Production Manager

Ambrosia Remedies; Waghodia; On-site; INR 3,50,000 - 4,50,000; Full time

Job summary

A leading pharmaceutical company in Gujarat is seeking a Production Chemist to manage production activities while adhering to SOPs and GMP guidelines. Candidates should have 13 years of experience in pharmaceutical production, with expertise in tablets and capsules. This role offers exposure to high-quality manufacturing practices and opportunities for career growth in a compliance-driven environment.

Benefits

Exposure to regulated pharmaceutical manufacturing practices

Opportunity for career growth

Qualifications

• 13 years of experience in pharmaceutical production.
• Expertise in tablets and capsules production and formulation development.

Responsibilities

• Carry out day-to-day production activities in accordance with SOPs and GMP guidelines.
• Monitor and operate production equipment for manufacturing of formulations.
• Ensure proper weighing, dispensing, granulation, compression, coating, and packaging processes.
• Maintain production records such as BMR and BPR.
• Coordinate with QC and QA teams to ensure product compliance.
• Maintain hygiene, safety, and discipline within the production area.
• Assist in process validation, scale-up, and continuous improvement initiatives.
• Adhere to regulatory standards during all production operations.

Skills

Knowledge of production processes in pharmaceutical formulations

Familiarity with GMP, GLP, and regulatory compliance

Good documentation and record-keeping abilities

Strong technical, analytical, and problem-solving skills

Team player with strong discipline and work ethics

Education

B.Sc. (Chemistry) / B.Pharm / M.Pharm

Job description

Job Title: Production Chemist
Company: Ambrosia Remedies Pvt. Ltd.
Location: Waghodia GIDC, Vadodara
Experience Required: 13 Years (in pharmaceutical production)
CTC: 3.5 4.5 LPA

Overview

Ambrosia Remedies Pvt. Ltd. is a growing pharmaceutical company committed to manufacturing high-quality medicines while adhering to international regulatory standards. We focus on innovation, compliance, and excellence in healthcare.

Responsibilities

• Carry out day-to-day production activities in accordance with SOPs and GMP guidelines.
• Monitor and operate production equipment for manufacturing of formulations.
• Ensure proper weighing, dispensing, granulation, compression, coating, and packaging processes.
• Maintain production records such as BMR (Batch Manufacturing Record) and BPR (Batch Packing Record).
• Coordinate with Quality Control (QC) and Quality Assurance (QA) teams to ensure product compliance.
• Maintain hygiene, safety, and discipline within the production area.
• Assist in process validation, scale-up, and continuous improvement initiatives.
• Adhere to regulatory standards (WHO, GMP) during all production operations.

Key Skills & Competencies

• Knowledge of production processes in pharmaceutical formulations.
• Familiarity with GMP, GLP, and regulatory compliance.
• Good documentation and record-keeping abilities.
• Strong technical, analytical, and problem-solving skills.
• Team player with strong discipline and work ethics.

• Reach Experience in tablets and capsules production and formulation development.
• Approval in tablet and capsule sections from FDA is essential.

Educational Qualification

• B.Sc. (Chemistry) / B.Pharm / M.Pharm

Why Join Us?

• Exposure to regulated pharmaceutical manufacturing practices.
• Opportunity to work on end-to-end production processes.
• Career growth in a professional and compliance-driven environment.