Stallion Laboratories Hiring for QA, Production, Packing & ADL Positions
Stallion Laboratories Pvt. Ltd., a well-established pharmaceutical formulation manufacturer, is conducting a walk-in interview for multiple key positions across various departments. With its state-of-the-art WHO GMP-approved production facility and a strong focus on quality management, Stallion Laboratories offers an exciting career opportunity for professionals looking to grow in the pharmaceutical industry.
Key Job Openings at Stallion Laboratories
Department | Position | Qualification | Experience Required | Location |
---|---|---|---|---|
QA (Validation, Qualification, IPQA, Vendor Audits) | Officer – Executive | M.Pharm / B.Pharm / M.Sc | 3-8 years | Gallops Industrial Park, Chachravadi Vasna, Matoda |
Production (QMS, Coating, Compression) | Officer – Sr. Officer | M.Pharm / B.Pharm | 2-5 years | Gallops Industrial Park, Chachravadi Vasna, Matoda |
Packing (Primary, Secondary) | Officer – Sr. Officer | M.Pharm / B.Pharm | 2-5 years | Gallops Industrial Park, Chachravadi Vasna, Matoda |
ADL (Documentation, Routine Analysis, AMV/AMD) | Officer – Executive | Relevant Experience | 3-8 years | Gallops Industrial Park, Chachravadi Vasna, Matoda |
Why Join Stallion Laboratories?
Established in 1988, Stallion Laboratories has become a trusted name in the pharmaceutical formulation manufacturing sector. The company’s strong focus on quality control, innovation, and strategic growth makes it an ideal place for professionals who want to advance their careers. With a WHO GMP-approved facility and a GLP-qualified quality control system, Stallion Laboratories ensures that every product meets international standards.
The company has a history of managing niche products and specializes in total quality management, zero-defect manufacturing, and customized selling concepts. These roles at Stallion Laboratories are an excellent opportunity for professionals with experience in USFDA-approved OSD (Oral Solid Dosage) facilities.
1. QA Department (Officer to Executive Level)
The Quality Assurance department is looking for candidates with 3 to 8 years of experience in validation, qualification, IPQA, APQR preparation, and vendor audit documentation. If you have a background in pharmaceutical QA processes and meet the required qualifications, this position offers a challenging and rewarding career.
This role will involve ensuring the highest standards of quality across various pharmaceutical operations, with a particular focus on USFDA regulations.
2. Production Department (Officer to Sr. Officer Level)
If you have 2 to 5 years of experience in pharmaceutical production, particularly in QMS, coating, and compression, Stallion Laboratories is looking for you. The company’s production team is responsible for ensuring that pharmaceutical formulations are manufactured efficiently while adhering to strict quality guidelines.
As a production officer, you will play a crucial role in maintaining the company’s reputation for quality by ensuring smooth manufacturing processes and compliance with regulatory standards.
3. Packing Department (Officer to Sr. Officer Level)
The packing department has openings for individuals with 2 to 5 years of experience in primary and secondary packing operations. Your responsibilities will include ensuring that products are packaged in line with regulatory standards, maintaining quality, and ensuring product safety.
This role is ideal for professionals with a background in pharmaceutical packing who are looking to work with a reputable pharmaceutical company.
4. ADL Department (Officer to Executive Level)
The Analytical Development Laboratory (ADL) is seeking candidates with 3 to 8 years of experience in documentation, routine analysis, and analytical method validation (AMV) and development (AMD). As part of the ADL team, you will ensure that the company’s products meet strict regulatory guidelines and maintain the high standards that Stallion Laboratories is known for.
This position offers a dynamic work environment where you’ll be involved in various critical aspects of pharmaceutical analysis.
Important Information for Candidates
Walk-In Interview Details:
- Date: 28th September 2024 (Saturday)
- Time: 9:00 AM to 2:00 PM
- Venue: Gallops Industrial Park – 2, Chachravadi Vasna, Matoda
What to Bring:
- Latest resume
- Recent photo
- Salary structure
- Last 3 months’ salary slips
Eligibility Criteria:
- Only candidates with experience in USFDA OSD facilities should appear for the interview.
- Candidates who have appeared for an interview in the last 6 months are not eligible to reapply.
If you are unable to attend the walk-in, you can still apply by sending your resume to:
- Email: aarti.oberoi@stallionlabs.com | darshan.mistry@stallionlabs.com
Conclusion
Stallion Laboratories provides a golden opportunity for experienced professionals in the pharmaceutical industry to advance their careers in Quality Assurance, Production, Packing, and ADL departments. With a focus on quality, innovation, and regulatory compliance, this is your chance to be a part of a leading company in the pharmaceutical formulation space. Don’t miss the walk-in interview on 28th September 2024, and take the next step in your career journey with Stallion Laboratories!