Manufacturing Supervisor

RecruitmentPlus; Newry; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading company in Newry is seeking a Manufacturing Supervisor to oversee production operations. The ideal candidate will have relevant manufacturing experience or a degree in a related field. Responsibilities include managing a team, ensuring compliance with quality standards, and driving improvements in production efficiency. This role requires excellent communication skills and the ability to motivate others. If you meet these qualifications, apply now to join a successful organization.

Benefits

Pension

Health assurance

Life assurance

Qualifications

• 4 years relevant manufacturing experience or a degree.
• 1 years+ experience in the pharmaceutical industry.

Responsibilities

• Assist in the day to day running of the production facility.
• Co-ordinate, plan and supervise a team of operators.
• Provide timely, detailed and accurate reports on manufacturing operations.

Skills

Excellent communication skills

Ability to motivate and train team members

Technical experience

Ability to prioritise and meet targets

Education

Degree in Pharmacy, Science, Engineering or Mathematics

Relevant manufacturing experience

Tools

Microsoft packages

Job description

Salary: Competitive plus pension, health, life assurance plus others

Job Type: Permanent Location: Newry Co. Down / Armagh Ref: S011724

RecruitmentPlus on behalf of our client have a great opportunity to join a highly successful organisation in Newry as a Manufacturing Supervisor.

Must be able to work on a rotating shift pattern including days and nights.

This role will be based in a site that produces and handles penicillin, and as such, this role would not be suitable for those that have a penicillin allergy.

Requirements:

• 4 years relevant manufacturing experience OR a degree or third level qualification in Pharmacy, Science, Engineering or Mathematics (or a closely related area)
• Technical experience in a related manufacturing environment.
• Able to demonstrate ability to motivate and train team members.
• Ability to issue and review technical reports and documents based on strong methodical rationale (either in an education or employment environment).
• Ability to prioritise and meet targets.
• Excellent communication skills both verbal and written
• Ability to work extra hours to meet the needs of the business.
• Proficient in all Microsoft packages.
• Applicants should be able to provide proof that they have a right to work in the UK at the time of their application.
• 1 years+ experience in the pharmaceutical industry.
• Experience of working in a regulated environment.
• Experience of control of cross contamination (microbial or chemical).
• Experience of controlling production documentation processes (including a document management system).
• Experience of documentation associated with a quality management system.

Key Duties & Responsibilities:

• Assist in the day to day running of the production facility.
• Comply with all aspects of the Quality, Environmental Management Systems and Health and Safety policies.
• Co-Ordinate, plan and supervise a team of operators ensuring that production goals and targets are met.
• Manage assigned personnel and provide feedback where required.
• Work to build strong cohesive teams both within the department and cross departments within the company.
• Provide input into the systems and procedures to ensure the efficient running of the production department.
• Maximise output and efficiency while looking for opportunities to drive improvements.
• 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.
• Ensure operatives maintain all records (e.g. Production Control Records, training records and log books).
• Create and review procedures and documentation associated with the manufacturing process for commercial products.
• Ensure cleaning of equipment and facilities is carried out in accordance with the relevant procedures to avoid contamination.
• Liaise with other departments such as Engineering, Process Excellence, Validations and Quality and actively engage in continuous improvement programs.
• 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.
• Ensure that team members are aware of issues which may affect them doing their duties and that information disseminates throughout the department.
• Assume responsibility for assigned Operational and Compliance metrics.
• Work towards the company mission, strategy and culture.
• Undertake any other duties, which may be assigned by Senior Management.

If you have the relevant qualifications and experience and are interested in this position, please apply now and Ciara who is based in our Northeast office will be in contact if you are suitable.

If you are living in Ireland and hold a VALID WORK PERMIT, please feel free to contact us directly. However, if you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search.

Recruitment Plus is not in a position to respond to each individual application due to the high volume of submissions. We will only contact those candidates whose CV matches the criteria for the vacancy. Thank you for your patience.

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