×
Register Here to Apply for Jobs or Post Jobs. X

Sr. Formulation Technician; nights, D shift, rotation

Job in Columbia, Lexington County, South Carolina, 29228, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-03
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering
Salary/Wage Range or Industry Benchmark: 45000 - 65000 USD Yearly USD 45000.00 65000.00 YEAR
Job Description & How to Apply Below
Position: Sr. Formulation Technician (12hr nights, D shift, 2-2-3 rotation)
Location: Columbia

Work Schedule

12 hr shift/nights

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, 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, 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.

Location/Division

Specific Information

Greenville, North Carolina/Steriles East

How Will You Make an Impact?

As a Sr Formulation Technician in our Greenville facility, you will play a crucial role in the development and production of sterile injectable drug products. Your expertise will contribute directly to bringing life‑saving medications to patients worldwide, ensuring the highest standards of quality and safety in pharmaceutical manufacturing.
Shift hours are 6pm-6am on a 2-2-3 rotating schedule.

A Day in the Life
  • Start your day by reviewing production schedules and preparing the clean room environment for sterile filling activities, including area cleaning and batch record review. Throughout the day, maintain detailed documentation of all processes and conduct in-process quality checks to ensure compliance with cGMP standards.

  • Participate in a cross‑functional team meeting to discuss upcoming production schedules, training, and Filling Work Orders revisions. Analyze filling operations data and contribute insights to optimize processes for efficiency and quality. Troubleshoot any issues that arise during the manufacturing process, working closely with quality assurance and engineering teams. Mentor junior technicians, sharing your expertise and ensuring adherence to safety protocols and standard operating procedures (SOPs) in the sterile manufacturing environment.

  • Engage in continuous improvement initiatives by participating in Lean Six Sigma projects aimed at enhancing production efficiency and reducing waste. Conduct end‑of‑batch reviews, training of new colleagues, and act as operations SME engaging in opportunities for process improvements. Stay updated on industry regulations and best practices, attending training sessions and sharing knowledge with your team to maintain Thermo Fisher Scientific’s position at the forefront of sterile drug manufacturing

Education

High school diploma or equivalent required.

Experience
  • Required:

    Minimum of 2 years of work experience in a manufacturing, operations, production, lab setting or related field

  • Preferred:
    Experience in a cGMP environment

  • Preferred:
    Experience working in a clean room environment

  • Preferred:
    Experience operating complex, technical, or fast‑paced manufacturing systems

  • Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities
  • Demonstrated knowledge of cGMP regulations and aseptic techniques required for sterile drug manufacturing. Proficiency in following complex SOPs, Work Instructions, and maintaining detailed documentation of manufacturing processes.

  • Strong analytical and collaborative problem‑solving skills with the ability to troubleshoot issues in real‑time during the production process. Excellent attention to detail and ability to maintain focus in a fast‑paced environment.

  • Proficient in using various operations filling equipment and machines relevant to pharmaceutical filling operations, such as Debaggers, Isolator filling machines, sterilizers, cappers, and Lyophilizers. Strong communication skills with the…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary