Sr QC Technician - 1st Shift

Thermo Fisher Scientific•Middletown, VA

1d•Onsite

About The Position

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. Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

Requirements

Minimum of 2 years of work experience in QA or QC or related field
Working knowledge of Excel, Word, PowerPoint and Outlook
Good organizational skills and the ability to multi-task
Excellent verbal and written communication skills
Strong cross functional relationship building
Independent self-motivated worker

Nice To Haves

Experience in a cGMP environment

Responsibilities

Testing and documentation of raw materials, intermediates, final kits, and stability samples on the c8000, Alinity c, and i2000 platforms
Comprehensive data review to ensure accuracy, compliance, and readiness for audit
Instrument troubleshooting to minimize downtime and prevent workflow disruption
Leading OOS investigations and reports, including mentoring junior analysts through investigation processes
Investigative testing and performance qualification activities, including control value assignments and validation of new test methods
Laboratory operational oversight, including reagent expiry monitoring and inventory management