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Kindeva 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.
Summary:
The Manufacturing Shift Leader is hands-on position . The Shift Leader is responsible for performing and leading manufacturing activities in a cGMP environment. The scope of the position includes writing and revising SOPs, Production Batch Records (PBRs), Forms and validation documents. This individual will train Manufacturing Technicians to perform work in a safe, accurate and timely manner, assuring cGMP compliance. Duties also include assisting with the development of processes, specifications, validation protocols and other validation and engineering related documentation. The person in this position may also perform routine preventive maintenance activities and manage validation and revalidation projects.
Essential Duties:
Qualifications:
EEOC Statement:
Kindeva Drug Delivery/Summit Biosciences is an equal opportunity employer and does not discriminate against any employee or applicant for employment based on race, color, religion, national origin, age, gender, sex, ancestry, citizenship status, mental or physical disability, genetic information, sexual orientation, veteran status, or any other characteristic protected by applicable law. We are committed to creating a diverse and inclusive workplace that values and supports all employees.
Full Time
$69k-91k (estimate)
06/29/2024
07/12/2024