Support the installation and qualification of new manufacturing equipment, and own/oversee assigned equipment packages.
Develop and implement operational procedures, including SOPs, master batch records, and work instructions.
Develop and manage manufacturing staff to support validation activities and batch execution.
Ensure adherence to quality standards and client requirements for aseptic processes such as cleaning and decontamination, sterilization, aseptic filling, and plunger stoppering.
Collaborate with Engineering and Maintenance to ensure timely calibration and validation of production equipment.
Work with Manufacturing Science & Technology (MSAT), Validation, Quality, and QC teams to ensure procedures are developed and personnel are trained for new product introductions.
Stay informed on global regulatory requirements (FDA, EMA, PIC/S, ICH) for aseptic manufacturing and product introduction, and remain up to date on current Good Manufacturing Practices (cGMP).
Maintain compliance with training requirements for self and staff.
Be accountable for the specified cleanroom environment and ensure adherence to stringent requirements, with flexibility to oversee execution during off-hours and work in a shift rotation, if needed.
Travel as necessary for project oversight, site visits, and training.
Be available for extended periods for overseas training.
Education
Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Biological Sciences or related field.
Master's degree or MBA is a plus.
Experience
6+ years in drug product manufacturing, with experience in aseptic processing.
2+ years of people management experience
Skills
Direct experience in aseptic qualification (e.g., media fill simulations) and drug product manufacturing such as decontamination, sterilization, aseptic filling and plunger stoppering.
Experience in a fast-paced CDMO (Contract Development and Manufacturing Organization) environment is desirable.
Strong interpersonal skills and ability to interact and manage team effectively.
