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Immacule Lifesciences Pvt. Ltd. has announced a significant hiring drive for its new project in Himachal Pradesh. The company is actively seeking seasoned professionals to join its growing team within its USFDA Approved Sterile Facility. This is a premier opportunity for senior-level pharmaceutical experts to contribute to a high-standard manufacturing environment focused on excellence and global compliance.
Job Overview: Quality Assurance – Sterile
The current opening is specifically tailored for the Quality Assurance (QA) department, focusing on sterile operations. The role is critical to maintaining the integrity of the production processes and ensuring that all products meet the rigorous standards required by international regulatory bodies.
- Department: Quality Assurance (Sterile)
- Specific Section: Qualification & Validation / Quality Management Systems (QMS)
- Location: Himachal Pradesh, India
Candidate Requirements and Qualifications
Immacule Lifesciences is looking for highly experienced candidates who possess a deep understanding of sterile manufacturing and regulatory protocols.
- Experience Level: 10 to 15 Years
- Educational Background: M.Pharm or B.Pharm degree from a recognized institution
- Core Competencies: Expertise in Qualification and Validation processes, as well as a robust background in managing Quality Management Systems (QMS).
Why Join Immacule Lifesciences?
Working with Immacule Lifesciences offers the chance to be part of a USFDA approved infrastructure. This designation indicates a commitment to the highest levels of quality and safety in the pharmaceutical industry. For professionals looking to advance their careers, this “New Project” phase offers a dynamic environment where leadership and technical expertise are highly valued.
How to Apply
Experienced Quality Assurance professionals who meet the criteria mentioned above are encouraged to share their updated CVs with the recruitment team.
- Email Address: recruitment@immacule.in
- Contact Number: +91 8580412182
Interested applicants should ensure their resumes highlight their specific experience in sterile facilities and their involvement in qualification and validation projects.
