Company Info

Job Description

As the 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 and Media & Buffer Preparation.  This position requires a 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 Tevas 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 and Media & Buffer Prep
• 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 support preparations and closure of GMP operations through the creation, update and approvals of GMP documents.  This include Standard Operating Procedures, Batch Records, Quality Investigations are related to production, and the like.  You will also be required to maintain 100% training compliance on all SOPs and safety procedures for self and team.
• This role will require standing, walking, bending and reaching for extended periods of time throughout the workday.
   

Qualifications

What you bring to the role:

• Associates 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
• Demonstration of strong management skills and capabilities
• 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 SOPs and batch documents.
• 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 SOPs, 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.
   

Function

Sub Function

Reports To

Senior Director, Manufacturing and Operations

Already Working @TEVA?

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

Tevas Equal Employment Opportunity Commitment