Looking for pharma jobs in Gujarat? Endoc Lifecare Pvt Ltd is urgently hiring Quality Assurance (QA) Executive/Sr. Executive and Regulatory Affairs (RA) Executive/Sr. Executive professionals for its API pharmaceutical operations in Rajkot.
Experienced candidates with expertise in GMP, QMS, regulatory compliance, and dossier preparation are encouraged to apply.
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About the Company
Endoc Lifecare Pvt Ltd is an ISO 9001 and WHO-GMP certified pharmaceutical company specializing in Active Pharmaceutical Ingredients (API) manufacturing. The company is committed to delivering high-quality pharmaceutical products while maintaining strict regulatory compliance and international quality standards.
With a strong focus on innovation, quality systems, and regulatory excellence, Endoc Lifecare continues to strengthen its position in the pharmaceutical industry. The organization offers professionals an opportunity to work in a compliance-driven environment with exposure to global regulatory requirements and industry best practices.
Job Details
- Company Name: Endoc Lifecare Pvt Ltd
- Positions: QA Executive/Sr. Executive & RA Executive/Sr. Executive
- Experience: 5–7 Years
- Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry or Relevant Discipline)
- Location: Shapar, Rajkot, Gujarat
- Work Type: On-Site
- Industry: API Pharmaceutical Manufacturing
- Vacancies: 2 Positions (1 QA, 1 RA)
Job Description
Endoc Lifecare Pvt Ltd is seeking experienced pharmaceutical professionals for its Quality Assurance and Regulatory Affairs departments. Selected candidates will play a critical role in ensuring regulatory compliance, maintaining quality systems, supporting audits, and managing pharmaceutical documentation in an API manufacturing environment.
Quality Assurance (QA) Executive / Sr. Executive
- Department: Quality Assurance
- Role: Executive / Sr. Executive
- Experience: 6–7 Years
- Education/Qualification: B.Pharm, M.Pharm, M.Sc.
- Industry: API Pharmaceutical Manufacturing
- Vacancies: 1
Regulatory Affairs (RA) Executive / Sr. Executive
- Department: Regulatory Affairs
- Role: Executive / Sr. Executive
- Experience: 5–6 Years
- Education/Qualification: B.Pharm, M.Pharm, M.Sc.
- Industry: API Pharmaceutical Manufacturing
- Vacancies: 1
Skills & Qualifications
Candidates should possess:
- Strong knowledge of GMP and QMS systems
- Experience with CAPA and change control management
- Understanding of deviations, OOS, OOT, and incidents
- Expertise in process and cleaning validation
- Vendor qualification experience
- Regulatory audit and inspection management skills
- Knowledge of DMF, CEP, CTD, and eCTD submissions
- Regulatory dossier preparation expertise
- Documentation and compliance management skills
- Strong communication and coordination abilities
- Understanding of API manufacturing processes
- Customer and regulatory audit handling experience
Key Responsibilities
Quality Assurance Role
- Review batch manufacturing records.
- Approve SOPs and specifications.
- Manage deviations and CAPA.
- Handle change controls and risk assessments.
- Conduct internal GMP audits.
- Support regulatory inspections.
- Review validation documents.
- Maintain QMS documentation.
- Qualify vendors and suppliers.
- Address audit observations.
Regulatory Affairs Role
- Prepare regulatory dossiers.
- Manage DMF and CEP submissions.
- Maintain regulatory documentation.
- Coordinate regulatory responses.
- Handle customer regulatory queries.
- Monitor global regulatory changes.
- Review declarations and statements.
- Support regulatory audits.
- Ensure submission compliance.
- Maintain regulatory records.
Benefits & Perks
- Opportunity to work in a WHO-GMP certified company
- Exposure to global regulatory standards
- Professional growth in API pharmaceutical sector
- Learning opportunities with experienced teams
- Competitive salary package
- Regulatory and compliance expertise development
- Stable and professional work environment
- Career advancement opportunities
- Exposure to USFDA and EU-GMP compliance systems
- Long-term professional growth
How to Apply
Interested candidates can share their updated resume directly with the HR department.
Email: hrd@endocpharma.com
Contact Number: +91 98750 91526
Candidates with relevant API pharmaceutical experience and immediate availability will be preferred.
For more pharma jobs, QA jobs, RA jobs, and pharmaceutical career opportunities, visit:
Apply today and advance your pharmaceutical career with Endoc Lifecare Pvt Ltd.
Why You Should Join Endoc Lifecare Pvt Ltd
Endoc Lifecare offers an excellent opportunity for experienced pharmaceutical professionals to work in a highly regulated API manufacturing environment. The company emphasizes quality, compliance, and continuous improvement while maintaining international standards.
Professionals joining Endoc Lifecare gain valuable exposure to regulatory submissions, quality systems, validation activities, and international audits. The organization’s commitment to excellence and employee development makes it an attractive destination for long-term pharmaceutical careers.
Frequently Asked Questions (FAQs)
Who can apply for these positions?
Candidates with B.Pharm, M.Pharm, or M.Sc. qualifications and relevant API pharmaceutical experience can apply.
Is API industry experience mandatory?
Yes. The company specifically requires experience within an API pharmaceutical manufacturing environment.
How can I apply for the job?
Interested candidates can email their updated resume to hrd@endocpharma.com or contact the HR team at +91 98750 91526.
What regulatory exposure is required for the QA role?
Candidates should have experience with GMP, QMS, CAPA, deviations, validation activities, and regulatory audits including USFDA, EU-GMP, and WHO-GMP inspections.
What regulatory documentation experience is required for the RA role?
Candidates should have hands-on experience with DMF, CEP, CTD/eCTD submissions, regulatory dossiers, and global regulatory compliance requirements.
