Innoheart is a preclinical Contract Research Organization (CRO) providing evaluation in the areas of Biomedical Devices (e.g. coronary stents), Biologics (including cell therapy for regenerative medicine) and other Medical Implants (e.g. pacemakers), particularly cardiovascular and orthopedic/spinal related type products.
In line with our expansion plans, we are inviting applications from suitably qualified persons for the following position to contribute to our quality management team in meeting our clients’ high expectations in regulatory compliance and standards conformation.
Contract/Perm Quality Assurance Executive
jobsDB Ref. JSG400003003028040
You will be responsible for conducting quality audits and quality assurance in a GLP environment that evaluates new implantable devices and explores medical technologies in cardiovascular medicine. You will work with surgeons, cardiologists, veterinarians, scientists, engineers and technicians in ensuring compliance with GLP principles and standards.
- Bachelor of Science degree or equivalent.
- At least 2 years of relevant working experience in quality management in GLP, GMP or ISO environments.
- Prior working experience in quality audits and assurance in the pharmaceutical and biotech industry will be an added advantage.
- Familiar with OECD GLP principles or FDA CFR 21 part 58 regulations.
Interested applicants please submit your detailed resume with a recent photograph, current and expected salary and availability date.
We regret that only shortlisted candidates will be notified