Manager/Senior Manager, GCP Quality
at Ascendis Pharma
København, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Sep, 2024 | Not Specified | 02 Jun, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
On-siteCopenhagen, Capital Region of Denmark, DenmarkProduct Supply & Quality, Quality AssuranceFull time
Description
Join theGCP Qualityteam in a leading and fast-growing biotech company.
Ascendis Pharma is a fast-growing biopharmaceutical company with locations in Denmark, Germany, and the United States.
We are applying our TransCon technology to build a leading, fully integrated biopharmaceutical company focused on making a meaningful difference in patients’ lives. Guided by our core values of patients, science, and passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Today, we have a growing pipeline of prodrug therapies in development, each designed to be a best-in-class therapy.
Ascendis Pharma is currently expanding its GCP and GVP Quality with a quality and compliance position.
In GCP Quality you will together with a growing & dynamic quality team take part in the oversight of the compliance, quality, standards and training for Clinical Development and Development Operations areas. You will maintain an up-to-date knowledge of external requirements and ensure implementation of these in internal corporate procedures. You will as quality assurance partner advise and support the Global Development and Development Operations to ensure compliance and continuous process optimization.
You will join a dedicated GCP team located in Hellerup, Denmark and Palo Alto, USA. This role is based in Hellerup, Denmark and reports directly to the Vice President, GCP and GVP Quality, based in Denmark (Hellerup).
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
København, Denmark