Career Opportunities
at Medcomp®
| Interested candidates should send their résumé
to: MEDCOMP Attn: Catherine Frayne, Human Resources Manager 1499 Delp Drive Harleysville, PA 19438 Phone: (215) 256-4201 Fax: (215) 256-4398 Medcomp® is an Equal Opportunity Employer. |
Current Openings:
Senior Product Engineer
Product Engineer
We are always accepting résumés, which can be emailed to resumes@medcompnet.com.
Medcomp® is one of the
world's leaders in dialysis access therapy. We are ISO13485 and CE certified. This
certification is recognized worldwide as indicative of an organization that places
quality, dependability, and customer satisfaction as their primary objectives.
We view our employees as
one of the main factors to our success. They contribute courteous, knowledgeable,
and efficient service. We encourage their participation in achieving Medcomp®'s
goals and their own aspirations.
Senior Product Engineer
Reports To:
Director of Engineering
Job Description:
The Senior Project Engineer shall be responsible for managing multiple development and product support programs. Responsibilities will include development of product concepts working in conjunction with customers and sales personnel, scheduling, product failure investigations, resource coordination, vendor evaluations and coordination, and assuring that all design control activities are completed in accordance with current GMP/QSR, ISO and MDD requirements.
Qualifications:
A (B.S.) or (M.S.) in Mechanical, Biomedical, Chemical Engineering or a combination of education and work experience, a minimum of 7-10 years experience in the medical device industry. Must be familiar with current QSR and EN 46001 compliance requirements.
Product Engineer
Reports To:
Director of Engineering
Job Description:
The Project Engineer shall be responsible for managing multiple development and product support programs. Responsibilities will include development of product concepts working in conjunction with customers and sales personnel, scheduling, product failure investigations, resource coordination, vendor evaluations and coordination, and assuring that all design control activities are completed in accordance with current GMP/QSR, ISO and MDD requirements.
Qualifications:
A (B.S.) or (M.S.) in Mechanical, Biomedical, Chemical Engineering or a combination of education and work experience, a minimum of 3-5 years experience in the medical device industry. Must be familiar with current QSR and EN 46001 compliance requirements.