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Immacule Lifesciences Hiring for Production / AQA / Microbiology / QA Validations

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Immacule Lifesciences, a leader in liquid and lyophilized injectables, is hiring for multiple pharmaceutical roles at its state-of-the-art facility in Nalagarh, Himachal Pradesh. Renowned for innovation, quality, and global partnerships, this fast-growing company offers an exciting opportunity to join a world-class team. If you’re a skilled professional with a passion for excellence in pharmaceuticals, explore these career openings in sterile production, analytical quality assurance, microbiology, and QA validation.

Job Openings at Immacule Lifesciences

1. Production QMS (Sterile)

Experience: 5–7 years
Qualification: B.Pharma
Responsibilities:

  • Oversee quality management systems for sterile manufacturing processes.
  • Ensure compliance with cGMP and regulatory standards.
  • Conduct risk assessments and implement corrective actions.
  • Collaborate with production teams to optimize workflows.
  • Maintain documentation for audits and inspections.

2. Analytical Quality Assurance (AQA)

Experience: 5–7 years
Key Skills: Stability Studies
Qualification: M.Sc
Responsibilities:

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  • Perform stability studies and analytical testing for injectables.
  • Validate analytical methods and ensure data integrity.
  • Prepare reports for regulatory submissions.
  • Monitor product quality and compliance with SOPs.

3. Microbiology (Environmental Monitoring)

Experience: 1–4 years
Qualification: M.Sc (Microbiology)
Responsibilities:

  • Conduct environmental monitoring in sterile facilities.
  • Perform microbial testing and ensure contamination control.
  • Analyze samples and document results per regulatory guidelines.
  • Support sterile process validations and investigations.

4. QA Validation (Sterile)

Experience: 5–7 years
Qualification: B.Pharma
Responsibilities:

  • Develop and execute validation protocols for sterile processes.
  • Ensure equipment and processes meet regulatory standards.
  • Conduct risk-based validation and qualification activities.
  • Maintain compliance with global regulatory requirements.

Qualifications

  • Education: B.Pharma for Production QMS and QA Validation; M.Sc for AQA and Microbiology (Microbiology for EM role).
  • Experience: 5–7 years for Production QMS, AQA, and QA Validation; 1–4 years for Microbiology.
  • Skills: Expertise in sterile manufacturing, cGMP, stability studies (for AQA), environmental monitoring (for Microbiology), and regulatory compliance.
  • Strong analytical, problem-solving, and communication skills.

Benefits of Working at Immacule Lifesciences

  • Join a globally recognized leader in pharmaceutical injectables.
  • Access cutting-edge technology and a collaborative work environment.
  • Competitive salary (₹5,00,000–₹10,00,000 annually, based on role and experience).
  • Opportunities for career growth and professional development.
  • Work in a scenic location in Nalagarh, Himachal Pradesh.

How to Apply

Interested candidates can share their updated CV via WhatsApp or call at 8278729004. Ensure your CV highlights relevant experience in pharmaceutical manufacturing, sterile processes, or quality assurance.

Location: Nalagarh, Himachal Pradesh
Application Deadline: September 18, 2025

FAQs

Q: What is the work environment like at Immacule Lifesciences?
A: Immacule Lifesciences fosters a collaborative and innovative culture, with a focus on quality and compliance. Employees work with advanced technology in a supportive, growth-oriented environment.

Q: Are there opportunities for career advancement?
A: Yes, Immacule Lifesciences encourages professional development and offers clear pathways for career growth within its global operations.

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