QC Lab Services Analyst, Radiopharmaceuticals & GMP Compliance
Overview
QC Lab Services Analyst will own daily lab operations at our Springfield NJ site, ensuring accurate sample tracking, materials management, and regulatory compliance for radiopharmaceutical processes. You will join a cross functional team supporting continuous improvement, workflow optimization, and partner with Quality, Operations, and Facilities. This role emphasizes on site presence five days a week and attention to GMP GLP OSHA standards. What makes this role different is the opportunity to contribute to a fast paced lab services function within a leading radiopharmaceutical company.
What You'll Do10
- 1Build and maintain sample tracking storage logistics and QC material control to ensure timely scheduled testing and material readiness
- 2Design and manage QC equipment management and waste control to support efficient lab operations
- 3Lead and support the stability program and QC inspection readiness activities to pass external audits
- 4Drive cross functional collaboration with Quality Operations and Facilities to align workflows with business priorities
- 5Own reporting of KPIs service requests and inventory accuracy to enable data driven decisions
- 6Support training and development of lab services staff to improve performance
- 7Coordinate with vendors and maintain inventory systems ensuring supply continuity
- 8Support general QC system procedure management and lab operations in compliance with GMP GLP and OSHA
- 9Assist in reference standards alert limit setting and materials management to support testing programs
- 10Contribute to continuous improvement projects aimed at increasing lab efficiency and reliability
Requirements10
- 1Bachelor’s degree in Life Sciences Chemistry Biology or related field or equivalent experience
- 23–5+ years of laboratory operations or lab services experience
- 3Radiopharmaceutical experience preferred
- 4Strong organizational and problem solving skills with ability to work under strict timelines
- 5Ability to convey complex ideas simply to management and customers and exercise independent judgement during method development or transfer
- 6Team oriented mindset with ability to work cross functionally
- 7Fluent in Microsoft Office and experienced with laboratory information management systems LIMS
- 8Preferred familiarity with quality control systems regulatory requirements and knowledge of cGMP FDA and EMEA environments
- 9Experience with electronic lab systems or inventory systems preferred
- 10Strong communication and time management skills and ability to adapt to a fast paced changing environment
Salary Insight
$72 - $107k per year
Location
Required Skills
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