HomeHead/VP/CEO/President/GMHead Production (Sterile Facility) | Immacule Formulations | Baddi | 20-30 L

Head Production (Sterile Facility) | Immacule Formulations | Baddi | 20-30 L


A Leading Pharma Group with Global Presence and approvals from EU-GMP, MHRA-UK, ANVISA Brazil, PICS Ukraine, WHO Geneva, INVIMA Colombia, USFDA*

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We have 3 facilities in North India and 1 R&D center at Bengaluru,

1. Immacule Lifesciences- Manufacturing of Liquid and Lyophilized injections approved from MHRA, ANVISA, PICS Ukraine, USFDA

2. Acme Formulation Pvt Ltd- Comprises of 2 blocks (General & Hormone), manufacturing Tablets, Capsules approved by WHO Geneva

3. Acme Generics LLP – Comprises of 2 blocks (General & Thyroxine), manufacturing Tablets, Capsules approved by EU-GMP

Position: Head Production – Sterile Facility

Location: Baddi, Himachal Pradesh. India

Job Description:

Experience in CNC/ Autoclave /Filling & Sealing / QMS/ Lyophilizer / Terminal Sterilizer / Tunnel Sterilizer and from USFDA approved Pharmaceutical Industries

  • Day to day planning, target achieving in the monthly production plan
  • Proper coordination and communication with other departments for better execution of processes.
  • Prepare Machine URS / DQ and execute the qualification of IQ/OQ/PQ.
  • Preparation of SOP’s and masterbatch packing records.
  • Handling of batch activity like- Media fill, Scaleup/Engineering, Exhibit, PPQ, and commercial batches.
  • Ensure the completion of the batch as per the production plan, Control on daily production output.
  • Review and Compliance of executed Batch Record and submit to QA in within time.
  • Immediate information to superiors in case of any anomalies found in the process.
  • Overseeing production related tasks including planning, control, and troubleshooting.
  • Setting up production targets and achieving the same within time and cost parameters.
  • Optimizing man & machine utilization to achieve pre-set production targets.
  • Any other job assignment allocated by the site head.
  • Documents preparation and changes in existing documents as per USFDA and cGMP requirements.
  • Responsible for investigation of non-conformities, identification of root cause, the suggestion of CAPA, preparation review, and compliance of investigation reports.
  • Responsible for raising and execution of change control and CAPA and its implementation through eQMS software.
  • Responsible for preparation and review of Risk assessment related to process and product attributes.
  • Maintained the discipline in the departments.

Qualification: B.Pharma

Experience: 18-25 Years

Salary: 20,00,000 to 30,00,000 INR CTC/PA

Contact Details:

Mr. Rahul Verma


hr@acmecgcnerics.in, rahul.verma@acmeformulation.com

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