QC Analyst Cover Letter

I submit this application to express my sincere interest in the QC analyst position.

In my previous role, I was responsible for support to maintain cGMP testing in support of stability out of specifications (OOS) investigations and Non-conformance investigations.

My experience is an excellent fit for the list of requirements in this job:

• Requires basic understanding of HPLC/GC and other scientific instrumentation
• Working knowledge of GMP
• Analytical Testing of Biopharmaceutical Products using Electrophoresis (CGE, cIEF), Biacore (SPR), or ELISA methods
• Knowledge of GMP and GLP
• Ensure QC team work in a safe manner and in accordance with GxP
• Training of QC team for specific tasks in accordance with GxP
• Highlighting issues to the Quality Control Manager, OQ Manager and Quality Director as appropriate
• Preparation and review of in-house procedures (SOPs)

I am excited to be applying for the position of QC analyst. Please accept this letter and the attached resume as my interest in this position.

Previously, I was responsible for organizational leadership, direction and training in areas such as QA, QC, safety, cGMP, GDP, productions, team leadership etc.

Please consider my experience and qualifications for this position:

• Have a good knowledge on GLP and cGMP
• Able to operate a computer (minimum Microsoft Word & Excel)
• Current Residential Appraisal License in good standing
• Innovative and quick thinking
• Cross functional exposure both on site and within Campus Ireland
• Regular one to ones and feedback from programme manager
• Introduction to new and innovative technologies
• Exposure to Senior Management Team

I submit this application to express my sincere interest in the QC analyst position.

In my previous role, I was responsible for leadership and accountability for the design, implementation and documentation of laboratory investigations to establish the root cause of observed out of specification, out of trend or atypical results from the cGMP testing requirements of the QC laboratory.

My experience is an excellent fit for the list of requirements in this job:

• Runs analytical method transfer and qualification/validation experiments per approved protocols and with general instruction
• Writes and revises Standard Operating Procedures, provides support to QC projects and trains other lab analysts on routine test methods
• Performs general lab support activities such as housekeeping, equipment maintenance, inventory/ordering of supplies
• Dependable and able to work well within a team
• Bachelor of Science in Chemistry or Biology
• Preferredexperience with HPLC and/or GC
• Minimum SMAK (Sekolah Menengah Analis Kimia)
• Have a good knowledge on GDP and GLP

I would like to submit my application for the QC analyst opening. Please accept this letter and the attached resume.

Previously, I was responsible for technical support to run and validate necessary test methods on laboratory equipment and later perform product testing under cGMP.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• BS in Biochemistry or life sciences related field
• Understanding of sterile/aseptic technique
• Requires a minimum high school or junior college level biology classes or related fields or an equivalent combination of education and experience
• Requires BS/BA in Life Sciences or equivalent
• Experience of GMP QC Operations
• Experience of area supervision
• Experience of performing troubleshooting and acting as an SME
• Analytical Testing of Biopharmaceutical Products using Biacore (SPR), or ELISA methods

I would like to submit my application for the QC analyst opening. Please accept this letter and the attached resume.

Previously, I was responsible for technical expertise and leadership to the QC group ensuring samples are tested under cGMP within specified timelines.

Please consider my experience and qualifications for this position:

• Able to identify the potential of improvement and implement improvement in working area and able to lead continuous improvement program in working area
• Knowledge in cell science
• Awareness of Cell lines and passaging
• Practical experience with HPLC and GC systems
• Experience working in an DS/DP facility, desirable but not essential
• Experienced in technical writing
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