Production Supervisor

DEPARTMENT:

PRODUCTION REPORTING TO:

PRODUCTION MANAGER HOURS 40 hours per week Monday to Friday Day shift 07:45 16:15 Evening shift 15:45 12:15 MAIN

DUTIES AND RESPONSIBILITIES:

The post holder will be responsible for the safe, efficient and economical operation of the Manufacturing processes for Commercial and Development products in accordance with Good Manufacturing Practice. Meeting manufacturing targets and ensuring that the correct systems and procedures are in place. The post holder will supervise and assist in the development of a team of Process Operators, Senior Operators and Technicians.

JOB PURPOSE:

To co-ordinate and plan the smooth running of the Production department, whilst complying with all aspects of the Millicent Pharma Quality and Environmental Health and Safety systems as well as to MHRA, FDA and cGMP Standards. GENERAL DUTIES Leadership:
Demonstrate high levels of leadership and people management skills to personnel with the Department and across the site. Coach, mentor and encourage all production personnel to ensure they reach their full potential. Proactively develop and sustain cross and inter-departmental co-operation. Personnel:
Supervise a team of operators / senior operators and technicians ensuring that production goals and targets are met. Ensure that all operators / senior operators and technicians are adequately trained and are competent in the tasks they are undertaking. Ensure that team members are aware of issues which may affect them doing their duties and that information disseminates throughout the department.

Departmental:
Ensure efficient use of all plant and personnel; maximising the efficiency of the Production Department by minimising reject product levels and maximising yields. Coordinate and plan the smooth running of the department. Ensure raw / packing material, equipment, facilities and personnel are available to meet market demands. Provide timely, detailed and accurate reports on the status of manufacturing and packing operations, alerting the senior management of any issues which may impact on finished product quantities and availabilities.

Provide technical supervision and guidance within the Production department. Manage the validation and maintenance of all Production Facilities and Equipment to ensure they are fit for use. Lead investigations and suggest Corrective and Preventative Actions for manufacturing issues. Lead the change management process for manufacturing issues. Author and review scientific / technical reports and documents based on strong scientific rationale.

Create and review procedures and documentation associated with the formulation, testing and manufacturing process for commercial and development products. Manage Production ERP master data. Adhere to the principles of Good Manufacturing Practice ensuring product is manufactured within the defined parameters of the Quality Management System. Where deviations occur suggest and implement CAPAs. Perform regular internal compliance audits against the appropriate regulations to ensure an audit ready Production facility.

Provide input into the systems and procedures to ensure the efficient running of the production department. Actively engage in continuous improvement programs to ensure that all manufacturing activities are carried out in the most cost-effective manner, minimising reject levels and maximising yields to ensuring that daily production targets and annual departmental goals are met. Assume responsibility for assigned Operational and Compliance metrics.

Undertake any other duties, which may be assigned by Management. A full job description is available on request ESSENTIAL CRITERIA: A degree in Pharmacy, Science, Engineering or Mathematics (or a closely related area) Strong attention to detail and accuracy. Previous experience supervising others in a manufacturing environment GMP experience Ability to work effectively as part of a team. Proficiency in Microsoft Office, particularly Word and Excel Right to work in the UK.

DESIRABLE CRITERIA:
Further qualifications in Maths, Science, or Engineering. Experience in the pharmaceutical or food industry. Proven ability to prioritise tasks and meet targets. Technical experience in a related manufacturing environment.

Experience of validation activities. BENEFITS:
Company sick pay Discretionary bonus scheme Length of service awards Health care plan On Site Parking Cycle to work scheme 34 days leave per year inclusive of public holidays (FTE)…