Quality and Compliance Manager
Primary Job Function
Responsible for product quality engineering activities providing high level of hands-on support throughout the product life cycle, from conception to commercialization and post-market evaluation in a cross-functional environment. Responsible for all aspects related to the quality of Company products, as well as Quality System processes, to establish and maintain compliance to all applicable regulatory requirements. The right candidate has quality engineering experience with electro-mechanical and software-based products and the ability to take on technical challenges through resolution.
Essential Duties and Responsibilities
Develops, maintains, improves, and audits a Quality Management System (QMS) that is functionally-compliant to ISO 9001:2015
Leads Design Quality and Compliance activities for new product development, working with PD Engineers to ensure compliance to ISO 9001:2015 and select medical device standards
Ensures products are developed to meet customer expectations and regulatory requirements
Applies knowledge of Design Control and Risk Management activities throughout the product lifecycle
Leads Manufacturing Quality and Compliance activities for production of new and existing products
Manages quality and compliance of Supply Chain, including qualifying all contract manufacturing and component suppliers, conducting supplier quality audits, and establishing Receiving and Outgoing Inspection methods, tests, and tools
Manages product non-conformances via SCAR process, complaint handling and post-market data collection and analysis, including root cause determination and coordination of associated CAPA activities
Manages quality and compliance of in-house Production and Servicing (as applicable)
Develops, implements, and maintains the Document Change Control system
Serves as Quality lead for business system implementations and other special projects
Roles and responsibilities may be shifted to maximize customer and Company success
Minimum Qualifications
Bachelor’s Degree in an applied science or engineering field
7+ years of Design and Manufacturing Quality Engineering experience with
electro-mechanical and software productsExperience establishing or maintaining a QMS compliant to ISO 9001:2015
Demonstrated competency utilizing 9001:2015, 21 CFR part 820, 14971, 60601, APQP, and PPAP on past projects
Understanding of HIPAA and cybersecurity-related standards and guidance documents
Proven track record of success working with a globally-distributed
manufacturing supply chainAbility to work in a fast-paced early-stage startup where “many hats” must be worn
Exceptional analytical, problem-solving, and interpersonal communication skills
Understands and can subsequently explain complex quality details to non-experts
Exceptional organizational skills and attention to detail
Knowledge and experience with ERP/MRP systems and their applications
Administrative and financial management skills relative to job expectations
Willing and able to travel when required, up to 40%, domestic and international
To apply, please send your resume/CV to careers@activeprotective.com with the job title in the description.
About ActiveProtective
We are a growing venture-backed startup based in the Philadelphia region developing new-to-the-world personal safety products. Our key focus is a wearable airbag for hip protection in the event of a fall, which represents a leading cause of disability and death in the elderly population. We’re looking for passionate individuals to join our mission to make hip fractures a preventable condition.