India Quality assurance managers Jobs – 1498 Open Jobs Today

Compliance Manager - APAC
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Microsoft Office
- Analysis skills
- Bachelor's degree
1d
Assistant Manager Quality
SA Management Services —Chakan, Pune, Maharashtra
- ₹8,00,000 - ₹12,00,000 a year
- Full-time
- Bachelor's degree
- In-person
- Manufacturing
- Commuter assistance
- Food provided
Quick apply
1d
Quality Manager
Shri Parmanand Steel Industries Pvt Ltd —Bawal, Haryana
- ₹10,00,000 - ₹12,00,000 a year
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Food provided
- Paid sick time
Quick apply
Quality Assurance Executive
VINT Foods & Beverages —Madhapur, Hyderabad, Telangana
- ₹35,000 - ₹39,000 a month
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
Quality Assurance Executive / Manager (Essential Oil)
NCR BACKUP ACADEMY —Greater Noida, Uttar Pradesh
- ₹25,000 - ₹70,000 a month
- Full-time
- Microsoft Word
- Microsoft Excel
- B.Sc
Quick apply
Quality manager|International|07082025
TGBPL TP India - IBU —Hyderabad, Telangana
- Full-time
- Remote
- Work from home
Quality & Compliance Manager
GD Goenka Healthcare Pvt Ltd —New Delhi District, Delhi
- ₹50,000 - ₹70,000 a month
- Full-time
- In-person
- Health insurance
- Paid time off
Quick apply
Assistant Manager - Quality Assurance
Jiaan Biotech —Pithampur, Madhya Pradesh
- ₹2,21,336.44 - ₹11,85,814.70 a year
- Full-time
- Quality control
- APIs
- In-person
Quick apply
Executive - Quality
Larsen & Toubro —Coimbatore, Tamil Nadu
- ₹5,50,000 - ₹6,50,000 a year
- Assembly
- Bachelor's degree
- Leadership
Quality general Manager
WELCORD COMPONENTS PVT. LTD. —Puducherry, Puducherry
- ₹20,000 - ₹60,000 a month
- Full-time
- Engineering
- Analysis skills
- Bachelor's degree
Quick apply
Head of Quality Assurance
Coppergate Consultants Private Limited —Vadodara, Gujarat
- ₹25,00,000 - ₹30,00,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Welding
- Commuter assistance
Quick apply
10d
Quality Manager
Frumar Agri Pvt Ltd —Hyderabad, Telangana
- ₹5,00,000 - ₹9,00,000 a year
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply
Asst. Manager Quality
Amber Enterprises India Ltd —Kancheepuram District, Tamil Nadu
- ₹5,00,000 - ₹9,00,000 a year
- Full-time
- Bachelor's degree
- Quality control
- In-person
Quick apply
Assistant Quality Manager
Bakewell industries pvt Ltd. —Kompally, Hyderabad, Telangana
- ₹30,000 - ₹45,000 a month
- Full-time
- Quality control
- In-person
- Manufacturing
- Health insurance
Quick apply
Officer/Executive - QA
Quality HR India Pvt Ltd —Silvassa, Daman and Diu
- Up to ₹4,00,000 a year
- Full-time
- B.Sc
- Microsoft Office
- Master's degree
Quick apply
Manager Quality Assurance
ANANNYA POWER —Vizianagaram, Andhra Pradesh
- ₹60,000 - ₹75,000 a year
- Full-time
- Bachelor's degree
- In-person
- Manufacturing
- Food provided
Quick apply
Quality Manager
BlueBerry Agro Products Pvt Ltd —Kanchad, Maharashtra
- ₹5,35,706.49 - ₹13,36,661.86 a year
- Full-time
- Management
- Master's degree
- Analysis skills
Quick apply
Quality Head
Shreem Talent Bridge —Gurugram, Haryana
- ₹15,00,000 - ₹30,00,000 a month
- Analysis skills
- Bachelor's degree
- Continuous improvement
Quick apply
Quality Manager
GURUPRIYA TELEAUTO PRIVATE LIMITED —Bommasandra Industrial Estate, Bengaluru, Karnataka
- ₹45,000 - ₹55,000 a month
- Full-time
- Quality control
- In-person
- Manufacturing
Quick apply
5d
Assistant General Manager – Quality Control (AGM - QC)
Sudeep Nutrition Pvt Ltd —Rania, Vadodara, Gujarat
- ₹18,00,000 - ₹21,00,000 a year
- Full-time
- Master's degree
- Quality control
- In-person
Quick apply

