Production Operator (11-Month Fixed Term Contract) Job Purpose: We are seeking an experienced Production Operator to join our team.
The successful candidate will work across multiple manufacturing activities, including manufacturing, filling, packaging, serialisation, inspections and in-process testing, to support the reliable production of high-quality pharmaceutical products.
This role requires full availability to work mainly day shifts, with early and late shifts as required.
A strong commitment to cGMP, safety, accuracy, and teamwork is essential.
Key Responsibilities: Operate, monitor, and adjust production, filling, packaging, and serialization equipment as trained.
Perform IPC (In-Process Control) tests, inspections, and quality checks.
Complete batch records, logbooks, and electronic documentation in accordance with cGMP.
Implement and maintain high standards of cGMP and SOP compliance in all activities.
Carry out area clearances, equipment cleaning, and housekeeping to ensure audit readiness.
Report any deviations, OOS results, inefficiencies, or breaches of SOPs, safety or environmental procedures.
Make minor machine adjustments where required to maintain efficient operations.
Support the Operations schedule by working collaboratively with team members and other departments (QS, QC, Engineering, Maintenance, Warehouse).
Assist in the training of new Operators and maintain your own training records up to date.
Participate in Continuous Improvement (CI) / Lean activities and site projects.
Wear appropriate PPE and work safely at all times, reporting any incidents, injuries, or material loss (spills/contamination).
Transfer between Operations areas as required to support business needs.
Qualification / Experience / Skills: The successful applicant must possess the following knowledge, skills, qualifications, attributes and experiences.
Previous experience in manufacturing operations (essential).
Experience in the pharmaceutical, medical device, food, or other GMP-regulated sector (strong advantage).
Strong understanding of cGMP and SOP-based working practices.
Experience with batch documentation, IPC testing or equipment operation.
Basic computer literacy.
Experience with ERP/MES systems (e.g., SAP) is beneficial.
Full availability to work early and late rotating shifts if required.
Leaving Certificate or equivalent.
Technical or manufacturing qualifications are an advantage.
Key Competencies Accuracy, strong attention to detail, and high standards of documentation.
Commitment to quality, safety, and compliance.
Ability to work effectively within a team and maintain positive working relationships.
Strong communication skills and a proactive attitude.
Flexibility to support different Operations areas and changing priorities.
Demonstrated initiative and willingness to contribute to CI / Lean activities.
Respect for confidentiality, professionalism, and alignment with company values.
Helsinn Birex Pharmaceuticals - we are a global pharmaceutical company and a leader in supportive care focused on improving the health and quality of life of patients with cancer and chronic diseases.
For more information, please visit our company website ( Skills: Production line GMP Manufacturing Pharmaceutical Production Operator Benefits: Health Insurance Performance Bonus Parking Space with EV Charger Subsidized Canteen Pension Scheme