The quality engineer will help lead all quality-driven activity associated with the design and manufacturing... of their industry! 5-7+ years of quality experience in medical device understanding of ISO13485 and FDA standards Experience...
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing...+ years of quality experience in medical device understanding of ISO13485 and FDA standards Experience with metal...
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing...+ years of quality experience in medical device understanding of ISO13485 and FDA standards Experience with metal...
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing...+ years of quality experience in medical device understanding of ISO13485 and FDA standards Experience with metal...
on , , , , and . Job Description We are looking for an experienced Scientist I/Mechanical Engineer to join our Injection Device Development team to help us accelerate AbbVie... (MS preferred) 3-5 years of experience (MS up to 2 years) ideally in the medical device, drug delivery or other regulated...
on , , , , and . Job Description We are looking for an experienced Scientist I/Mechanical Engineer to join our Injection Device Development team to help us accelerate AbbVie... (MS preferred) 3-5 years of experience (MS up to 2 years) ideally in the medical device, drug delivery or other regulated...
on , , , , and . Job Description Purpose: We are looking for experienced Development Engineer to join our Late-Stage Injection Device Development team... CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing, and other cross-functional colleagues...
on , , , , and . Job Description Purpose: We are looking for experienced Development Engineer to join our Late-Stage Injection Device Development team... CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing, and other cross-functional colleagues...
of relevant experience in the medical device industry; at least 5+ years in Quality Assurance experience required. Working... Product Quality Assurance strategy to support device and combination products produced at *** plants as well as contract...
reviews as needed. Qualifications 8+ years of experience in Quality Assurance within the pharmaceutical or medical device... with internal teams to ensure timely and effective closure of quality issues. Participate in general quality and manufacturing...
of relevant experience in the medical device industry; at least 5+ years in Quality Assurance experience required. Working... Product Quality Assurance strategy to support device and combination products produced at Client plants as well as contract...
Thermoforming and IBC bottle filling a plus as well as custom medical device sub-assembly and final assembly technology solutions... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...
pharmaceutical or medical device industries. Demonstrated problem solving skills and innovative thinking to develop and implement... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...
pharmaceutical or medical device industries. Demonstrated problem solving skills and innovative thinking to develop and implement... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...
Thermoforming and IBC bottle filling a plus as well as custom medical device sub-assembly and final assembly technology solutions... serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives...
Responsibilities: The Combination and Medical Device Products team is developing a replacement infusion system...-mechanical medical device design requirements, risk management, design verification and DHF traceability required. Proficiency...
: Manage device design changes by interfacing with cross-functional teams both at manufacturing partners and within Client... development partners. Propose device refinements based upon patient feedback, manufacturing records, and feedback...
of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing... of experience (MS 8-10 years, PhD 2-4 years) ideally in the medical device, drug delivery or other regulated industry...
of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs, Internal and External Manufacturing... of experience (MS 8-10 years, PhD 2-4 years) ideally in the medical device, drug delivery or other regulated industry...