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 2,000 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
Position performs daily QA activities to support GMP Analytical projects, nonGMP/GMP Manufacturing Facility operations, and other duties as needed.
Responsibilities Perform approval process for analytical procedures. Perform approval process for analytical protocols/reports. Maintain controlled documents. Perform approval and release of regulated raw materials and intermediates. Review and approve analytical data used in the support of raw material, intermediate, and final product batch release. Knowledge and use of computerized quality systems such as Empower, MasterControl, TrackWise, and SAP. Develop and issue Certificates of Analysis. Assist with management and issuance of notebook system. Ensure compliance with company policies and SOPs, as well as FDA and other applicable guidelines. Assist with developing and maintaining Cambrex's quality system. Assist with developing and performing training activities. Qualifications/Skills Assist with development and writing of standard operating procedures. Serve as a backup to Senior Quality Assurance Scientist and management. Other duties as assigned and/or developed by Quality Management. In the absence of Manager/Associate Director, Quality, sign certificates and forms following written authorization from management
Education, Experience & Licensing Requirements
BS or MS in Chemistry (or closely related discipline) or relevant experience. A minimum of 5 years of relevant background in GXP compliant pharmaceutical laboratory environment or related quality area. Ability to create and interpret SOPs. Ability to work with minimal supervision.
The daily work is performed in an office setting and involves sitting most of the time. Walking and standing are required only occasionally.
All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.
