Officer / Sr. Officer / Executive / Sr. Executive-Production

Dishman Carbogen Amcis; Ahmedabad District; On-site; INR 300,000 - 500,000; Full time

Job summary

Dishman Carbogen Amcis is seeking a candidate with hands‑on API, intermediate, or bulk drug manufacturing experience to operate and monitor manufacturing processes. You will ensure equipment cleanliness, follow strict SOPs, and adhere to GMP guidelines for product quality and safety.

The role requires a science, engineering, or related graduate with strong problem‑solving abilities and teamwork to support a compliant, efficient manufacturing operation within a GMP environment.

Qualifications

• GMP knowledge and compliance with regulatory standards.
• Hands‑on API, intermediate or bulk drug manufacturing experience.
• Strong problem‑solving and troubleshooting skills.

Responsibilities

• Operate and monitor manufacturing processes with understanding of unit operations and unit processes.
• Ensure proper cleaning and maintenance of manufacturing equipment per SOPs.
• Follow safety standards and PPE requirements.
• Adhere to GMP guidelines to maintain product quality, compliance, and safety.
• Identify and resolve production-related issues to minimize downtime.
• Maintain accurate documentation and support continuous improvement initiatives.

Skills

GMP knowledge

ALCOA principles

Data integrity

Troubleshooting

Teamwork

Education

Science/Engineering graduate

Job description

Role & responsibilities

• Operate and monitor manufacturing processes with a sound understanding of unit operations and unit processes.
• Ensure proper cleaning and maintenance of manufacturing equipment as per SOPs.
• Follow safety standards and ensure compliance with PPE requirements.
• Adhere to GMP guidelines to maintain product quality, compliance, and safety.
• Demonstrate knowledge of:
• GMP (Good Manufacturing Practices)
• GDP (Good Documentation Practices)
• GEP (Good Engineering Practices)
• GHP (Good Hygiene Practices)
• ALCOA Principles
• Data Integrity (DI)
• HAZOP
• Cleanroom/Clean Area Practices
• Manufacturing Area Hygiene Standards
• Understand and comply with regulatory requirements related to manufacturing operations.
• Identify and resolve production-related issues promptly to minimize downtime and improve operational efficiency.
• Maintain accurate documentation and support continuous improvement initiatives.

Preferred candidate profile

• Science Graduate, Postgraduate, or Engineering Graduate.
• Hands‑on experience in API, Intermediate, or Bulk Drug Manufacturing is mandatory.
• Good understanding of pharmaceutical manufacturing processes and compliance requirements.
• Strong problem‑solving and troubleshooting skills.
• Ability to work effectively in a team‑oriented manufacturing environment.