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Compliance Manager - APAC

Thermo Fisher Scientific -
Remote

Apply Now

Job details

Full-time
1 day ago

Qualifications

Clinical research
Quality management
Microsoft Office
Analysis skills
Quality assurance
Bachelor's degree
Conflict management
Root cause analysis
Project leadership
Negotiation
Time management

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

As a Compliance Manager within the Audits and Inspections team, you will be responsible for managing all aspects of GxP audits and Regulatory Authority inspections for the company, investigator sites, and clients. The Compliance Manager leads and/or reviews complex internal and external audits and inspections to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Majority of the work is focused on the APAC region; however, inspection support in other regions is also in scope.

What you will do:

Provide consultation to project teams and clients on GxP audit and inspection readiness, preparation, management, and follow-up activities.
Serve as the primary point of contact for audit and inspection-related discussions with clients.
Support client audits and GxP regulatory authority inspections of the company, investigator sites, and sponsors, including risk assessment and mitigation strategies, training of involved staff and conducting mock interviews, internal preparation, pre-inspection / mock inspection activities, review of documentation requested by inspectors, audit/inspection hosting and facilitation, and post-inspection follow-up.
Lead, review, and approve reports for a variety of client, internal, or GxP audits and regulatory inspections.
Support project teams in investigating root causes of findings/non-conformances and in developing CAPAs to address identified issues; follow up on action implementation, effectiveness checks, and the collection and review of supporting evidence.
Contribute to lessons learned discussions and participate in company-wide improvement initiatives.
Develop and effectively share guidance and reference information, repositories, and communication channels including policies, procedures, guidance documents, or quality management systems training.
Lead process improvement initiatives and collaborate with a variety of cross functional staff to ensure appropriate execution and completion and continuous improvement.
Develop tools and other materials for tracking of compliance management activities and analyse trends.
Mentor less experienced staff and serve as project lead for group projects.
Identify and resolve issues impacting the quality and/or integrity of clinical research programs, determine root cause of non-conformance and develop strategies to address issues.
Prepare and present audit findings and/or other related information at departmental, internal operations or client meetings.

Education & Experience

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Preferred Fields of Study: Biology, Pharmacy or related
5+ years of quality assurance experience that provides the knowledge, skills, and abilities to perform the job or equivalent combination of education, training, & experience.
1+ years of experience in management/leadership roles preferred

Knowledge, Skills, Abilities

Extensive knowledge of GxP, with GCP required, along with a strong understanding of applicable regional clinical research regulations, requirements and guidelines, along with applicable global guidelines / requirements
Proven expertise and experience in quality management systems and regulatory frameworks, conducting internal audits, supporting, hosting/management of client audits and GxP regulatory inspections across the region
Proven experience in root cause analysis
Strong problem solving, critical thinking, risk assessment and impact analysis abilities
Detail oriented with ability to deal with multiple and changing priorities
Exceptional communication (verbal and written) and presentation skills (including appropriate use of medical and scientific terminology)
Strong negotiation and conflict management skills
Ability to effectively mentor and provide direction to staff and to work independently or in a team environment
Strong organizational and time management skills, flexibility and ability to multi-task and prioritize complex demands/workload
Advanced proficiency in Microsoft Office Suite and compliance-related software. Veeva QMS experience is a plus

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Apply Now

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