QC Analyst - Pharmaceutical
- Employer
- Anonymous
- Location
- Runcorn
- Salary
- Competitive
- Closing date
- 21 Aug 2019
View more
- Sector
- Pharmaceutical (Sector)
- Job Type
- Permanent
- Category
- Pharmaceautical (Category)
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QC Analyst - Pharmaceuticals - Runcorn
An established Pharmaceutical CDMO in Runcorn are currently looking to add a QC Analyst to their team, primarily responsible for QC testing of inhalation products using HPLC, GC, UV-vis and other analytical techniques.
As a QC Analyst you will have university level experience with various analytical techniques including HPLC, GC and UV-vis and will be looking to join a company who can offer robust training in GMP practices and processes while offering progression and development opportunities.
Responsibilities
Perform analysis on raw materials, in-process, finished products and stability samples using various analytical techniques including HPLC, GC and UV-vis.
Preparation and completion of GMP related documentation (SOPs, batch records, etc.)
Report any out of spec/out of trend results and assist in their investigationRequirements
BSc or equivalent in a Chemistry related subject is essential
Practical experience with HPLC, GC and wet chemistry techniques is essential
Prior experience within a Pharmaceutical QC lab is desired but not essentialInterviews for this QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information
An established Pharmaceutical CDMO in Runcorn are currently looking to add a QC Analyst to their team, primarily responsible for QC testing of inhalation products using HPLC, GC, UV-vis and other analytical techniques.
As a QC Analyst you will have university level experience with various analytical techniques including HPLC, GC and UV-vis and will be looking to join a company who can offer robust training in GMP practices and processes while offering progression and development opportunities.
Responsibilities
Perform analysis on raw materials, in-process, finished products and stability samples using various analytical techniques including HPLC, GC and UV-vis.
Preparation and completion of GMP related documentation (SOPs, batch records, etc.)
Report any out of spec/out of trend results and assist in their investigationRequirements
BSc or equivalent in a Chemistry related subject is essential
Practical experience with HPLC, GC and wet chemistry techniques is essential
Prior experience within a Pharmaceutical QC lab is desired but not essentialInterviews for this QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information
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