Job Details

ID #51040584
Estado South Carolina
Ciudad Columbia
Full-time
Salario USD TBD TBD
Fuente Integra LifeSciences
Showed 2024-02-11
Fecha 2024-02-12
Fecha tope 2024-04-12
Categoría Etcétera
Crear un currículum vítae

Supervisor, Production - 2nd Shift

South Carolina, Columbia, 29201 Columbia USA

Vacancy caducado!

Changing lives. Building Careers.Joining us is a chance for you 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, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.SUMMARY DESCRIPTIONThe Supervisor, Production - 2nd Shift, 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 QUALIFICATIONSThe 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

TOOLS AND EQUIPMENT USEDOperation of specialty equipment (ex: lyophilizer, condenser, die press, etc.)PHYSICAL REQUIREMENTS

Repetitive motion of wrists, arms, and hands

Lifting of up to 40 lbs.

Standing for two hours or more; sitting for two hours or more

TRAVEL REQUIREMENTS

Less than 5%

ADVERSE WORKING CONDITIONSThe adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position, which is that of a general plant environment.

Clean room environment; must be able to properly gown and de-gown

Handling of raw materials (porcine bladder) required

May encounter strong odor of strong cleaning material

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/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/adaveteransemployers.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] or call us at 855-936-2666.Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)

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