Website:
stavrospharma.com
Job details:
Company Description Stavros Pharmaceuticals Pvt. Ltd. is a new-age pharmaceutical company focused on becoming a global healthcare leader through innovation and quality. The organization emphasizes scientific excellence and continuous improvement to deliver advanced healthcare solutions. A dedicated team works on developing products that address the evolving needs of patients, healthcare professionals, and the wider medical community. Every product is designed to meet stringent quality standards and incorporate the latest developments in science and technology. This strong commitment to research, development, and improving lives positions Stavros as a forward-thinking trailblazer in the pharmaceutical industry.
Role Description This is a full-time, on-site role based in Palghar, covering positions in Pharma QC, QA, Microbiology, Maintenance, Lab QA, QMS, F&D, and ADL for professionals with 1 to 7 years of experience. Team members will perform routine testing, documentation, and review of raw materials, in-process samples, and finished products in accordance with established protocols and regulatory requirements. Daily responsibilities may include implementing and monitoring quality systems, performing microbiological analyses, supporting equipment and facility maintenance, and contributing to formulation development and analytical method validation. The role involves close collaboration with cross-functional teams to maintain compliance with GMP, support internal and external audits, and ensure timely resolution of quality-related issues. Personnel are expected to actively participate in continuous improvement initiatives and support training and knowledge-sharing within the department.
Qualifications
- Strong foundation in Quality Control and Quality Assurance, with practical experience in pharmaceutical testing and documentation.
- Proficiency in Quality Management practices, including implementation, monitoring, and improvement of quality systems and SOPs.
- Sound knowledge of Good Manufacturing Practice (GMP) standards and their application in day-to-day operations.
- Experience in Quality Auditing, including participation in internal and external audits and corrective and preventive actions (CAPA).
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Microbiology, or a related scientific discipline.
- 1 to 7 years of relevant experience in pharmaceutical QC, QA, Microbiology, Maintenance, Lab QA, QMS, F&D, or ADL roles.
- Familiarity with regulatory guidelines, validation procedures, and data integrity principles.
- Strong attention to detail, analytical thinking, and ability to work effectively in a fast-paced, regulated environment.
- Effective communication skills and ability to collaborate with cross-functional teams on-site in Palghar.
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