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 2,000 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!

Job Overview

The AD Technical Writer will be responsible for consistently generating high quality technical documents, such as test procedures, protocols, and reports based on data collected by other members of the Analytical Development department that meet the needs of other departments, clients, and regulators.  Compliance with SOPs, cGMP, ICH, and other regulatory guidelines is required to perform most job tasks. 

Responsibilities

Drafting and revising controlled documents such as test procedures, method evaluation protocols, reports, and SOPs while following established guidelines for correctness, completeness, clarity, and format. 

• Coordinate the approvals of these documents through the use of software such as MasterControl and TrackWise. 
• Compile and present data from multiple sources such as laboratory notebooks and various laboratory instrumentation software. 
• Maintain open communication with members of AD, QC, and QA to ensure timely delivery of high quality documents to support evolving business needs. 
• Continuously improve documentation systems to increase efficiency and compliance with cGMP and/or other regulatory requirements. 

Qualifications/Skills

Advanced technical writing skills and the ability to communicate effectively with peers, department management, and cross-functional coworkers. 

• Fluent in written English. 
• Familiarity with compliance requirements within cGMP with an emphasis on method validation and reporting requirements preferred. 
• Demonstrated excellence in advanced word processing using Microsoft Word. 
• Demonstrated computer literacy, including spreadsheets, structural drawings, databases, and communication packages preferably in a Windows environment. 
• Ability to work in a highly independent and self-directed work environment. 

Education, Experience & Licensing Requirements

Bachelor’s degree in Chemistry or closely related field required. 

• Minimum of 2 or more years of experience in a cGMP regulated laboratory environment highly preferred. 

This position works with and handles hazardous materials and wastes at Cambrex. This person has the appropriate qualifications to read, understand, apply and communicate written and verbal information regarding handling and managing hazardous wastes. He/She is also responsible for recognizing emergency situations concerning hazardous materials and wastes.