Lead Operator

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.

TheLeadManufacturing Operator will provide daily directions to the manufacturing floor based on production schedule, available resources, and department priorities. Engage and support manufacturingprocessto ensure timely completion and quality throughput.Leadand support administrative activities such as training, investigations, procedure development, and inventory management within the manufacturing area. Drive a positive culture within the manufacturing environment through teamwork, engagement, and respect.

SUPERVISION EXERCISED

Indirectly supervise the Manufacturing Operators

ESSENTIAL DUTIES AND RESPONSIBILITIES

People:

· Allocate resources to meet daily schedule needs and supportrecoverplan development and execution.

· Partner with area management toidentifyovertime needs in advance.

· Communicate with support groups on daily processing needs.

· Provide feedback to department management on operator and process performance.

· Interface with support departments toestablishclear/consistent manufacturingobjectivesand needs.

Process:

· Perform all requirements of a Manufacturing Operator.

· Provide daily oversight of manufacturing operations inside the skin suite.

· Actively engage in all areas of the manufacturing process.

·Identifyand resolve training gaps (process, performance, paperwork) through the execution of a training plan.

· Own operator training for all new Manufacturing Operators.

·Leadtroubleshooting initiatives to minimize equipment/process downtime.

· Perform manufacturing suite walk through activities toidentifyequipment deficiencies andobserveoperator execution.

· Support investigations as a subject matter expert.

·Maintainprocess andcomponentinventories.

· Support time management around start/stop,breaksandtimelycompletion of tasks.

Paperwork:

· Obtain batch records in advance for associated manufacturing operations to prevent delays.

· Document manufacturing activities in real time and perform daily in-process checks of paperwork.

· Supply and receive paperwork from support groups when necessary to keep manufacturing operations on track and progressive.

· Perform daily, in-process reviews of batch records to support good documentation practices.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

DESIRED MINIMUM QUALIFICATIONS

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

· High School diploma or equivalent. Degree in related science a plus.

· 3+ years of experience in manufacturingenvironmentin the Medical Device or Pharmaceutical industry preferred.

· Basic computer skills for email and data entry.

· Must read,writeand speak in English, and communicate clearly and concisely.

· Fundamental understanding of mathematics and chemistry.

· Able toparticipatein a team-oriented environment, willingness toassistand train others.

· Able to work independently with minimal supervision.

· Understand product flow and understand chemical processes and their impact.

· Able to work overtime.

Salary Pay Range:

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation . Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

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 [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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