Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

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.

• Perform analytical and functional testing of raw materials, intermediates, finished goods kits, and/or filled bottle reagents/calibrators according to approved standard operating procedures (SOPs).
• Use chemistry clinical analyzers for product testing, and accurately document test results using Excel spreadsheets and workbooks.
• Document test results, complete batch records in compliance with current Good Manufacturing Practices (cGMPs).
• Perform revisions and updates to QC SOPs and/or worksheets as part of our continuous improvement culture and initiate document change orders.
• Summarize test data, maintain lot histories, and evaluate data for trends and discrepancies.
• Perform out of specification investigations (OOS), and participate in investigations on nonconforming material. Document investigations using established procedures and processes.
• Support the needs of the department by performing assigned responsibilities as directed by the Supervisor.
• Actively participate in PPI, Lean, and 5S programs, when required.

• BS/BA in Chemistry, Biochemistry, or Bioscience preferred (equivalent combinations of education, training, and relevant work experience may be considered).
• Experience in Quality Assurance/Quality Control, preferably in the medical diagnostics industry preferred.
• Strong laboratory skills, including pipetting, safety, and hazardous chemical handling.
• Understanding of cGMP and its application in the work environment is preferred.
• High level of reading comprehension and ability to follow written and verbal directions with a high level of accuracy.
• Excellent written communication skills to produce clear and understandable documentation.
• Strong verbal communication skills for effective collaboration with team members.
• Intermediate word processing and spreadsheet software skills.
• Ability to manage multiple tasks simultaneously and work independently.
• Proficiency in performing simple data analysis and summarizing results.
• Basic math skills, including calculation of concentrations and dilutions, and a strong grasp of algebraic concepts.

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
• Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount