Senior Manufacturing Engineer

Integra LifeSciences Corporation; Prospect (CT); On-site; USD 71,000 - 98,000; Full time

Job summary

Integra LifeSciences Corporation in Prospect, CT is seeking a Senior Manufacturing Engineer to design and optimize manufacturing processes for medical device components, and to improve production efficiency. The role involves documenting systems, writing test protocols, and collaborating with technicians, machinists, and management.

The ideal candidate has a BS in Mechanical Engineering with 8+ years of related experience (or MS with 5+), strong problem-solving, and proficiency with SolidWorks

Qualifications

• Education: BS in Mechanical Engineering or equivalent; MS is a plus.
• Knowledge of GMPs, ISO 13485 Design Control, and Manufacturing Process IQ/OQ/PQ qualifications.
• Ability to lead teams and communicate across all functional groups.

Responsibilities

• Plans and designs manufacturing processes for medical device components.
• Documents systems and equipment functions; writes and tests equipment.
• Leads and implements projects for transfers, new product introductions, and CapEx.
• Collaborates with RA/QA, Marketing and cross-functional teams to define and introduce new products.

Skills

Problem solving

Cross-functional communication

Leadership

Regulatory understanding

Education

BS in Mechanical Engineering or equivalent

MS in relevant discipline

Tools

SolidWorks

AutoCAD

MRP/ERP systems

Job description

Senior Manufacturing EngineerBy clicking \"Accept All Cookies\", you agree to the storing of cooking on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts.Privacy Policy# Integra LifeSciences Careers## Senior Manufacturing EngineerApply: US-CT-Prospect-facility: Full time: Posted Today: JR-6792Changing 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.**SUMMARY DESCRIPTION**Plans and designs manufacturing processes as well as design methods to support medical device component manufacturing and improve efficiency in production. This position supports operation’s goals by analyzing and managing change of existing processes, machining steps, product related drawings, specifications, standards, and tooling required in the manufacture of components. Duties will include documenting existing systems and equipment functions, writing and performing testing of equipment to perform its intended functions, and working with senior staff of technicians, machinists, and management to document existing methods and tools. This position acts as the subject matter expert (SME) for assigned product lines which includes supporting audit activities and first response for shop floor alerts. **ESSENTIAL DUTIES AND RESPONSIBILITIES**To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.· Works with Harmonic materials for the manufacture of medical devices. Knowledge of machining and ability to analyze data and draw cause and effect conclusions is part of responsibilities. Learn the product mix and machining steps and build institutional knowledge.· Designs and works with other engineering personnel to create and develop engineering prototypes of new products/processes.· Executes tactical implementation of strategic plans.· Prepares cost and time estimates for engineering and project schedules.· Instructs engineers and technical support staff on engineering test and build requirements.· Works as a team leader (and as a team member when required) in the development of engineering designs and tests.· Writes engineering test protocols for testing of component parts and integrated systems.· Develops and writes specifications for components/systems, product, processes and packaging/labeling.· Authors various type of qualification protocols and reports (IQ/OQ/PQ) and PV.· Works with engineering personnel on production problems and changes as necessary.· Works with RA/QA and Documentation departments to establish proper regulatory and quality documentation procedures.· Works with Marketing and cross-functional teams to define and introduce new products.· Works directly with finish goods suppliers in all aspects of product/process development, release and sustaining activities.· Leads and implements projects for transfers, new product introductions and CapEx spend.**DESIRED MINIMUM QUALIFICATIONS**The requirements listed below are representative of the knowledge, skill and/or ability required for this position.**Education & Experience:**· BS degree in Mechanical Engineering or Equivalent discipline with at least eight (8) years of related engineering experience; or MS in relevant discipline with at least five (5) years of related engineering experience.· Ability to effectively solve complex problems and ability to influence and communicate across all functional groups and levels.· Excellent verbal and written communication skills.· Medical device experience is desired.· Proficiency with development tools (e.g. SolidWorks, autocad) used by the department.· Knowledge of Engineering Change Order System.· Knowledge of engineering test protocols.· Ability to lead teams through complex projects.· Knowledge of GMPs, ISO 13485 Design Control, and Manufacturing Process IQ, OQ, PQ qualifications as related to medical devices is required.· Ability to make presentations at company meetings.· Ability to communicate effectively with internal and external personnel.· Ability to provide departmental technical leadership.· Ability to review and analyze engineering reports.TOOLS AND EQUIPMENT USEDAbility to utilize a telephone, fax, copier and desktop computer with finance and other typical business programs installed, including spreadsheets, word processing and MRP/ERP systems.Strong computer skills are required. Knowledge and experience with MRP/ERP systems is required. PHYSICAL REQUIREMENTSThe physical requirements listed in this section include, but are not limited to, the motor/physical abilities and skills required of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and have the mobile ability move throughout the building. Candidates must be capable of using a keyboard for computer purposes. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 25lbs.This position is expected to require 10% travel.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.Adverse exposure may result from the handling of hazardous and bio-hazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps and medical wastes.Salary Pay Range:$71,000.00 - $98,000.00 USD SalaryOur 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 LifeSciencesIntegra 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 [e-mail] Agency SubmissionIntegra 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.