Senior Manager, Corporate Quality Policy
Sun Pharmaceutical Industries Ltd —Tandalja, Vadodara, Gujarat
- Doctoral degree
- English
- Master's degree
5d
Plant Operator
Life Chem Pharma —Ankleshwar, Gujarat
- ₹15,000 - ₹35,000 a month
- Full-time
- B.Sc
- Bachelor's degree
- Computer skills
- Paid time off
Quick apply
QC Chemist
Babyorgano —Makarba, Ahmedabad, Gujarat
- ₹45,000 - ₹50,000 a month
- Full-time
- Analysis skills
- Bachelor's degree
- Quality control
Quick apply
Comm Ops Quality Specialist
Zentiva Group, a.s. —Ankleshwar, Gujarat
- Full-time
- English
- Bachelor's degree
- Agile
Officer, Quality Control
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Bachelor's degree
2d
QC - G12C
Sun Pharmaceutical Industries Ltd —Halol, Gujarat
- Master's degree
Deputy Manager - Quality Assurance / API - WHO-GMP Facility
RELIANCE RASAYAN PVT LTD —Naroda Gidc, Ahmedabad, Gujarat
- ₹45,000 - ₹50,000 a month
- Full-time
- Master's degree
- Bachelor's degree
- EMR systems
Quick apply
Executive
Cadila Pharmaceuticals Ltd —Ankleshwar, Gujarat
- Full-time
3d
Senior Executive, Quality Control
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
Quality Operations Specialist
Zentiva Group, a.s. —Ankleshwar, Gujarat
- Full-time
- English
- Bachelor's degree
- Organizational skills
Manager - QA/QC and R&D
Girnar Ayurvedic Pharmacy Pvt. Ltd. —Bavla, Ahmedabad, Gujarat
- ₹45,000 - ₹50,000 a month
- Full-time
- Master's degree
- Bachelor's degree
- In-person
- Health insurance
Quick apply
Sr. Quality Operations Specialist
Zentiva Group, a.s. —Ankleshwar, Gujarat
- Full-time
- English
- Bachelor's degree
- Organizational skills
Store Officer
Galentic pharma —Gandhidham, Gujarat
- ₹3,00,000 - ₹5,00,000 a year
- Full-time
- B.Sc
- ERP systems
- Master's degree
- Health insurance
- Flexible schedule
Quick apply
Manager -2
Sun Pharmaceutical Industries Ltd —Halol, Gujarat
- Bachelor's degree
- Manufacturing
Executive, Manufacturing Process Operations
Amneal Pharmaceuticals —Dahej, Gujarat
- Full-time
- Master's degree
- Bachelor's degree
- APIs
Lab Technician
EXCELLENT WEBWORLD —Ahmedabad, Gujarat
- Laboratory experience
- Bachelor's degree
- Quality control
9d
Boiler Operator
People Human Resource Development Foundation —Bharuch, Gujarat
- ₹2,00,000 - ₹3,00,000 a year
- Full-time
- Electrical experience
- In-person
- Manufacturing
- Flexible schedule
- Food provided
Quick apply
3d
QC Officer
Briyosis Softcaps Pvt Ltd —Jarod, Vadodara, Gujarat
- ₹2,50,000 - ₹3,50,000 a year
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply
Senior Officer, Administrative Support
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Executive Quality Assurance
Contract Pharmacal Corp. —Ahmedabad, Gujarat
- From ₹25,000 a month
- Full-time
- Microsoft Word
- Microsoft Excel
- Master's degree
- Health insurance
Quick apply

I want to receive the latest job alerts for pharmaceutical quality control in gujarat

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

pharmaceutical quality control jobs near gujarat

Plant Operator jobs in Ankleshwar, Gujarat

Quality Assurance Analyst jobs in Ahmedabad, Gujarat

Laboratory Technician jobs in Ahmedabad, Gujarat

Control Officer jobs in Jarod, Vadodara, Gujarat

Policy Manager jobs in Delhi, Delhi

Public Policy Intern jobs in Delhi, Delhi

Food Quality Manager jobs in Bengaluru, Karnataka

Policy Manager jobs in Mumbai, Maharashtra

Hr Manager jobs in Salem, Tamil Nadu

It Project Manager jobs in Chennai, Tamil Nadu

Policy Manager jobs in Kolkata, West Bengal

Policy Manager jobs in Delhi

Trainee Quality Control jobs in Kerala

Quality Specialist jobs in Hyderabad District, Telangana

Quality Specialist jobs in Bengaluru, Karnataka

Food Quality jobs in Calicut, Kerala

Garment Quality jobs in Okhla, Delhi, Delhi

Quality Assurance jobs in Kerala

Quality Specialist jobs in Chennai, Tamil Nadu

Quality Specialist jobs in Maharashtra

Senior Manager, Corporate Quality Policy

Sun Pharmaceutical Industries Ltd -
Tandalja, Vadodara, Gujarat

Apply Now

Job details

5 days ago

Qualifications

Doctoral degree
English
Master's degree
Quality assurance
M.Pharma
Pharmacy
Technical writing

