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O firmie AbbVie
Misją AbbVie jest odkrywanie i dostarczanie innowacyjnych leków, które już dziś rozwiązują poważne problemy zdrowotne i stanowią odpowiedź na medyczne wyzwania jutra. Dążymy do wywarcia znaczącego wpływu na życie ludzi w kilku kluczowych obszarach terapeutycznych: immunologii, onkologii, neurobiologii, pielęgnacji oczu, wirusologii, zdrowia kobiet i gastroenterologii, a także w zakresie produktów i usług z portfolio Allergan Aesthetics. Aby uzyskać więcej informacji o AbbVie odwiedź nas na www.abbvie.com. Obserwuj @abbvie na portalach Twitter, Facebook, Instagram, YouTube i LinkedIn.
Supervisor, Manufacturing III
Worcester, Massachusetts Identyfikator oferty 2202275 Kategoria Manufacturing & Operations Dział AbbVie- • Reviews daily production schedule and priorities to determine unit (suite) assignments and critical actions.
- • Reviews all materials and batch records required to support shift and any off-shift needs for the day.
- • Provides on the floor training to support formalized technical and cGMP training. Checks that operator training files match and support the processes they are required to carry out.
- • Monitors operator training files and works with compliance specialist to keep files up to date.
- • Works with QA and Subject Matter Expert (Tech Ops or Process Sciences) to resolve exceptions.
- • Works with technology transfer team to incorporate new processes in the plant.
- • Reviews new Batch records and SOPs.
- • Provides supervision primarily to skilled nonexempt and junior level exempt employees. Acts as advisor to unit or sub-unit, becomes actively involved as required. Acts as mentor for less senior personnel.
- • Evaluates staff performance.
- • Requires a Bachelor’s degree or equivalent. • Five plus years’ experience in all aspects of manufacturing/ production processes
- • Computer proficiency and scheduling experience required; good writing skills required.
- • Familiarity with industrial automation (e.g., distributed control and PLC-based systems)
- • Working knowledge of safety, quality systems, and cGMPs is required
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