Senior Manager, Manufacturing Services Details

Senior Manager, Manufacturing Services

Teva Pharmaceuticals - West Chester, PA

Employment Type : Full-Time

As the Senior Manager you will lead the Manufacturing Services group within the state-of-the art Biologics Manufacturing Facility (BMF) located in West Chester, PA. You will oversee Manufacturing Services functional groups including Weigh & Dispense, Media & Buffer Preparation, Warehouse Operations and Critical Cleaning. This position requires a highly motivated team player willing to contribute to the operation and overall success of the manufacturing operations group.

This is a high-visibility and critical position that supports manufacturing of Teva’s fast-growing innovative and biosimiliar biologics pipeline.

In this role you will:

• Lead in developing processes and procedures for the Manufacturing Services group that includes Weigh and Dispense, Media & Buffer Prep, Warehouse Operations & Critical Cleaning
• Lead and Perform cGMP operations within Clinical Manufacturing
• Contribute to the qualification and manufacturing readiness activities for the Manufacturing Service team
• Build and develop the Manufacturing Services Team

In addition to the above you will also oversee stocking of gowning supplies and removal of spent gowning from the Manufacturing facility, oversee removal and management of waste from the Warehouse and Manufacturing facility and oversee and coordinate facility cleaning and sanitization activities within the Manufacturing facility. You will also be required to maintain 100% training compliance on all SOP’s and safety procedures for self and team.

This role will require standing, walking, bending and reaching for extended periods of time throughout the workday.

What you bring to the role:

• Bachelor’s degree in Life Science or related field of study
• Minimum 6 years of experience in lead/supervisor role within GMP manufacturing environment
• Minimum 2 years of experience with formulating media and buffer solution preparations within a GMP environment

Preferred Qualifications:

• Minimum 6 years combined experience within cGMP Lead manufacturing role
• Experience with CGMP-compliant Warehouse operation
• Demonstration of continuous improvement initiatives
• Experience with process control SCADA software (e.g., WonderWare ).
• Experience with single use equipment and consumables.
• Experience authoring controlled documents, such as SOP’s and batch documents.
• Experience with biologics logistics, supply chain and warehouse operations.
• Experience with performance of parts washer and/or autoclave.
• Strong background in aseptic technique and microbial controls.
• Strong understanding of cGMPs as applicable to biologic operations.
• Ability to read, interpret, and follow SOP’s, batch documents and other procedures.
• Strong documentation skills to direct/generate process and procedure SOP, batch records and work instructions along with Experience in all areas of TrackWise system.
  

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.