Thermofisher
Direct Workday career site

Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation)

Location
Greenville, NC · On-site
Job type
Full-time
Level
Lead / Staff
Experience
2+ years
Education
High school diploma or equivalent
Listed
7 days ago

Skills & highlights for this role

  • GMP compliance
  • cGMP
  • equipment troubleshooting
  • root cause analysis
  • production scheduling
  • team leadership

Also useful

  • Oral Solid Dose manufacturing
  • sterile manufacturing
  • SAP
  • lean manufacturing
  • 5S
  • on-the-job training

About the role

  • Work Schedule
  • 12 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, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.)

About the role

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.

Location/Division Specific Information: Greenville, NC

How Will You Make an Impact?

Uses appropriate interpersonal styles, training methods, and leadership to guide individuals and groups (subordinate, peers, or superiors) toward task accomplishment in the optimum operations of manufacturing areas. Coordinates the efficient operation of bulk manufacturing/filling area including compounding, sterile filtration, and maintenance of pharmaceutical products. Shift hours are 6am-6pm or 6pm-6am on a 2-2-3 rotating schedule.

A Day in the Life

  • Ensure operations are performed in a safe and responsible manner striving to create an injury-free and incident-free workplace.
  • Comply with all job-related safety, Current Good Manufacturing Practices (cGMPs), and other department procedural requirements.
  • Coordinates and motivates personnel to ensure finished product is in accordance with GMP requirements.
  • Commits to action or develop an alternative course of action that is based on logical assumptions and factual information to meet production schedules and targets in accordance with changing priorities. Take corrective action in a timely manner.
  • Plans, prepares and executes a work routing that will ensure that all necessary tasks are completed accurately and in a timely manner to ensure a quality product as well as schedule adherence. Take into consideration resources and constraints.
  • Gathers information to accurately identify the root cause of problems in equipment or work processes. Coordinates entry and follow up for area maintenance tickets to ensure timely completion of equipment maintenance to minimize impact to production schedule.
  • Troubleshoots operational and production problems in order to identify appropriate corrective actions. Disassembles, assembles, cleans and operates area manufacturing equipment.
  • Provides leadership and coordination for parts preparation, parts maintenance, and the implementation and sustainment of 5S practices across PFS parts storage areas.
  • Communicates and works to resolve any production, quality or safety issues.
  • Fosters crew teamwork in such a way that promotes increasing employee knowledge and skills.
  • Manages primary interface with data entry into Systems, Applications and Products (SAP) system.
  • Functions as Champion of the On-the-Job Training (OJT) program, area safety initiatives, and area lean manufacturing initiatives. Functions as Subject Matter Expert (SME) for area of responsibility.

How Will You Get Here

Education

  • High school diploma or equivalent required.

Experience

  • Required: Minimum of two (2) years of work experience in a pharmaceutical, biopharmaceutical, operations, lab setting or sterile manufacturing is required.
  • Preferred: Experience in Oral Solid Dose or Steriles or leadership experience.
  • Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities

  • Excels in a team environment.
  • Basic math skills.
  • Attention to detail while maintaining a quality product.
  • Ability to perform repetitive work duties.
  • Ability to follow SOPs.
  • Ability to concisely communicate with Production leadership to accept daily assignments and report any relevant production-related information.
  • Ability to schedule the team’s activities and drive priorities
  • Strong communication skills
  • Proactive in identifying quality opportunities
  • Flexibility/willingness to adapt to operational needs

Physical Requirements / Work Environment

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 25-50 pounds, occasionally pushing or pulling more than 100 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Read the original posting

From Thermofisher's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.

How Rolev.ai helps with this application

Rolev.ai is a job search and application tool for US job seekers. For this Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) role at Thermofisher, it shows how your resume fits, tailors your resume to the posting, and prepares the application for you to review.

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Common questions

Where is the Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) job at Thermofisher located?

This Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) position at Thermofisher is located in Greenville, NC (On-site). Always check Thermofisher's application page for specific state eligibility or relocation policies.

What qualifications are required for Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) at Thermofisher?

For the Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) role, Thermofisher highlights 2+ years of relevant experience; a high school diploma or equivalent; experience with GMP compliance, cGMP, equipment troubleshooting, root cause analysis, production scheduling, team leadership. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the Sr Formulation Technician (12hr days or 12hr nights; 2-2-3 rotation) position at Thermofisher?

This listing links directly to Thermofisher's Workday application page. You can apply directly on Thermofisher's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.