Manufacturing Supervisor

1 month ago

Newry, United Kingdom Norbrook Laboratories Full time

In Norbrook we pride ourselves in being one of the top companies in Northern Ireland and one of

the top veterinary pharmaceutical companies globally. We develop & manufacture veterinary

medicines, supplying products to 120 countries globally. With a strong portfolio of existing products

and significant investment in R&D to launch new products annually, we have opportunities for

individuals to join us and develop their career in a global company.

Our business strategy is supported by our Values - Customer Value, One Team, Results Driven,

Excellence, Innovation, and Quality - and we support our employees to live the behaviours that

creates our culture. Our on-going success is based on the expertise, knowledge and innovation of

our employees. If you are interested in joining our team here at Norbrook and supporting our vision,

**Job Overview**

Norbrook laboratories are looking to fill the role of Manufacturing Supervisor. The main duties of the
role are:
To manage a team of people in all aspects of manufacturing in order to produce products complying

with all aspects of the Norbrook Quality and Environmental Health and Safety systems.

This role will improve the performance of the Production department providing supervision and

support.

**Main Activities/Tasks
**SAFETY **

Understand and follow the company’s Health & Safety policies.

Comply with the environmental management system and minimise environmental impact

where possible.

Ensure a ‘safe culture’ and an appreciation of the materials, processes and systems is

embedded within the organisation.

Coordinate and plan the smooth running of the department.

Supervise a team of operators ensuring that production goals and targets are met.

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 products are produced according to the appropriate Production Control Record in

order to obtain the required quality.

Ensure operatives maintain all records (e.g. Production Control Records, training records and

log books).

Ensure documentation is signed and countersigned at each stage of the process as required.

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 to ensure all production equipment and areas are fully compliant with all GMP and

customer requirements.

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.

Undertake any other duties, which may be assigned by Senior Management.

**OPERATIONAL **

Assist in the day to day running of the Norbrook production facility.

**QUALITY **

Comply with all aspects of the Norbrook Quality System.

Ensure that a ‘quality culture’ and an appreciation of the quality system is embedded within
the organisation.

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.

Participate in investigations and suggest CAPAs for manufacturing issues.

Ensure all documentation (e.g. production control records, log books, training records etc) are
completed in line with good manufacturing practices and expectations.

Ensure all assigned quality events (e.g. deviations, complaints, CAPAs, change controls etc) are
addressed in a timely manner.

Identify true root cause in all quality related investigations to prevent reoccurrence and
improve compliance, product quality and safety.

Perform regular internal compliance audits against the appropriate regulations to ensure an
audit ready Production facility.

**PERSONNEL MANAGEMENT **

Manage one shift on various shift rotations, which may include but is not limited to three shift
patterns or four shift continental style shift patterns.

Manage assigned personnel and provide feedback where required.

Work to build strong cohesive teams both within the department and cross departments
within the company.

**LEARNING & DEVELOPMENT **

Ensure

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