Sun Pharmaceutical Industries Ltd has announced an excellent career opportunity for experienced life sciences professionals to join its R&D Quality division as Executive โ R&D Quality GCP QA at Gurugram, Haryana. Candidates with a graduate or postgraduate degree in basic sciences and relevant experience in the BA/BE environment can apply for this quality assurance position.
If you are looking for a pharmaceutical quality assurance career with one of India’s leading pharmaceutical companies, this opportunity offers exposure to GCP/GLP compliance, bioanalytical audits, regulatory inspections, and global quality systems.
Job Overview
- Company: Sun Pharmaceutical Industries Ltd
- Position: Executive โ R&D Quality GCP QA
- Business Unit: Sun R&D Quality
- Job Grade: G12A
- Department: Quality Assurance
- Job Location: Gurugram, Haryana, India
- Experience Required: Minimum 2โ3 years
- Qualification: Graduate or Postgraduate Degree in Basic Sciences
- Travel Requirement: Nil
About Sun Pharmaceutical Industries Ltd
Sun Pharmaceutical Industries Ltd is one of India’s largest pharmaceutical companies with a strong global presence. The company promotes continuous learning, collaboration, and employee development through its culture of innovation and quality excellence.
Key Roles & Responsibilities
The selected candidate will be responsible for:
- Conducting BA/BE study audits including bioanalytical in-process audits, retrospective audits, pharmacokinetic audits, and statistical audits.
- Performing system, facility, and process-based QA audits.
- Reviewing, coordinating, and implementing Quality Assurance SOPs, GSOPs, and other global quality documents.
- Supporting the preparation and review of operational SOPs with cross-functional stakeholders.
- Conducting qualification and re-qualification audits of CROs, CSPs, and material suppliers.
- Reviewing study protocols, method validation documents, raw data, and study reports for regulatory compliance.
- Reviewing PBPK and PBBM model reports generated within the organization.
- Reviewing SOPs, GSOPs, ATP documents, instrument qualification records (IQ/OQ/PQ/DQ), and validation documents.
- Reviewing Quality Management System records including deviations, incidents, investigations, CAPA, temporary change controls, and change controls.
- Preparing audit reports and escalating critical compliance observations.
- Supporting regulatory inspections and coordinating CAPA implementation.
- Assisting in training programs related to applicable regulations, SOPs, and quality guidelines.
Required Qualifications
Candidates should possess:
- Graduate or Postgraduate Degree in Basic Sciences.
Experience Required
Applicants should have:
- Minimum 2โ3 years of experience in the BA/BE environment.
- Preference will be given to candidates with QA experience.
- Experience in PBPK/PBBM studies will be an added advantage.
Technical Skills
Candidates should have knowledge of:
- International GCP and GLP regulations
- Clinical research processes
- Quality Assurance systems
- Auditing techniques
- Pharmacokinetics
- Statistical analysis and related tools
- Computer and IT systems
Desired Soft Skills
- Strong result orientation
- Teamwork and collaboration
- Customer-centric mindset
- Excellent written and verbal communication
- Problem-solving ability
Salary & Benefits
Although the company has not officially disclosed the salary, candidates with similar experience can expect an estimated annual compensation in the range of โน7,00,000 โ โน11,00,000, depending on qualifications, experience, and company policies.
Employees may also receive benefits such as:
- Career development opportunities
- Learning and training programs
- Exposure to global quality systems
- Collaborative work environment
- Performance-based growth opportunities
- Employee wellness initiatives
Selection Process
The selection process may include:
- Application Screening
- Technical Evaluation
- Interview Rounds
- HR Discussion
- Final Offer