Biopharmaceutical Production Supervisor

Category:

Manufacturing & Production

Employment Type:

Direct Hire

Reference:

BH-383834

Yoh is seeking a Biopharmaceutical Production Supervisor
for our Pharmaceutical Client in Saint Louis, MO. This is a direct-hire opportunity to join their growing team!

Industry:
Pharmaceutical
Location:
Saint Louis, MO
Type:
Direct Hire

Responsibilities

• Responsible for management of direct reports
• Responsible for executing the production protocols, scheduling activities, troubleshooting process anomalies
• Adhering to Quality Management Systems and completing associated documentation
• Collaborate daily with teams across the client site
• Execution of manufacturing batch records, work instructions / 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.
• 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.
• 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.
• Coordinates training with team either in class or on the floor, as needed.

• Bachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering, or related field is required
• 2+ years supervisory/leadership experience preferred (pharmaceutical industry preferred)
• 3-5 years' industry experience (ex. operating in a gowned, clean room)
• Experience in identifying deviations, aiding in investigations/root cause analysis, and providing input on major/critical deviations.
• cGMP exposure and experience
• Biologics experience is highly preferred
• Extensive knowledge of Downstream Production
• Knowledge of deviation investigations
• Knowledge of chromatography, cell culture, and aseptic techniques is strongly desired