GMP Production Supervisor - 6 month contract

Job Title: GMP Production Supervisor

Location: Nottingham

Contract: 6 months

Hours: 5 days per week - alternating shifts (6am-2pm, 2pm-10pm)

Salary: Experience dependent - via Umbrella Inside IR35 +17.5% shift uplift

Please note: this role does not offer any VISA sponsorship, to be eligible for the role you must have the right to work in the UK.

i-pharm consulting is working with a multinational corporation. They are a global provider of delivery technologies, development, drug manufacturing, biologics, gene therapies and consumer health products. They are the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. Join them today as a GMP Production Supervisor at their site in Nottingham.

Overview:

To support and manage the manufacturing operators, schedule operator workload for short to medium term and compliance of GMP Manufacturing and cleaning activities. Responsible for directing manufacturing staff to ensure the timely delivery and Right First-Time execution of manufacturing operations for development projects and manufacturing batches.

Responsibilities:

• To manage the 'hands-on' day-to-day running of the Production area to ensure all operations are undertaken and facilities maintained in accordance with company Quality Management System and Standard Operating Procedures (SOP`s).
• To carry out GMP Manufacturing activities according to clearly defined documentation and cleaning validation processes.
• Ensuring that the recording of tasks and events on the batch manufacturing documentation is carried out both timely and accurately in accordance with GMP's.
• Support the Clinical Manufacturing Management team, undertaking direct supervision of Pharmaceutical Operators within the GMP Manufacturing Facility ensuring that all clinical manufacturing activities are undertaken to a high standard of quality in accordance with exemplary Good Manufacturing Practice (cGMP) across a full range of dosage forms (solid, semi-solids, solutions, suspensions, ointments and creams).
• Batch Sampling Activities
• Daily compliance checks of Batch documentation, equipment and facility logbooks to ensure continual compliance.
• Ensuring tasks are undertaken and completed in full and in a compliant manner in line with scheduled activities as directed by GMP Production Manager.
• cGMP compliance activities related to manufacturing equipment, documentation and facilities
• Assisting in internal audit programmes, Unplanned Deviation Investigations and Corrective and Preventative Action (CAPA) Management as directed by Clinical Manufacturing Senior Management Team.
• Cross functional collaboration with Validation, Quality Assurance, Analytical Services, Engineering, and Project Management functional areas to plan and implement the execution of cGMP activities in Manufacturing Operations for both development processes and commercial operations.
• Ensure all departmental staff are appropriately trained with training records to corroborate this in a timely manner across all GMP Manufacturing activities.
• Ensure timely and compliant GMP room clean-down/cleaning verification activities undertaken.
• Ensure all key processing equipment are appropriately validated and calibrated to meet GMP Manufacturing needs.
• Ensure compliant GMP Facility, including, but not limited to Management of the Environmental Monitoring System (EMS), investigation and reporting of out of specification incidents.

Education or Equivalent Requirements:

• A minimum of 5 years' experience in a GMP Pharmaceutical Manufacturing environment, preferably across a broad range of dosage forms, with some supervisory experience.

Knowledge/Skills Requirements:

• Ability to work effectively under pressure to meet deadlines
• Proficient (excellent) in English verbal and written communication skills to convey and receive ideas and instructions to/from others within and outside the organization
• Ability to effectively present information and respond to questions from peers, management, suppliers and customers.
• Proficient skills in Microsoft Office applications (Word, Excel, PowerPoint, Access).
• Strong GMP Compliance.
• Excellent numerical skills.

If you are interested in finding out more about this role or others, please contact Manpreet Bhullar at mbhullar@i-pharmconsulting.com or call +44020 7551 0802