GlaxoSmithKline Pharmaceuticals Limited Posted September 2, 2026

Supplier Quality Specialist

Nashik, India Full time
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About this opportunity

Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.

Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary You will manage supplier quality activities across our India operations to protect product quality and support reliable supply. You will work closely with suppliers, procurement, site teams and regulatory partners. You will lead investigations, track corrective actions, and drive supplier improvement. We value clear communication, practical problem solving and collaboration. This role offers clear growth, meaningful impact, and aligns with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Maintain and manage the approved supplier database and supplier compliance documentation. - Lead supplier investigations, manage corrective and preventive actions (CAPAs), and ensure timely closure. - Negotiate, create and maintain Quality Agreements and manage supplier change controls. - Plan and execute supplier audits and self-inspections, and support regulatory inspection readiness. - Monitor supplier performance using key quality indicators and prepare summary reports for governance. - Support onboarding of new suppliers and coordinate technical transfers and change implementations.

Responsibilities - Act as the main point of contact for supplier quality issues, coordinating internally and with suppliers. - Review supplier documentation, certificates of analysis and compliance records to ensure conformity. - Drive root cause analysis and implement effective corrective actions with clear timelines and owners. - Track and escalate supplier risks that could affect product quality or supply continuity. - Support cross-functional teams during supplier selection, qualification and supplier transitions. - Prepare clear, timely updates and reports for stakeholders and governance forums.

Why You?

Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals - Bachelor’s degree in Pharmacy, Science, Engineering or a related technical discipline. - Minimum 3 years’ experience in supplier quality, quality assurance, or a relevant manufacturing role. - Experience working in a regulated manufacturing environment with knowledge of Good Manufacturing Practices (GMP). - Practical experience with supplier audits, CAPA management and change control processes. - Strong written and verbal communication skills in English and ability to work with cross-functional teams. - This role is on-site at a GSK India location and will require travel to supplier sites as needed.

Preferred Qualification If you have the following characteristics, it would be a plus - Advanced degree in Pharmacy, Microbiology, Chemistry or a quality-related field. - Experience with supplier qualification for APIs, excipients or packaging materials. - Familiarity with quality management systems and risk management tools. - Proven track record of leading supplier improvement projects and audit remediation. - Experience with quality or data systems and tools for reporting and tracking. - Prior experience in the pharmaceutical or life sciences industry with exposure to regulatory inspections.

What we value in you - A practical, evidence-based approach to solving problems. - Clear and concise communication that makes complex information easy to use. - Collaboration and respect for different perspectives and experiences. - Commitment to learning and growing your skills. - A focus on quality and patient safety in every decision.

How to apply If this role feels like the next step in your career, we would love to hear from you. Please apply with your CV and a short note explaining why you are interested. We welcome applicants from all backgrounds and encourage people who value inclusion and teamwork to apply.

Skills

Data Integrity, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Supplier Auditing, Supplier Quality Management, Technical Writing

Why GSK?

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.

Inclusion at GSK:

As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.

Please contact our Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss your needs.

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.

It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way.

GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable.

If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com , so that we can confirm to you if the job is genuine.

Job details

Seniority
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Nashik, India
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 1473 comparable Quality roles across 143 biopharma companies.

1473Comparable roles tracked
1323Currently active
143Companies hiring similar roles
53Countries represented

Salary context

261 of 1473 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · QC Lab Technician (Lilly Contractor - Fixed Term) · Lilly $13/hr – $29/hr (≈ $26,998–$60,507/yr)
Highest disclosed · VP, Quality Assurance · City Therapeutics $340,000/yr – $360,000/yr
Peer group range $43,753 – $350,000 (median $123,250)

Where these roles are based

Top locations among the 1473 comparable roles

United States590
Ireland91
Germany72
China69
France67
India55

+ 47 more countries

Seniority mix

726 of 1473 peers have a known seniority level

Manager220
Senior187
Intern/Fellow/Postdoc98
Associate66
Director47
Associate Director45
Principal31
Senior Director25
Executive/VP7

Therapeutic area mix

3 of 1473 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease2
Respiratory1

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.