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SUMMARY DESCRIPTION
The Production Supervisor is responsible for the direct supervision of all Tissue Processing Technician team members.
Oversee the quantity and quality of the production staff including recommending hires, promotions and disciplinary actions as well as conducting performance reviews.
Ensures the daily efficient running of Integra’s production function with oversight from management.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Ensure proper inspection and handling of raw materials
Oversee Tissue removal processes
Monitor disinfection process in a class 7 clean room environment
Use of laboratory equipment for measuring solutions
Document and track materials; ensure entry into appropriate software
Oversee processing of raw materials for final product including but not limited to cutting/trimming to size, lyophilizing, and packaging
Supervise clean room processing and procedures
Continually monitor for proper aseptic techniques
Conduct and/or oversee Inspection processes
Ensure that team members follow all standard operating procedures
Provide direction for cleaning a sterile environment
Instruct and supervise training of new and current employees in multiple work environments
Ensure all tasks required by the Quality Management System are conducted in a timely manner
Assist in the creation and/or revision of training methods, procedures, processes, job descriptions, etc.
Provide ongoing feedback to employees
Draft and conduct reviews with staff
Administer disciplinary action, when necessary, in a fair and empathic manner
Strive for continuous improvement of the work environment and material processing
Create management reports including appropriate metrics
Suggest improvements in workflow process, equipment, technology, etc.
Perform other tasks as assigned
DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
Education & Experience:
Bachelor’s degree or equivalent experience
Minimum of 2+ years of supervisory experience
Prior lean manufacturing experience preferred
Prior clean room experience preferred
Prior production experience preferred
Required Knowledge, Skills, and Abilities
Solid understanding of a clean-room production environment
Must be highly detail oriented
Must be punctual, reliable, and efficient
Able to multi-task
Able to effectively communicate in verbal, written, and electronic form
Must demonstrate proactive problem-solving skills
Ability to influence the behavior and performance of others by giving feedback and instruction
Ability to work in full sterile gowning and function in a sterile environment
Ability to work with illuminated magnification
Understanding of cGMP regulations and how they impact production
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.
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