Equipment Operator, Print & Auto Inspection - 2nd Shift

Equipment Operator, Print and Auto Inspection

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Clinical Labeling Services, part of the Clinical Trials Division, located in Bohemia, New York provides leading clinical label design, production, and management services for the pharmaceutical and biotechnology industry. Our advanced inspection software, full in-house variable and non-variable print capabilities, and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times.

The Equipment Operator, Print and Auto Inspection role plays a crucial part in ensuring smooth clinical label manufacturing processes by computerizing (print) variable/static text on labels using niche automated inspection inkjet equipment within a team that is dynamic and fast-paced.

Demonstrates a solid understanding of the label manufacturing process of a wide array of label constructions using both automated and non-automated inkjet equipment following client-approved proofs and associated documents to manufacture labels per established specifications.

Sets up computerization production runs using the proprietary software application CLPS, as per department Standard Operating Procedures (SOPs) and Work Instructions (WIs) while monitoring all label production processing for accuracy and completeness by applying current Good Manufacturing Practices (cGMPs) in all areas of responsibility safely and efficiently.

High school diploma or equivalent required.

Required:

Minimum of 2 years of work experience in a manufacturing, operations, production, lab setting or related field.

Preferred:
Experience in a cGMP environment.

Knowledge and experience in the printing or manufacturing industry with proficiency in computer operations of transferring data, MS excel and outlook, file management, are required.

Candidates should be mechanically inclined with the ability to accurately read measurements, troubleshoot issues, strong analytical and problem-solving abilities to identify potential solutions associated with various label constructions, skills in handling fanfold and rolled materials, performing roll splicing using manual equipment, and operating computerized digital inkjet equipment are also important.

Computer Literacy - Vision System & File Manipulation

Quality Orientation - 100% Accountable for Finished Product

GMP Expertise – Extensive Documentation Requirements

Cross Training – Expectation to operate multiple pieces of equipment

Use Personal Protective Equipment (PPE), be able to stand and move about including reaching, bending, stooping, grasping and understand chemical hygiene.

Use hand tools and equipment including forceful gripping, grasping, pushing, and pulling.

Lifts and maneuver materials weighing up to 50 pounds max unassisted.

Competitive Hourly Pay Rate

Additional shift differential for 2nd shift and 3rd shift positions

Annual performance-based bonus

Annual merit performance-based increase

Medical, Dental, & Vision benefits-effective Day 1

Paid Time Off & Designated Paid Holidays

Retirement Savings Plan

Tuition Reimbursement

Employee Referral Bonus

Career Advancement Opportunities

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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