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

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

work outline icon2 - 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: Officer/Sr. Officer-QA
  2. Qualification: MPharm/BPharm
  3. Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
  4. Work Experience: 2 to 5 Years

Job Description

  1. Review and approve batch manufacturing & packaging records.
  2. Ensure compliance with GMP and regulatory requirements.
  3. Prepare, review & control SOPs and quality documents.
  4. Handle deviations, OOS/OOT, CAPA & change control activities.
  5. Support internal audits and regulatory inspections.
  6. Monitor quality systems and continuous improvement.
  7. Coordinate with QC, Production & Validation teams.
  8. Ensure data integrity and documentation accuracy.
  9. Train staff on GMP & quality procedures.

Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Officer/Sr. Officer-QA 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

Risk Management SkillsGood CommunicationCoordination SkillsTeamwork

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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