QC Specialist
at QNTM Labs
5220 Odense, Region Syddanmark, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Jan, 2025 | Not Specified | 30 Oct, 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:
QC SPECIALIST FOR QUALITY CONTROL
Are you passionate about quality control and do you like to be challenged? Then you may be the chemist with LC/GC/MS experience we’re looking for!
QNTM Labs is an advanced analytical laboratory providing research, development, and regulatory compliance services to pharmaceutical and biotechnology companies. Headquartered in Odense, Denmark, QNTM is dedicated to developing innovative analytical methods while maintaining the highest quality levels to forge new pharmaceutical industry standards. Our mission is to improve transparency and access to robust scientific analysis, working hand-in-hand with global drug producers, API manufacturers, and pharmaceutical industry stakeholders through analytical testing, contract research and clinical trial support.
How To Apply:
Incase you would like to apply to this job directly from the source, please click here
Responsibilities:
- Developing and maintain analytical methods that can either be based on pharmacopoeias or developed in house.
- Writing appropriate methods and approving of analytical data.
- Preparing protocols and reports to ensure validation or verification of methods.
- Giving the customers a superior service by ensuring close cooperation and transparency.
- Ensuring that methods are carried out according to current relevant standards and that analyses are being performed according to internal procedures
- Responsible for maintenance and periodic qualification of equipment.
- Work closely with the laboratory technicians and assist the broader laboratory operations, including equipment and method investigations and troubleshooting.
- Taking responsibility for change controls processes, deviation handling and for investigations related to your work.
- Collaborating with the Quality Assurance (QA) team when adapting and maintaining documentation, e.g., instruction and SOPs, equipment qualification protocols and relevant reports
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Biology
Proficient
1
5220 Odense, Denmark