Website:
stavrospharma.com
Job details:
Company Description Stavros Pharmaceuticals Pvt. Ltd. is a modern pharmaceutical company with a clear ambition to become a global healthcare leader. Built on a strong foundation of quality and innovation, the organization focuses on developing advanced medicines that address evolving patient and healthcare needs. The company emphasizes scientific excellence, continuous improvement, and breakthrough healthcare solutions across its portfolio. Every product is designed to meet rigorous quality standards while incorporating the latest developments in science and technology. Stavros fosters a professional environment where team members contribute to meaningful advancements in medicine and improved health outcomes.
Role Description This is a full-time, on-site role for Pharma QC Professionals located in Kathua, with opportunities for individuals having 1 to 10 years of experience, preferably in injectable manufacturing companies. The role involves performing routine and batch-wise quality control testing of raw materials, in-process samples, and finished injectable products in accordance with GMP and regulatory guidelines. Professionals will be responsible for operating and maintaining QC instruments, documenting test results, preparing and reviewing analytical reports, and supporting investigations related to deviations, OOS, and OOT results. Daily tasks include coordinating with production and QA teams to ensure product quality, participating in method validation and stability studies, and supporting compliance during internal and external audits. The position requires meticulous attention to detail, adherence to safety procedures, and commitment to continuous improvement in QC processes.
Qualifications
- Candidates should possess strong knowledge of pharmaceutical quality control principles, especially related to injectable dosage forms and sterile manufacturing practices.
- Candidates should possess skills in operating and handling QC instruments (e.g., HPLC, UV, dissolution apparatus, microbiological testing tools) and performing routine analytical testing.
- Candidates should possess proficiency in documentation, data integrity practices, and preparation/review of analytical reports in compliance with GMP and regulatory standards.
- Candidates should possess understanding of validation activities, stability studies, and quality risk management related to injectable products.
- Candidates should possess the ability to collaborate effectively with cross-functional teams, manage time efficiently, and follow established SOPs and safety protocols.
- Diploma or Bachelor’s degree in Pharmacy, Chemistry, Microbiology, or a related scientific discipline is preferred.
- 1 to 10 years of relevant experience in pharmaceutical QC, with injectable company experience strongly preferred.
- Familiarity with regulatory requirements (e.g., WHO, GMP, Schedule M) and experience in facing regulatory or customer audits will be an advantage.
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