Production Manager / Asstt. Production Manager /

Medipol Pharmaceutical; Solan; Presencial; INR 1 200 000 - 2 200 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Air conditioned accommodation

Canteen facility (paid)

Laundry facility (subsidised)

On-site housing guidance

Resumo da oferta

Medipol Pharmaceutical seeks an experienced Production Head to lead and coordinate daily pharma manufacturing activities in Solan, Himachal Pradesh. You will supervise staff, ensure cGMP compliance, manage inventory, and drive efficiency and quality across tablets, capsules, liquids, and syrups.

This role requires strong leadership, regulatory knowledge, and hands-on problem-solving, with fluency in English and Hindi. Working hours are long; accommodation and canteen facilities may be available.

Qualificações

• 5+ years of hands-on experience managing production in a pharmaceutical manufacturing facility with tablets, hard gelatin capsules, liquids, and dry syrups.
• Approval from drugs control department in Tablet, Hard Gelatine Capsule, Liquid Orals, External Application, Dry Syrup Sections.
• Strong knowledge of cGMP, regulatory guidelines, process control, and documentation systems.
• Excellent leadership, analytical, and problem-solving abilities.
• Proficiency with MS Office (Excel, Word, PowerPoint).
• Fluent in English and Hindi; additional certifications are a plus.

Responsabilidades

• Plan, schedule, and coordinate daily production activities, ensuring timely output and adherence to quality standards.
• Supervise, coach, and develop production staff, fostering a culture of safety, compliance, and teamwork.
• Ensure strict compliance with cGMP, EHS, and regulatory norms throughout production operations.
• Oversee inventory, raw material usage, and procurement of production supplies, collaborating with purchase and supply chain teams.
• Monitor equipment performance, manage repairs and maintenance, and initiate upgrades for operational efficiency.
• Implement and improve standard operating procedures (SOPs) for manufacturing, documentation, and process control.
• Manage budgets, control production costs, and report performance metrics to management.
• Troubleshoot production issues, resolve delays, and guide corrective or preventive action.
• Coordinate with QA/QC, R&D, regulatory, and engineering teams for tech transfers, audits, new product launches, and change controls.
• Lead continuous improvement initiatives in compliance, process efficiency, automation, and sustainability.
• To act as responsible person under section 34 of Drugs and cosmetics Act. To act as in charge and responsible to the company for the conduct of the business of the company as per the requirement.
• Maintain all production records and documentation for audits and regulatory reviews.

Conhecimentos

cGMP knowledge

Regulatory knowledge

Process control

Documentation systems

MS Office

Leadership

Problem solving

English + Hindi

Formação académica

Bachelor’s or Master’s in Pharmacy/Chemical Eng

Ferramentas

MS Office

Descrição da oferta de emprego

Role & responsibilities

The role encompasses a variety of responsibilities, including but not limited to:

• Plan, schedule, and coordinate daily production activities, ensuring timely output and adherence to quality standards.
• Supervise, coach, and develop production staff, fostering a culture of safety, compliance, and teamwork.
• Ensure strict compliance with cGMP, EHS, and regulatory norms throughout production operations.
• Oversee inventory, raw material usage, and procurement of production supplies, collaborating with purchase and supply chain teams.
• Monitor equipment performance, manage repairs and maintenance, and initiate upgrades for operational efficiency.
• Implement and improve standard operating procedures (SOPs) for manufacturing, documentation, and process control.
• Manage budgets, control production costs, and report performance metrics to management.
• Troubleshoot production issues, resolve delays, and guide corrective or preventive action.
• Coordinate with QA/QC, R&D, regulatory, and engineering teams for tech transfers, audits, new product launches, and change controls.
• Lead continuous improvement initiatives in compliance, process efficiency, automation, and sustainability.
• To act as responsible person under section 34 of Drugs and cosmetics Act. To act as in charge and responsible to the company for the conduct of the business of the company as per the requirement.
• Maintain all production records and documentation for audits and regulatory reviews.

Preferred candidate profile

• Minimum 5 years of hands-on experience managing production in a pharmaceutical manufacturing facility with tablet, Hard Gelatine Capsule, Liquid Orals, External Application, Dry Syrup Sections.
• Approval from drugs control department in any one or more sections namely : Tablet, Hard Gelatine Capsule, Liquid Orals, External Application, Dry Syrup Sections.
• Bachelors or Masters degree in Pharmacy, Chemical Engineering, or related field.
• Strong knowledge of cGMP, regulatory guidelines, process control, and documentation systems.
• Excellent leadership, analytical, and problem-solving abilities.
• Proficiency with MS Office (Excel, Word, PowerPoint).
• Fluent in English and Hindi; additional technical or regulatory certifications are a plus.

Working Hours: This is a full-time position. The job requires you to work from 8:15am till 7:15pm from Monday to Saturday .
Accomodation: Airconditioned Room with attached bathroom available ( Bare) for willing candidate ( Subject to availability) ( independent or on sharing basis).
Canteen : Facility on to pay basis available for breakfast, lunch and dinner.
Laundry : Laundry facility available ( On subsudised rates) (On to pay basis)