Job ref: CC240625 Job type: Permanent Location: Monaghan Closing date: Tuesday 08 Jul 2025 13:00 Job Overview To assist in the day to day running of the Norbrook production facility and help improve output and efficiencies.
Main Activities/Tasks Review and record relevant production KPls.
Processing and reviewing PCRs and SPRS on site in a timely manner.
Ensure all records such as cleaning records, logbooks and calibration records are maintained by operatives.
SOP Custodian for site.
Ensure training of staff on most recent versions of SOPs is carried out.
Responsible Employee, issuing Working Copy stamped documentation on site e.g.
appendices, generating logbooks etc.
Request and review PCR's, SPRS and relevant appendices.
Safety Understand and follow the company's Health & Safety policies.
Ensure a 'safe culture' and an appreciation of the materials, processes and systems is embedded within the organisation.
Act as point of contact for external contractors and fill out work orders on site.
Operational 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.
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.
Assume responsibility for assigned Operational and Compliance metrics.
Undertake any other duties, which may be assigned by Senior Management.
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.
Reporting through the QA Department, you will have the responsibility to approve and control the issuing of Working Copy Documents for the recording of data within the GMP environment Corporate Work towards the company mission, strategy and culture Essential Criteria: A level qualification in English and Maths (or a closely related area) Able to demonstrate ability to motivate and train team members.
Ability to prioritise and meet targets.
Excellent communication skills both verbal and written Proficient in all Microsoft packages Duration: Full time, Permanent Location: Newry Additional Information: Applicants should be able to provide proof that they have a right to work in the Ireland at the time of their application.
Applicants who are unable to provide this proof will not be considered.
We regret that applications received after the closing date and time will not be accepted.
We are unable to sponsor or take over sponsorship of a Visa at this time.
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