Thermo Fisher Scientific In Process Inspector 2, Finishing Operations in Bohemia, New York
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Fisher Clinical Services, part of Thermo Fisher Scientific, is a leading provider of global clinical supply chain. With unwavering commitment to service, science and process engineering, Fisher Clinical Services is powered by people with an exceptional commitment to quality, deeply instilled ethics of personal responsibility and unrivaled expertise. We are exclusively focused on serving the packaging and distribution requirements of clinical trials across the world. Whether planning, packaging, labeling, storing, or distributing the important supplies needed to perform clinical research, for more than 27 years Fisher Clinical Services has been committed to delivering the highest possible value while ensuring adherence to the highest level of quality, performance, reliability and sustainability standards. http://www.fisherclinicalservices.com/
What will you do?
A quality control inspector responsible for operating various pieces of inspection and finishing equipment to ensure clinical labels meet established quality standards.Requires demonstrated knowledge and expertise in verifying the physical attributes of manufactured labels including their construction, print quality and quantity. Responsibilities include inspection of labels produced by cold fusion and/or digital printers, label application machines and booklet presses.Ability to operate vision inspection and finishing machines, such as slitters, is a major function of this position.This position also calls for completion of finishing operations including but not limited to the pack out of inspected material, slitting of labels to their finished dimensions, and blinding panel application.
Ensures all In Process Inspection SOPs and Work Instructions are current and followed, as well as adheres to Quality Assurance standards
Performs Start-Up & Re-Start Verifications of Computerized Runs as well as Guardian verifications as applicable
Performs 100% inspection of all computerized material via visual inspection. Understands what constitutes a defective label that must be rejected prior to passing on to the client.
Ability to accurately count out labels to verify the quantity shipping is what is being requested by the client.
Performs all required activities associated with labels which must be reprinted; included but not limited to: identification of defective labels, reprint file generation, and label integration
Releases inspected materials which have met required inspection standards for further processing or shipping.
Assists with the packaging of released finished or computerized materials; including, but not limited to shrink wrapping, generating material ID tags and boxing of labels
Assists with the mentoring of new In Process Inspectors to familiarize them with department practices and policies
Follows all safety procedures when operating all manufacturing equipment or when handling chemicals.
Adherence to good attendance policy and the ability to work overtime to meet company timelines
Ability to efficiently use the finishing machines to aid in the finishing operations associated with roll labels. Specifically this includes the table top rewind machine for roll label reprint integration and the Rotoflex System for roll label reprint integration, roll slitting and roll rewinding.
Full working knowledge of the label Vision System including, but not limited to: proper machine set-up, run monitoring, roll slitting (as applicable), and run close-out.
Ability to trouble shoot and problem solving knowledge to facilitate job execution
Issues IRQ for digital materials
Ability to work in a fast paced environment and demonstrate team work when necessary to insure jobs are completed per established timelines.
Maintains the finishing area and label storage area in a constant state of cleanliness.
Applies current Good Manufacturing Practices (cGMPs) in all areas of responsibility.
Ability to work independently in planning, setting up and equipment and meeting DPS schedules
Maintains daily and monthly production goals and schedules proactively relaying any obstacles encountered to management to insure smooth operations
Offers process improvement suggestions to improve products, processes and environment.
Conducts all activities in a safe and efficient manner.
Other duties may be assigned to meet business needs as they arise.
How will you get here?
Minimum Qualifications :
Designated position for mandatory vision testing every two years
High School Diploma or GED
2+ years’ experience in a quality inspection and/or GMP environment
Ability to lift 30 lbs.
Ability to perform basic mathematical calculation with the assistance of a calculator
Comprehension of specifications
Machine Operator experience preferred
Execute measurements using a ruler
Associates Degree preferred but not required
At Thermo Fisher Scientific, each one of our 65,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
Apply today! http://jobs.thermofisher.com
If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here at https://jobs.thermofisher.com/page/show/eeo-affirmative-action-statement#accessibility for further assistance.
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.