Full job description

Title: Senior Manager, Corporate Quality Policy

Date: Jun 1, 2026

Location: Tandalja - R&D

Company: Sun Pharmaceutical Industries Ltd

Title: Senior Manager, Corporate Quality Policy

Business Unit: Quality

Job Grade: G9

Location: Baroda

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

JOB DESCRIPTION:

Job Summary:

Author Global Documents in partnership with functional area SMEs and business co-owners ensuring that global documents are designed to a comprehensive level, and agreed upon by stakeholders.

Responsible for working with corporate functions, influencing process, tool and template improvement and helping to facilitate alignment across multiple functional manuals.

Additionally, this role will ensure all documents authored are aligned to compendial, ICH, FDA and other regulatory guidance expectations. The role requires to work independently and manage multiple assignments simultaneously with business co-owners and functional key SMEs.

Essential Job Functions:

Author and fully manage the lifecycle (development, review, change control, execution, approval, effective status, training activities, revision, obsoletion, periodic review etc.) of global documents.

Ensure all written documents are aligned and confirmed to an approved document format, standards, style, methodology and terminology.

Work using Sun Pharma’s eDMS system ensuring proper workflows are utilized with appropriate review and approval for all global documents.

Function as the SME and keep abreast of updates on the applicable health agency regulations and best industry practices. Provide technical and regulatory guidance with respect to global regulations to internal and external stakeholders ensuring overall quality and compliance.

Oversee and drive implementation of global documents with regulated market site representatives in order to direct and facilitate implementation and guide sites to overcome hurdles in implementation as required by effectively facilitating discussions to attain consensus between business stakeholders.

Ensure that target dates for updates on Global document implementation to regulatory bodies, e.g., FDA, are met by timely preparation and site data collection.

Monitor progress of commitments made to regulatory bodies and GxP consultants for Global document creation/revision ensuring the effective document availability within committed timelines.

Own, execute or support the projects and initiatives to enhance processes, compliance and the global document collection e.g., review of site global documents implementation practices and harmonization/reduction/simplification/enhancement of Global documents,

Support site deployment and implementation of process sustainability and effectiveness as a continuous improvement efforts.

Perform periodic assessment of global documents regarding implementation feedback, status based on site inputs, observations based on site self-inspections, corporate audit and regulatory inspections as well as update to regulatory requirements.

Act as a contributing member of the global document SPOC forum, ensuring consistent approaches to document development and site implementation as appropriate.

Develop and manage global documentation implementation packages, request and review site gap assessment forms when necessary.

Conduct and attend cross-functional meetings, quality management review meetings to present global document strategy, status, implementation plan and progress on continuous improvement approach for global documents life cycle management.

Support the upgrade/enhancement of enterprise electronic systems by ensuring timely communications to aid site preparedness, e.g., notification of approved status of system GSOPs, to enable alignment of site readiness to Go-Live target dates.

Carry out effectiveness checks of Global document implementation e.g., performing spot checks on site/function procedures to assess alignment against the requirements in the Global Documents as applicable.

Experience:

Atleast 15 years of experience, good knowledge of GxP regulations (US, EU, Health Canada, TGA, Schedule M, WHO, PIC/S, ICH, etc.) related to 6 quality systems, especially manufacturing, compliance, quality assurance and QMS.
The candidate should be a dynamic result driven and performance oriented professional with excellent competencies of collaboration & empowerment, decision-making, change management and vision.
The candidate would primarily be responsible for authoring global documents and hence should have a good command over English language, with clear technical writing skills. A candidate with primary education in English medium is preferred.

Education: M.Sc./Master of Pharmacy/ Ph.D.

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Apply Now

Refine Your Search

pharmaceutical quality control jobs in gujarat

Senior Manager, Corporate Quality Policy

Plant Operator

QC Chemist

Comm Ops Quality Specialist

Officer, Quality Control

QC - G12C

Deputy Manager - Quality Assurance / API - WHO-GMP Facility

Executive

Senior Executive, Quality Control

Quality Operations Specialist

Manager - QA/QC and R&D

Sr. Quality Operations Specialist

Store Officer

Manager -2

Executive, Manufacturing Process Operations

Lab Technician

Boiler Operator

QC Officer

Senior Officer, Administrative Support

Executive Quality Assurance

I want to receive the latest job alerts for pharmaceutical quality control in gujarat

Explore jobs in more locations

Title: Senior Manager, Corporate Quality Policy

Jobseeker tools

Employer Tools

Browse

Stay Connected