Executive/Sr. Executive-Formulation & Development Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

institute logo

Executive/Sr. Executive-Formulation & Development Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad

work outline icon4 - 8 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: Executive/Sr. Executive-Formulation & Development
  2. Qualification: MPharm
  3. Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
  4. Work Experience: 4 to 8 Years

Job Description

  1. Perform formulation development for new products.
  2. Conduct pre-formulation and compatibility studies.
  3. Develop robust, stable and cost-effective formulations.
  4. Execute lab-scale, pilot-scale & scale-up batches.
  5. Prepare development protocols, reports & SOPs.
  6. Support technology transfer to manufacturing.
  7. Coordinate with ADL for method development & validation.
  8. Monitor stability studies and recommend improvements.
  9. Assist in regulatory submissions (CTD/ANDA support).
  10. Ensure compliance with cGMP & data integrity.
  11. Provide technical support during process validation.

Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Executive/Sr. Executive-Formulation & Development 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)

Key Skills

Communication SkillsDocumentationCoordinationTeamwork

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