Supervisor, Formulation Manufacturing (12hr Nights 2-2-3 schedule)
Greenville, NC - USA
Job Summary
Work Schedule
12 hr shift/nightsEnvironmental 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 Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job 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.
Discover Impactful Work:
The Formulation Supervisor provides leadership to production teams in the manufacturing filling and packaging of high-quality pharmaceutical products. This role ensures operations meet schedule cost and quality standards while maintaining safety compliance and strong team engagement.
Excellent Benefits Package
Review our companys Total Rewards
Medical Dental & Vision benefits-effective Day 1
Paid Time Off & Holidays
401K Company Match up to 5%
Tuition Reimbursement eligible after 90 days!
Employee Referral Bonus
Employee Discount Program
Recognition Program
Charitable Gift Matching
Company Paid Parental Leave
Career Advancement Opportunities
Location/Division Specific Information
Greenville NC
Hours: 6pm-6am (2-2-3 schedule) 15% shift differential
RELOCATION ASSISTANCE IS NOT PROVIDED
- Must be legally authorized to work in the United States WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
- Must be able to pass a comprehensive background check which includes a drug screen.
A Day in the Life:
- Lead develop and empower production staff while fostering engagement and teamwork.
- Ensure production quality and quantity standards are consistently achieved.
- Monitor production performance and take corrective actions as needed.
- Ensure compliance with cGMPs and readiness for FDA QAT and OSHA inspections.
- Plan and adjust production schedules for efficiency and quality output.
- Promote and enforce safety programs to maintain an incident-free workplace.
- Evaluate employee performance and conduct annual reviews.
- Support technical teams and validate new processes.
- Approve production documentation including SOPs and validation protocols.
- Drive cost reduction and efficiency improvement initiatives.
- Track attendance training and timekeeping.
- Perform additional duties as assigned.
Keys to Success:
Education
Bachelors degree in Physical Biological Chemical or Production-related science preferred. Equivalent combinations of education training and relevant work experience may be considered.
Experience
5 years of manufacturing experience with 2 years of leadership experience required. Sterile pharmaceutical manufacturing experience preferred.
Knowledge Skills Abilities
- Technical knowledge of aseptic processing operations.
- Strong attention to detail and organizational skills.
- Ability to manage multiple priorities in a fast-paced environment.
- Strong interpersonal and communication skills.
- Ability to lead motivate and develop teams.
- Effective time management and decision-making skills.
- Ability to handle confidential information with discretion.
Required Experience:
Manager
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