A leading life sciences company is looking for two Senior QMS Process Engineers to enhance their Quality Management System. The role involves authoring and optimizing procedures and ensuring compliance with regulations. Ideal candidates have experience in the medical device industry and are familiar with ISO standards and Codebeamer. This is a remote, 3-month contract position requiring 40 hours per week.
Qualifications
Proven experience in the medical device industry.
Strong knowledge of QMS documentation and procedures.
Ability to work independently and manage multiple priorities.
Responsibilities
Draft, update, and optimize QMS procedures.
Collaborate with cross-functional teams for compliance.
Translate regulatory requirements into clear documentation.
Skills
QMS documentation
ISO 13485
regulatory knowledge
technical writing
project management
Tools
Codebeamer
Polarion
Jama
Job description
A leading life sciences company is looking for two Senior QMS Process Engineers to enhance their Quality Management System. The role involves authoring and optimizing procedures and ensuring compliance with regulations. Ideal candidates have experience in the medical device industry and are familiar with ISO standards and Codebeamer. This is a remote, 3-month contract position requiring 40 hours per week.