Full-Time

Quality Manager

Digital Systems

Updated on 9/12/2026

Deadline 9/17/26
Pfizer

Pfizer

10,001+ employees

Biopharmaceutical company develops medicines and vaccines

No salary listed

Remote in India + 2 more

More locations: Mumbai, Maharashtra, India | Chennai, Tamil Nadu, India

Remote

Bachelor's, Master's

Category
Biology & Biotech (1)
Required Skills
Power BI
Dataiku
Data Visualization
SQL
Data Engineering
Snowflake

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Requirements
  • A bachelor's degree in Life Sciences, Information Systems, Computer Science, or a related field, plus 5 or more years of relevant industry experience.
  • The ability to produce clear documentation, user-facing guidance, and stakeholder-ready reports through excellent written and verbal communication.
  • Demonstrated experience working directly and iteratively with business stakeholders to understand their underlying needs and workflows.
  • Working knowledge of Veeva Vault eQMS or a comparable enterprise quality/GxP system, including vault object relationships and configuration dependencies.
  • Hands-on experience or concrete examples of applying AI-enabled tools, automation, or advanced analytics to improve processes and drive innovation.
  • Experience in a GxP-regulated pharmaceutical or biotech environment and understanding of quality management system processes.
  • The ability to operate autonomously and collaboratively on complex, cross-functional work.
  • Strong analytical and problem-solving skills, including the ability to assess the downstream impact of system changes and translate business needs into actionable decisions.
Responsibilities
  • Serve as the primary business administrator for Veeva eQMS on behalf of Regulatory Quality Assurance.
  • Triage and resolve business administration requests requiring business-level judgment, partnering with technical teams on complex issues.
  • Own access request intake and provisioning across RQA digital systems environments.
  • Support Veeva release coordination through user acceptance testing, business approvals and communications, and production deployments.
  • Maintain and continuously improve job aids, quick reference guides, and user-facing documentation for Veeva eQMS and integrated supporting tools across system releases.
  • Develop, prepare, and deliver reporting across functional areas.
  • Provide guidance on Veeva Vault configuration options, including object relationships, shared configuration dependencies, and downstream impacts of proposed changes.
  • Support triage and formulation of eQMS enhancement requests by providing business context and impact assessment to inform prioritization and decision-making.
  • Stay current on Veeva platform developments and GxP digital systems best practices, including emerging AI technologies, and identify opportunities to modernize system design and operations.
  • Participate in eQMS governance forums and represent RQA Digital Systems’ interests.
  • Represent the RQA Digital Systems team within enterprise programs and initiatives, scope team responsibilities, develop execution plans, and deliver against them.
  • Maintain ownership of workstream status and decisions and proactively surface blockers or escalation points to leadership.
  • Coordinate with Pfizer Digital and cross-functional teams to support enterprise quality data integrity and system continuity efforts.
  • Issue clear and timely communications so stakeholders are informed and aligned on timelines and expected outcomes.
  • Execute periodic data extracts and reporting tasks, including basic dashboarding and data queries, for regulatory and quality operations.
  • Develop and maintain operational documentation and user guidance for current and legacy quality systems.
  • Gather, synthesize, and prepare materials for stakeholder communications and leadership briefings.
  • Identify opportunities for process improvement and digital transformation within quality systems operations.
  • Apply practical AI knowledge to evaluate use cases, partner with technical teams, and drive adoption of AI-enabled solutions.
  • Support organizational transformation initiatives, including AI integration into quality workflows, eQMS process redesign, and platform evolution.
  • Apply emerging Veeva, GxP, and regulatory best practices to improve team operations and delivery.
Desired Qualifications
  • Basic coding, scripting, and/or dashboarding experience, such as SQL, Power BI, Spotfire, or similar tools.
  • Experience as a Veeva Vault business administrator, business analyst, or similar business-technology liaison.
  • Experience with Veeva Vault configuration in a pharmaceutical or contract research organization setting, including system releases, eQMS governance forums, or enhancement request management.
  • Familiarity with Pfizer enterprise data and/or source systems.
  • Exposure to data platforms such as Snowflake and DSS/Dataiku or related data engineering tools.
  • Working knowledge of Microsoft Power Automate or similar automation tools.
  • An advanced degree.

Pfizer is a global biopharmaceutical company that discovers, develops, manufactures, and sells medicines and vaccines for a range of health needs, including vaccines, oncology, and other specialized therapies. Its products work by using biological mechanisms to prevent or treat diseases—vaccines train the immune system to fight infections, while medicines target cancer and other conditions. Pfizer differentiates itself through its large worldwide footprint, broad portfolio across multiple therapeutic areas, and partnerships (notably with BioNTech) that expanded its reach in vaccines and cutting-edge therapies. The company also engages in public health initiatives, such as efforts to provide vaccines to underserved populations. Pfizer’s broad goal is to improve global health by delivering safe and effective medicines and vaccines through research, development, and wide international distribution.

Company Size

10,001+

Company Stage

IPO

Headquarters

New York City, New York

Founded

1849

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue rose to $15 billion, and non-COVID products grew 5% operationally.
  • Pfizer raised 2026 guidance to $60.5 billion-$62.5 billion after Eliquis, Padcev, Vyndaqel strength.
  • Berobenatide entered Phase 3 planning, giving Pfizer a credible obesity franchise before 2028.

