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Description

The incumbent is responsible for supporting the operations in our cGMP clinical manufacturing site producing plasmids, viral vectors, and autologous cell therapies. This role is responsible for performing day to day operations. KEY ROLE AND RESPONSIBILITIES: Execute the Day-to-Day Manufacturing Processing ● Execute manufacturing operations safely, as scheduled, and right the first time for delivery of treatment to patients. ● Adhere to the current Good Manufacturing Practices (cGMP) and standard operating procedures (SOPs). ● Escalate manufacturing operations issues to management and quality assurance in a timely manner. ● Maintain production facilities at a high standard of cleanliness and organization. ● Perform equipment maintenance and calibrations as required. ● Complete and review GMP documentation in a timely manner. ● Maintain appropriate level of training for assigned responsibilities. ● Assist with inventory management of supplies in the manufacturing facility. ● Assist with daily tasks and support manufacturing. Collaborate Effectively ● Be a team player, offer assistance, and respond well to requests for help from team members. ● Use strong communication and build relationships. ● Demonstrate technical acumen, operational understanding, and GMP compliance. ● Support operational excellence initiatives. ● Support a culture of safety and GMP compliance. ● Identify opportunities for continuous improvement.

Skills

Gmp, cell therapy

Top Skills Details

Gmp,cell therapy

Additional Skills & Qualifications

• A Minimum of 4 years’ experience in GMP biopharmaceutical operations preferably with experience in cell therapy, mammalian cell culture, and/or microbial fermentation. ● Experience with quality management systems (e.g. Deviations, CAPAs, Change Management). ● Experience with electronic systems such as MES and ERP. Lyell Immunopharma ROLE DESCRIPTION KNOWLEDGE, SKILLS AND ABILITIES: ● Familiar with regulations for GMP manufacturing of drug substance, drug products, cellular and gene therapies, and viral vectors for clinical phase therapies. ● Proven track record in cGMP manufacturing operations, including producing therapies safely and right the first time. ● Fast learner, adaptable, and excellent cross-collaboration and inter-personal skills. ● The desire and ability to work in a fast-paced, start-up environment. PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. While performing their duties, the employee must be able to do the following: ● Confirm visual information in the environment such as batch record and SOP steps were completed properly, parameters on equipment and computer screens, status of materials and equipment, and perform visual inspection of materials and product. A vision test may be required. Use of corrective lenses is acceptable. ● Stand and step over a gowning bench (12-24”) and aseptically don head-to-toe nonsterile and sterile gowns.

Experience Level

Intermediate Level

Job Type & Location

This is a Contract position based out of Bothell, WA.

Pay and Benefits

The pay range for this position is $36.06 - $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 Dec 5, 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.