Quality lead
Waukegan, IL - USA
Job Summary
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. This Client is mission is to discover and deliver innovative medicines and solutions that address complex health issues and enhance peoples lives.
Position: Quality lead
Location: Waukegan IL 60085
Duration: 7 Months
Job Type: Temporary Assignment
Work Type: Hybrid
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. This Client is mission is to discover and deliver innovative medicines and solutions that address complex health issues and enhance peoples lives.
Position: Quality lead
Location: Waukegan IL 60085
Duration: 7 Months
Job Type: Temporary Assignment
Work Type: Hybrid
Job Responsibilites
- Serves as the primary quality lead for project activities to achieve on-time quality deliverables high customer value and profitable results.
- Primary driver for the quality and compliance aspects of the project.
- Assure proper integration and support of device regulations drug regulations and as appropriate biologics regulations.
- Responsible for compliance with company policies and procedures.
- Ensure design control documentation (Traceability/Linkages) & design change control requirements are met.
- Assess the impact of a change on the safety efficacy of the combination product/device.
- Analyze and justify the impact on cumulative changes.
Years of experience/education and/or certifications required:
- Bachelors Degree in relevant Engineering Life Science or other technical discipline or equivalent job experience required.
- 5 years of total combined experience. At least 3 years in Device Design Quality Assurance
- What are the top 3-5 skills requirements should this person have
- Deep understanding of DHF structure and traceability between DHF elements.
- Knowledge and a comprehensive understanding of combination products medical devices and design controls.
- Sound technical understanding of product development (e.g. approaches for definition of requirements and specification setting for verification and validation) and/or practical experience in design control.
- Well-versed in risk management methodologies and their application.
- Work independently and in a global team environment and with all levels of personnel within the organization.
What is a nice to have (but not required) regarding skills requirements experience education or certification
Examples: Bachelor of Science; 4-year pharma health care or regulated industry
1. Systems Engineering experience
2. Relational database experience.
2. Relational database experience.
TekWissen Group is an equal opportunity employer supporting workforce diversity.