Full-Time

Quality Head

Global Shared Services, Quality Systems

Posted on 10/6/2025

Deadline 11/7/25
Merck

Merck

10,001+ employees

Pharmaceutical company developing medicines and vaccines

No salary listed

Hyderabad, Telangana, India + 1 more

More locations: Pune, Maharashtra, India

Hybrid

This hybrid role requires in-person attendance at the Pune Global Capability Center for three days each week.

Category
Medical, Clinical & Veterinary (5)
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Requirements
  • BS degree required with concentrations in Science, Engineering, or Pharmacy
  • Minimum of 15 years of experience within the pharmaceutical industry (or equivalent regulated environment)
  • Previous management experience is required along with a minimum of 5 years in a significant leadership role
  • Strong preference for previous quality/compliance experience in the pharmaceutical industry
  • Requires established ability to manage and implement multiple projects/tasks simultaneously with competing priorities
  • Requires established ability to identify and implement Lean Six Sigma principles
  • Demonstrated experience of continuous improvement efforts successfully implemented
  • Excellent problem-solving skills, based on science, facts, data, and understanding of regulatory requirements in complex and evolving environments
  • Ability to be decisive and influence management with demonstrated leadership skills to drive change in a compliance culture
  • Auditing organization support or participation experience
Responsibilities
  • Ensure execution and alignment of the Quality organization with all corporate policies and procedures and other division policies and regulatory laws related to the management of quality systems
  • Interact and deliver Quality Shared Services strategy to GQLT (Global Quality Leadership team), and Divisional Quality Councils
  • Provide quality and technical knowledge and expertise to the Pune Quality organization and the Pune Shared Services structure
  • Perform as the Quality Head, primary liaison, and representative for regulatory inspections and other internal and external audits
  • Oversee the GQSS internal auditing program and ensure compliance within the Shared Services Operations model
  • Responsible for the Pune Quality Plan, which will outline Quality areas of focus
  • Actively lead, engage, and monitor Quality team outputs, deliverables, and performance against targets and requirements in established Quality Systems
  • Establish and manage Pune Quality Council and deliverables
  • Renders executive quality decisions related to Pune Quality issues, QNs, deviations, deficiencies, and escalations
  • Partners with key stakeholders, sites and functions and drives significant Shared Services issues to completion
  • Sponsors and works with Shared Services in the identification of new work as well as efficiency improvement projects
  • Owns and operates Pune Quality Hoshin activities
  • Establishes and manages organizational and capacity forecasts
  • Support and actively engage with QMS in the development of digitalized approaches to Quality System topics
  • Lead standardization methodologies regarding the implementation and integration of QMS topic adoption
  • Oversee Pune Quality organizational budgets
  • Develop and establish Pune Quality as a Quality Center of Excellence
  • Develop training methodologies to sustain current talent and provide opportunities for future growth
  • Foster an attitude of embracing change
  • Providing direction and guidance for direct reports and groups under their management
  • Overall responsibility for recruiting and hiring activities for new employees into the GQSS - Delivery Team at the Pune Capability Center (PCC)
  • Providing subject matter expertise in alignment with applicable principles in the Pharmaceutical Quality System and ICH Q10
  • Ensuring GMP activities in the Delivery Team are consistent with current regulatory expectations
  • Maintaining awareness of evolving industry and regulatory trends associated with quality and compliance
  • Establish and maintain a high-performing organization that provides the highest customer satisfaction level to site, functions, and stakeholders
  • Monitoring and constant engagement an appropriate suite of metrics, KPIs, and SLAs in place across all activities in scope for all regions
  • Responsible for governance, coordinating meetings, and overseeing the transition of activities to GQSS
  • Serving as Quality Lead for internal and business representation
  • Identifying, driving, and implementing continuous improvement initiatives to streamline delivery team processes
  • Managing quality agreements and overseeing complaint handling processes for divested products
  • Ensuring that GQSS adheres to all relevant topics within the Company’s Quality Management Systems
Desired Qualifications
  • Demonstrated ability to lead and drive results impacting critical business and compliance initiatives
  • 15 plus years of experience in the Pharmaceutical industry as a Quality leader
  • Lean Six Sigma Certified
  • Provide leadership, vision, and direction to create best-in-class Quality Shared Services
  • Builds and maintains effective partnerships with diverse business stakeholders
  • Embraces the value of bringing diverse, talented, and committed people together
  • Strong preference for previous quality/compliance experience, previous complaint management, product release and inspection readiness experience
  • Significant knowledge of Quality Systems and associated regulations
  • Experience working in a Global, complex and fast paced organization

Merck is a global healthcare company that develops medicines, vaccines, and animal health products. It advances long-term health by conducting research and development to create new treatments for diseases such as cardiovascular disease, diabetes, and cancer, then brings these medicines to patients, healthcare professionals, and institutions worldwide. The company’s products work by undergoing scientific discovery, clinical testing, and regulatory approval before being manufactured and sold or distributed through patient assistance programs. What sets Merck apart is its large, diversified portfolio across human medicines, vaccines, and animal health, along with a strong emphasis on R&D, global reach, and support services like Merck Connect and Merck Manuals that provide professional resources. Merck’s goal is to tackle major health threats by applying science to discover and deliver therapies that improve patient outcomes and public health across the globe.

