Benefits
- Competitive salary
- Annual bonus based on company performance
- Health care and wellbeing programmes
- Pension plan membership
- Shares and savings programme
In this role you will…
- Work with a range of equipment and technology within a Steriles Business Unit, including inspect, assembly, and packaging of vials.
- Work shift‑based, likely 24/7 or 24/5.
- Support day‑to‑day breakdown repairs of production and plant equipment.
- Complete Planned Preventative Maintenance (PPM) schedules and breakdown maintenance activities.
- Provide support for localised area projects, including new product introductions.
- Complete tasks within Engineering Change Controls.
- Prepare, complete, and own GMP safety and quality documentation.
- Be accountable for the delivery of SAP/MERPS activities such as work orders, notifications, data maintenance, and ordering of plant spares.
- Deliver continuous improvement to drive increased performance in line with EHS and quality improvement objectives and KPIs via the use of GPS tools.
- Engage in equipment upgrades and obsolescence management through continuous improvement.
- Self‑manage training compliance metrics.
- Perform calibration of equipment instrumentation.
- Supervise internal and external contractors, ensuring GMP standards and reviewing contract company details for accuracy.
- Manage sterile and terminally sterilised processes of products, including boundary control and contamination prevention.
- Handle building infrastructure specific tasks concerning building fabric, electricity, piped services supply, and drainage.
- Operate and maintain systems such as air compressors, VHP, and refrigeration systems.
- Positively engage with stakeholders, ensuring relevant contract details are accurate.
- Deliver data cleansing activities to ensure optimum data maintenance.
- Maintain compliance with the role, department, and site procedures, processes, and systems.
- Manage the creation and changes to SAP vendor data.
Basic Qualifications & Skills
- Multi‑skilled technician with an industry‑recognised apprenticeship and post‑apprenticeship industry‑based knowledge and experience.
- Minimum of an HNC level qualification in an engineering discipline.
- Hands‑on experience of GSK/Pharmaceutical processes and procedures.
- Experience with the SAP business system.
- Demonstrable experience working with cross‑functional teams in a complex organisation.
- Required to demonstrate competence in current Good Manufacturing Practice (cGMP).
- Strong experience of working in a complex GMP environment.
Preferred Qualifications & Skills
- Experience working in classified areas such as ISO 5 or ISO 7 (working in a sterile manufacturing environment).
- Good communication and teamwork skills.
- Ability to implement plans and hold yourself and team accountable for delivery goals.
- Ability to work under pressure.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service, or any basis prohibited under federal, state, or local law.
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