Overview
Hybrid
Depends on Experience
Contract - Independent
Contract - W2
Skills
ISO 13485
QSR
MDSAP
CAPA
Audit programs
21 CFR Part 820
ISO 14971
5+ years Quality Assurance
FDA Regulations
Job Details
Job Title: Sr. Quality Systems Engineer
Rate: Open based on Experience
Location : Onsite- Danvers, MA (Hybrid)
Principle Duties and Responsibilities:
- Must have in depth knowledge of and ability to apply quality system regulation, including QSR, ISO 13485, MDSAP and MDD/MDR.Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues as related to the position responsibilities.
- Contribute to the development of Quality System performance measures, data collection, trending and reporting.
- Assures that data obtained during all quality activities is complete, accurate and documented consistently with company policies and procedures.
- Provide support during Corrective and Preventive Action (CAPA) activities and manage the CAPA system as necessary.
- Support and/or lead 3rd party audits, including follow-up on actions.
- Lead Back Room, communicate and coordinate associated activities across the organization.Support Internal Audit program, e.g., participate/lead Internal audits, follow up on the finding with auditee through effective closure, present the data for trending, etc.
- Ensure compliance of QMS through authoring and updating Standard Operating Procedures (SOP).
- Establish and support to client global training program.Support New Product Development projects, as needed.Other Duties as assigned
Job Qualifications:
- BS degree is required. MS preferred.
- Lead Auditor Certification highly preferred.5+ years Quality Assurance / Quality Systems experience in an FDA regulated industry (Medical device).
- Must be proactive and able to work independently with minimal supervision; strong collaboration skills are essentialKnowledge and application of QSR/GMP/Google Cloud Platform/ISO regulations as related to medical device manufacturing.
- Working knowledge and practical application of 21 CFR Part 820, ISO 13485, and ISO 14971.
- Strong analytical and statistical skillsAbility to Communicate ideas and information clearly, effectively, and frequently (oral and written)Ability to exercise judgment to determine methods, techniques, and evaluation criteria for obtaining results.Able to work in a fast-paced work environment, prioritize tasks and manage multiple projects at once.
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