QC Technician II - 1st Shift

Work Schedule Flex 10 hr shift/days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse Job Description Compensation: $18.65 - 25.00/HR Work Schedule Shift: 1st Shift, Monday-Thursday Shift Hours: 7:00AM – 5:30PM QC Raw Materials Technician II As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Division/Site Specific Information Thermo Fisher Scientific - Viral Vector Services (VVS) is a multifaceted gene therapy contract development and manufacturing organization (CDMO) that is seeking sharp individuals to bring the highest quality processes, products and testing to our clients. Our employees are committed to making a difference in our organization for our client partners and the patients we serve. Pharma Services | Viral Vectors | 5 Commerce Drive, Plainville, MA | How will you make an impact? The QC Raw Material Technician II provides critical sampling activities of the raw materials that will be used to manufacture leading edge viral vector therapies to our clients. the Plainville, Massachusetts site has become a key manufacturing facility, and this team will be instrumental in supporting the production and timely delivery of critical therapies to patients. What will you do? • Raw Materials Inspection: to include but not limited to; Review of received goods, documenting appropriate particulars (e.g. lot numbers, expiry dates, etc), cross-referencing information against documentation, detecting incorrect goods and notifying appropriate personnel • Raw Material Sampling: Arrange and collection, labeling and storage of samples where required as per material Specifications, and perform sample adjustments in SAP • Perform material transfer and gown into clean rooms • Perform equipment cleaning • Ability to create purchase requests and ship raw materials for testing to external/internal laboratories • Reconcile test results for release of GMP materials • Identify, escalate, and support investigations for any identified internal and/or external non-conformances identified during QC checks, or notified to QC by another function • Performing documentation review of general processing documents such as, but not limited to; Receipt Records and Laboratory Processing Records • Performing additional QC check duties as identified by the QC Team Manager and governing SOPs • To ensure during review documentation is correct, GMP compliant, error-free, and entered operating systems appropriately • Perform ad hoc duties, as requested by the QC Team Manager or Senior Manager, Quality, to support activities of the Quality department …