We are seeking a motivated Manufacturing Technician to join a production team in a high-growth biotechnology environment. This role is instrumental in executing the daily manufacturing schedule for clinical and commercial-grade viral vectors and cell therapies. Operating within an ISO-classified cGMP cleanroom, you will handle critical upstream and downstream unit operations-from cell expansion to final fill/finish. The ideal candidate is a disciplined professional who thrives in a fast-paced environment and is committed to maintaining the highest standards of safety and quality to deliver life-altering therapies to patients.
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Responsibilities:
Execute aseptic processing tasks within Grade B/C cleanrooms and Biological Safety Cabinets (BSCs).
Support cell culture activities, including cell expansion, media preparation, and the operation of various bioreactor platforms.
Perform purification techniques such as chromatography (column packing and running) and Tangential Flow Filtration (TFF).
Complete Batch Records, equipment logs, and other production forms in real-time following Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).
Set up, calibrate, and troubleshoot semi-automated and automated manufacturing equipment; perform specialized cleaning and sterilization (autoclave/VHP).
Assist in room and isolator monitoring to ensure the integrity of the controlled environment.
Participate in deviation investigations and identify opportunities for continuous improvement in facility operations.
Monitor and kit raw materials and reagents to ensure readiness for upcoming production runs.
Working hours: 7:00 AM - 5:00 PM
Skills:
1-3 years of experience in a pharmaceutical or biotech manufacturing environment (CDMO experience is a plus).
Associate's or Bachelor's degree in Biotechnology, Biology, Chemistry, or a related science discipline.
Prior experience with upstream (bioreactors) or downstream (chromatography/filtration) operations.
Familiarity with Laboratory Information Management Systems (LIMS), ERP systems (like SAP), or electronic batch records.
Strong critical thinking skills and the ability to act as a subject matter expert for specific equipment or assays.
Education:
Bachelors
Experience:
1-4 years
Qualifications:
Ability to operate and troubleshoot complex laboratory or manufacturing instrumentation.
Understanding of cGMP principles and the importance of following Standard Operating Procedures (SOPs) without deviation.
Demonstrated ability to work safely with biological materials and maintain sterility in a cleanroom setting.
Ability to stand for long periods, work in full cleanroom gowning (including respirators if required), and lift up to 40 lbs.
Excellent verbal and written communication skills; ability to work effectively within a cross-functional team (QA, QC, and MSAT).
High School Diploma or GED (with relevant experience) or an Associate???s degree in a scientific field.
Apply today! #wka123
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Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).