Formulation Technician II (12hr nights, 2-2-3 rotation)

Thermo Fisher Scientific • Greenville, NC

5d • 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.

Location/Division Specific Information:
Greenville, NC

How Will You Make an Impact?: Support and maintain aseptic/non-aseptic manufacturing areas. 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. The candidate will also need to be flexible to support other shifts as needed. Initial start will be on day shift for several months then move to night shift (6pm-6am).
A Day in the Life:
Ensure pharmaceutical products are manufactured in accordance to area SOPs and current cGMP.
Verify and document production activities in batch records, logbooks and controlled forms.
Complete tasks vital to manufacture drug products in an aseptic filling area, including:
Cleaning cGMP Areas
Parts Preparation
Filter Integrity Testing
Operating Parts Washers and Autoclaves
Performing Tray Loading
Operating the Filling Isolator
General Material Handling
Troubleshooting Equipment Alarms
Designated Trainer/Certified SME

Requirements

• High school diploma or equivalent required.
• Minimum of 1 year of work experience in a manufacturing, operations, production, or lab setting or related field.
• Basic math skills.
• 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.
• Ability to lift 40 lbs. without assistance.
• Adherence to all Good Manufacturing Practices (GMP) Safety Standards.
• Cleanroom restrictions: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed.

Nice To Haves

• Experience in a cGMP environment.
• Equivalent combinations of education, training, and relevant work experience may be considered.
• Excels in a team environment.
• Attention to detail while maintaining a quality product.
• Proactive in identifying quality opportunities.
• Flexibility/willingness to adapt to operational needs.

Responsibilities

• Support and maintain aseptic/non-aseptic manufacturing areas.
• Coordinate the efficient operation of bulk manufacturing/filling area including compounding, sterile filtration, and maintenance of pharmaceutical products.
• Ensure pharmaceutical products are manufactured in accordance to area SOPs and current cGMP.
• Verify and document production activities in batch records, logbooks and controlled forms.
• Complete tasks vital to manufacture drug products in an aseptic filling area, including: Cleaning cGMP Areas, Parts Preparation, Filter Integrity Testing, Operating Parts Washers and Autoclaves, Performing Tray Loading, Operating the Filling Isolator, General Material Handling, Troubleshooting Equipment Alarms.
• Act as a Designated Trainer/Certified SME.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED