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Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
This Manufacturing Operator I role is responsible for executing manufacturing operations on site. Responsible for maintaining a clean and orderly work environment. Completes work in a timely manner and performs all tasks with emphasis on safety. Works collaboratively with Manufacturing, Engineering, Quality Assurance, and other functional experts to support all daily operational activities. Consults with management to resolve quality, production, and efficiency problems. Functions in conjunction with manager and functional experts on special department projects. Works with internal departments to ensure implementation, maintenance, and improvement of the quality management system. Performs the essential duties and responsibilities as listed in section below.
SHIFT SCHEDULE
Monday-Friday, 8hrs, 6:00AM-2:30PM. Potentially moving to a two-shift operation in 2026.
LOCATION NOTIFICATION:
Role is for a brand-new manufacturing facility that was opened in Braintree, MA to replace the Boston, MA facility. Initial training may be conducted out of the Boston, MA facility.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are to:
Manufacture biologically derived medical devices in a clean room environment (must be willing and able to follow clean room dress code requirements).Accurately and completely fill out required documentation, following GDP GSOP requirementsMaintain compliance to cGMP/ISO systemsFollow batch processing per procedures and forms trained toOperate processing inspection equipmentMaintain inventories of materialsParticipate in process improvement and validation activitiesComplete and pass all training and re-training requirements on-timePerform general cleaning of the clean rooms and other manufacturing spacesPerform general maintenance tasks as requiredMust be comfortable in working with animal tissue (skin and/or biological fluid)Perform all tasks with the emphasis on safety – Be respective of a ZERO tolerance policyPerform all tasks safely and thoroughly in a timely mannerFollow SOP’s, Work Instructions, and other company policies and instructions at all timesUse company provided PPE, manufacturing equipment, chemicals, and other equipment safely, responsibly, and compliantlyMaintain good attendance and scheduled work hoursMust be comfortable working with sharp rotary bladesMust be comfortable working in a cleanroom with required PPEMust be able to work in teams and assist site with additional tasks as requestedMust be able to have good vision and ability to read measurement instrumentation for inspectionMust be able to safely lift and place items up to 50-60lbs.Must be computer literate/Word/Excel, etc.DESIRED MINIMUM QUALIFICATIONSThe requirements listed below are representative of the knowledge, skill and/or ability required for his position.
Minimum required education and experience: High School Diploma or equivalent with 0-2 years of experience Excellent Attendance RecordAbility to read, write and understand EnglishComputer literacy is requiredAbility to work overtime as requiredReliable TransportationIntegra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
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