Cambrex

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Job Locations US-NC-Durham
As an Analytical Scientist, you will develop and validate analytical methods for testing of drug substances and drug products.
Job Locations US-CO-Longmont
The Supervisor, Drug Substance Manufacturing plays an important leadership role and is responsible for successfully meeting client and departmental objectives in a timely manner. The Supervisor is responsible for leading the technical staff to enable the goals of the organization in Drug Substance Manufacturing with a focus on safety, quality, and right first-time metrics.
Job Locations US-NC-Durham
Our Analytical Services Department is seeking a high-level management candidate to oversee of a core-team of scientists focused on supporting a wide range of testing services for clients in late phase and commercial operations. The person’s primary responsibilities will include overseeing and planning resourcing across  this Analytical team, delivery of project milestones, development of personnel and operational excellence initiatives within analytical. This role will interact with clients and is responsible for successfully meeting client and departmental objectives in a timely manner.
Job Locations US-CO-Longmont
Support Quality System Management Review planning and review process.
Job Locations US-CO-Longmont
Cambrex in Longmont Colorado is seeking a Research Scientist for our process chemistry research group.  This position requires expertise in synthetic organic chemistry as well as the analytical instrumentation used in this field (for ex. NMR, HPLC, GC, FTIR).  The process chemistry group conducts research into new synthetic routes and optimizes existing processes for the generation of the active pharmaceutical ingredient (API) in developmental drugs for clinical evaluation.
Job Locations US-NC-Durham
As a Project Manager, you will be responsible for managing cross-functional project teams to ensure that projects are completed with the deliverables and timeline described in the project’s scope of work.  These projects may cover individual or multiple services including analytical chemistry, process chemistry, formulation development, and manufacturing.  Some projects may span multiple locations.
Job Locations US-IA-Charles City
Cambrex Charles City, Inc. is seeking an Environmental Engineer to work at our manufacturing plant in Charles City, Iowa who shares the values and principles that characterize who we are and how we work. It’s time to join our world-class team.    
Job Locations UK-Edinburgh
The main purpose of the Solid Form Screening Team Leader is to lead, develop and direct a team of solid form scientists. 
Job Locations US-CO-Longmont
The Technical writer will author and edit Master Batch Records for pilot plant and process labs manufacturing.  They will be responsible for progressing them through peer review/approval process. The Technical writer assures that all documents are consistent with the approved format meeting the RFT goals.
Job Locations US-CO-Longmont
As a Manufacturing API Technician, you will be responsible for cGMP and non-GMP manufacturing and conducting chemical reactions with direct guidance.
Job Locations US-NC-Durham
Support a diverse range of client programs within a highly cross-trained analytical core team
Job Locations US-NJ-Whippany
The Manager Quality Assurance Training  and Process Improvement is responsible for managing the Training Department, overseeing development and administration of TMS training curricula that provides comprehensive training to employees. This position will also promote compliance and a continuous improvement culture to drive process and cost improvement.  
Job Locations US-CO-Longmont
As an Analytical Scientist, you will develop and validate analytical methods for testing of drug substances and drug products.
Job Locations US-IA-Charles City
Reporting to the Production Supervisor, the Chem I Operator will be expected to successfully produce chemical and pharmaceutical products in our manufacturing environment.
Job Locations US-IA-Charles City
The Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production.
Job Locations US-IA-Charles City
The Senior Process Engineer will be responsible for implementation of projects for the manufacture of APIs and bulk intermediates and other products from development through piloting and/or commercial production.
Job Locations US-NC-Durham
Develop biopharmaceutical assays, bioassays, and validate the methods for GMP use
Job Locations US-CO-Longmont
The Manager, Drug Substance Manufacturing plays an important leadership role and is responsible for successfully meeting client and departmental objectives in a timely manner. The Manager is responsible for leading team members to enable the goals of the organization in Drug Substance Manufacturing with a focus on safety, quality, and right first-time metrics.
Job Locations US-CO-Longmont
We are seeking an Associate Scientist to support formulation design and development activities within the Formulation team. This role will be responsible for executing oral solid dosage formulation experiments for drug product process development and analytical testing to primarily support early stages of the CDMO projects.
Job Locations US-NC-Durham
About this opportunity Build, improve and integrate  quality management system (QMS) for all of Cambrex US locations. Design and implement strategy for quality certifications and interfaces among entities. Create visibility and accountability for QMS process indicators (KPIs) for all sites and reporting to executive management. Leverage US Quality leadership team in sharing best practices and coordinating US efforts. Lead evaluation of best in class processes and tools. Oversee implementation of QMS process tools such as electronic document control, change control, and CAPA solutions to leverage the buying power of a US entity. Coordinate and streamline site-to-site interfaces including change control and design transfer activities. This person must establish effective partnerships within and outside of the quality team to facilitate the timely identification and resolution of quality matters as well as opportunities for quality process improvement.