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QC ANALYST/ NATIONWIDE
Company:RFT GROUP |
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Job Reference Number |
10414388 |
Client ID: |
RI/RFT71921JF |
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Posted On: |
May 9 2008 |
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Last Updated: |
May 16 2008 |
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Location: |
MUNSTER, LEINSTER, NATIONWIDE |
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Job Type: |
Contract/Permanent |
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Salary: |
€ NEG |
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Benefits: |
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QC Analyst/ Nationwide
Our client’s, large Bluechip Multinational’s based Nationwide are looking for permanent and contract Quality Control Analyst, Quality Chemist Analyst to join team’s whose responsibility it is to ensure that their products are manufactured to the highest international standards.
Responsibilities:
To observe GLP/cGMP at all times. Testing of all laboratory samples including in-process, finished products, Validation, Stability, and Environmental.
Performance of laboratory tests as per written procedure or as per pharmacopeia. Recording of analytical results accurately.
Operation, maintenance and calibration of laboratory instruments.
Preparation and execution of instrument and method validation protocols.
To maintain written training records.
To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior.
Requirements:
The ideal candidate must have a third level qualification in chemistry, analytical chemistry or a related subject.
They must have 1-2 years previous laboratory experience.
Strong technical ability and the ability to troubleshoot GC, HPLC and Dissolution testing methods are essential.
Experience in pharmacopeial testing, along with method development, validation experience in accordance with ICH guidelines and working knowledge of cGMP, GLP, FDA would be advantageous.
For Further details please contact; John on 01 2302400 or email: john@rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. No CV or details will be submitted to any potential client without prior knowledge, discussion and consent from “every” candidate. For a list of all our current vacancies, view our website http://www.rftgroup.ie/ Key Words: HPLC QC GC QA GMP FDA Documentation Pharmaceutical Validation
Apply for this jobOur client’s, large Bluechip Multinational’s based Nationwide are looking for permanent and contract Quality Control Analyst, Quality Chemist Analyst to join team’s whose responsibility it is to ensure that their products are manufactured to the highest international standards.
Responsibilities:
To observe GLP/cGMP at all times. Testing of all laboratory samples including in-process, finished products, Validation, Stability, and Environmental.
Performance of laboratory tests as per written procedure or as per pharmacopeia. Recording of analytical results accurately.
Operation, maintenance and calibration of laboratory instruments.
Preparation and execution of instrument and method validation protocols.
To maintain written training records.
To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior.
Requirements:
The ideal candidate must have a third level qualification in chemistry, analytical chemistry or a related subject.
They must have 1-2 years previous laboratory experience.
Strong technical ability and the ability to troubleshoot GC, HPLC and Dissolution testing methods are essential.
Experience in pharmacopeial testing, along with method development, validation experience in accordance with ICH guidelines and working knowledge of cGMP, GLP, FDA would be advantageous.
For Further details please contact; John on 01 2302400 or email: john@rftgroup.ie
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. No CV or details will be submitted to any potential client without prior knowledge, discussion and consent from “every” candidate. For a list of all our current vacancies, view our website http://www.rftgroup.ie/ Key Words: HPLC QC GC QA GMP FDA Documentation Pharmaceutical Validation
