Sr. Executive-Quality Control Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

institute logo

Sr. Executive-Quality Control Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

work outline icon8 - 12 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. Executive-Quality Control
  2. Qualification: MPharm/BPharm
  3. Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
  4. Work Experience: 8 to 12 Years

Job Description

  1. Perform and supervise QC testing activities.
  2. Review analytical results, worksheets & reports.
  3. Ensure compliance with GMP / GLP & SOPs.
  4. Investigate and close OOS / OOT / deviations.
  5. Support method validation and stability studies.
  6. Ensure proper operation, calibration & upkeep of QC instruments.
  7. Maintain accurate documentation and data integrity.
  8. Train and guide junior QC staff.
  9. Coordinate with QA, Production & ADL teams.

Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Sr. Executive-Quality Control 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 Control (QC)

Preferred Education

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

Key Skills

Communication SkillsProblem Solving SkillsAnalytical SkillsDocumentation

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.

Aggregated job.

Learn more