QC Sr Manager- Pharma Formulations OSD Injectable Plant- CTC Range 10-12 LPA

Company Description Jaidev Pharma Placement is Indias leading hiring partner for the pharmaceutical and healthcare industry, specializing in building high-performing teams that drive long-term growth and impact. In just five years, the firm has earned the trust of over 75 organizations across India, supported by a network of more than 350,000 pharma professionals. With over 20 years of pharma industry experience and dedicated recruitment expertise, Jaidev Pharma Placement offers strategic hiring solutions aligned with business and market needs. The company operates from Gurgaon, Mumbai, and Hyderabad, backed by a focused team of experienced pharma professionals and dynamic talent. Its services cover leadership, sales and marketing, technical and plant roles, and healthcare staffing, along with training and performance enhancement support.

Role Description The QC Sr Manager – Pharma Formulations (OSD and Injectable Plant) will lead and oversee all quality control operations at the Bahadurgarh manufacturing facility in a full-time, on-site capacity. Responsibilities include planning and managing QC activities for oral solid dosage and injectable formulations, ensuring compliance with regulatory standards, and maintaining robust documentation and audit readiness. The role involves supervising and mentoring QC teams, reviewing and approving test reports, and driving continuous improvement in laboratory processes and quality systems. The QC Sr Manager will collaborate closely with QA, Production, R&D, and regulatory teams to resolve quality issues, support validations, and ensure timely release of materials and finished products. The position also requires implementing best practices in data integrity, safety, and GMP, while supporting inspections by internal and external regulatory bodies.

Qualifications

• Candidates should possess strong quality control and laboratory management skills, including method validation, routine testing of raw materials, intermediates, and finished products, and data integrity practices.
• Candidates should possess expertise in OSD and injectable formulations, including familiarity with formulation processes, sterilization and aseptic practices, and product-specific quality requirements.
• Candidates should possess sound knowledge of GMP, GLP, and regulatory guidelines (such as WHO, EU, USFDA), along with experience in handling audits, inspections, and compliance-related documentation.
• Candidates should possess proficiency in analytical instruments and techniques (such as HPLC, GC, UV, dissolution, and related pharmacopeial methods) and troubleshooting skills for equipment and methods.
• Candidates should possess strong leadership and people management capabilities, including team supervision, performance monitoring, coaching, and cross-functional collaboration.
• Candidates should possess effective communication, reporting, and documentation skills, with attention to detail and the ability to prepare and review SOPs, protocols, and investigation reports.
• Candidates should possess a graduate or postgraduate degree in Pharmacy, Chemistry, or a related scientific discipline, with substantial experience in QC management in