1 Temporary, Biotechnology / Life Sciences jobs in Largs, North Ayrshire

The Operational Quality Advisor plays a crucial role in maintaining the quality and compliance of various materials and processes within the GSK Irvine site. You will be responsible for the release of raw materials, starting materials, intermediates, drug substance and blends. This role is critical for ensuring that the products manufactured by the organisation are safe, effective, and of high quality, ultimately protecting patient safety and maintaining the overall quality assurance., Release raw materials and products for downstream manufacturing to ensure all quality standards and market restrictions are met and appropriately signed off.

• Participate in assessment of non-conformances with cGMP, deviations and customer complaints investigations and ensure that appropriate CAPA has been identified and verification of CAPA effectiveness and deviation trending is carried out.
• Approve master batch sheets, SOPs, specifications and methods to ensure compliance with GMP and licence registrations.
• Participate in Operational Quality approval of changes in a compliant manner to ensure that proposed changes are planned and evaluated.
• Plan, conduct and document internal quality audits to ensure GMP compliance.
• Evaluate site Right First time performance and drive improvements in the RFT figures
• Complete product stability protocols and periodically evaluate the stability profiles to ensure the quality of the products manufactured.
• Provide support and advice both informally and through quality councils to Operations to ensure continued business compliance.
• Review of batch documentation, test results and all other documentation associated with certification (for EU) and release of Finished Product
• Provide Batch certification for release.
• Review and approve of Technical Terms of Supply (TTS) and associated quality agreements to include review and approval of changes and assessment of deviations and trends.
• Approve distribution risk assessments to assure compliance with cGMP.
  
  Degree or HNC/HND or equivalent with relevant GMP experience
• Strong organizational and decision-making skills, excellent communication skills, and ability to manage change.
• Experience within the Pharmaceutical Industry including an in-depth knowledge of cGMP/GQLP and Quality issues.
Preferred Qualifications: Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:
• Experience of working in the GMP operational environment.
• Experience in systems utilized for role, such as SAP / M-ERP, VQMS.
  
  We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021.
We continue to modernise, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together., Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. 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). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, 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. 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., Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov