• The QCM will perform release testing on finished products following Standard Operating Procedures (SOPs) and in-house test methods.
• The QCM II will review and approve documentation to include but not be limited to Data Control Reports, Notebooks, and Certificates of Analysis (C of A's).
• The QCM II will be assigned a specific area (determined by upper management) and become the Subject matter Expert (SME). These areas include but are not limited to microbial identification, probiotics, Environmental Monitoring (EM) risk evaluation, etc.
• The QCM will be responsible for submitting samples to contract labs as necessary with appropriate documentation. The QCM will follow Current Good Manufacturing Practice (cGMP) documentation guidelines to record all procedures in a timely fashion. The analyst will be responsible for reporting the results of analyses on finished product Certificates of Analysis (COAs).
• The QCM will perform evaluation/ validation testing on Nutramax Laboratories, Inc. finished products and raw materials following Standard Operating Procedures (SOPs), in-house test methods, and industry guidelines. (S)he will be responsible for the execution of Evaluation Protocols as well as Evaluation/ Validation Reports and Summaries, following Current Good Manufacturing Practice (cGMP) documentation guidelines, to be presented to QC and Upper Management.

Leveraging the power of relationship building and the Adecco brand, we work to align candidates with permanent positions based on skillset and job requirements. Our personal and tailored approach assures that our candidates are placed into positions that align with their long-term goals. We specialize in recruiting for permanent positions within the Life Sciences industry. Here are just some of the roles we specialize in: - Biotechnology - Pharmaceutical - Clinical Research/Trials - Medical Devices - Quality Assurance - Engineering