Process Support Technician
4 weeks ago
GSK Barnard Castle is a key secondary manufacturing site that has invested heavily in industry 4.0 state-of-the-art equipment to support sustained new product introductions and volume increases. As a key supplier of some of GSK's blockbuster products, the site contributes revenues of ~$2Bn annually.
We strive to create a workplace where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programs.
We embrace modern work practices, including a hybrid working model that empowers employees to find the optimal balance between remote and in-office work.
Discover more about our company-wide benefits and life at GSK on our webpage Life at GSK | GSK.
There is an exciting opportunity for a Process Support Technician within C Block Inhalations and Derms at GSK's manufacturing site, Barnard Castle.
As a Process Support Technician, you will be responsible for ensuring the Production areas are fully supported in terms of Compliance, Project, Digital, OE, and NPI activity. You will provide the support required to be Audit Ready and fully compliant with Safety and Quality standards, while monitoring and issuing feedback on all Health and Safety, Quality, and compliance systems.
Key Responsibilities:
- Support MSAT/capital projects as a customer representative, including design development, factory acceptance testing, installation, validation, commissioning, and associated documentation.
- Work with the MES & MSAT teams to create digital recipes, flows, config specs, etc.
- Dry running and testing of digital systems in the MES and eBRS environments and the raising & completion of Method Statements using the Kneat Digital System.
- Ensure Compliance with QMS/Group Quality Policies (G.Q.P.'s), EHS policies, and Site Procedures, and that the area is continually in an audit-ready state and fully compliant with Quality and Health and Safety Standards, support the area during audits.
- Complete actions arising from Audits, local improvement initiatives, project plans, and liaise with Contractors on matters concerning work/projects.
- Change/update GXP parts reference manuals for Equipment Preparation/Manufacturing areas and support the effective use of the Operational Support budget.
Requirements:
- Ability to apply current Good Manufacturing Practice (cGMP), explaining its fundamental importance to pharmaceutical manufacture.
- Operate complex, technical processes, both manual and automatic, adhering to safety and GMP standards.
- Flexible to working hours that suit the needs of the business.
- Ability to troubleshoot problems and drive continuous improvement.
- Good written skills to write SOPs, training packages.
- Demonstrated commitment to safety, assessing safety risks, and implementing process improvements.
Preferred Qualifications:
- Computer literacy with experience or ability to quickly learn a number of different systems such as MERP, electronic batch record, and Dispense/Weigh Systems, Siemens PCS7, PIMMS, Erwin Case wise, Microsoft Office, Veeva.
Why GSK?
At GSK, we unite science, technology, and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty, and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/immunology, and oncology).
We want GSK to be a place where people can thrive. We strive to create a workplace where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programs.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, color, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status, or any other federal, state, or local protected class.* (*US only)
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