Asst. Manager / Manager-Production (Liquid) Jobs in Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
12 - 15 Years of Experience
Not disclosed 
Full TimeStallion Laboratories Pvt Ltd
Bavla, Gujarat, India
Posted on 28-01-2026
1 Vacancy
Description
- Job Title: Asst. Manager / Manager-Production (Liquid)
- Qualification: MPharm/BPharm
- Location: Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad
- Work Experience: 12 to 15 Years
Job Description
- Plan, execute & supervise liquid production operations.
- Ensure manufacturing activities are as per approved BMR/BPR & SOPs.
- Monitor critical process parameters and product quality.
- Ensure compliance with GMP, safety & regulatory standards.
- Handle deviations, investigations & CAPA related to production.
- Support process validation, cleaning validation & scale-up activities.
- Coordinate with QA/QC for in-process controls and batch release.
- Manage manpower, training & shift schedules.
- Ensure equipment qualification, maintenance & line clearance.
- Drive productivity, efficiency & continuous improvement initiatives.
- Maintain audit readiness and support regulatory inspections.
Take this opportunity to join Stallion Laboratories Pvt Ltd - Bavla, Ahmedabad as a Asst. Manager / Manager-Production (Liquid) 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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