Quality Control Raw Materials Coordinator (Biotech)

 

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The QC Raw Material Coordinator will represent the Quality Control department and act as a liaison between Raw Materials Planning, Receiving, Sampling and QA to expedite release of raw materials.   Responsible for the coordination and communication of priorities for raw material to ensure continuity of raw material supply for use in Production. Uses abilities in accordance with company policies and procedures to complete tasks in creative and effective ways. Works on where initiative are required in resolving problems and making recommendations. Works on analysis of data requiring an in-depth evaluation of various factors.

This position has a schedule of M-F 1st shift business hours

Must be within (or able to relocate to) commuting range of our Portsmouth NH facility, as regular on-site presence is required for this role 

Key Responsibilities:

• Collaborates with internal and external teams to meet timelines
• Interfaces with contract laboratories to prioritize testing
• Monitors the completion of contract laboratory investigations, including incremental steps to ensure timely completion of GMP records
• Enters and reviews data in electronic systems (LIMS, etc)
• Perform other duties as assigned
• Level of this role is dependent on experience

Key Requirements:

• Bachelor or Associates Degree required, area of study in Chemistry, Biochemistry or Related Science Fields
• Previous experience working in a QC laboratory
• Knowledge of QC testing
• Experience with MS Suite applications, particularly Word and Excel
• Strong organizational skills and time management abilities
• Experience with document management systems (DMS)/document control practices preferred
• Experience in technical writing (protocols, reports, specifications and methods) preferred
• Coherent and effective interpretation of written and verbal instructions

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.