QC Associate
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Job Description
Job Title: Senior QC Associate
Requirements
Responsibilities include but are not limited to:
Testing of raw materials in process stability and finished product samples. Eg Ph Appearance Colour Clarity Sub Visible Particle testing Osmolality Protein Concentration Polysorbate Moisture and Device testing.
Review and authorisation of Lab Data
Support Analytical Technical Transfer activity testing reports and documentation.
Document review/updates when required.
Monitoring of site water and Nitrogen systems.
Equipment Calibration Maintenance and Trouble Shooting.
Method Validation/Verification.
Training of QC Chemistry Laboratory colleagues.
Laboratory Investigation support
Laboratory Housekeeping and maintaining GMP standards.
Assisting in regulatory audits.
Commitment tracking and follow up.
The successful candidate will:
Hold a third level qualification (Degree/Diploma) in Biochemistry Chemistry Biology Biotechnology or similar Scientific Subject.
Have at least 2 years relevant experience in a pharmaceutical/healthcare environment.
Be very proficient in the use of Microsoft Word Excel etc.
Have strong technical writing skills.
Be detail oriented selfmotivated with good troubleshooting and problemsolving abilities.
Be a selfstarter and capable of working on own initiative.
Strong teamwork skills.
Proven track record of meeting deadlines.
Experience with analytical techniques such as Compendial testing would also be advantageous.
Responsibilities include but are not limited to: Testing of raw materials, in process, stability and finished product samples. Eg Ph, Appearance, Colour, Clarity, Sub Visible Particle testing, Osmolality, Protein Concentration, Polysorbate, Moisture and Device testing. Review and authorisation of Lab Data Support Analytical Technical Transfer activity testing reports and documentation. Document review/updates when required. Monitoring of site water and Nitrogen systems. Equipment Calibration, Maintenance and Trouble Shooting. Method Validation/Verification. Training of QC Chemistry Laboratory colleagues. Laboratory Investigation support Laboratory Housekeeping and maintaining GMP standards. Assisting in regulatory audits. Commitment tracking and follow up. The successful candidate will: Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology, or similar Scientific Subject. Have at least 2 years relevant experience in a pharmaceutical/healthcare environment. Be very proficient in the use of Microsoft Word, Excel etc. Have strong technical writing skills. Be detail oriented, self-motivated with good troubleshooting and problem-solving abilities. Be a self-starter and capable of working on own initiative. Strong teamwork skills. Proven track record of meeting deadlines. Experience with analytical techniques such as Compendial testing would also be advantageous. #LI-XA1
Employment Type
Full Time
