Biopharma Manufacturing Technician: Upstream/Downstream

Partner Therapeutics, Inc.; Lynnwood (WA); Ibrido; USD 60.000 - 72.000; Tempo pieno

Vantaggi offerti da questo lavoro

Hybrid/Remote workplace program

Annual bonuses

401k matching

Wellness program

Paid time off

Gym subsidy

Tuition assistance

Free parking

Orca pass

Descrizione del lavoro

Partner Therapeutics, Inc. in Lynnwood, WA is seeking Senior Manufacturing Technicians to support cGMP operations, upstream (fermenters and filtration) and downstream (HPLC and low-pressure chromatography) activities.

You will perform a variety of GMP tasks, operate production equipment per SOPs, prepare media and buffers, conduct CIP/SIP, test filters, maintain clean areas, comply with safety standards, and complete required training on time.

Competenze

• High School Diploma or GED required.
• 2+ years of relevant work experience or certification/degree in biopharmaceutical manufacturing.
• Associate or BA/BS in science/engineering preferred.
• GMP/cGMP manufacturing environment experience is a plus.

Mansioni

• Operate process equipment (fermenters, chromatography systems) per SOPs.
• Operate autoclaves, media and buffer prep equipment per SOPs.
• Perform CIP/SIP to prepare equipment for manufacturing.
• Prepare media and buffers (weighing, measuring, mixing, filtering).
• Test filter integrity and perform regular equipment maintenance.
• Maintain tidy, compliant work area and follow safety policies.
• Complete mandatory Quality and Compliance training on schedule.
• When not manufacturing Leukine, revise controlled documents and maintain training.

Conoscenze

Respirator use

PPE compliance

Problem solving

Teamwork

English communication

MS Office

Formazione

High School Diploma or GED

Associate degree in science/engineering (preferred)

BA/BS in science/engineering (preferred)

Strumenti

MS Office

Descrizione del lavoro

Partner Therapeutics, Inc. in Lynnwood, WA is seeking Senior Manufacturing Technicians to support cGMP operations, upstream (fermenters and filtration) and downstream (HPLC and low-pressure chromatography) activities.

You will perform a variety of GMP tasks, operate production equipment per SOPs, prepare media and buffers, conduct CIP/SIP, test filters, maintain clean areas, comply with safety standards, and complete required training on time.