• Manufacturing Associate II

    Actalent (Bothell, WA)


    Job Title: Manufacturing Associate IIJob Description

     

    The Manufacturing Associate II is tasked with supporting operations at our cGMP clinical manufacturing site, focusing on the production of plasmids, viral vectors, and autologous cell therapies. This role involves performing day-to-day operations while ensuring compliance with industry standards.

    Responsibilities

    + Execute manufacturing operations safely, on schedule, and correctly to ensure timely delivery of treatments to patients.

    + Adhere to the current Good Manufacturing Practices (cGMP) and standard operating procedures.

    + Escalate manufacturing operations issues to management and quality assurance promptly.

    + Maintain production facilities in a clean and organized manner.

    + Perform equipment maintenance and calibrations as required.

    + Complete and review GMP documentation in a timely manner.

    + Maintain an appropriate level of training for assigned responsibilities.

    + Assist with inventory management of supplies within the manufacturing facility.

    + Support daily tasks and collaborate effectively within the manufacturing team.

    + Communicate effectively to build strong relationships and demonstrate technical acumen.

    + Support operational excellence initiatives and uphold a culture of safety and GMP compliance.

    + Identify opportunities for continuous improvement.

    Essential Skills

    + Knowledge of GMP and quality management systems.

    + Minimum of 2 years' experience in GMP biopharmaceutical operations, preferably in cell therapy, mammalian cell culture, and/or microbial fermentation.

    + Experience with quality management systems, including Deviations, CAPAs, and Change Management.

    + Proficiency in electronic systems such as MES and ERP.

    + Familiarity with regulations for GMP manufacturing of drug substances, drug products, cellular and gene therapies, and viral vectors for clinical phase therapies.

    + Proven track record in cGMP manufacturing operations.

    Additional Skills & Qualifications

    + BSc degree in a relevant field such as biochemistry, chemical engineering, bioengineering, or a related scientific field.

    + Fast learner with adaptability and excellent cross-collaboration and interpersonal skills.

    + Desire and ability to work in a fast-paced, start-up environment.

    Work Environment

    This position requires working from Sunday to Wednesday, with four 10-hour shifts from 0700 to 1730. Overtime is often available due to extended operations or shift coverage opportunities.

    Pay and Benefits

    The pay range for this position is $34.00 - $38.46/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Bothell,WA.

     

    Application Deadline

     

    This position is anticipated to close on Aug 4, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.