VP, Manufacturing and Technical Operations

🕒 May 8

🏈 Alabama, North Carolina, +2 more states – Remote

🏈 Alabama – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote ❄️ Minnesota – Remote

💵 $200k - $250k / year

⏰ Full Time

🔴 Lead

⚙️ Operations

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PerkinElmer

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1938

🔬 Science

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Science • Pharmaceuticals • Healthcare Insurance

PerkinElmer is a global leader in providing analytical and testing solutions for a wide range of industries, including pharmaceuticals, food safety, environmental analysis, and industrial testing. The company offers advanced equipment and consumables, including mass spectrometers, chromatography instruments, and spectroscopy systems. With over 85 years of experience, PerkinElmer is committed to innovation and dedicated to partnering with laboratories worldwide to enhance scientific discovery and ensure product quality and safety. Their services support industries like healthcare, food and beverage, environmental testing, and industrial applications, helping clients meet compliance and quality standards.

📋 Description

• Lead end-to-end program management for complex technical operations initiatives including new product introductions, technology transfers, process validations, and facility fit assessments • Develop integrated program plans, critical path analyses, risk registers, and resource plans; proactively identify and escalate risks and issues • Own stage-gate processes and governance deliverables, ensuring milestones are met on time, within scope, and aligned to regulatory commitments • Coordinate cross-functional workstreams across Manufacturing, Process Development, Quality, Regulatory Affairs, Supply Chain, and Engineering • Partner with technical subject matter experts to translate scientific and process requirements into executable operational plans

🎯 Requirements

• Bachelor’s Degree in Life Science, Engineering, or related discipline • 20+ years of experience in operations management within pharmaceutical, biotech, or regulated manufacturing environments • Strong understanding of pharmaceutical development and manufacturing processes (biologics, small molecule, or both) • Ability to interpret technical documentation and engineering drawings • Working knowledge of cGMP regulations (FDA 21 CFR Parts 210/211, ICH guidelines, EMA requirements) • Exceptional organizational, communication, and stakeholder management skills

🏖️ Benefits

• Health insurance • Professional development opportunities • Flexible work arrangements • Paid time off