Job Description
Manufacturing Biotech Associate – a site-based role on a 24/7 shift. This position is responsible for the production of biologic drug substance within a self‑directed shift team, ensuring compliance with GMP, EHS, and continuous improvement practices.
Responsibilities
Prepare, operate and monitor equipment, use business systems, and perform tasks including cleaning, validation, and in‑process testing.
Execute automated recipes using paperless technology to produce drug substance through inoculation, cell culturing, filtration, and purification.
Set up single‑use equipment between runs and follow GMP and EHS standards, optimizing processes with standard work and lean techniques.
Contribute to a culture that prioritizes patient delivery, safety, right‑first‑time execution, and peer engagement.
Qualifications & Experience
Scientific or engineering qualification or equivalent.
0–3 years’ experience in the biotechnology and/or pharmaceutical industry or equivalent.
Experience in a highly regulated pharmaceutical manufacturing environment.
Knowledge of biologic drug substance production; experience is an advantage.
Strong teamwork, initiative, logical thinking, and the ability to perform under pressure.
Flexible, self‑motivated, and proactive mindset.
As an equal opportunity employer, we embrace diversity, talent, and commitment across all roles.
Required skills include analytical problem solving, GMP compliance, manufacturing operations, quality control, and related technical competencies.
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