Qa qms experienced only
BDL - Beta Drugs Ltd.
Job Description
Company Description Beta Drugs Ltd. (BDL) is a global leader dedicated to oncology, focused on developing enabling products supported by strong scientific knowledge and technical expertise. The organization operates across a wide range of applications, working to bring high-value oncology solutions to market efficiently. BDL emphasizes accelerating product launch timelines while maximizing value for healthcare partners and customers. A newly formed breakthrough innovation group drives initiatives that push business and technology boundaries, creating opportunities for continuous advancement in cancer care.
Role Description The QA QMS role at BDL is a full-time, on-site position based in Baddi. This role is responsible for implementing, maintaining, and continuously improving the Quality Management System in line with regulatory and company standards. Day-to-day activities include drafting and reviewing SOPs, overseeing documentation control, coordinating and supporting internal and external quality audits, and monitoring compliance with Good Manufacturing Practices (GMP). The role involves investigating deviations, managing CAPA (Corrective and Preventive Actions), performing risk assessments, and collaborating with cross-functional teams such as production, QC, and regulatory affairs to ensure consistent product quality. The QA QMS professional will also contribute to training initiatives, support inspections, and help drive quality-focused process improvements.
Qualifications
- Candidates should possess strong skills in Quality Assurance and Quality Management, with experience in pharmaceutical or oncology manufacturing environments.
- Candidates should possess skills in Quality Control and Quality Auditing, including experience with inspections, deviation handling, and CAPA management.
- Candidates should possess a solid understanding of Good Manufacturing Practice (GMP) and regulatory requirements relevant to pharmaceutical production.
- Candidates should possess strong documentation, analytical, and problem-solving skills, with attention to detail and a focus on continuous improvement.
- Relevant qualifications such as a degree in Pharmacy, Chemistry, Life Sciences, or a related discipline; prior experience in QA/QMS roles in the pharmaceutical industry is highly preferred.
- Ability to work collaboratively with cross-functional teams, good communication skills, and readiness to support audits and regulatory inspections on-site in Baddi.
Required Skills
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