Lead Formulation Technician (12hr Day Shift, 2-2-3)
Greenville, NC - USA
Job Summary
Work Schedule
12 hr shift/daysEnvironmental 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 Fluctuating Temps hot/cold Laboratory Setting Loud Noises (Equipment/Machinery) Office Rapid flashing lights 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.) Various outside weather conditions Warehouse Will work with hazardous/toxic materials Working at heightsJob Description
As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
Greenville NC (USA) DPD
How You Will Make an Impact
As aTeam Leader in Formulation Manufacturing you will lead a skilled team of manufacturing technicians dedicated to producing sterile pharmaceutical products that meet the highest standards of quality and compliance. Youll coordinate daily operations mentor and develop team members and help ensure that every batch meets safety and quality expectations. Shift hours are 6am-6pm on a 2-2-3 rotating schedule.
What You Will Do
Lead and develop a team of manufacturing operators to achieve production safety and quality goals.
Plan daily work assign resources and supervise progress to ensure schedule adherence.
Ensure compliance with cGMP SOPs and data integrity standards through accurate documentation and process execution.
Partner with Quality Engineering and Maintenance to resolve process and equipment issues.
Oversee batch record accuracy documentation and adherence to all cGMP SOP and regulatory requirements.
Ensure data integrity and compliance across all operational processes.
Support deviation investigations root cause analysis and corrective actions.
Promote a culture of safety inclusion and continuous improvement through active engagement and example.
Track and report key production metrics finding opportunities for efficiency and improvement.
Maintain a clean safe and compliant workspace aligned with EHS and regulatory requirements.
Communicate effectively between operators line leads and supervisors to ensure smooth operations.
Support the Manager as a delegate during absences and assist with onboarding and training of new employees.
How You Will Get Here
Education:
High School Diploma or equivalent required.
Experience:
Minimum of three (3) years of experience in pharmaceutical biopharmaceutical or sterile manufacturing four (4) years preferred.
Equivalent combinations of education training and relevant work experience may be considered.
Hands-on experience in aseptic or sterile product formulation and using SAP or other manufacturing systems strongly preferred.
Knowledge Skills and Abilities:
Deep understanding of cGMP aseptic technique and regulatory compliance. Strong interpersonal and communication skills with the ability to inspire and engage others. Organized and adaptable skilled at balancing various priorities in a fast-paced setting. Analytical thinker with problem-solving skills and attention to detail. Proficiency in Microsoft Office applications (Excel Word PowerPoint). Commitment to teamwork accountability and Thermo Fishers 4i Values: Integrity Intensity Innovation and Involvement.
Physical Requirements:
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 20-50 pounds occasionally pushing and pulling over 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. Occasional weekend shifts required.
Required Experience:
IC
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more