Explore 13 Jobs at AtomVie
Open Positions at AtomVie
Posted 10 days ago
The Logistics & Packaging Coordinator coordinates domestic and international shipments of radiopharmaceutical products, prepares shipping and customs documentation, and arranges transport with logistics providers. The role also packages patient doses and hazardous materials, ensures regulatory and quality-system compliance, monitors deliveries, and supports process improvement.
Key Details
- full time Jobs
- $60,000+ per year
- 3+ years experience
Top Skills Required
Top Benefits
Posted 16 days ago
The CQV Specialist I (Lab) supports laboratory equipment qualification, calibration, recertification, and documentation in a GMP pharmaceutical environment. Responsibilities include maintaining calibration and preventive maintenance programs, executing equipment qualification and validation, developing SOPs and maintenance programs, troubleshooting equipment and compliance issues, and authoring deviation, change control, and CAPA documentation.
Key Details
- full time Jobs
- $64,000+ per year
- 2+ years experience
Top Skills Required
Top Benefits
Posted 23 days ago
The QA – Data Reviewer, Associate ensures GMP compliance and data integrity by reviewing analytical laboratory records, audit trails, and reported results for radiopharmaceuticals. The role supports investigations, verifies adherence to methods and SOPs, and guides laboratory staff on data integrity and regulatory requirements.
Key Details
- full time Jobs
- $70,000+ per year
- 5+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The QA Associate for Batch Release determines the final disposition of incoming materials and radiopharmaceutical batches, ensuring documentation, specifications, validated processes, and regulatory requirements are met. The role also supports SOP and product quality review work, client batch-related issues, audits and inspections, new product launches, and continuous improvement in a GMP production environment.
Key Details
- full time Jobs
- $65,000+ per year
- 3+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The Production Technician supports radiopharmaceutical manufacturing by preparing and sanitizing production materials, maintaining aseptic and cleanroom areas, packaging dangerous goods, and managing radioactive waste. The role also includes inventory counts, adherence to safety and radiation protocols, and assisting production at other facilities as needed, with rotational or fixed shifts and weekend availability required.
Key Details
Top Skills Required
Top Benefits
Posted a month ago
The Microbiology Technical Writer and Data Reviewer supports Microbiology and Sterility Assurance operations by authoring, reviewing, and managing GMP documentation and reviewing microbiological laboratory data for accuracy, traceability, and regulatory compliance. The role also supports investigations, CAPAs, change controls, audits, training, client requests, and continuous improvement initiatives.
Key Details
- full time Jobs
- $79,000+ per year
- 2+ years experience
Top Skills Required
Top Benefits
Posted a month ago
The Analytical Development Chemist conducts analytical method development, transfer, validation, stability testing, and quality investigations for radiopharmaceutical products in a GMP environment. The role also supports regulatory documentation, laboratory operations, product release testing, process improvements, and collaboration with production and stability teams.
Key Details
- full time Jobs
- $74,000+ per year
- 3+ years experience
Top Skills Required
Top Benefits
Posted 2 months ago
The AD Laboratory Technologist supports an analytical development and radiopharmaceutical quality control laboratory by maintaining a clean, organized, and GMP-compliant facility. Responsibilities include laboratory housekeeping, material and equipment management, sample preparation, basic testing, data entry, documentation, and support for protocols and final reports.
Key Details
Top Skills Required
Top Benefits
Posted 2 months ago
The QC Analyst performs quality control testing of finished drug products, raw materials, and in-process materials using analytical chemistry, microbiology, and biology techniques in a GMP-regulated environment. The role includes documenting results, supporting investigations and corrective actions, maintaining laboratory equipment and materials, coordinating testing with contract laboratories, and ensuring compliance with nuclear safety, health and safety, and regulatory requirements.
Key Details
- full time Jobs
- $60,000+ per year
- 1+ years experience
Top Skills Required
Top Benefits
Posted 2 months ago
The CQV Specialist I (Lab) supports laboratory equipment qualifications, calibrations, recertifications, and documentation in compliance with GMP practices. The role executes validation activities, manages calibration and preventive maintenance programs, coordinates contractors, troubleshoots equipment and validation issues, and supports compliance documentation such as deviations, change controls, nonconformance reports, and CAPAs.
Key Details
- full time Jobs
- $64,000+ per year
- 2+ years experience
Top Skills Required
Top Benefits
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