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Changing lives. Building Careers.

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.

The **Manufacturing Operator/Warehouse Associate** will verify and keep records of all incoming and outgoing shipments, physically move material to all required inventory locations, and perform all associated transactions in ORACLE. The warehouse associate will perform all required duties in compliance with company policies, U.S. Food and Drug Administration and DOT/IATA, ISO 13485, and other applicable regulatory agencies.

This is a Weekend Shift, Friday through Sunday (6:00 a.m. - 6:00 p.m.) role.

ESSENTIAL DUTIES AND RESPONSIBILITIESTo perform this job successfully, an individual must be able to perform each essential duty satisfactory.

+ Work with internal and external parties to insure the proper items are received in a timely manner and documented

+ Verifies all incoming materials and paperwork against purchase orders, notifies Buyer of any missing documentation, damages, shortages, and problem receipts.

+ Performs receipt transactions and material moves ensuring receipt and inventory accuracy in ORACLE.

+ Process all required receiving paperwork; affix all appropriate labeling to stock items.

+ Sort and distribute miscellaneous items received to appropriate individuals or departments.

+ Prepare and pack case and pallet size shipments and all associated documentation as per written standard operating procedures.

+ Pick material work orders to be delivered to shop floor.

+ Stock all warehouse and KANBAN locations. Move materials as necessary to maintain neat, organized warehouse.

+ Perform inventory counts and cycle counts dictated by established periodic schedule.

+ Drive the company vehicle.

+ Other related duties as assigned in support of department/organizational duties and initiatives.

+ Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and be able to make minor equipment adjustments as needed.

+ Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.

+ Responsible for the cross linking, cutting, packaging and boxing of the product in its finished goods form, which includes performing visual product and component inspections to identify and remove defects.

+ Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.

+ Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.

+ Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.

+ Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.

+ Follow applicable Standard Operating Procedures, Quality System Regulations and ISO 13485 requirements.

+ Responsible for reporting all discrepancies to the Supervisor or Group Leader.

+ Support department and plant Safety goals by continuously demonstrating safe behavior.

+ Maintain a clean and orderly work area

+ Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements

+ Perform other manufacturing activities as assigned by the department leadership

Primary responsibilities are to:

+ Work with internal and external parties to insure the proper items are received in a timely manner and documented appropriately.

+ Verifies all incoming materials and paperwork against purchase orders, notifies Buyer of any missing documentation, damages, shortages, and problem receipts.

+ Performs receipt transactions and material moves ensuring receipt and inventory accuracy in ORACLE.

+ Process all required receiving paperwork; affix all appropriate labeling to stock items.

+ Sort and distribute miscellaneous items received to appropriate individuals or departments.

DESIRED MINIMUM QUALIFICATIONS

+ High School diploma or equivalent

+ Minimum1 to 3 years of shipping/receiving/warehouse experience in Pharmaceutical/Medical device environment.

+ Forklift experience

+ Valid drivers license

+ Demonstrated organizational and communication skill

+ Must possess a team focused attitude

+ Demonstrated knowledge of FDA regulations, ISO 9001, ISO 13485, preferred

+ Demonstrated computer skills (MS Office, Excel). Must be capable of working in an Oracle Enterprise Resource Planning (ERP) system.

Integra 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.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:

EEO Is the Law (https://www.eeoc.gov) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada\_veterans\_employers.cfm)

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at [email protected].

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

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