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.

Perform manufacturing activities as assigned by the area supervisor. Daily interaction with hazardous materials used in a controlled environment. Responsible for maintaining legible and accurate records and other procedures to comply with regulatory requirements, Good Manufacturing Practices (Quality Systems Regulations) and Standard Operating Procedures. Ability to operate, maintain, and troubleshoot process equipment, and make minor adjustments as needed. To execute and to visualize the Lyophilization process according with the established parameters in the SOP. To handle and to treat the waste water prior to be discarded.  Maintain a clean and orderly work area, and perform all work in compliance with Good Manufacturing Practices (Quality Systems Regulations), and Standard Operating Procedures, and Health and Safety requirements. Maintain all required logs, books and records pertaining to the manufacturing department accurately. Responsible for maintaining process and component inventories. Interface with QA/QC department during normal course of work to coordinate inspections of completed product and to interface with the Materials Management Department to ensure efficient flow of materials through operations. Initiate and/or propose revisions to standard operating procedures involving new processes or equipment. Experience with process equipment is necessary, not only to operate, maintain, and train but analyze problems. Ability to gown in a surgical scrubs and/or additional Cleanroom clothing, climb step ladders, lift 30-60 lbs. without assistance, bend, and stand for long periods of time. Performs other activities as required by the supervisor.

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.

Associate degree in the science field (Chemistry, Biology etc.) or High School diploma or equivalent at least.

Must read, write and speak in English.

Fundamental understanding of mathematics and chemistry.

Demonstrate safe behavior and support department/plant Safety goals in a continuous improvement process.

Possess the ability to participate in a team-oriented environment, willingness to assist and train others, flexible and able to work overtime.

Make effective use of work time, and be a self-starter and work independently when necessary.

Recognize the importance of punctuality and good attendance on a daily basis.

Must be able to follow the policies set forth by Integra.

Willing to travel out of the country

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 | EOE including Disability/Protected Veterans

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. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.

Integra - Employer Branding from Integra LifeSciences on Vimeo