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Job Information

ThermoFisher Scientific Lead Formulation Technician in High Point, North Carolina

Work Schedule

12 hr shift/nights

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), Office, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Job Description

Lead Machine Operator (Nights)

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 humankind by enabling our customers to make the world healthier, cleaner and safer.

Watch as our colleagues explain 5 reasons to work with us (https://jobs.thermofisher.com/global/en/5-reasons-to-work-at-thermo-fisher-scientific) . As one team of 100,000+ colleagues, we are working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Incredible Benefits!

Medical, Dental, and Vision – effective day1

Paid time off and holidays

401k company match up to 6%

Tuition Reimbursement – available after 90 days

Employee referral bonus

Employee discount program

Employee recognition program

Charitable gift matching

Company paid parental leave

Career advancement opportunities

Location/Division Specific Information

High Point, NC

Hours: 7:00pm - 7:00am (2-2-3 schedule)

What will you do?

  • Performs tactical planning to make decisions based on encapsulation schedule, staffing, product mix, and manufacturing priorities in order to meet high Quality, high Productivity, and On Time Delivery dates.

  • Checks encapsulation schedule daily in order to plan for effective execution of activities.

  • Assigns associates to work stations to meet production requirements.

  • Checks log books in each room for proper completion and accuracy.

  • Verifies that no foreign capsules are remaining in any room following a changeover and that all equipment is clean and the documentation is complete and accurate.

  • Notifies supervisor of any problems, including poor quality, compliance risks, data integrity concerns etc.

  • Collects data for shift production and inputs information into computer

  • Verifies, inputs and corrects information in SAP.

  • Reviews Batch Production Records (BPRs) accurately and thoroughly, with Right First Pass metrics in mind. Submits detailed review of completed BPR paperwork to In Process Quality Assurance (IPQA).

  • Investigates and writes events and CAPAs in Trackwise, must be able to efficiently and effectively write and obtain approval of GMP notes and memos as needed.

  • Coordinates and/or supplies materials (towels, paperwork, etc.) to the encapsulation rooms to minimize down time.

  • Verifies the product quality of in process batches multiple times throughout their shift. Quality checks include review of fill weight statistics, seam thickness values, and physical capsule attributes.

  • Conducts periodic checks throughout shift of all fill weight scales, seam microscopes, and all associated equipment for proper set-up and operation.

  • Meets with supervisor to receive instructions and to exchange production information. Provides back-up for supervisor in their absence.

  • Conducts detailed Training sessions for workers in equipment operation and when SOPs have been revised.

  • May perform duties of absent associates in order to maintain production standards and goals.

  • May perform other reasonable, related business duties as assigned.

  • Perform periodic GEMBA walks of the encapsulation area in order to find opportunities for improvement and GMP compliance.

How will you get there?

  • High School diploma or GED

  • Ability to pass DEA requirements

  • Ability to read, write, and speak English fluently

Experience

Two years of production experience

At Thermo Fisher Scientific, each one of our 70,000 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!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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