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Over AbbVie
De missie van AbbVie is het ontdekken en leveren van innovatieve geneesmiddelen die vandaag een oplossing bieden voor ernstige gezondheidsproblemen en de medische uitdagingen van morgen aanpakken. We streven ernaar om een grote impact te hebben op het leven van mensen in verschillende belangrijke therapeutische domeinen: immunologie, oncologie, neurowetenschappen, oogzorg, virologie, vrouwengezondheid en gastro-enterologie, naast producten en diensten uit de portefeuille van Allergan Aesthetics. Bezoek www.abbvie.com voor meer informatie over AbbVie. Volg @abbvie op Twitter, Facebook, Instagram, YouTube en LinkedIn.
Supervisor, Manufacturing III
Worcester, Massachusetts Job ID 2202275 Categorie Manufacturing & Operations Afdeling 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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