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Candidate will be assigned to the Biopatch Wet Processing Area to perform various processing steps required to produce Biopatch products. Drug Preparation, Drug Loading, Lyophilization and Packaging Process.

• Perform manufacturing activities as assigned by the area group leader.

• Daily interaction with minimally 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.

• Maintain a clean and orderly work area, and perform all work in compliance with Good Manufacturing Practices (Quality Systems Regulations), 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.

Qualifications:

• Must be able to lift 15 to 30 lbs. on a daily basis.

• Ability to stand for 8 hours in a working posture.

• High School diploma or equivalent.

• Reading comprehension of English.

• Basic understanding of mathematics

• 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.

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.

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EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | 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 careers@integralife.com or call us at 855-936-2666.

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