Gujarat Associate manager quality assurance Jobs – 15 Open Jobs Today

Associate manager - Quality Assurance
Pfizer —Ahmedabad, Gujarat
- Full-time
- Microsoft Office
- Master's degree
- Analysis skills
18h
IT Technical Project Coordinator / Associate Project Manager / Assistant Project Manager
Design'N'Buy —Ahmedabad, Gujarat
- Master's degree
- Project management
- Bachelor's degree
Associate Manager – CSR & Skilling Programs
CSRBOX —Ahmedabad, Gujarat
- ₹60,000 - ₹70,000 a month
- Full-time
- Engineering
- Master's degree
- Project management
Quick apply
Associate Manager- QA
Apollo Tyres —Limda, Vadodara, Gujarat
- Master's degree
- Bachelor's degree
- Communication skills
5d
Associate Consultant - Angular
Dynamic Elements —Ahmedabad, Gujarat
- Azure
- Computer Science
- Software troubleshooting
Quick apply
Help Desk Specialist
Stemmons Business Services Private Limited —Vadodara, Gujarat
- Up to ₹35,000 a month
- Full-time
- Computer Science
- Software troubleshooting
- Customer service
Quick apply
Associate BIM
Mott MacDonald —Ahmedabad, Gujarat
- Full-time
- B.Sc
- Analysis skills
- Bachelor's degree
- Health insurance
- Paid sick time
13d
Associate Manager - Yarn Dyeing
The Anup Engineering —Gandhinagar, Gujarat
- ₹4 - ₹6 an hour
- Full-time
10d
Loss Prevention Associate
Marriott International, Inc —Alkapuri, Vadodara, Gujarat
- Full-time
- Hospitality
- 12th Pass
- Supervising experience
Associate Manager - Yarn Dyeing
Arvind Envisol —Gandhinagar, Gujarat
- ₹4 - ₹6 an hour
- Full-time
10d
IT Helpdesk Specialist
Stemmons Business Services —Vadodara, Gujarat
- Rotational shift
- Computer Science
- Software troubleshooting
- Customer service
Draftsman
Stemmons Business Services —Vadodara, Gujarat
- Project management
- Bachelor's degree
- Diploma
Bell Boy
Marriott International, Inc —Ahmedabad, Gujarat
- Full-time
- 12th Pass
- Supervising experience
Export Sales
Jivika Agri —Ahmedabad, Gujarat
- English
Quick apply

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Associate manager - Quality Assurance

Pfizer -
Ahmedabad, Gujarat

Apply Now

Job details

Full-time
18 hours ago

Qualifications

Statistical software
Statistics
Microsoft Office
Master's degree
Analysis skills
Quality assurance
Presentation skills
Bachelor's degree
Risk management
Mentoring
Technical writing
APIs
Manufacturing
Microsoft Project
AI
Communication skills

Full job description

Use Your Power for Purpose

Pfizer is driven by an unwavering commitment to delivering safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Your contributions will be vital and will have a direct impact on patient care, ensuring we deliver on our promise of quality and safety.

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 & 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.
Supplier Quality Management
- Assist with supplier related activties for API, excipient & critical processing aid as per Pfizer Quality standards.
- Ad-hoc activities related to supplier.

Quality Management System (QMS) compliance functions: Assist as required for Review and approval of Investigations (QARs) initiated at ZHOPL.To be part of SQRT and involve in the Investigations.
To provide Quality support for review of documents for new product launches and Tech transfers as needed
Support review of Process validation related documentation performed at ZHOPL.
Training Management for Team.
Assisting with QMS related activities, Including GSOP review and assessment and implementation at site and for Pfizer team.
Other: To support any additional and urgent activity in absence of primary responsible person as assigned by the Manager. As needed to provide Quality support for new product launches and Tech transfer as and when needed.
Assisting with review and approval of investigations.
Managing various Pfizer share points and Pfizer digital systems for activities related to support complaints, Change controls, Investigations, supplier management, Etc.

Here Is What You Need (Minimum Requirements)

B. Pharm/ M. Pharm / M.Sc. with minimum 6+ years of experience
Strong understanding of Quality System functions, manufacturing and packaging processes, validations, batch documents , customer complaints, investigations, Training management, change controls, document Management.
Ability to apply mathematical concepts, particularly statistics and probability, to Quality Engineering tasks
Excellent technical writing, communication, and presentation skills
Proficiency in Microsoft Office, Microsoft Project, and Statistical Software
Experience in preparing and participating in audits and inspections

Bonus Points If You Have (Preferred Requirements)

Background in handling complaints and utilizing electronic lab systems
Strong analytical and problem-solving skills
Ability to work independently and as part of a team
Strong interpersonal skills and the ability to communicate effectively with all levels of the organization
Ability to adapt to changing priorities and manage multiple tasks simultaneously
Experience in mentoring and training colleagues
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

Apply Now

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