Sterile Fill Finish Manufacturing Support

Job Description

The purpose of this position is to be the subject matter expert in supporting of Sterile Fill Finish operation and be a recognised expert in this industry.

She/He needs to also ensure equipment is maintained in a validated state meeting cGMP requirements. Development, deployment and improvement of validation processes is key to ensure the maximum levels of performance and compliance are maintained.

Qualifications & Experience

• Preferred candidate to be Qualified to a minimum of higher degree level in Operations Management, Manufacturing engineering or related Science discipline.
• Minimum 10 year's Manufacturing experience at operational lead or supervisor level within a Sterile Manufacturing environment.

Skills

• Ability to understand Manufacturing processes through a logical, data driven, hands on approach.
• Knowledge of sterile Manufacturing and aseptic processing techniques
• Can interact with audits (internal and external)
• Excellent report writing skills.
• Ability to develop and coach more junior members of team.