Job Details
Pegasus Laboratories, Inc., part of PBI-Gordon Corporation, is excited to welcome a 2nd Shift Production Supervisor to the team in Pensacola, FL.
Pegasus Laboratories, Inc., is an innovative veterinary pharmaceutical and medical product company committed to supporting veterinarians and the animal health industry. This role is located in Pensacola, FL.
As a Production Supervisor, you will oversee plant operations to ensure compounding, compression, and packaging activities are completed per the production schedule and meet cGMP, SOP, and safety requirements in accordance with corporate policies.
Job Responsibilities:
Lead and direct plant employees to include staffing and performance management
Manage employee training, workforce ladder qualification assessments, ladder advancements, and workforce ladder updates
Effectively prioritize workloads and manage time to complete multiple projects within established timelines and communicate priorities to Team Leads to ensure proper planning of equipment, materials, and labor requirements
Authors system investigation reports (SIRs), reviews executed batch records and logbooks, reviews, updates, and approves cGMP documents
Benefits and perks:
Competitive compensation
401(K) retirement
Flexible Spending Account
Disability insurance
Tuition reimbursement
Healthcare coverage
Pet insurance
Employee Stock Ownership Plan (ESOP)
o What is ESOP? It's an ownership stake in the company that provides an additional form of compensation directly tied to PBI-Gordon's financial success. All regular employees are eligible to participate in the ESOP and will be partially vested after two years with the companies; all employees are 100% vested after six years of service
Qualifications:
High school diploma or GED equivalent required; bachelor's degree in business administration, project management, or engineering preferred
Ability to work on-site in Pensacola, FL during a typical 2nd shift schedule, Monday-Friday
3+ years of experience in manufacturing and plant operations required
Experience overseeing FDA/cGMP pharmaceutical manufacturing operations with people leadership responsibilities preferred
Intermediate knowledge of Microsoft Office Suite (Word, Excel, Outlook) required
Basic knowledge of quality management systems preferred
If you are ready to lead and develop a team of professionals while upholding exceptional manufacturing and production processes, apply today.
This organization is an Equal Employment Opportunity employer and a supporter of affirmative action with a strong commitment to diversity, equity, and inclusion. All qualified applicants are considered for employment without regard to membership in any protected class by federal, state, and/or local laws.