Manufacturing Supervisor - Second Shift

Job Summary:
Kindeva Drug Delivery, formerly Summit Biosciences, is seeking a highly motivated and experienced Manufacturing Supervisor for our Second Shift team in Lexington, Kentucky. This individual contributor role will oversee our manufacturing facility's daily operations on the second shift (3:00 PM - 11:30 PM) ensuring efficient production and maintaining high-quality standards. The Manufacturing Supervisor will report to the Production Manager and work closely with cross-functional teams to achieve production goals.

Compensation & Benefits:
This is a full-time, salaried position with a competitive compensation and benefits package. Benefits include medical, dental, and vision insurance, a 401(k) retirement plan, paid time off, and opportunities for career advancement within the company.

Responsibilities:
- Oversee the day-to-day production activities of the manufacturing facility on the Second Shift.
- Monitor production schedules and allocate resources accordingly to meet production goals.
- Train, coach, and mentor manufacturing operators to ensure high-quality standards and adherence to standard operating procedures.
- Identify and troubleshoot production issues, provide solutions, and escalate to appropriate personnel when necessary.
- Maintain a safe and clean working environment by enforcing safety procedures and regulations.
- Work closely with cross-functional teams (Quality, Engineering, Supply Chain) to optimize production processes and implement improvements.
- Conduct performance evaluations, identify training needs, and provide feedback for team members.
- Manage inventory levels and ensure materials are properly stored and utilized.
- Collaborate with the Production Manager to develop and implement production plans and strategies.

Requirements:
- Bachelor's degree in Engineering, Science, or a related field.
- 3-5 years of experience in a pharmaceutical manufacturing leadership role including hands-on manufacturing or validation experience
- Strong knowledge of cGMP guidelines and FDA regulations, HVAC systems and cleanrooms, & pharmaceutical processing and plant equipment.
- Excellent leadership, communication, and problem-solving skills.
- Ability to work independently and manage multiple tasks effectively.

EEOC Statement:
Kindeva Drug Delivery is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability status, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.