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Ipca Laboratories Hiring Quality Assurance Executive/Senior Executive

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Ipca Laboratories

B.Pharm, M.Pharm, Post Graduate (Biotechnology/Microbiology)

Sector 3, Pithampur, Dhar, Madhya Pradesh

5โ€“10 Years

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Ipca Laboratories Limited has announced a recruitment opportunity for experienced Quality Assurance professionals at its Bio-Manufacturing facility located in Pithampur, Dhar, Madhya Pradesh. Candidates with experience in biotechnology, biosimilar, or injectable manufacturing and exposure to regulated markets such as USFDA or EU can apply for this opportunity.

If you have strong expertise in Quality Assurance, IPQA, QMS, CAPA, and pharmaceutical manufacturing processes, this could be an excellent career opportunity with one of India’s leading pharmaceutical companies.


Job Overview

Company Name: Ipca Laboratories Limited

Department: Quality Assurance

Position: Executive / Senior Executive

Job Location: Bio-Manufacturing Unit, Sector 3, Pithampur, Dhar, Madhya Pradesh, India

Employment Type: Full-Time

Industry: Pharmaceutical / Biotechnology / Injectable Manufacturing


Eligibility Criteria

Educational Qualification

Candidates should possess any of the following qualifications:

  • B.Pharm
  • M.Pharm
  • Post Graduate in Biotechnology
  • Post Graduate in Microbiology

Experience Required

  • 5โ€“10 Years
  • Experience in Biotech, Biosimilar, or Injectable manufacturing plant.
  • Regulatory exposure to USFDA and EU guidelines is preferred.

Roles & Responsibilities

IPQA Responsibilities

  • Develop and execute IPQA strategy.
  • Analyze in-process quality data to improve manufacturing processes.
  • Ensure area clearance according to SOP for fill-finish and packing sections.
  • Ensure sampling activities are performed as per BMR and specifications.
  • Participate in investigations related to process execution and market complaints.

QMS Responsibilities

  • Handle QMS e-modules efficiently.
  • Manage Change Control, Deviations, CAPA, and QRM activities.
  • Support investigations and monitor CAPA effectiveness.
  • Review executed documents including BMRs and protocols.
  • Prepare Annual Product Quality Reviews (APQRs).
  • Ensure timely closure of QMS activities.
  • Familiarity with EDMS, LIMS, TrackWise, and SCM will be an added advantage.

Required Skills

  • Strong knowledge of Pharmaceutical Quality Assurance
  • Good understanding of GMP and regulatory compliance
  • Experience in Injectable/Biotech manufacturing
  • Documentation review and compliance management
  • Investigation handling and CAPA implementation
  • Analytical and problem-solving skills
  • Teamwork and communication skills

Salary

The official notification has not disclosed the salary package.

Expected Salary: โ‚น8,00,000 โ€“ โ‚น14,00,000 per annum (Approx.), depending on experience, skills, and company policies.


Benefits

  • Opportunity to work with a leading pharmaceutical company
  • Exposure to regulated manufacturing environments
  • Career growth in Quality Assurance
  • Learning opportunities in biotechnology and injectable manufacturing
  • Professional work culture

How to Apply

Interested and eligible candidates can send their updated resume to the following email addresses:

Candidates are advised to mention the applied position in the email subject line and ensure that their resume highlights relevant Quality Assurance experience.

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