Pharmaceutical Manufacturing Specialist

Berry Recruitment; Oxford; On-site; GBP 40,000; Full time

Job summary

A recruitment agency is seeking a Pharmaceutical Manufacturing Specialist for a pharmaceutical company in Oxford. This full-time permanent role involves supervising production, ensuring compliance with regulations, and assisting in the training of operators. The ideal candidate will have experience in a CGMP environment, strong communication skills, and proficiency in Microsoft Office. Salary is £40,000 per annum, and applications can be made through Berry Recruitment.

Qualifications

• Experience in supervision within a CGMP environment is essential.
• Must understand quality, environmental, and health & safety compliance.
• Excellent communication and interpersonal skills are required.

Responsibilities

• Support the Production Department to ensure compliance.
• Supervise the Production department when needed.
• Assist with manufacturing cleanroom schedule control.

Skills

Experience in the supervision of Production Operators within a CGMP environment

Sound understanding of regulatory and compliance requirements

Good communication and interpersonal skills

Proficient use of Microsoft Office

Job description

Overview

Berry Recruitment are NOW hiring for a committed and experienced Pharmaceutical Manufacturing Specialist to work for a pharmaceutical company in Oxford.

Role: Pharmaceutical Manufacturing Specialist

Salary: £40,000 per annum

Location: Oxford, Oxfordshire

Hours: Full time - Permanent

Key Responsibilities

• To support and assist in an effective Right First-Time approach within the Production Department to ensure compliant delivery of processes on time and in full.
• In the absence of the Production Supervisor, Supervision of the Production department.
• Assist the Production Supervisor with the implementation and control of the manufacturing cleanroom schedule
• Ensuring that all equipment is in a state of readiness to perform batch manufacture
• Effective communication to staff of requirements as stated in standard operating procedures and assuring compliance with these procedures
• Training Production Operators in line with written procedures and maintenance of training records.
• Providing motivation for individual staff members to develop technically
• To ensure effective departmental communications
• Assuring high standards of technical performance within the Production Department by effective interaction with line management to best serve clients.
• Assisting in local projects to optimise site performance and regulatory compliance.
• Updating production documentation as required via the change control process
• Raise, investigate and document deviations to the manufacturing processes
• Utilise the software available for stock control, ensuring accurate deductions and additions to stock levels
• To assist wherever required within the Production department

About you

• Experience in the supervision of Production Operators within a CGMP environment
• Sound understanding of the regulatory and compliance requirements of the business particularly with regards to Quality, Environmental and H&S (Health & Safety)
• Good communicate and interpersonal skills
• Proficient use of Microsoft Office

No candidate will meet every single desired qualification we have listed. If your experience looks a little different but you think you can role; value to the role, we'd love to learn more about you!

For more information and to apply, contact the Oxford branch of Berry Recruitment – 01865 777733 or click 'Apply Now' to submit your application.

Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job.