Job Summary
Responsible for leading all phases of the product development process in support of immediate, mid-term, and long-term innovation and product design strategies. Provide expertise to guide product divisions to navigate the development of new products and technologies.Job Description
Manage the design control process including investigation of user need and product requirement/specifications, coordinate verification and validation activities, coordinate design transfer activities and multi-source projects, determine performance impacts and process change of new materials and designs, conduct risk assessment activities, and resolve residual risk.
Investigate root causes and provide corrective actions on product failures. Work with manufacturers to implement corrective actions.
Coordinate with end users and marketing to identify product opportunities and establish a vetted business case.
Oversee product development timelines and balance corporate priorities to ensure that deadlines and goals are met.
Work with internal or external design teams to generate product designs and technical specifications.
Evaluate prototypes for usability, manufacturability, performance, and quality.
Work with legal to identify opportunities to protect product designs through patents, trademarks, or other intellectual property techniques.
Generate Protocols, Reports, and Technical Documentation as necessary.
REQUIRED EXPERIENCE
Education
Bachelor's degree in Engineering or Science.
Work Experience
At least 2 years of product development experience.
PREFERRED QUALIFICATIONS
Experience in the development and launch of new medical/pharma products.
Experience with medical device requirements (Class I-II), design controls, risk assessments, and the 510k process.
21 CFR Part 11, 21 CFR Part 820 basic knowledge.
Experience with project management and Microsoft project.
Experience utilizing Minitab to perform analysis of test data.
Experience with CAD systems (Solid Works preferred), FEA, Six Sigma, ANDA, ISO/CE Mark, GLP, GMP, GDP, USP testing, and high volume manufacturing processes.
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$72,280.00 - $105,040.00 AnnualThe actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
Every day, we're focused on building a more diverse and inclusive company, one that recognizes, values and respects the differences we all bring to the workplace. From doing what's right to delivering business results, together, we're better. Explore our Diversity, Equity and Inclusion page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
