SBS - The best value in QMS software

Medical Devices Jobs - Abbott is currently hiring

L

lise22

#1
Abbott is currently hiring for the following positions: Quality Assurance Professionals Quality Engineers R&D Engineers Regulatory Affairs Professionals Clinical Research Professionals.
 
Elsmar Forum Sponsor

Wes Bucey

Quite Involved in Discussions
#2
Re: Medical Devices Jobs

Abbott is currently hiring for the following positions: Quality Assurance Professionals Quality Engineers R&D Engineers Regulatory Affairs Professionals Clinical Research Professionals.
I am leaving this post in the current Forum because it is phrased as a FYI rather than a recruitment. The poster has mentioned in her Profile she is visiting the Cove to learn about aerospace, not pharmaceuticals. It would seem, therefore, she is NOT the hiring agent or recruiter.

If you are in the market for a job, this is one of those "tips" we talk about in the threads listed below for a candidate to use in targeting potential employers.
Thinking about a New Job for New Year?
http://elsmar.com/Forums/showthread.php?t=19619
Resume and cover letter - How good are yours?
http://elsmar.com/Forums/showthread.php?t=10169
The Job Hunt - Care and feeding of references
http://elsmar.com/Forums/showthread.php?t=19094
Tips to get past the "gatekeeper" when job hunting
http://elsmar.com/Forums/showthread.php?t=9325
 
Thread starter Similar threads Forum Replies Date
B Free Sales Certificate for Non Medical Devices Other Medical Device Related Standards 0
K Usability for custom made medical devices IEC 62366 - Medical Device Usability Engineering 4
dgrainger Informational MHRA - Regulating medical devices in the UK - Post Brexit - 2021-02 UK Medical Device Regulations 0
M Europe GMP medical devices - Combination products - Ancillary medicinal substance CE Marking (Conformité Européene) / CB Scheme 4
L Shelf life of medical devices Other Medical Device Related Standards 4
M Medical Devices - Ancillary - ISO 10993-17 Medical Device and FDA Regulations and Standards News 6
S How is the service life for class I reusable medical devices described in MDR? EU Medical Device Regulations 7
S How is the service life described for class I reusable medical devices in MDR? Elsmar Xenforo Forum Software Instructions and Help 1
M Brexit The Medical Devices (Amendment etc.) (EU Exit) Regulations 2020 UK Medical Device Regulations 1
P New Global HQ Suggestions for Virtual manufacturing/own brand labelling of medical devices? EU Medical Device Regulations 0
N Chemical Testing on Medical Devices - Solutions in a container closure system (bag) EU Medical Device Regulations 1
M Is IEC 60601-1-2 required by FDA for all electronic medical devices? IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
M Subcontracting a repair of Medical Devices Canada Medical Device Regulations 0
S Regrind Material in Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 1
R Product Recall - medical devices in the hospital warehouse Canada Medical Device Regulations 2
P Monolithic application and medical devices ISO 13485:2016 - Medical Device Quality Management Systems 2
N Medical Devices in oxygen rich environment IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
M Medical Devices Shelf Life ---INDIA Other Medical Device Regulations World-Wide 3
JoCam Warranty of Medical Devices EU Medical Device Regulations 2
R Obsolesce medical devices ISO 13485:2016 - Medical Device Quality Management Systems 1
dgrainger Informational UK - Medicines and Medical Devices Bill 2019-21 UK Medical Device Regulations 0
S Call it refurbish or not? Medical Devices Manufacturing and Related Processes 2
C Registering Medical Devices in Australia and New Zealand - ANZTPA Other Medical Device Regulations World-Wide 0
S Requirements for "Claims Guide" for medical devices Medical Device and FDA Regulations and Standards News 6
C FDA Establishment registration - Buying some medical devices from another manufacturer Medical Device and FDA Regulations and Standards News 5
G Accelerated stability of medical devices Other Medical Device Related Standards 1
A Medical Device Vigilance decision tree for Japan for class 2 devices. Japan Medical Device Regulations 1
K Contamination Control - Class Is medical devices (Clause 6.4.2 ISO 13485:2016 (E)) ISO 13485:2016 - Medical Device Quality Management Systems 12
W Seeking Guidance Verification Test Strategy for Class B Medical Devices IEC 62304 - Medical Device Software Life Cycle Processes 1
G Free Sales certificates for Medical Devices - List of countries EU Medical Device Regulations 4
dgrainger Informational Parliament to vote on postponing new requirements for medical devices -17th April Medical Device and FDA Regulations and Standards News 1
K Old medical devices -> 7.3.7. Design and development validation ISO 13485:2016 - Medical Device Quality Management Systems 1
M Who needs a MDEL? How to buy and sell medical devices on my own Canada Medical Device Regulations 14
D Social Media Feedback process for Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 6
M Post Market Surveillance for Class II Medical Devices Medical Device and FDA Regulations and Standards News 2
M Special Controls and Class II Medical Devices Medical Device and FDA Regulations and Standards News 18
dgrainger Informational Have your say on the UK's Medicines and Medical Devices Bill Medical Device and FDA Regulations and Standards News 0
L Packaging unsterile medical devices ISO 13485:2016 - Medical Device Quality Management Systems 6
R Expected life span of Medical devices - X-Ray based diagnostic medical devices ISO 13485:2016 - Medical Device Quality Management Systems 6
Marc Medical device vulnerability highlights problem of third-party code in IoT devices Other Medical Device and Orthopedic Related Topics 1
J UK Medicines and Medical Devices Bill - 2019 ISO 13485:2016 - Medical Device Quality Management Systems 0
dgrainger Informational UK's new Medicines and Medical Devices Bill Medical Device and FDA Regulations and Standards News 0
O Is it mandatory for Medical Devices to work properly after dielectric strength tests? IEC 60601 - Medical Electrical Equipment Safety Standards Series 5
F Medical Devices - Hong Kong - Post approval changes regulation (China's MOH) Other Medical Device Regulations World-Wide 3
F Medical Devices-South Africa _Post approval changes and Software Other Medical Device Regulations World-Wide 0
S IVF medical devices standards and test methods Medical Device and FDA Regulations and Standards News 4
J Looking for a template SOP for UDI implementation for EU Medical Devices EU Medical Device Regulations 0
M Selling Medical Devices in Puerto Rico US Food and Drug Administration (FDA) 3
J Searching Registered Medical Devices in Argentina Other Medical Device Regulations World-Wide 0
M Advertising medical devices in the U.S - Advertising regulations or guidance documents Other US Medical Device Regulations 3

Similar threads

Top Bottom