Company Size

10,001+

Company Stage

IPO

Headquarters

Kenilworth, Illinois

Founded

1891

Simplify Jobs

Simplify's Take

What believers are saying

  • FDA approves IDVYNSO HIV therapy launching post-May 11, 2026.
  • Keytruda Qlex adds $128 million Q1 sales with administration advantages.
  • Peenya facility expands for filtration, targeting $14.06B market by 2035.

What critics are saying

  • Keytruda patent expires 2028, biosimilars slash $8B quarterly sales 70%.
  • Gardasil trial starts July 27, 2026, erodes trust amid RFK Jr. involvement.
  • Gardasil sales drop 19% Q1 2026 from Chinese competition permanently.

What makes Merck unique

  • Keytruda generates $8 billion in Q1 2026 sales, up 12% year-over-year.
  • Winrevair surges 88% to $525 million in Q1 2026 across US, Japan, Europe.
  • Cidara Therapeutics $9.2 billion acquisition bolsters antifungal pipeline.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Hybrid Work Options

Company News

Castlefield
Apr 27th, 2026
Engagement update with Merck & co on animal testing and packaging.

Engagement update with Merck & co on animal testing and packaging. By Ffion Spencer * Share * April 27/04/2026, 12:00 AM As part of its ongoing efforts to improve performance across key environmental, social, transparency and governance (E.S.T.) metrics, Castlefield Partners Limited recently engaged with US pharmaceutical company Merck & co., held in the castlefield thoughtful World Equity Fund, to discuss its approach to animal testing, the use of animal-derived ingredients, and packaging practices. At a recent External Advisory Committee meeting, the committee highlighted increasing numbers of animals being used in animal testing across the pharmaceutical sector. Around the same time, Castlefield Partners Limited also received a client query relating to the use of animal derived ingredients in pharmaceutical products. This engagement therefore focused on three material topics for the pharmaceutical industry: animal testing, the use of animal derived ingredients in products, and plastic use. In its initial response, Merck explained that it makes extensive use of non animal research methods, including in vitro techniques, computer modelling and advanced imaging, prior to or instead of animal studies. The company shared that approximately 96% of its research animals are rodents and confirmed that it maintains detailed records on animal use across species, purpose and site, including research carried out by third party organisations on Merck's behalf. As Merck has confirmed that it maintains this data internally, Castlefield Partners Limited has encouraged greater transparency through public disclosure. Castlefield Partners Limited also encouraged the company to consider setting reduction targets on this topic. While this response suggests a baseline level of governance and oversight, Castlefield Partners Limited believe there is scope for further progress. Castlefield Partners Limited has followed up and are awaiting further written responses.Castlefield Partners Limited note that some peers, including French pharmaceutical company Sanofi, which is also held in the World Equity Fund, publish the total number of animals used for scientific research on an annual basis. As Merck has confirmed that it maintains this data internally, Castlefield Partners Limited has encouraged greater transparency through public disclosure. Castlefield Partners Limited also encouraged the company to consider setting reduction targets on this topic. On animal derived ingredients, Merck highlighted the use of specialised tools to identify potential non animal alternatives, indicating consideration of reduction and substitution where scientifically feasible. On plastics, the company shared that it has developed a long term roadmap aimed at reducing the environmental impact of its packaging, suggesting an acknowledgement of plastics as a material environmental issue within its operations. Overall, while Merck provided high level information across all three topics, the most detailed discussion related to animal testing, reflecting its materiality to the sector. Outcome: Its engagement confirmed that Merck has a level of baseline governance on these topics. However, further engagement with the company is required, particularly in relation to transparency and disclosure on the number of animals used in scientific testing. Information is accurate as at 20.04.2026. Opinions constitute the fund manager's judgement as of this date and are subject to change without warning. The officers, employees and agents of CIP may have positions in any securities mentioned herein. This material may not be distributed, published or reproduced in whole or in part. With investment, capital is at risk.

Yahoo Finance
Apr 14th, 2026
Merck keeps Keytruda cancer drug prices high as single dose reaches $163K

Merck's cancer drug Keytruda has become a pricing flashpoint in US healthcare, with a single 400mg dose billed at $162,567 at a California clinic, despite Merck's list price of $24,000. The drug generated $31.7 billion in worldwide sales in 2025, representing nearly half of Merck's revenue. A joint investigation by the International Consortium of Investigative Journalists and USA TODAY found Merck employs multiple tactics to maintain high prices, including building patent walls against generic competition, lobbying against Medicare price negotiations, and maintaining higher dosing despite studies suggesting weight-based dosing would be effective and cheaper. Whilst Merck CEO Robert Davis pledged support for President Trump's drug pricing initiatives in December, he made no commitments regarding Keytruda. Merck attributes US price inflation to pharmacy benefit managers and insurers who add fees and rebates.

