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Cambrex


TALENT PIPELINE - Materials Characterization (Particle size / ICP-MS) - Future Opportunities

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Job ID: 2025-4138
Type: Regular Full-Time
Category: Material Characterization
Cambrex - Remote

Overview

Thank you for considering a future opportunity with Cambrex! If you are interested in joining our team but don't see a current role that fits your background, please submit your resume here. If we have future opportunities that match your skillset, we will contact you.

While we are not currently hiring for a role linked to this specific posting, we would love to connect with talented individuals who are interested in potential future positions. By joining this talent pipeline, you will be the first to be notified when suitable opportunities arise within our Materials Characterization function.

Cambrex's Materials Characterization positions will be on-site at one of our 14 locations. Locations include: Agawam, Massachusetts, Charles City, Iowa, Durham, North Carolina, East Rutherford, New Jersey (HQ), Edinburgh, UK, High Point, North Carolina, Karlskoga, Sweden, Liege, Belgium, Longmont, Colorado, Paullo, Milan, Italy, Tallinn, Estonia, Waltham, Massachusetts, Waterford, Ireland, and Wiesbaden, Germany.

Sample Job Description:

As a Scientist within our Materials Characterization department, you will execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products.

Responsibilities

• Execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products.
• Execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines.
• Develop and implement test methods utilizing U/HPLC, GC, HPLC/MS, ICP-MS, XRD, LPS and/or various analytical techniques.
• Write standard operating procedures (SOPs), method qualification/validation protocols and reports (GMP/GLP), and research study reports.
• Follow SOPs and clearly documents all procedures and results in a GMP notebook.
• Develop and validate analytical methods for testing of drug substances and drug products.
• Perform technical review of notebooks.
• Operate HPLC, GC, ICP-MS, XRD, LPS, and other laboratory equipment.
• Additionally, you will write standard operating procedures (SOPs), method validation protocols, method validation reports and specifications.
• Supply weekly updates on long-term projects.
• With guidance, you will prepare well written and organized development reports to convey the quality of the methods to clients.

Qualifications/Skills

• Experience in chromatography and wet analytical chemistry is required.
• QC Release, Method development and validation experience with drug substance and drug product is preferred.
• Excellent academic and professional record with demonstrated laboratory skills and the ability to work in an interdisciplinary team environment.
• Minimum of 2+ years of experience in chromatography and wet analytical chemistry is required.
• Strong analytical chemistry skills, including HPLC, GC, and wet chemical methods.
• Experience operating HPLC and GC equipment and executing method validations and transfers.
• Experience in a cGMP environment is required.
• Knowledge of USP, EP, FDA and ICH requirements as they apply to production of drug substances and drug products is preferred.

Success Factors:

• Excellent customer service and communication skills are required.
• Ability to write reports and business correspondences.
• Ability to listen and respond well to external customers, partners and colleagues at all levels.
• Prioritizes tasks according to business objectives and can pursue several objectives simultaneously.
• Highly goal and result oriented.
• Tackles problems with enthusiasm and curiosity.

Education, Experience & Licensing Requirements

• BS Degree or MS Degree in Chemistry or related discipline plus 1-5 years of industrial experience in a GMP environment is required.

Search Tags: PSD, particle size distribution, LPS, Laser Particle size, Malvern Mastersizer 3000, SympaTec, Horiba, ICP-MS, XRD, Method Development, particle size