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Location: 100% Remote in the USA
Residency: US Citizen/permanent resident required for US.
Status: Independent Contractor Role.
#lifesciences #consultant #RAQA
This exciting role is for independent contractors with significant experience in the RA/QA aspects of life sciences industry subsectors such as medical device in vitro diagnostics labdeveloped tests pharmaceuticals clinical manufacturing and cosmetics.
You will likely be an expert in auditing the design manufacture and monitoring of RA/QA under 21 CFR 2XX and/or 8XX sections and have wide life sciences experience. We are particularly looking for people with global regulatory coverage multiple jurisdictions in addition to US UK EU.
We seek consultants auditors and instructors and those who have expertise and a passion for patient safety and population health improvement. We have good rates of compensation defined by the project and a toprated team to work alongside you.
The roles are homebased and require the ability to travel to client sites for delivery or the ability to deliver through virtual technology. We therefore seek highly organized individuals who are selfstarters good communicators and are open to flexible work arrangements seeking variety in the work they do.
You would be responsible for planning and delivering Life Science consulting engagements related to quality/regulatory affairs infrastructure appropriate to the level of risk in a target product. The role is primarily that of an individual contributor although teamwork is expected.
Person Description
Essential Base Qualifications
Essential Industry Requirements
Travel
Ability to travel extensively domestically (25% 50%). Occasional international travel may be required.
Remote Work :
No
Full Time