Pfizer

Manager Compliance

Posted 3 Hours Ago

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Ahmedabad, Gujarat, IND

In-Office

Expert/Leader

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Lead and ensure GMP and QMS compliance for Pfizer products manufactured at ZHOPL. Authorize batch release, review/approve change controls, submissions, investigations, complaints, and validation activities. Act as SCNM and LPO for processes, support tech transfers, supplier management, recalls, and quality governance, and provide backup for urgent quality activities.

Summary Generated by Built In

Use Your Power for Purpose
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve.
What You Will Achieve
In this role, you will:

Overall responsibilities for quality assurance compliance at the Zydus Hospira Oncology Private Limited (ZHOPL) site and Pfizer Quality at & ensure sustainable GMP compliance for Pfizer Products manufactured at ZHOPL site as per Quality agreement.
Batch record review and release authorization compliance functions:
- Responsible for review and authorize the packed batch lot(s) for distribution in respective market from ZHOPL.
- To be part of SQRT as needed for any Batch related issue discussion.
Regulatory impact assessment for all types of change related to Pfizer products
- Responsible for Review and approval of Change controls at ZHOPL as per the Pfizer requirements.
- Responsible for performing the SCNM (Site Compliance Network Member) activities at ZHOPL and create the PAC and PCF in the PDM systems.
- Responsible for the review and approval of submission package as per procedure REG-459.
- Review BoH Queries & response and compendial/scientific data changes
- Responsible for review and approval for NPL assessment and dossier handover to ZHOPL
Complaint Management for Pfizer Product
- To coordinate and ensure that ZHOPL comply with the requirements for managing complaint.
- To review and approve the ZHOPL complaint investigation reports and upload investigation reports in the Pfizer electronic complaint database.
- Support for activities including co-ordination committee meeting and share the applicable information/ distribution details to site & & Pfizer market action leader function during market action and mock recall activity.
Quality Management System (QMS) compliance functions: Responsible for Review and approval of Investigations (QARs) initiated at ZHOPL. To be part of SQRT and involve in the Investigations. Provide support for Supplier management. To provide Quality support for review of documents for new product launches and Tech transfers as needed Responsible for reviewing and approval of Process validation related performed at ZHOPL.

Other: To support any additional and urgent activity in absence of primary responsible person as assigned by the Manager. Responsible to support with the AQRT /ESQRT process as and when required. To provide Quality support for new product launches and Tech transfer as and when needed
Pfizer Revolution Global SOPs management activities: Responsible for role of LPO for processes for Pfizer, Accountable for local process performance. Several LPOs could be assign to each L2 process, depending on local process requirements.
Any other responsibilities assigned by the Manager.

Here Is What You Need (Minimum Requirements)

B. Pharm/ M. Pharm / M.Sc.
10 + years of pharmaceutical industrial experience .
Exceptional organizational and project management skills
Demonstrated strength in analytical skills and meticulous attention to detail
A solid understanding of the regulatory and audit frameworks pertinent to biopharmaceutical operations
Proficiency in taking decisive action based on quality and compliance metrics and trends
Capable of managing multiple complex projects with a strong sense of business acumen
Excellent interpersonal effectiveness, coupled with superior written and verbal communication skills

Bonus Points If You Have (Preferred Requirements):

Master's degree
Experience in aseptic processes and operational knowledge
Knowledge of training design and tools and experience in applying training methodology
Ability to adapt to changing priorities and manage multiple tasks simultaneously
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control

Skills Required

B. Pharm/ M. Pharm / M.Sc.
10+ years of pharmaceutical industry experience
Knowledge of regulatory and audit frameworks for biopharmaceutical operations
Experience in GMP compliance, batch record review, and release authorization
Experience reviewing and approving change controls and regulatory submission packages
Strong organizational and project management skills
Analytical skills and meticulous attention to detail
Ability to act on quality and compliance metrics and trends
Capability to manage multiple complex projects with business acumen
Excellent written and verbal communication and interpersonal effectiveness
Master's degree
Experience in aseptic processes and operational knowledge
Knowledge of training design, tools, and training methodology
Experience using AI tools (e.g., ChatGPT, Microsoft Copilot) and understanding of responsible AI practices
Ability to adapt to changing priorities and manage multiple tasks simultaneously

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Healthcare Strength — Multiple U.S. medical plan options include telehealth, comprehensive mental‑health support, fertility/family‑building benefits, transgender‑inclusive coverage, and certain Pfizer medications at no cost. A Wellbeing Wallet and wellness resources broaden the health and wellbeing offering.
Retirement Support — A 401(k) with company matching is paired with an additional Pfizer Retirement Savings Contribution, alongside company‑paid life and disability insurance. One‑on‑one financial planning support is provided through Fidelity.
Leave & Time Off Breadth — Paid time off spans vacation, holidays, and personal days, with additional caregiver and medical leave. U.S. parental leave commonly includes 12 weeks paid with options for additional unpaid bonding time and a return‑to‑work transition.

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.