Officer/Sr. Officer-ADL Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

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Officer/Sr. Officer-ADL Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

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

Job Description

  1. Develop and optimize analytical methods for API / formulations.
  2. Perform method validation & verification as per ICH.
  3. Conduct stability & forced degradation studies.
  4. Prepare analytical protocols, STPs & validation reports.
  5. Support analytical troubleshooting during development.
  6. Transfer validated methods to QC and provide support.
  7. Ensure compliance with GMP, GLP & data integrity requirements.
  8. Maintain ADL documentation & laboratory records.
  9. Support regulatory submissions & queries.
  10. Participate in audits and inspections.

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

R&D / F&D / ADL

Preferred Education

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

Key Skills

DocumentationAnalytical SkillsProblem Solving SkillsCoordination Skills

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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