Job Description

Job Title: Downstream Processing Supervisor (Band 6)

Location/Division Specific Information

St. Louis, MO/ Drug Substance Division (Biologics)

Discover Impactful Work:

• The supervisor is accountable for the success and oversight of downstream manufacturing processes. This means being responsible for the carrying out a variety of functions related to Downstream Biopharmaceutical Manufacturing. These functions may include but are not limited to activities such as conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance.

• Execution of manufacturing batch records, work instructions and/or SOPs, with minimal instruction on a day-to-day basis and a focus on proactive 'right the first time' executions. Assist with batch record reconciliation.
• Able to complete all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.
• Documentation of all activities to meet cGMP requirements. Daily record review, tasks, and databases.
• Forecast and resolve supply and raw material deficiencies. Identify and resolve scheduling conflicts with one week outlook.
• Identify deviations, aid in investigations/root cause analysis, and provide input on major/critical deviations.
• Represent manufacturing team at tier meetings.
• Practices and promotes safe work habits and adheres to safety procedures and guidelines.
• Utilizes manufacturing process knowledge and investigational skills to identify and resolve manufacturing issues and drive continuous improvement in process operations.
• Provides feedback on document revisions and/or document management including batch production records and manufacturing procedures.
• Maintain safe and clean work environment by educating and directing personnel to ensure compliance with established policies and procedures.
• Coordinates training with team either in class or on the floor, as needed.
• Helps build cross-functional relationships and enhances relationships with team members.
• Provides frequent feedback and coaching to others on ways to improve performance.
• Complete production plan by scheduling and assigning personnel, prioritizing tasks, supervising progress, revising schedules, resolving problems, and reporting results.
• Lead shift exchanges and daily huddles for team as required. Act as liaison with other groups within the manufacturing organization and a Subject Matter Expert on various techniques.

• HS Diploma/ GED required, Bachelor's degree preferred

• 5 - 9 years relevant work experience required based on education
• 2+ years supervisory/leadership experience preferred (pharmaceutical industry preferred)
• Experience in cGMP environment preferred

• Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred

• Strong math skills
• Critical thinking and problem-solving capabilities
• Detail Oriented
• Results Driven
• Efficient in MS Office

• Critical evaluation of processes, including foresight and thinking ahead.
• Able to read, write, and communicate in English
• Able to understand and carry out instructions
• Reliable
• Effectively multi-task
• Able to work in an environment of change
• Able to work independently and as part of a team
• Able to recognize problems developing, not just occurring
• Seeks and welcomes feedback and responds to coaching.

• Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions or hair care products, etc.)
• Able to adhere to clean room gowning requirements, including wearing Tyvek, Nitrile, and/or Latex gloves
• Ability to lift minimum of 25 lbs independently
• Ability to stand for 80% of shift