Job Description

Job Description

Role Overview

The Eastman Kodak Life Sciences group is seeking a Reagent Clean Room Manufacturing Technician to execute the manufacturing process from mixing chemicals, filling, and labeling in a semi-automated system. This individual will play a pivotal role in executing manufacturing and quality control tasks according to our established procedures. Maintaining high standards of quality and safety at all phases of production is critical in this role. We are looking for candidates with a solid background in reagent manufacturing in a cGMP environment.

This is an onsite role in Rochester, New York.

Specific Duties and Responsibilities:
• Weighs, measures, subdivides, and dispenses raw ingredients into the processing equipment by following company recipes and procedures.
• Monitor processing equipment to maintain product quality standards.
• React to any type of alarm or malfunctions of the equipment as necessary.
• Comprehend written instructions and recipes from the company when putting together ingredients and starting each process.
• Clean/Sanitize all product-contact materials and equipment, as well as the workspace, by following company cleanliness standards.
• Completes documentation, including logbooks and batch production and control records as required.
• Work in a team environment with the ability to communicate in a concise, polite and respectful manner.
• Ability to rotate to other areas of operations such as logistics, shipping/receiving, etc., as needed.
• Works closely with the QC Manager and other technicians
• Complies with all Current Good Manufacturing Practice (cGMP) regulations and other company and industry policies and procedures.
• Operating and maintaining semi-automated manufacturing equipment
• Performs other duties as assigned.

Qualifications (Education, Experiences and Skills):
• Bachelor's degree in relevant science (chemistry, biochemistry, biology), or related field or equivalent experience in manufacturing disciplines
• Previous work environment to include cGMP and FDA.
• Experience with SAP and automated manufacturing systems
• Mechanical aptitude
• Excellent written and verbal skills.
• Self-motivated, solution-oriented personality with ability to work well under pressure.
• Ability to comply with the company's safety and quality SOP's/Policies.
• Experience working in start-up/small companies is a plus.
• Six plus years of relevant experience.

Physical Requirements:
• Fifty (50) pound lifting, carry, push, pull, or otherwise move objects.
• Ability to climb a platform/ladder.
• Ability to stand/walk for long periods of time.

EOE Policy Statement:
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

Estimated Salary : $24.00 - $27.00

Experience Level: 0-5 Years

Requisition ID: 1641

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