Quality & Regulatory Consultant Medical Devices & Biotechnology
- Medical Devices (ISO 13485, ISO 14971, MDR, Quality Management Systems, QMS) - Regulatory Affairs (RA) - Quality (QA/QC) - Internal Auditing - CV & Job Interviews
Setting up Quality Management Systems for compliance to ISO 13485, EU MDR & FDA CFR 820
Remediation of Technical Files, Clinical Evaluation and overall implementation of MDR
I can work with you to develop a clear job search strategy as well as CV that will make you stand out over other candidates
Was discussing quality management systems and way forward for a regulatory career. Karandeep was super helpful in pin pointing what ot do next and gave me overall good suggestions.
Fantastic knowledge of the medical sector. Karandeep gave me sound advice and guidance on how to start my career in medical device Industry.
Karandeep has a wealth of knowledge within Medical Devices Regulatory Affairs. This has been highlighted with his ability to answer all my queries honestly and provide strong advice. I have no hesitation in recommending and involving Karandeep in any future relevant regulatory work.
Finally got myself back into work! Karandeep helped me find unadvertised roles landing me an even better role than the one I was made redundant from
Lost my job due to Cover 19, karandeep gave me the roadmap to get me a new job
It was a breath of fresh air having Karandeep breakdown the criteria needed to set up a new QMS in a manner that made sense to me
