Qc Chemist I Jobs

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

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!

Responsibilities

• Write controlled documents such as stability reports, test procedures, SOPs, SAPs, et
• Follow all OSHA and company safety rules and practices.
• Provide on-call coverage as directed.
• Perform instrument maintenance and troubleshoot equipment as
• Review and enter data for Inventory Control
• Handle, analyze and dispose of hazardous samples and
• Perform in-depth laboratory investigations of non-complying test
• Working knowledge of chromatography.
• Recommend, develop and maintain laboratory programs, including stability, calibration, preventive maintenance, reduced testing, check sample, IQ/OQ, etc., to comply with cGMP regulations and audits.
• Evaluate performance of instrumentation and validity of test results
• Perform statistical evaluation of data including SPC (statistical process control), system suitability, instrument and method
• Adhere to all EPA, FDA, cGMP, cGLP DEA regulations and internal SOP's as they relate to the operation of the Quality Control lab and general operation of the chemical production
• Responsible for coverage of all job duties for QC Tech I Chemist.
• Follow all OSHA and company safety rules and practices.
• Perform method development including instrument parameters, new instruments and method improvement
• Review and enter data for Inventory Control
• Perform and document method transfer from Analytical Development
• Perform a wide variety of chemical analyses for release of raw materials, intermediates and finished
• Maintain laboratory solutions, inventory and notebooks.

Education, Experience & Licensing Requirements

• Strong chemistry theory
• Experience in a laboratory environment preferred
• Effective communication skills (oral, written)
• Proven ability to handle various project load is preferred
• Strong attention to detail
• BS/BA in Chemistry/Biology or related science field.
• Ability to work in a fast-paced, deadline driven work environment
• Knowledge of analytical instrumentation (GC, HPLC preferred)
• Ability to work well with others in a team environment