Laboratory Technician, Finished Products
at Custom Pharma Services
Brighton BN2, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Dec, 2024 | GBP 28024 Annual | 05 Oct, 2024 | N/A | Excel,Communication Skills,Gmp,Stability Testing,Chemistry,Pharmaceutical Industry,Microsoft Word,Documentation | 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 TECHNICIAN - FINISHED PRODUCTS - PHARMACEUTICALS
We are now looking for an additional experienced Technician to join us to work within our Finished Products Team. The role involves carrying out hands-on analyses (including HPLC and various wet chemistry techniques) of finished products to ensure regulatory requirements for the product are met; supporting the Finished Products Team Manager to achieve the appropriate throughput of samples for testing; output of consistently accurate data and reports to meet quality standards through conformance with up-to-date procedures, methods, internal SOP’s, Health & Safety and current principles of GMP/GLP.
WE WOULD LIKE TO HEAR FROM YOU IF YOUR BACKGROUND, EXPERIENCE, AND SKILLS INCLUDE:
- A degree in chemistry or other closely related science discipline
- A chemistry background and previous experience in finished products and/or stability testing with solid dose finished products is preferable. Or other pharmaceutical medicinal products will also be considered
- Previous experience within a QC or development environment in the pharmaceutical industry or similar GMP environment
- HPLC experience
- Working knowledge of GMP and GLP
- A familiarity with laboratory equipment/ techniques/ procedures and documentation systems
- The ability to plan and prioritise workload
- Competence in Microsoft Word and Excel i.e., Basic level
- Attention to detail
- The ability to follow written procedures with accuracy and efficiency
- Able to work effectively with minimum supervision in a team or alone
- Good verbal and written communication skills
- Adaptable and flexible to meet changing priorities
- Understanding of UK, EU and other specific analytical regulations for the pharmaceutical industry would be a bonus.
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
Chemistry
Proficient
1
Brighton BN2, United Kingdom