Officer / Sr. Officer-Production Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
2 - 4 Years of Experience
Not disclosed 
Full TimeStallion Laboratories Pvt Ltd
Bavla, Gujarat, India
Posted on 28-01-2026
1 Vacancy
Description
- Job Title: Officer / Sr. Officer-Production
- Qualification: MPharm/BPharm
- Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
- Work Experience: 2 to 4 Years
Job Description
- Execute and supervise production activities as per BMR/BPR & SOPs.
- Operate and monitor production equipment and processes.
- Ensure compliance with GMP & safety standards.
- Complete batch documentation accurately and timely.
- Perform line clearance and equipment cleaning verification.
- Identify, report & support closure of deviations.
- Support process validation and continuous improvement.
- Coordinate with QA/QC for in-process checks and release.
- Guide and train operators & junior staff.
- Maintain housekeeping, safety & productivity standards.
Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Officer / Sr. Officer-Production 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
Production / Manufacturing
Preferred Education
Key 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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