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Company Description Jaidev Pharma Placement is a specialized pharma and healthcare hiring partner recognized as one of India’s leading recruitment firms in this domain. In just five years, the organization has built strong partnerships with over 75 pharma and healthcare companies across India, supported by a wide network of more than 350,000 pharma professionals. With over 20 years of pharma industry experience and dedicated expertise in recruitment, the team focuses on aligning talent with business needs for long-term success. Operating from offices in Gurgaon, Mumbai, and Hyderabad, and supported by a focused nine-member team, Jaidev Pharma Placement delivers strategic hiring solutions, leadership recruitment, and performance-focused support. The company is committed to values-driven, results-oriented collaboration to help organizations build winning teams and scale efficiently.
Role Description The ADL Head – OSD Formulations will lead the Analytical Development Laboratory (ADL) for oral solid dosage (OSD) formulations, with potential exposure to injectables, at a leading pharmaceutical manufacturing site in Roorkee. This is a full-time, on-site leadership role responsible for planning, executing, and supervising analytical development activities for new and existing formulations, including method development, validation, and transfer in line with regulatory requirements. The role involves managing and mentoring the ADL team, allocating resources, reviewing analytical data and reports, and ensuring compliance with quality standards, GMP, and global regulatory guidelines. The ADL Head will collaborate closely with R&D, QA, QC, Production, and Regulatory Affairs to support product development, submissions, and troubleshooting of analytical issues. Additional responsibilities include continuous improvement of lab practices, technology adoption, audit readiness, and maintaining robust documentation and data integrity.
Qualifications
Candidates should possess strong pharmaceutical analytical expertise, including method development, method validation, and analytical troubleshooting for OSD formulations and preferably injectables.
Candidates should possess solid leadership and people-management skills, including team mentoring, performance management, and cross-functional collaboration.
Candidates should possess sound knowledge of GMP, regulatory guidelines (e.g., ICH, WHO, USFDA, EMA), quality systems, and data integrity requirements.
Candidates should possess experience with chromatographic and spectroscopic techniques (such as HPLC, GC, UV, dissolution testing) and relevant analytical instrumentation.
Candidates should possess strong documentation, reporting, and communication skills, including preparation and review of SOPs, protocols, and analytical reports.
Candidates should possess excellent problem-solving, planning, and decision-making abilities, with a focus on operational efficiency and continuous improvement.
10+ years of progressive experience in pharmaceutical analytical development, with significant exposure to OSD formulations; injectable experience will be an added advantage.
Master
Work arrangement
No
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