QA Data Coordinator

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

• engage in work that matters to our customers and the patients they serve
• learn new skills and enjoy new experiences in an engaging and safe environment
• strengthen connections with coworkers and the community

We’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

This position provides critical administrative and documentation support for pharmaceutical manufacturing operations by managing batch records, labels, training documentation, and controlled records in compliance with cGMP, FDA, DEA, and EPA requirements. The role ensures production documentation is accurate, organized, and available to support daily manufacturing activities while maintaining filing systems, logbooks, and compliance records. Working closely with Production and other departments, this individual coordinates documentation, tracks training and supplements, and provides backup support for operational administrative functions. Success in this role requires strong organizational skills, attention to detail, computer proficiency, and the ability to thrive in a regulated manufacturing environment.

• Issue requested batch records for next day’s production and attach necessary stamped labels 
• Label coordination/management-design, etc. 
• Order labels for Production, check in labels, maintenance of label storage according to cGMP regulations. 
• Issue and track training records for all records, including batch records, SOPs and other miscellaneous required training 
• Maintain MSDS Sheets 
• WFI auditing and document maintenance 
• Filing of SOPs, Product specs, RM specs and other miscellaneous filing as needed 
• Log book updates and auditing 
• Maintain work center logs and equipment logs in an orderly manner 
• Track supplements and ensure proper closure and follow up 
• Back  up Admin Assistant as needed on batch record entry and other miscellaneous operations assignments 
• File completed batch records and other filing as necessary.  Maintain tight control of batch record files  

• Strong computer skills 
• Manufacturing office background preferred