Qualified Person
GSK
Date: 12 hours ago
City: Harlow
Contract type: Full time

Site Name: UK - Essex - Harlow
Posted Date: Oct 10 2025
We have a new opportunity for a Qualified Person (or trainee QP close to eligibility) to join our team on a permanent basis at Harlow. The successful person will perform the quality assurance activities and quality oversight of the GMP functions performed within Pharma R&D.
You’ll provide expert oversight, certification, and release of products, ensuring they meet regulatory standards and support GSK’s mission to get ahead of disease together. Collaborating with cross-functional teams and external partners, you’ll contribute to innovation, continuous improvement, and patient safety. This is an opportunity to grow your career, make a meaningful impact, and be part of a team that values inclusion, integrity, and excellence.
In this role you will…
Basic Qualifications
We are looking for professionals with these required skills to achieve our goals:
If you have the following characteristics, it would be a plus:
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 on [email protected] 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/
Posted Date: Oct 10 2025
We have a new opportunity for a Qualified Person (or trainee QP close to eligibility) to join our team on a permanent basis at Harlow. The successful person will perform the quality assurance activities and quality oversight of the GMP functions performed within Pharma R&D.
You’ll provide expert oversight, certification, and release of products, ensuring they meet regulatory standards and support GSK’s mission to get ahead of disease together. Collaborating with cross-functional teams and external partners, you’ll contribute to innovation, continuous improvement, and patient safety. This is an opportunity to grow your career, make a meaningful impact, and be part of a team that values inclusion, integrity, and excellence.
In this role you will…
- Provide QP certification and release investigational medicinal products in compliance with EU and UK regulations.
- Ensure compliant operations to meet regulatory standards, guaranteeing product quality and conformity to submissions.
- Stay ahead of legislative changes, assess their impact, and implement mitigation strategies.
- Offer expert QP advice to internal teams, external collaborators, and sponsors, reducing regulatory risks and ensuring critical assurances.
- Build strong relationships across GSK and with external partners, contributing to process improvements and mentoring others within the organization.
- Participate in audits, investigations, and quality reviews, recommending and implementing corrective actions where necessary.
Basic Qualifications
We are looking for professionals with these required skills to achieve our goals:
- Science degree and extensive experience in pharmaceutical manufacturing and quality operations.
- Eligible to act as Qualified Person in the UK (or imminently ready to submit for Viva)
- Extensive experience working alongside QP’s certifying major dose forms such as Tablets, aseptic sterile manufacture and biopharm products
- Broad knowledge of quality management
- Capable of working in multi-disciplinary teams
If you have the following characteristics, it would be a plus:
- Previous experience of working with external partners.
- Experience in QP certification of Investigational Medicinal products.
- Experienced of Regulatory Inspections
- Certification of Investigational Medicinal Products
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 on [email protected] 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/
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resumeSimilar jobs
Design Sales Assistant
Nobia,
Harlow
3 weeks ago
This role will be based in one of our Magnet showrooms, working closely as part of a fast paced, motivated team. With more than 100 years’ experience behind us, Magnet is one of the UK’s biggest and best known kitchen brands and is part of the wider Nobia group.What’s on offer?For this role you will earn a starting salary of...

Senior Formulation Scientist
Charles River Laboratories,
Harlow
3 weeks ago
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play...

Team Manager
Matalan,
Harlow
3 weeks ago
Salary: From £25,969Working Pattern: Full TimeContract Type: PermanentHours: 38.0About MatalanFrom humble beginnings to disruptive innovations in the retail industry, find out about how Matalan is ever-evolving here on our careers site.We know as a team, we are stronger together – we champion equality for all and make lasting connections that go beyond work. We thrive off our inclusive culture, encouraging...
