Website:
vhabiopharma.com
Job details:
Company Description VHA Biopharma Private Limited is dedicated to providing quality healthcare solutions that make a meaningful difference in patients’ lives. The organization focuses on delivering effective therapies across multiple segments, including antibiotics, pain management, gastrointestinal, gynecological, and nutritional and health supplements. VHA emphasizes customer satisfaction for both external stakeholders and internal teams through a strong commitment to excellence. As the company grows, it continues to expand into additional therapeutic categories, creating opportunities for professionals to contribute to its mission-driven work.
Role Description The QC Manager for the OSD (Oral Solid Dosage) Pharma Plant at VHA Biopharma is a full-time, on-site role based in New Delhi. The role involves overseeing quality control operations for OSD manufacturing, including routine testing of raw materials, in-process samples, and finished products to ensure compliance with regulatory and internal standards. The QC Manager will develop, implement, and monitor QC procedures, manage documentation, and coordinate with production, QA, and regulatory teams to maintain GMP and safety standards. Daily responsibilities include supervising laboratory staff, reviewing and approving analytical reports, handling deviations and OOS investigations, and supporting audits and inspections. The role also includes continuous improvement initiatives to enhance process efficiency, product quality, and adherence to industry best practices.
Qualifications
- Strong knowledge of quality control processes and systems for OSD (tablets, capsules), including stability studies, validation, and routine analytical testing.
- Hands-on experience with analytical techniques and instruments (e.g., HPLC, UV, dissolution testing) and related documentation practices.
- Proficiency in GMP, GLP, and relevant regulatory guidelines (e.g., WHO, FDA, ICH) applicable to pharmaceutical manufacturing.
- Skills in QC documentation management, SOP development, deviation handling, change control, and CAPA implementation.
- Leadership and team management abilities, including planning workloads, mentoring staff, and fostering a culture of quality and safety.
- Strong analytical, problem-solving, and decision-making skills, with attention to detail and a structured approach to investigations.
- Effective communication and collaboration skills for working with cross-functional teams and supporting internal and external audits.
- Educational background in Pharmacy, Chemistry, or a related field (Bachelor’s or Master’s degree); prior experience as QC Manager or senior QC professional in a pharma OSD plant is highly desirable.
- Comfort with using laboratory software, data integrity principles, and basic MS Office tools to manage reports and QC metrics.
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