Longevity.Technology
Apr 9th, 2026
Merck bets $838M on antibody startup Infinimmune for faster drug discovery

Merck has announced a collaboration with Infinimmune, a California-based biotech founded in 2022, worth up to $838 million to discover new antibody drug candidates. The deal targets multiple undisclosed targets selected by Merck, though upfront payment details were not disclosed. Infinimmune's platform identifies promising antibodies by studying memory B cells from the human immune system. The company claims it can identify antibodies binding to a target within one week and prepare candidates for animal studies in roughly three months. Chief executive Wyatt McDonnell described the approach as building a massive database of immune cell information that can be searched for matching antibodies. The 10-person startup is also developing IFX-101, its lead candidate for moderate-to-severe atopic dermatitis, designed for quarterly or twice-yearly dosing.

Yahoo Finance
Apr 7th, 2026
JPMorgan raises Merck price target to $135 as EU approves KEYTRUDA for ovarian cancer

Merck & Co. (NYSE: MRK) received a price target increase from JPMorgan to $135 from $125 on 6 April, maintaining an Overweight rating ahead of its 30 April earnings report. The firm highlighted Merck's pipeline as the primary focus, citing a favourable risk-return setup with key data readouts expected in 2026 and 2027. On 2 April, Merck announced EU approval for KEYTRUDA combined with paclitaxel for adults with platinum-resistant ovarian, fallopian tube or primary peritoneal carcinoma. The approval marks the first PD-1 inhibitor-based option for eligible patients with platinum-resistant ovarian cancer in the EU and extends across all 27 member states plus Iceland, Liechtenstein and Norway.

Ophthalmology Times
Apr 7th, 2026
Merck launches phase 2b/3 MALBEC trial of MK-8748 in wet AMD.

Merck launches phase 2b/3 MALBEC trial of MK-8748 in wet AMD. MALBEC (NCT07440225) is a randomized, double-masked trial evaluating the safety and efficacy of MK-8748 at 2 dose levels versus control (aflibercept 2mg). Merck has initiated MALBEC, its phase 2b/3 clinical trial evaluating MK-8748 (also known as Tiespectus, EYE201) for the treatment of neovascular (wet) age-related macular degeneration (AMD). MK-8748 is defined by the company as a "novel investigational bispecific antibody with a dual mechanism that directly activates the Tie2 pathway and inhibits VEGF with the goal of stabilizing retinal and choroidal blood vessels and reducing fluid accumulation in the macula." According to the company, preclinical evidence may suggest that dual pathway modulation helps improve vascular stability in the retina and supports vision preservation in patients with certain vascular retinal diseases.[1] MALBEC is a randomized, double-masked trial evaluating the safety and efficacy of MK-8748 at 2 dose levels versus control (aflibercept 2mg). The primary endpoint of the trial is mean change in best-corrected visual acuity (BCVA) from baseline to Year 1 in the study eye of the participants, using standardized Early Treatment of Diabetic Retinopathy Study (ETDRS) vision. Patients will be randomized 1:1:1 to receive 2 dose regimens of MK-8748 or aflibercept 2mg. Patients will initially receive 3 monthly doses of MK-8748 or aflibercept 2mg. These doses will be followed by treatments every 8 weeks until week 48. Following week 48, patients will be treated at intervals determined based on individualized response to treatment, with the last study visit at week 96. David Guyer, MD, founder, CEO and president of, commented on the trial in a press release from the company, saying, "Despite available therapies, many patients with neovascular age-related macular degeneration remain at risk of further vision loss due to continued vascular leakage. With its differentiated dual mechanism directly agonizing Tie2 and inhibiting VEGF, MK-8748 has the potential to offer a novel approach to maintain vascular stability for patients with serious retinal diseases." In addition to MALBEC, the company intends to initiate a second study in wet AMD in 2026. The company noted that the plan to advance into pivotal studies is based on results from the Phase 1/2a RIOJA trial, which was a 2-part study evaluating MK-8748 in patients with either wet AMD, macular edema secondary to branch retinal vein occlusion (BRVO), or diabetic macular edema (DME). In addition to MK-8748, Merck is developing MK-3000 (also known as Restoret, EYE103) for the treatment of DME. MK-3000 is currently being evaluated in the BRUNELLO trial, a randomized, double-masked trial evaluating the efficacy and safety of 2 dose levels of intravitreal MK-3000 versus active control ranibizumab.[2] References: Don't miss out - get Ophthalmology Times updates on the latest clinical advancements and expert interviews, straight to your inbox.

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