What are the responsibilities and job description for the Manufacturing Supervisor - Third Shift position at Kindeva Drug Delivery?
Manufacturing Supervisor/Shift Lead
Kindeva Drug Delivery is a leading global contract developer and manufacturing organization (CDMO) with delivery platform experience expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch, and Nasal Spray Technologies. The Lexington location develops, manufactures, and commercializes prescription nasal spray products and is experiencing increasing continuous growth. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture more tomorrows.
MUST HAVES: 3-5 years of experience in a pharmaceutical manufacturing leadership role including hands-on manufacturing or validation experience
Third Shift Hours: 11:00 PM - 7:30 AM.
Compensation and Benefits: This is a full-time, salaried position with a competitive compensation package including benefits such as health insurance, 401(k) plan, paid time off, and opportunities for professional development.
Job Summary: If you are ready to work for a purpose, the Manufacturing Supervisor/Shift Lead position is a crucial individual contributor role and will oversee our manufacturing facility's daily operations on the third shift. This position ensures 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 for the production of pharmaceutical nasal spray drug products ensuring that all products are produced efficiently, safely, and in compliance with regulatory standards in an FDA regulated cGMP pharmaceutical manufacturing environment. Position 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:
BS in Engineering, Science, or a related field.
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/Summit Biosciences is an equal opportunity employer and considers all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. We are committed to creating a diverse and inclusive workplace and encourage individuals of all backgrounds to apply.
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