QC Specialist I Job at Thermo Fisher Scientific
Job Title: Quality Control Specialist I (10hr nights)
Requisition ID: 221386BR
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer.
Location/Division Specific Information: 1200 Darrell Waltrip Drive, Lebanon, TN
Our new Lebanon site will be Thermo Fisher Scientific’s largest designated Single-Use Technology (SUT) manufacturing facility in the world! The biotherapeutic market has been rapidly adopting single-use technologies to reduce risk and improve operational efficiencies. Our new innovative Lebanon facility is helping strengthen our position as one of the market leaders in SUT manufacturing.
This is an exciting opportunity to become part of our Lebanon team for candidates who are looking to expand their skills, have exciting career growth opportunities, and be able to improve their communities and lives of patients around the world, with opportunities to contribute directly to the fight against COVID-19 and other diseases like cancer, Crohn’s disease, heart disease, arthritis and more!
How will you make an impact?
Our employees share a common set of values - Integrity, Intensity, Innovation and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve mankind by enabling our customers to make the world healthier, cleaner and safer. This position is a 10-hr night shift from 8:00pm to 6:30am, Monday-Thursday and Friday is optional overtime.
The QC Specialist I, is responsible for giving direction in the Inspection of BPCs (BioProcess containers) in a highly regulated production environment, must manage workflow for quality to efficiently achieve team goals and utilize quality and production resources. A QC Specialist I must be able to motivate and inspire the team with an emphasis on continuously improving quality processes to adapt to changing customer needs in a dynamic and profitable industry.
What you will do?
- Coordinate activities of QC labs and Quality Control with Team Lead and Production Spec II to meet production goals, quality and cost objectives.
- Coordinate staffing, interviewing and planning to meet company objectives and work load.
- Manage deployment of personnel across all work areas, prioritizing Quality and department schedules.
- Assist in the direction of a team of QC In-process Associates.
- Inspection of product to drawings, specifications and procedures.
- Maintain good documentation practices.
- Correctly and accurately document inspection in process control documents and inspection forms.
- Verify OOS and verify chambers that are QC observations and chambers that fail.
- Train QC in process Associates.
- Participate on special projects as assigned.
- May be required to perform other related duties as required and/or assigned.
- Review WID, SOP and recommend improvements, communicate and train entire team on any changes.
- Participate in Spec review and approval as needed.
- Support in-coming inspection, film testing, disposal forms.
How will you get here?
Education:
- High School Diploma or GED minimally required.
- 0-1 years of manufacturing experience required; 1+ years of regulated manufacturing experience preferred.
- Knowledge of computer applications and current software is desirable.
- Strong attention to detail is crucial, excellent oral and written communication skills required.
- Ability to read and interpret important documentation and directions: including critical details with drawings and special instructions, in order to properly inspect products.
- Good Interpersonal Skills and time management.
- Demonstrate reliability through exceptional attendance.
- Ability to work with production personnel to ensure good quality and workflow.
- Knowledge of BPC film and familiarity with their common associated defects.
- Desire to meet and/or exceed set performance goals and requirements.
- Objective thinking and rational decision making.
- Ability to accept and use constructive criticism to improve performance.
Physical and Environmental Requirements and Information
- Work in a fast-paced environment for 8-12 hours a night, depending on shift, with additional overtime as required.
- Ability to enter the clean room as needed. Clean room is a controlled environment with a humidity of 30% or greater and a temperature between 60⁰ and 70⁰ F and some ambient noise.
- Specific gowning requirements include, but are not limited to: gloves, hair net, beard net, face cover, safety glasses with no makeup / jewelry or piercings.
- Use PPE (Personal Protective Equipment) and understand chemical hygiene including labels and SDS (Safety Data Sheets), common chemicals used include: disinfectants, solvents and IPA (Isopropyl Alcohol 70% and 99%).
- Must have the ability to inspect bio-process containers on a light table for an entire shift, stand and move about including reaching, bending, stooping, grasping and lifting.
- Must have the ability to use hand tools and equipment including forceful gripping, grasping, pushing, pulling and repetitive motion along with frequently lifting and manipulating up to 40 pounds unassisted.
At Thermo Fisher Scientific, each one of our 95,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
For more information, please visit www.thermofisher.com.
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.
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