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- Tasks: Ensure product quality and patient safety through proactive oversight and compliance checks.
- Company: GSK is a global biopharma company dedicated to improving lives through innovative medicines.
- Benefits: Enjoy flexible working options, a collaborative culture, and opportunities for personal growth.
- Why this job: Make a real impact on health while thriving in a supportive, purpose-driven environment.
- Qualifications: A scientific qualification or significant experience in quality/compliance within pharmaceutical manufacturing is required.
- Other info: Join a diverse team committed to innovation and patient care.
The predicted salary is between 36000 - 60000 £ per year.
Site Name: UK – Angus – Montrose
Posted Date: Aug 8 2025
Are you ready to help deliver quality that makes a difference? At GSK, we are united by our mission to improve lives through our innovative pharmaceutical products. Join us as aShift Quality Oversight Specialistand take on a pivotal role in ensuring patient safety and product quality while driving a proactive quality culture.
This role is based at our Montrose site and the successful candidate will work 7 shifts in 14 days – 12 hour shifts including evenings and weekends.
As aShift Quality Oversight Specialist, you will:
- Be the first line of contact for quality issue management, offering rapid response and timely interventions across GMP areas like production, warehouse, utilities, and laboratories.
- Ensure compliance with GMP standards, procedures, and inspection readiness through independent checks and proactive oversight.
- Perform quality process confirmations and maintain adherence to ALCOA+ principles for documentation and records.
- Foster aQuality Starts With Me (QSWM)culture through coaching, mentoring, and emphasizing the importance of compliance for patient safety.
- Provide oversight of equipment cleaning, inspection activities, and support batch release processes for smooth, compliant material flow.
- Participate in activities related to non-sterile microbiology, including water/environmental monitoring and deviation management.
- Role model GSK’sGlobal Production System (GPS)standards and contribute to change management initiatives and continuous improvement.
Qualifications
Basic Qualifications
- A scientific qualification (HNC, HND, BSc, BEng) or significant experience in quality/compliance within pharmaceutical manufacturing.
- Proven experience in deviation management, coaching and mentoring, and continuous improvement initiatives.
- Strong knowledge of QMS, cGMP principles, and API manufacturing processes.
- Excellent communication skills to engage teams across all levels.
Preferred qualifications
- Experience in non-sterile microbiology and delivering change management projects.
Why GSK?
At GSK, we put patients first. As a Shift Quality Oversight Specialist, you’ll play a key role in ensuring our products are safe, effective, and delivered with excellence. You’ll thrive in a collaborative environment where quality, innovation, and integrity are at the heart of everything we do.
Ready to make a difference?Apply nowto be part of a diverse, purpose-driven team where your expertise in quality oversight will impact lives worldwide.
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.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on UKRecruitment.Adjustments@gsk.com or 0808 234 4391. The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.
Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive .
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK\’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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/
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Shift Quality Oversight Specialist employer: GlaxoSmithKline
Contact Detail:
GlaxoSmithKline Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Shift Quality Oversight Specialist
✨Tip Number 1
Familiarise yourself with GSK's Global Production System (GPS) standards. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality and compliance, which is crucial for the Shift Quality Oversight Specialist role.
✨Tip Number 2
Network with current or former employees of GSK, especially those in quality oversight roles. They can provide valuable insights into the company culture and expectations, which can help you tailor your approach during the interview process.
✨Tip Number 3
Prepare to discuss specific examples of your experience with deviation management and continuous improvement initiatives. Being able to articulate your past successes in these areas will showcase your expertise and fit for the role.
✨Tip Number 4
Demonstrate your understanding of ALCOA+ principles during discussions. This shows that you are not only knowledgeable about documentation standards but also committed to maintaining high-quality practices in pharmaceutical manufacturing.
We think you need these skills to ace Shift Quality Oversight Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality oversight, GMP compliance, and any scientific qualifications. Use keywords from the job description to demonstrate your fit for the role.
Craft a Strong Cover Letter: In your cover letter, express your passion for quality assurance in pharmaceuticals. Mention specific experiences that align with the responsibilities of the Shift Quality Oversight Specialist, such as deviation management or coaching.
Showcase Relevant Skills: Emphasise your knowledge of QMS and cGMP principles. Provide examples of how you've contributed to continuous improvement initiatives or change management projects in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on quality.
How to prepare for a job interview at GlaxoSmithKline
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) standards and how they apply to the role. Be prepared to discuss specific examples of how you've ensured compliance in previous positions.
✨Showcase Your Coaching Skills
As a Shift Quality Oversight Specialist, you'll need to mentor others. Think of instances where you've successfully coached team members or led initiatives that improved quality processes.
✨Prepare for Scenario Questions
Expect scenario-based questions related to quality issue management and deviation handling. Prepare by thinking through how you would respond to potential challenges in a GMP environment.
✨Communicate Effectively
Strong communication skills are essential for this role. Practice articulating your thoughts clearly and confidently, especially when discussing complex quality concepts or past experiences.
