Website:
stavrospharma.com
Job details:
Company Description
Stavros Pharmaceuticals Pvt. Ltd. is a forward-thinking pharmaceutical company dedicated to making a global impact in the healthcare industry. Guided by a commitment to innovation and quality, we strive to deliver groundbreaking healthcare solutions that address the changing needs of patients and medical professionals worldwide. With a focus on research, scientific excellence, and cutting-edge technology, Stavros sets industry-leading standards in pharmaceutical development. Our mission is to improve lives through the creation of high-quality, science-driven products, reflecting our dedication to advancing the future of medicine.
Role Description
This is a full-time, on-site role located in Roorkee for an experienced professional in Pharma Formulations Developmental Quality Assurance. The role involves overseeing quality assurance processes for pharmaceutical formulations, ensuring compliance with regulatory standards, and conducting quality audits. Responsibilities include collaborating with the research and development team, documenting procedures, and implementing quality control protocols for product development. The candidate will play a critical role in identifying quality improvements and ensuring consistent adherence to company and industry standards.
Qualifications
- Strong knowledge and experience in Pharma Formulations Development and Quality Assurance processes.
- Proficiency in communication and collaboration skills for effective team coordination and reporting.
- Understanding of and experience with Early Intervention approaches and handling developmental disabilities in product development.
- Experience in training processes to ensure compliance with regulatory guidelines and quality objectives.
- M.Pharm degree, preferably in Pharmaceutics or related field.
- 5-6 years of relevant professional experience in the pharmaceutical or healthcare industry.
- Strong analytical and problem-solving skills, with a keen focus on quality and compliance.
- Knowledge of regulatory standards and documentation practices in the pharmaceutical sector.
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