Job description

Well known Medical Device company seeks Quality Assurance Document Control Specialist II to join outstanding company. This is an excellent opportunity to utilize current skills in Document Control and be part of a thriving and stimulating environment.

Qualifications:

-5+ years of experience in an FDA regulated environment in the Quality department (Medical Device, Biotech, Pharmaceutical industry)
-4+ years of experience with managing Change Controls review, approval and release
-4+ years of experience with various document types (Procedures, Work Instructions, Bill of Materials, Part, Blueprints,
etc.) and managing the lifecycle of release, redlines and archiving
-Experience with electronic data management systems such as Greenlight Guru, eLeap, Agile, SAP, MasterControl, Pilgrim, etc.
-Experience setting up training courses for newly created or revised documents
-Ability to prioritize urgent events and manage competing priorities
-Attention to detail and ability to concentrate in an open cubicle environment
-Excellent verbal and written communication skills
-Ability to organize paper records and documentation
-Ability to work in a team environment as well as perform independently

Job Types: Full-time, Temporary

Pay: $28.00 - $30.00 per hour

Benefits:

• Health insurance

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: In person

seankuhnke.com is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, seankuhnke.com provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, seankuhnke.com is the ideal place to find your next job.