Inventory Control Specialist

ROLE SUMMARY

The Andover Clinical Manufacturing Facility (ACMF) is a new facility located on the Pfizer Andover, MA campus responsible for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio.

The IM Coordinator is part of the ACMF Inventory Management team, which is responsible for forecasting, procuring, receiving, maintaining and distributing cGMP materials in support of ACMF clinical drug substance manufacturing.

ROLE RESPONSIBILITIES

• Serve as the primary owner for development and ownership of Inventory Management processes (senior role).
• Forecasting raw material / consumable needs in cooperation with the ACMF Tech Transfer and Operations teams.
• Establishing sophisticated tracking mechanisms for materials inventory, forecasts, burn rates and order status tracking.
• Procurement of materials. Keeping close contact with materials vendors to update delivery timelines and collect receipt documentation.
• Working with ACMF Tech Transfer team to present "campaign enabling" status reports for material deliveries.
• Supporting ACMF Warehouse Technicians in all warehouse functions when needed (material moves, material receipts, shipping, etc.).
• Authorship of SOP's for inventory management processes.
• Training of colleagues as needed.
• Support implementation of new technologies and equipment.
• Support and author investigations as needed.
• Support facility audits as needed.

BASIC QUALIFICATIONS

• BS/BA in Chemical Engineering, Biotechnology, Microbiology, Cell Biology, Biochemistry, Supply Chain Management or related field.
• 4-8 years of experience in a laboratory or GMP manufacturing environment.
• Advanced Microsoft Excel skills (and/or similar programs).
• Ability to execute against SOP's and document entries in a compliant manner.
• Demonstrated capability to work as a team member in a matrix manufacturing team.
• Excellent oral and written communication skills.
• Ability to work under minimal supervision.
• Must be able to climb flights of stairs, and remain standing for 1-2 hours.
• Must be able to lift up to 50 lbs.
• Ability to work off shift (Nights and Weekends) as needed; non-routine.
• Ability to work in a clean room environment as needed; non-routine.

PREFERRED QUALIFICATIONS

• Experience with Warehouse operations and concepts.
• Experience with purchasing, procurement and vendor relationships.
• Experience in a GMP manufacturing role.
• Experience with Production Control Systems (i.e. DeltaV), ERP Systems (i.e. Microsoft Dynamics and/or SAP) and other business systems (Document Management Systems, LIMS, Microsoft Word, Excel, etc.)

Other Job Details:

• Last Date to Apply for Job: 1/26/21
• Eligible for Employee Referral Bonus: YES

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EEO & Employment Eligibility

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Research and Development

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