Executive – Quality Assurance

Please Note:

• We strongly advice you to read the entire Job Description before applying
• Please rename your Resume/CV to your first name + Job Title to avoid spamming or being quarantined by the system.
• Applications submitted for this position may also be considered for suitable roles within Natural Capsules Limited (NCL), the parent company of NBPL.
• Management have the right to alter any specification as deemed suited for the organisation.

This job is under scope for our API (Active Pharmaceutical Ingredient) manufacturing division under Pharmaceutical industry.

Job Title
: Assistant Manager – Quality Assurance (QA)

Location
: Vasanthnarasapura KIADB Industrial Area, Tumkur, Karnataka

Experience
: 2 to 4 years in API Manufacturing (Active Pharmaceutical Ingredients)

Qualification
: BSc. in Chemistry

Industry
: API (Active Pharmaceutical Ingredient) Manufacturing

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

No of Position Available
: - 2

About Natural Biogenex Private Limited. (NBPL)

Natural Biogenex Pvt. Ltd. (NBPL), a subsidiary of Natural Capsules Limited, is a specialised API manufacturing company with state-of-the-art facilities in Tumkur, Karnataka. We are committed to delivering high-quality steroidal APIs and intermediates while strictly adhering to global regulatory and compliance standards.

As we continue to expand, we seek, Executive – Quality Assurance (QA) to strengthen our QA team and uphold our commitment to excellence, compliance, and continuous improvement.

Role Summary

The
QA Executive
will be responsible for supporting all day-to-day activities within the Quality Assurance department. The role involves ensuring compliance with GMP guidelines, maintaining documentation accuracy, assisting in audits, and supporting quality control and manufacturing teams.

Key Responsiblities

• Support the implementation and maintenance of the Quality Management System (QMS).
• Ensure compliance with
  Good Manufacturing Practices (GMP)
  and standard operating procedures (SOPs).
• Review and maintain batch manufacturing records, test reports, and related QA documentation.
• Assist in handling deviations, change controls, CAPAs, and internal audits.
• Monitor in-process quality checks and ensure adherence to quality parameters.
• Participate in the qualification and validation activities of equipment and processes.
• Coordinate with production, QC, and warehouse departments to ensure product quality compliance.
• Maintain records for document control and ensure timely issuance and retrieval of controlled documents.
• Assist in preparing for customer and regulatory audits.
• Support the QA Manager and Assistant Manager in day-to-day departmental functions.

Educational Qualification

• B.Sc. in Chemistry
  (or equivalent scientific discipline).
• 2–4 years of experience
  in
  Quality Assurance
  within the
  pharmaceutical industry
  (preferably API or formulations).
• Good knowledge of
  GMP
  ,
  GDP
  , and
  regulatory guidelines
  .
• Familiarity with QA documentation, audit readiness, and compliance systems.
• Strong analytical and observational skills.
• Good written and verbal communication skills.

Preferred Skills

• Hands-on experience in document review, validation support, and batch record checks.
• Exposure to handling deviations, CAPA, and OOS investigations.
• Understanding of change control and risk management processes.
• Proficiency in MS Office (Word, Excel, PowerPoint).

What we offer

• Competitive remuneration package.
• Opportunities for learning, career development, and internal growth.
• Exposure to best-in-class QA practices in an expanding pharmaceutical setup.
• Supportive and professional work environment.