Cambrex
Quality Control Chemist – Cambrex
Apply for the Quality Control Chemist position at Cambrex.
Company Information 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, and 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!
Job Overview Reporting to the QC Supervisor, the QC Chemist is responsible for raw material, in‑process, isolated intermediate, or finished good testing in a GMP laboratory environment. The QC Chemist III will provide technical knowledge to the role and assist junior staff with troubleshooting activities as necessary.
Responsibilities
Follow all FDA, ICH, cGMP, cGLP, DEA, and internal SOP requirements as they relate to Phase III and commercial GMP laboratory operation.
Adhere to all OSHA and company safety requirements and practices.
Perform a wide variety of chemical analyses for release of raw materials, in‑process, intermediates, finished goods, and stability.
Support/maintain laboratory programs such as calibration/preventive maintenance, IQ/OQ/PQ.
Perform in‑depth out of specification or out of trend laboratory investigations of non‑complying or aberrant results.
Support the implementation and training efforts for new laboratory instrumentation or software.
Perform data review of QC data as necessary.
Independently perform troubleshooting of laboratory equipment.
Strong working knowledge of H
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Company Information 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, and 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!
Job Overview Reporting to the QC Supervisor, the QC Chemist is responsible for raw material, in‑process, isolated intermediate, or finished good testing in a GMP laboratory environment. The QC Chemist III will provide technical knowledge to the role and assist junior staff with troubleshooting activities as necessary.
Responsibilities
Follow all FDA, ICH, cGMP, cGLP, DEA, and internal SOP requirements as they relate to Phase III and commercial GMP laboratory operation.
Adhere to all OSHA and company safety requirements and practices.
Perform a wide variety of chemical analyses for release of raw materials, in‑process, intermediates, finished goods, and stability.
Support/maintain laboratory programs such as calibration/preventive maintenance, IQ/OQ/PQ.
Perform in‑depth out of specification or out of trend laboratory investigations of non‑complying or aberrant results.
Support the implementation and training efforts for new laboratory instrumentation or software.
Perform data review of QC data as necessary.
Independently perform troubleshooting of laboratory equipment.
Strong working knowledge of H
#J-18808-Ljbffr