Engineer II, Collagen

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

Job Overview

Job Responsibilities and Essential Duties

• Perform technical and product-related sustaining activities using knowledge of biomaterials, Design Controls, engineering principles and compliance writing
• Responsible for creating technical specifications for new product or product improvements.
• Prepare experimental protocols and reports in response to development needs.
• Evaluate prototypes, collect, analyze and report data.
• Perform basic remediation activities using Design Controls principles, new product development knowledge and our internal procedures.
• Support the transition from product development to manufacturing including technical training of personnel in order to ensure a smooth manufacturing start-up.
• Identify and record any problems relating to the product, process and quality system.
• Provide technical support for product registrations using product knowledge and the scientific literature.
• Collaborate with material science lab located in Merrimack, NH to support development and testing activities.

Minimum Requirements

• Bachelor's Degree in Engineering (preferably Biomedical), or related field, or possess the equivalent combination of education and experience
• Minimum 3 years of medical device industry experience, preferably in a new product development engineering position

Required Knowledge, Skills and Abilities

• Ability to effectively navigate technical documents focusing on timely completion
• Ability to access clean room environment (OEM collagen manufacturing site) in Mahwah, NJ
• Experience with biomaterial technology or experience developing or refining biological implantable materials preferred
• Experience in generating test plans, writing protocols, conducting design verification/validation, and processing validation testing
• Experience/familiarity with U.S. FDA, GMP, and ISO requirements for the design, validation, manufacturing processes and assembly of medical components and devices
• Good cross collaboration skills within internal departments
• Ability to effectively communicate with external suppliers
• Ability to prioritize tasks in a fast-paced environment
• Intermediate skills using Microsoft Office products such as Outlook, Word, Excel, MS Project and PowerPoint
• Possesses a consistently positive and solution-oriented attitude, approaching challenges with enthusiasm and a willingness to learn

Salary Range: $92,000 - $115,000

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About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge:

At Getinge, we offer a comprehensive benefits package, which includes:

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off
• Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Commuter Benefits
• Parental and Caregiver Leave
• Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.