At a Glance
- Tasks: Manage quality systems for pharmaceutical materials and ensure supplier compliance.
- Company: GSK, a global biopharma leader focused on innovative medicines and vaccines.
- Benefits: Competitive salary, annual bonus, healthcare, pension plan, and shares programme.
- Other info: Agile working culture with opportunities for growth and inclusivity.
- Why this job: Join a mission-driven team impacting global health and advancing your career.
- Qualifications: Degree in Science or equivalent experience; strong communication and attention to detail.
The predicted salary is between 49500 - 60500 £ per year.
As a Quality Governance & Partnership Senior Specialist, you will be responsible for managing and maintaining the systems used to release starting materials for our finished products.
You will provide expert advice on supplier changes, vendor complaints and Corrective and Preventative Actions (CAPA), this includes the creation and review of Raw Material Specifications alongside the monitoring of the Supplier Quality Workflow.
- In this role you will…
- Oversight of new Active Pharmaceutical Ingredients (API)/Raw Materials, raising Change Controls in VQMS and allocating actions to ensure the Supplier is suitable and the material specifications are created.
- Providing annual updates of the Supply Chain Management (SCM) documents in VQD containing all Suppliers of materials for a given product.
- Active management of Vendor Complaints working closely with the suppliers to ensure appropriate actions are progressed.
- Raising, managing and completing Change Controls for progression of new and existing excipients and non-GSK API testing requirements against pharma/regulatory standards.
- Checks on the Supplier of a Packaging or Raw Material to ensure they meet the expected quality standards.
- Creating and approving the relevant Certificate of Analysis (C of A) acceptance reports to allow material deliveries to be accepted.
Reports must be reviewed and updated as required.
- Review and update Distribution Risk Assessment (DRA) as required by assessing transportation to site from the Supplier ensuring compliance.
- Reviewing the quality systems in place for Suppliers not within scope of the audit process by performing desktop audits and generating the subsequent reports.
- Creating and reviewing agreements between Suppliers and site for specifications and purchase requirements.
- Ensuring all Suppliers have been audited in accordance with expected frequency, reviewing audits performed and ensuring that the reports are in line with site requirements.
- Degree in Science related discipline or equivalent experience.
- The ability to approach and discuss scientific data.
- Strong communications skills, able to communicate at all levels internally and externally.
- Experience using various electronic systems e. g., SAP.
- Good attention to detail, able to multitask., Data Integrity, Digital Fluency, Gx P Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Supplier Auditing, Supplier Quality Management, Technical Writing
GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases, and as a key supplier of some of GSK's blockbuster products, the site contributes revenues of ~\$2Bn annually., Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together.
We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive.
We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines.
We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most.
Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.
Adjustments@gsk. com where you can also request a call.
Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels.
We create a place 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 programmes, pension plan membership, and shares and savings programme.
Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK
#J-18808-Ljbffr
Quality Governance & Partnership Senior Specialist in Eggleston employer: GSK
GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Governance & Partnership Senior Specialist in Eggleston
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like GSK. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like GSK.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like GSK. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what GSK is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Quality Governance & Partnership Senior Specialist in Eggleston
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at GSK!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show GSK that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at GSK!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At GSK, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at GSK
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at GSK that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with GSK’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.