As the Lab Supervisor, you will be responsible for the staffing, maintenance, performance and scheduling of Laboratory Technicians, while ensuring all safety, quality, cost and production requirements are met.
Key Responsibilities
-Adheres to production schedule and ensures adequate coverage for the daily manufacturing of finished goods to meet customer and shipping requirements.
-Ensures raw materials and required staff are available to fill production orders using inventory management tools.
-Distributes production orders to the floor and prepares work order packages, ensuring completion by shipment date.
-Monitors progress of ongoing production and expedites orders or modifies schedule to meet customer demands, as required.
-Utilizes the ERP system to properly handle builds and reporting.
-Ensures the production team achieves the annual Quality goals.
-Health & Safety Responsibilities:
Ensure compliance within the plant premises
Participates in developing, implements and monitors Health & Safety policies included in the program.
-Supervisory Responsibilities:
Manage human and material resources to meet production targets and deadlines.
Implement standard operating procedures for production operations.
Implement product quality standards and track programs to meet said quality standards.
Manage production and quality control to detect and correct problems.
Prepare and maintain production reports.
Monitor performance of production staff and organize necessary interventions for improvement and help create a positive work environment.
Authority to suggest or carry through with hiring, terminating, promoting or granting change in employment status for other employees.
Arrange employee trainings.
Review and approve timesheets and manage time off.
Minimum Qualifications
High School Diploma or GED. Associates/Bachelor’s degree in Life Sciences, Chemistry, Biology, Molecular Biology, Biochemistry, or Business is preferred.
A minimum of 2-5 years related experience and/or training particularly in a cGMP Lab Supervisor role in Pharmaceutical, Biotechnology or diagnostic industry background.
Must have technical skills, knowledge of cGMP, manufacturing and shipping processes and basic computer skills.
Required Competencies
Strong leadership skills.
Detail-Oriented.
Excellent Organizational skills.
Time-management skills. Ability to multi-task and shift priorities.
Extreme regard for quality, quality control, safety procedures and requirements.
Working knowledge of Microsoft Office Suite.
Why Join Us:
Our comprehensive benefits package includes:
Medical, Dental, and Vision Insurance
Health Savings Account
Flexible Spending Account
Voluntary Accident, Hospital Indemnity, and Critical Illness Insurance
Basic & Voluntary Life and AD&D Insurance
Short-Term & Long-Term Disability
Pet Insurance
Commuter Transit Benefits
401(k) Retirement Plan
Paid Time Off
Paid Holidays
It is our policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Science and Manufacturing
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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