19 Sep
|
Stavros Pharmaceuticals
|
Chandigarh
19 Sep
Stavros Pharmaceuticals
Chandigarh
Company Description Stavros Pharmaceuticals Pvt. Ltd. is a new-age pharmaceutical company with a vision to become a global healthcare leader. Built on the foundations of quality and innovation, the organization focuses on scientific excellence and continuous improvement in the field of medicine.
A dedicated team develops and delivers advanced healthcare solutions that address the changing needs of patients, healthcare professionals, and the wider medical community. Every product is designed to meet stringent quality standards while incorporating the latest developments in science and technology. This commitment to research, development, and better health outcomes positions Stavros as an emerging trailblazer in the pharmaceutical industry.
Role Description This is a full-time, on-site role based in Chandigarh, India, for multiple pharmaceutical profiles across QA, QMS, Compliance, Exports, Process, and Purchase, with a CTC of up to ₹15 LPA. The role involves overseeing and maintaining quality systems, ensuring adherence to regulatory and GMP requirements, and supporting internal and external audits.
Team members will manage documentation, SOPs, and records related to quality, compliance, and processes, while coordinating with cross-functional departments such as production, R&D;, logistics, and procurement.
Responsibilities also include supporting export documentation and regulatory submissions, optimizing manufacturing and procurement processes,
and contributing to continuous improvement initiatives that enhance product quality and operational efficiency.
Qualifications
- Candidates should possess strong skills in Quality Assurance and Quality Control to ensure consistent product quality and compliance with specifications.
- Candidates should possess solid expertise in Quality Management and Quality Auditing to maintain robust QMS frameworks and support internal and external audits.
- Candidates should possess thorough knowledge of Good Manufacturing Practice (GMP) to uphold regulatory standards and ensure safe, compliant manufacturing operations.
- Relevant experience in pharmaceutical QA/QC/QMS, compliance, exports, process optimization, or purchase functions in a regulated environment.
- Degree in Pharmacy, Chemistry, Life Sciences, or a related discipline; advanced qualifications or professional certifications in quality or regulatory fields are an advantage.
- Strong documentation, analytical, and problem-solving skills, with proficiency in MS Office and familiarity with ERP or quality management systems.
- Ability to collaborate effectively with cross-functional teams, manage multiple priorities, and maintain high ethical and qualified standards.
- Knowledge of Indian and international regulatory requirements relevant to pharmaceutical manufacturing and exports is beneficial.
📌 Pharma Exp Candidates-QA/QMS/Compliance/Exports/Process/Purchase- Baddi/Chandigarh- CTC upto ₹15 LPA
🏢 Stavros Pharmaceuticals
📍 Chandigarh