Job Opportunity: Multiple Openings at Stallion Laboratories Pvt. Ltd.

Job Summary:
Stallion Laboratories Pvt. Ltd., a premier pharmaceutical manufacturing company established in 1988, is currently seeking dedicated professionals to join our team. We operate state-of-the-art, WHO-GMP-approved manufacturing facilities in Gujarat and are looking for both fresh graduates and experienced industry veterans to contribute to our growth. If you are passionate about quality, innovation, and professional excellence in the pharmaceutical sector, we invite you to explore these career-defining opportunities across various departments.

About the Company

Since our inception, Stallion Laboratories has been committed to producing high-quality pharmaceutical formulations. With rigorous quality control systems and a focus on regulatory compliance, we provide a robust professional environment where employees can develop their skills and advance their careers within the global pharmaceutical landscape.

Available Departments

We are hiring across the following functional areas:

• Production
• Quality Assurance (QA)
• Quality Control (QC) & QC Microbiology
• Engineering
• Packing
• Analytical Development Lab (ADL)
• Computer System Validation (CSV) / IT Infrastructure

Roles and Responsibilities

Depending on your department, your key duties may include:

• Production: Managing granulation, compression, and coating processes; ensuring optimal manufacturing efficiency while strictly adhering to SOPs and GMP standards.
• Quality Assurance (QA): Overseeing In-Process Quality Assurance (IPQA), managing regulatory audits, and ensuring total compliance with international quality standards.
• Quality Control (QC): Performing advanced analytical testing, including HPLC, to ensure product quality, consistency, and safety.
• Engineering: Maintaining manufacturing equipment and plant infrastructure to ensure uninterrupted, high-efficiency technical operations.
• Packing: Supervising and executing primary and secondary packaging processes to ensure strict adherence to safety and quality packaging standards.
• CSV / IT: Managing computer system validation, ensuring data integrity, and maintaining compliance with 21 CFR Part 11 requirements.

Requirements

We are looking for candidates with relevant educational backgrounds and experience levels:

• Education: B.Pharm / M.Pharm, B.Sc / M.Sc, B.Tech, MCA, BCA, or Diploma/ITI holders.
• Experience: We offer roles suitable for all career stages, ranging from entry-level positions (Freshers/Trainees) to senior leadership roles:
  • Freshers (Helper/Trainee positions)
  • 1 to 3 years of experience
  • 2 to 5 years of experience
  • 5 to 10 years of experience
  • 10+ years (Manager/DGM roles)

Benefits

At Stallion Laboratories, we invest in our people by offering:

• Competitive Compensation: Salary packages ranging from ₹1.8 LPA to ₹12 LPA, commensurate with experience and role.
• Global Exposure: Hands-on experience working within a WHO-GMP-approved facility.
• Professional Development: Clear career growth trajectories and continuous learning in regulatory and quality-driven environments.
• Supportive Culture: A professional work environment that values efficiency, integrity, and employee well-being.

How to Apply

If you are interested in joining our team, please submit your updated resume to our recruitment team.

• Email: [email protected]
• Contact Number: +91 94093 09964

Important: Please mention the department and specific position you are applying for in the subject line of your email to ensure your application is directed to the appropriate hiring manager.

Stallion Laboratories is an equal opportunity employer committed to workforce diversity and maintaining a safe and productive work environment.