Technical Transfer Lead

Responsibilities

• Lead end-to-end technical transfer projects, ensuring timelines, scope, and quality objectives are achieved.
• Serve as site point of contact for transfer activities, aligning stakeholders across Technical Development, Supply Chain, Manufacturing, Quality, HSE, and other sites.
• Develop and execute transfer and validation strategies, including process, cleaning, packaging, and supportive studies.
• Coordinate technical, regulatory, and validation batches, ensuring documentation readiness and compliance.
• Establish and lead cross-functional project teams, driving execution, risk mitigation, and decision-making.
• Ensure compliance with cGMP and readiness for inspections and pre-approval audits.
• Drive process improvements and optimization to support successful product launches and ongoing manufacturing excellence.

• Bachelor of Science in Pharmacy, Pharmaceutical Technology, Chemistry, or equivalent scientific degree.
• Minimum 5 years of experience in oral solid dosage pharmaceutical manufacturing.
• Demonstrated experience in technical transfer, process scale-up, and validation activities.
• Strong knowledge of current Good Manufacturing Practices and regulatory requirements.
• Proven project management skills with ability to lead cross-functional teams.
• Strong technical expertise in pharmaceutical processes, with ability to solve complex manufacturing challenges.

• Master of Science or equivalent experience.

• Performance-based cash incentive; eligibility for annual equity awards (depending on level).
• Comprehensive benefits package (health, life, disability), 401(k) with company contribution and match; time off (vacation, personal days, holidays, and other leaves).