical products, including operating equipment, following strict safety and quality protocols, and documenting processes. They work in controlled environments and often require knowledge of Good Manufacturing Practices (GMP) and attention to detail. The role supports ensuring the efficient and compliant manufacturing of biotech products.

What are 5 careers in biotechnology?

Biotech manufacturing associates work in roles such as research scientist, quality control analyst, process development engineer, regulatory affairs specialist, and bioprocess technician. These careers involve working with laboratory equipment, manufacturing processes, and compliance standards in a biotech production environment.

What is the highest paying job in biotech?

In biotech manufacturing, senior roles such as Biotech Manufacturing Director or Vice President of Manufacturing tend to be the highest paying positions, often earning six-figure salaries. These roles require extensive experience, leadership skills, and knowledge of regulatory compliance and process optimization.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

How to get into biotech sales with no experience?

Biotech sales roles typically require knowledge of the industry and strong communication skills. To enter with no experience, candidates can pursue relevant certifications, such as in biology or sales, and gain familiarity with biotech products through online courses or networking. Entry-level positions often value transferable skills like customer service or technical aptitude, and internships or entry-level roles can provide valuable industry exposure.
What job categories do people searching Biotech Manufacturing Associate jobs in Bothell, WA look for? The top searched job categories for Biotech Manufacturing Associate jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Manufacturing Associate jobs? Cities near Bothell, WA with the most Biotech Manufacturing Associate job openings:
Infographic showing various Biotech Manufacturing Associate job openings in Bothell, WA as of June 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Contract, and 2% Nights. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $49,268 per year, or $23.7 per hour.
Quality Control Associate II

Quality Control Associate II

Lyell Immunopharma

Seattle, WA

$75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Using living cells to treat – and sometimes even cure – cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response. We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyell's product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission's urgency.

We are seeking a highly motivated and detail-oriented QC Associate II to join our dynamic team at the Lyell Manufacturing Facility, LyFE in Bothell, WA. The ideal candidate will have hands-on experience in a GMP-regulated facility and be proficient in conducting cell-based and flow cytometry-based assays. Experience in cell therapy is highly desirable.

This role requires working a Wednesday through Saturday shift, 10 hours per day, and involves routine laboratory work supporting ongoing preclinical and clinical development programs. This is an onsite role with no remote option.

Key Responsibilities:

  • Perform cell-based release and stability assays for cell count, viability and cytotoxicity.
  • Execute release lentiviral vector assay to determine titer and potency
  • Perform flow cytometry in-process, release and stability testing
  • Support and execute method transfer, qualification and validation
  • Participate in authoring test methods and developing and validating blueprints for testing in LIMS
  • Maintain compliance with GMP regulations and internal SOPs and methods during all QC operations.
  • Initiate, lead and participate in deviations, Change Controls and CAPAs. Experience with MasterControl is a plus.
  • Perform preventative maintenance of QC equipment, and ensure clean and organized, laboratories. Experience with BMRAM is a plus.
  • Perform other QC support duties as assigned.

Requirements:

  • 3-5 years of experience in a GMP-regulated pharmaceutical, biotech, or related industry.
  • Prior experience in cell therapy environments is a plus.
  • Working knowledge of LIMS systems is strongly preferred.
  • Detail-oriented with strong organizational and GDP skills.
  • Ability to work independently on a fixed schedule (Weds-Sat, 10 hours/day).
  • Overtime may be required occasionally, based on business needs.
  • Ability to stand for extended periods and work in a laboratory environment wearing personal protective equipment.
  • Work involves repetitive tasks and occasional lifting (up to 25 lbs).

Qualifications:

  • Bachelor's or Master's degree in biology, Immunology, Cell Biology, or related field.
  • 3–5+ years of experience working in a GMP-regulated laboratory environment.
  • Experience with cell and flow cytometry-based assays is required.
  • Familiarity with software tools for flow cytometry data analysis (e.g. FCS Express).
  • Strong attention to detail, organizational skills, and ability to work independently on a fixed schedule (Weds-Sat.).

Additional Information:

  • This is an onsite role with no remote option.
  • Candidates must be authorized to work in the U.S. without sponsorship.
Shift: Weds– Saturday, 10 hours/day
The salary range for this position is $75,000 to 85,000 per year with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell's compensation practices and an applicant's qualifications and experience. Employees are also eligible to participate in Lyell's Equity Incentive Plan.
Our Employee Benefits program is extensive and includes subsidized medical, dental and vision plans from your first day of employment, FSA, Company provided Life and AD&D Insurance as well as STD and LTD Insurance, ESPP, a 401(k) Plan with Company match, mass transit commuter benefits, cell phone reimbursement and a range of supplemental benefits that you may choose to elect. Our paid time-off benefits currently include 18 days' vacation, 9 day's sick leave, 8 observed holidays as well as a floating holiday. We also have a summer and a winter office shutdown.
At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees. Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.
We've learned from experience that some of the best people don't always match our requirements perfectly - if you're interested and think you could fit, please don't hesitate to apply.