Sr QC Analyst
Aequor JD ·www.aequor.com
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This role will be on 100% Onsite.
Senior Quality Control Analysts have the following responsibilities:
Perform laboratory activities to support method validation.
Write method validation protocols and reports.
Generate and revise analytical test procedures.
Senior Quality Control Analysts should have the following skill set:
Familiar with current Good Manufacturing Practices and Good Lab Practices.
Familiar with current ICH and USP guidance for analytical method validation.
Familiar with analytical lab equipment and analytical lab techniques (e.g. HPLC, TLC, UV)
The ability to work independently following an approved protocol.
The ability to function in a team environment.
The flexibility to work overtime as required.
The ability to demonstrate creative and innovative thinking to solve analytical problems.
Good technical writing skills and the ability to communicate technical issues to project lead and team.
Minimum Qualifications:
Bachelors of Science degree in Chemistry or other science
5 years of analytical laboratory experience
3 years analytical method validation experience
Proficient in MS Word and Excel.
Preferred Qualifications:
3 years of experience in a Pharmaceutical manufacturing facility
7 years of analytical laboratory experience
5 years analytical method validation experience
Senior Quality Control Analysts have the following responsibilities:
Perform laboratory activities to support method validation.
Write method validation protocols and reports.
Generate and revise analytical test procedures.
Senior Quality Control Analysts should have the following skill set:
Familiar with current Good Manufacturing Practices and Good Lab Practices.
Familiar with current ICH and USP guidance for analytical method validation.
Familiar with analytical lab equipment and analytical lab techniques (e.g. HPLC, TLC, UV)
The ability to work independently following an approved protocol.
The ability to function in a team environment.
The flexibility to work overtime as required.
The ability to demonstrate creative and innovative thinking to solve analytical problems.
Good technical writing skills and the ability to communicate technical issues to project lead and team.
Minimum Qualifications:
Bachelors of Science degree in Chemistry or other science
5 years of analytical laboratory experience
3 years analytical method validation experience
Proficient in MS Word and Excel.
Preferred Qualifications:
3 years of experience in a Pharmaceutical manufacturing facility
7 years of analytical laboratory experience
5 years analytical method validation experience
Frequently asked questions
Who is hiring for the Sr QC Analyst role?
Aequor JD is hiring for the Sr QC Analyst position, a Shazamme client. Apply directly on the employer's career site.
Where is the Sr QC Analyst job located?
The Sr QC Analyst role with Aequor JD is based in Fort Worth, TX, US.
Is the Sr QC Analyst role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Sr QC Analyst role?
The Sr QC Analyst position is aimed at senior-level candidates.
How do I apply for the Sr QC Analyst role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.