Checking and reviewing the compliance and completeness of documentary requirements for CPR application.Submission of initial, variation, and renewal
**BASIC PURPOSE OF THE JOB**:The Regulatory Compliance Staff shall oversee and coordinate the overall management of all company-related regulatory and
Checking and reviewing the compliance and completeness of documentary requirements for CPR application.· Submission of initial, variation, and renewal
HIRING: MEDICAL AND REGULATORY HEAD Qualifications: With at least 10 years work experience in Regulatory Affairs Must be a QPIRA (Qualified Persons in Industry
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my
Food Technology & Safety (Science & Technology) Lead the HACCP Team of GMP Officer(s), GMP Inspectors, Food Safety Document Controller and Food Safety
About the roleRole location - homebasedThe Senior Study Leader is responsible for the execution and delivery of the Global Clinical Operations (GCO), clinical
About the roleLooking to turn breakthrough science into transformative treatments? Join our team. The SSO Study Start-Up Team Lead is accountable for the
Bachelor's degree in pharmacy, chemistry, or a science-related field.with at least one year (1) of experience in the cosmetic industry or a related field such
- Licensed pharmacist or graduate of any allied science or engineering course- With 5 years experience particularly in the medical device manufacturing
**JOB SUMMARY**Quality Assurance Supervisor reports directly to the Plant Manager by which the main function is to ensure strict compliance to Product Quality,
COMPANY PHARMACIST Job Qualifications: Must be a Licensed Pharmacist with valid PRC IDPreferably with work experience as Regulatory or with experience in
Job Title: Quality Engineer Work location: San Jose CA Duration: 12 Months Work day/hours: 40 hours M F day shift Hybrid (at least 3 days onsite) ***LOCALS
Sr. Statistical Data Programmer at ClinChoice (View all jobs) Philippines ClinChoice is a global full-service CRO dedicated to professional development and
Preparation of government documents to be submitted in securing and renewing permits & licenses- Preparation of RFPs for fees to be paid in relation to
ANDAMAN MEDICAL PHILIPPINES CORPORATION Quality Assurance & Control (Science & Technology) We Are Looking for Applicants Residing in Philippines. Andaman
•Responsible for sourcing and purchasing of business unit local product and service requirements•Responsible for managing all governmental and regulatory
Position Purpose- Individual filling the position are responsible for the project management of safety aggregate reports submitted to regulators that include
Abbott Rapid Diagnostics (ARDx) is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading
Propose and implement effective strategies to minimize the timing of and optimize the commercial viability of product licenses from the relevant regulatory