Immacule Lifesciences-Opening for QA, QC, Engineering, Regulatory Affairs 

Immacule Lifesciences-Opening for QA, QC, Engineering, Regulatory Affairs 

Immacule Lifesciences is rapidly expanding and is a top provider of liquid and lyophilized injectables. Our core values revolve around innovation, quality, and long-lasting collaborations. With a state-of-the-art manufacturing plant and extensive experience in the field, we are the preferred choice for pharmaceutical companies worldwide.

Immacule Lifescience, Nalagarh HP offers exciting job opportunities in Quality Control, Quality Assurance, Engineering, and Regulatory Affairs. If you have 1 to 7 years of experience in these fields, we want to hear from you. Contact us at 8278729004 or send your resume to gurdas@acmegenerics.in. Early joiners preferred.

Quality Control

  • Officer: 1 to 3 years experience

Quality Assurance

  • IPQA Executive: 4 to 7 years experience
  • Validation Executive: 3 to 7 years experience
  • QMS Executive: 5 to 7 Years

Engineering

  • Fitter: 4 to 7 years experience (Process)
  • Plant Maintenance Executive: 4 to 7 years experience (Electrical Side)
  • Executive (Water System / HVAC / Utility): Electrical Side
  • BMS/UTILITY Executive 5 to 7 Years

Regulatory Affairs

  • EU/US/ROW 3 to 6. Years

Requirements:
– Experience with audits like USFDA, MHRA, EU-GMP
– Early joiners preferred

📧 Send your resume to: gurdas@acmegenerics.in
📞 Contact: 8278729004
Please forward to your network!

Job Category: pharma
Job Type: Full Time
Job Location: - Nalagarh (HP)

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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