Title : Project Manager
Location : Tucson AZ
Duration : 1Year
Description:
- Bachelors degree preferably in a Life Sciences field.
- You have 4 years of experience in project management / engineering/ business in the diagnostic medical device pharmaceutical or biotech industry leading product development and product care projects.
- You have at least one year of experience in the following areas: clinical biomarker or In Vitro Diagnostic development companion diagnostic development analytical and clinical validations regulatory submissions instrument/systems development or program management)
- You have one year of experience in a regulated industry (e.g. FDA 21 CFR part 820 ISO 13485 ISO 9001).
Preferred Qualifications: - You hold a Masters degree preferably in a Life Sciences field and 6 years project management / engineering/ business experience in the diagnostic medical device pharmaceutical or biotech industry leading product development and product care projects. Alternatively you hold a Ph.D with 3 years project management experience in those areas.
- Prior 3 years in clinical biomarker or In Vitro Diagnostic development experience in companion diagnostic development analytical and clinical validations and regulatory submissions or instrument development and program management.
Title : Project Manager Location : Tucson AZ Duration : 1Year Description: Bachelors degree preferably in a Life Sciences field. You have 4 years of experience in project management / engineering/ business in the diagnostic medical device pharmaceutical or biotech industry leading product develop...
Title : Project Manager
Location : Tucson AZ
Duration : 1Year
Description:
- Bachelors degree preferably in a Life Sciences field.
- You have 4 years of experience in project management / engineering/ business in the diagnostic medical device pharmaceutical or biotech industry leading product development and product care projects.
- You have at least one year of experience in the following areas: clinical biomarker or In Vitro Diagnostic development companion diagnostic development analytical and clinical validations regulatory submissions instrument/systems development or program management)
- You have one year of experience in a regulated industry (e.g. FDA 21 CFR part 820 ISO 13485 ISO 9001).
Preferred Qualifications: - You hold a Masters degree preferably in a Life Sciences field and 6 years project management / engineering/ business experience in the diagnostic medical device pharmaceutical or biotech industry leading product development and product care projects. Alternatively you hold a Ph.D with 3 years project management experience in those areas.
- Prior 3 years in clinical biomarker or In Vitro Diagnostic development experience in companion diagnostic development analytical and clinical validations and regulatory submissions or instrument development and program management.
View more
View less