Sr. Officer-QA (AQA) Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

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Sr. Officer-QA (AQA) Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Stallion Laboratories Pvt Ltd

time outline iconBavla, Gujarat, India

Posted on 28-01-2026

1 Vacancy

Description

  1. Job Title: Sr. Officer-QA (AQA)
  2. Qualification: MPharm/BPharm
  3. Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
  4. Work Experience: 0 to 5 Years

Job Description

  1. Review and approve analytical data generated by QC.
  2. Evaluate and close analytical OOS / OOT / deviations.
  3. Review STPs, SOPs, specifications, and test methods.
  4. Ensure compliance with data integrity & GMP requirements.
  5. Support method validation, transfer & verification activities.
  6. Review stability data and prepare trend analysis.
  7. Participate in internal audits and regulatory inspections.
  8. Coordinate with QC, QA & regulatory teams.
  9. Ensure timely closure of CAPA & change controls.
  10. Maintain QA documentation and ensure audit readiness.

Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Sr. Officer-QA (AQA) in Bavla, Ahmedabad and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

TeamworkGood CommunicationCoordinationProblem Solving

About Organization

Stallion Laboratories Pvt Ltd, Bavla, Ahmedabad, Gujarat, is a reputed pharmaceutical manufacturing company focused on quality, compliance, and regulatory excellence. The company is expanding its quality assurance team and inviting applications for this role. The responsibilities include preparation and execution of validation protocols, review of validation documentation, handling deviations, change control and CAPA activities, ensuring compliance with cGMP and regulatory guidelines, coordination with production and quality control departments, support during internal and external audits, and maintenance of accurate quality records. This opportunity offers strong exposure to pharmaceutical validation systems, professional growth, and long-term career development in a structured and quality-driven work environment.

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