What critics are saying

  • Depo-Provera MDL exceeded 5,800 cases by July 2026, with late-2026 bellwethers looming.
  • Vyndamax still faces Apotex litigation in Delaware, preserving generic-entry uncertainty beyond 2031.
  • Ringaskiddy and Catania cuts show manufacturing contraction, signaling more restructuring through 2029.

What makes Pfizer unique

  • Seagen gives Pfizer leading ADCs: Padcev, Tivdak, Adcetris, Tucysa across oncology.
  • Pfizer still owns COMIRNATY distribution scale, with XFG vaccine approved August 27, 2026.
  • Vyndamax settlement extends U.S. exclusivity to June 1, 2031, stabilizing cardiomyopathy cash flows.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

401(k) Company Match

Paid Vacation

Paid Sick Leave

Paid Holidays

Hybrid Work Options

Relocation Assistance

Growth & Insights and Company News

Headcount

6 month growth

-5%

1 year growth

-5%

2 year growth

-5%
Yahoo Finance
Sep 10th, 2026
Medicus Pharma secures Pfizer ADC deal with $2M funding, advances SkinJect for rare cancer treatment

Medicus Pharma has secured a development and licensing agreement with Pfizer for a CD228-targeted antibody-drug conjugate programme focused on solid tumours, including refractory melanoma. Pfizer is providing approximately $2 million in development funding, plus inventory and infrastructure support. CEO Dr Raza Bokhari said the deal allows Medicus to continue from where Pfizer concluded its Phase 1 dose-escalation work, strengthening the company's position in precision oncology. Medicus is also advancing its SkinJect programme for basal cell carcinoma. Final clinical trial results identified the 200-microgram patch as the optimal dose for future studies. The company is preparing for the FDA-approved pivotal SkinJect 005 study whilst recruiting patients. An independent reimbursement analysis suggests SkinJect could achieve reimbursement levels of $25,000 or more per patient.

Yahoo Finance
Sep 8th, 2026
AbbVie beats Pfizer as top dividend stock with 53-year payout streak and 203% growth

AbbVie offers a smarter long-term dividend investment than Pfizer, despite Pfizer's higher 6.1% yield. AbbVie holds Dividend King status with 53 consecutive years of dividend increases and raised its payout by 5.5% this year to $1.73 per share. Over the past decade, AbbVie increased its dividend by more than 203% compared to Pfizer's 51%. AbbVie's revenue grew 138% during this period, whilst Pfizer's rose just 18%. AbbVie successfully navigated Humira's patent cliff through home-grown immunology drugs Skyrizi and Rinvoq. By 2025, these two drugs generated combined annual sales exceeding $25 billion, replacing Humira's peak revenue and pushing total company revenue to record highs. AbbVie's free-cash-flow dividend payout ratio stands at 65%, lower than Pfizer's 89%.

Yahoo Finance
Aug 28th, 2026
Pfizer's updated COVID vaccine ships as FDA approves narrower rollout for over-65s and high-risk groups

Pfizer received FDA approval for its updated Comirnaty COVID-19 vaccine on Thursday, with deliveries to pharmacies and clinics beginning immediately. The company's shares were trading at $27.9079 on 28 August. However, the market opportunity has significantly narrowed from pandemic levels. Eligibility is now limited to adults aged 65 and older, plus higher-risk patients aged 5 through 64. Despite Comirnaty having distributed over five billion doses worldwide historically, today's revenue potential is considerably more constrained. Pfizer faces competition from Moderna and the Novavax-Sanofi protein vaccine for this smaller patient pool. The company's current share price sits 5.27% above its estimated value of $26.51, suggesting investors are paying a premium before actual uptake and commercial results become clear.

Associated Press
Aug 27th, 2026
FDA approves Pfizer-BioNTech XFG-adapted COVID-19 vaccine for high-risk groups

Pfizer and BioNTech have received US Food and Drug Administration (FDA) approval for their 2026-2027 COVID-19 vaccine targeting the XFG variant. The vaccine is approved for adults aged 65 and older, and individuals aged 5 to 64 with underlying conditions that increase risk of severe COVID-19 outcomes. The FDA approval is based on clinical, non-clinical and real-world data demonstrating the vaccine generates strong immune responses against currently circulating SARS-CoV-2 variants, including XFG and other contemporary lineages. The XFG variant was selected following FDA guidance for fall 2026 vaccine composition. The vaccine will begin shipping immediately and will be available in US pharmacies, hospitals and clinics within days. To date, more than five billion doses of COMIRNATY have been distributed globally.

Yahoo Finance
Aug 24th, 2026
Pfizer and J&J navigate patent cliffs with newer drugs offsetting blockbuster losses

Pfizer and Johnson & Johnson are navigating patent cliffs as key drugs lose exclusivity, with their latest results showing differing stages of transition. Pfizer's revenue excluding COVID products grew 5% operationally in Q2 2026, with newer medicines like Padcev and Vyndaqel contributing. The company expects $9.7 billion in cost savings through 2029 to support margins during the transition. Johnson & Johnson's Innovative Medicine sales rose 7.8%, despite Stelara revenue declining 55%. Tremfya sales surged 72.5% to $2 billion, helping offset losses alongside growth from oncology and neuroscience products. Johnson & Johnson raised 2026 guidance, with reported sales expected to reach $101.1 billion and adjusted EPS of $11.68. Its MedTech division provides additional diversification that pure pharmaceutical company Pfizer lacks, suggesting Johnson & Johnson's transition is more advanced.