Executive QA - Documentation

Natural Capsules Limited

Website: naturalcapsules.com
Job details:

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Job Title: Executive - QA Documentation

Location: Attibele, Bengaluru, Karnataka

Experience: 2-3 years of experience.

Qualification: BSc Graduate (Any Stream), B Pharma

Compensation: Compensation commensurate to the experience and qualification of the candidate

No of Position Available: - 2

ABOUT US

Natural Capsules Limited (NCL) is a leading manufacturer of high-quality Hard Gelatin (EHG) and HPMC capsules, serving pharmaceutical, nutraceutical, and herbal industries across India and global markets. With decades of expertise, advanced manufacturing facilities, and a strong commitment to quality, we deliver innovative and reliable capsule solutions that meet international standards.

Our subsidiary, Natural Biogenex Private Limited (NBPL), strengthens our portfolio by offering Steroid API and its Intermediaries, ensuring end-to-end support for our partners in the healthcare sector.

At NCL and NBPL, we believe in operational excellence, continuous improvement, and a people-first culture. We are committed to fostering a professional, inclusive, and growth-oriented work environment where talent is recognised, nurtured, and empowered.

JOB SUMMARY

As a QA Documentation Executive / Reviewer, you will be responsible for managing and reviewing critical QMS documents while supporting validation, qualification, and audit readiness activities. The ideal candidate should have strong attention to detail and the ability to maintain high-quality standards throughout the process. The ideal candidate will have strong functional knowledge, technical capability, and excellent communication skills suitable for client-facing engagements.

KEY RESPONSIBILITIES:

· Handling QMS documents – Deviation, OOS, OOT, BMR, BPR

· Ensuring compliance with GMP and regulatory standards

· Supporting validation & calibration of instruments

· Managing qualification & requalification of equipment

· Maintaining audit-ready documentation and assisting in audits

· Coordinating with cross-functional teams for documentation accuracy

WHAT WE’RE LOOKING FOR:

• Strong knowledge of QMS & GMP practices
• High attention to detail
• Good analytical and documentation skills
• Team player with strong communication abilities

ELIGIBILITY CRITERIA:

• B.Sc / M.Sc / B.Pharm
• 2–3 years of experience in QA (Pharma preferred)

WHY JOIN US?

🔹 Be a part of a leading API manufacturing company with cutting-edge technology and compliance standards.

🔹 Work in a state-of-the-art Quality Control Laboratory with global regulatory standards.

🔹 Opportunity to contribute to regulatory audits and pharmaceutical quality excellence.

🔹 Competitive salary and professional development opportunities.

Click on Apply to know more.