Our client is seeking a Quality Control Scientist as they continue to expand their Quality Control Department. This is a large CMO based out of Portsmouth, New Hampshire that is one of the world's leading suppliers to the Pharmaceutical & Biotechnology and Specialty Ingredients markets. They are currently in the process of building out their cell therapy group which is the reason for this hire.
As a QC Analyst II, you will help the Quality Control department to upkeep production with the release of raw materials. The QC Analyst II will provide high quality and on time results to meet the manufacturing demands of the company. The QC Analyst will use company policies and procedures as well as applied job skills to complete various task.
Performing test samples for Raw Materials
Providing training to other employees
Writing Test Methods and Quality Records (Deviations, Change Control, CAPA)
Accountable for various duties as assigned.
Minimum Required Qualifications:
Bachelor/Associates degree with preferred area of study in Chem, Biochem, or Related Science field
2-4+ years industry experience, preferably in a cGMP environment
Use of Laboratory computer systems
Preferably, candidate has previously used GMP Quality Systems such as: TrackWise, LIMS
Strong data analytics skills.
Ability to perform assigned, multifaceted and/or wide-ranging tasks with guidance from Supervisor.
EPM Scientific is a global specialist recruitment company working exclusively in the Life Sciences industry. As an industry expert we understand that the ongoing changes within the Life Sciences industry make the ability to attract and maintain industry-leading talent a key priority.
As of today EPM Scientific has consultants based all over the world, from our own fully licensed and compliant offices in New York, Boston, San Francisco, Chicago, Dallas, London, Zurich, Berlin, Singapore, and Hong Kong, and unlike many other companies, we have grown organically.
Role: QC Analyst Raw Materials
Apply for this job now.