Aseptic Technician III

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Bio Life Solutions is repeatedly named one of Washington’s 100 Best Companies to Work For, a list curated by Seattle Business Magazine. We welcome you to apply to join our dynamic, high-energy team. Here you will find a performance‑based, family‑oriented environment where authentic communication and treating colleagues with respect are required. Our employees receive a competitive benefits package, which includes generous company stock awards and a 401k matching program.

Bio Life Solutions is a leading developer, manufacturer and supplier of class‑defining cell and gene therapy bioproduction tools and services. Our solutions facilitate basic and applied research and commercialization of new therapies by maintaining the health of biologic source material and finished products during manufacturing, storage, and distribution. Our solutions offer commercial companies and clinical researchers significant improvement in shelf life and post‑preservation viability and function of biologic materials.

Our tools portfolio includes our proprietary, serum‑free and protein‑free, fully defined Cryo Stor freeze media and Hypo Thermosol shipping and storage media, ThawSTAR family of automated, water‑free thawing products. For more information, visit

The Aseptic Technician III is a core team member of the manufacturing team. The role is responsible for daily production including environmental monitoring, formulation, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem‑solving skills. It provides an opportunity to solve challenges in a fast‑growing industry.

60‑70% of job duties are directly related to routine processes of bulk formulation, filling, and packaging of Quality System regulated compliant media products. This includes but is not limited to:

• Disinfecting and transferring materials and equipment into the cleanroom for production.
• Working inside cleanroom suites on your feet for several hours at a time.
• Performing environmental monitoring.
• Weighing, measuring, and checking raw materials to ensure batches manufactured contain proper ingredients and quantities.
• Aseptically filling solutions into finished product containers under sterile conditions.
• Performing washing of labware used in GMP manufacture.
• Cleaning equipment and classified cleanroom facility (ceiling, walls, critical surfaces, and floors).
• Performing repetitive tasks while gowned (hood, mask, coveralls, boots, gloves, etc.).
• Operating equipment such as balances, volumetric glassware, peristaltic pumps, filters, pH meter, and pipettes.
• Performing all tasks while following all SOPs, batch records, and safety policies.
• Accurately completing batch record documentation, all appropriate logbook entries, and GMP documentation.

30‑40% of job duties include indirect manufacturing support projects. This includes but is not limited to:

• Performing preventive maintenance on manufacturing equipment.
• Conducting root‑cause investigations for quality issues.
• Performing validation activities as needed.
• Revising batch record and SOPs.
• Proposing champions and implementing process improvements.
• Supporting training programs and sharing knowledge of processes.
• Training new manufacturing team members and serving as a source of knowledge and information.
• Real‑time reviewing production records (GDP) to ensure operators are documenting procedures in real time.
• Leading cross‑departmental projects.

Additional responsibilities may include:

• May be required to work either day or evening shift as needed.
• May occasionally be required to work weekends and overtime as needed.
• Required to be on‑call for equipment monitoring on a rotation.
• Duties, responsibilities, and activities may change at any time with or without notice.

• Bachelor’s degree and 2 years of manufacturing experience; or Associate degree/biotech certification and 3 years of relevant experience; or…