Executive / Sr. Executive – QA Documentation

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• Kindly rename your Resume/CV as: First Name + Job Title to avoid system filtering.
• Applications may also be considered for suitable roles within Natural Biogenex Private Limited (NBPL), a subsidiary of NCL.
• Management reserves the right to modify specifications as deemed appropriate for the organization.

Job Title: Sr Executive/Executive QA Documentation

Location: Attibele, Bengaluru, Karnataka

Experience: 2-3 year experience.

Qualification: BSc/MSc or 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 Gelatine (EHG) and HPMC capsules, catering to pharmaceutical, nutraceutical, and herbal industries across India and global markets. With decades of expertise, advanced manufacturing facilities, and a strong commitment to quality, NCL delivers reliable and innovative capsule solutions aligned with international standards.

Our subsidiary, Natural Biogenex Private Limited (NBPL), expands our capabilities into Steroid APIs and intermediates, providing integrated solutions across the pharmaceutical value chain.

At NCL and NBPL, we emphasize operational excellence, continuous improvement, and a people-centric culture that promotes growth, accountability, and innovation.

JOB SUMMARY

We are seeking a detail-oriented and quality-focused professional for the role of Executive / Sr. Executive QA Documentation. The candidate will be responsible for handling and reviewing critical Quality Management System (QMS) documents while supporting validation, qualification, calibration, and audit readiness activities in compliance with GMP and regulatory requirements.

KEY RESPONSIBILITIES:

Handle and review QMS documents including Deviation, OOS, OOT, BMR, and BPR

Ensure documentation compliance with GMP guidelines and regulatory standards

Support validation and calibration activities of instruments and equipment

Perform qualification and requalification of equipment

Maintain accurate, complete, and audit-ready documentation

Support internal and external audit activities

Coordinate with cross-functional departments to ensure documentation accuracy and compliance

ELIGIBILITY CRITERIA:

• B.Sc / M.Sc in Microbiology or Biotechnology
• Candidates with relevant experience of 2-3 years is mandatory
• Must know to leverage technology and AI for day to day activity in order to get result accurate and swiftly.

What we are looking for:

Strong understanding of QMS documentation practices

Knowledge of GMP and pharmaceutical compliance requirements

Familiarity with validation and calibration procedures

High attention to detail and documentation accuracy

Good analytical, communication, and coordination skills

Ability to work effectively in a regulated pharmaceutical environment.

WHY JOIN US?

Be part of a leading pharmaceutical/API manufacturing organization

Exposure to global regulatory standards and audit practices

Opportunity to work in a high-performance, growth-driven environment

Competitive compensation with career advancement opportunities