Data Verification Officer

**Analytical Data Verification Officer**with an excellent eye for detail, the ability to successfully manage multiple tasks simultaneously and previous laboratory experience with a good solid understanding of a wide range of analytical techniquesis required for a well-established pharmaceutical company based in Abingdon, Oxfordshire.

**SALARY**:Competitive (Depending on experience) + Bonus + Excellent Benefits

**LOCATION**:Abingdon, Oxfordshire

**JOB TYPE**:Full-Time, Permanent

**WORKING HOURS**:40 hours per week, Monday to Friday

**JOB OVERVIEW**

We have a fantastic new job opportunity for an Analytical Data Verification Officer with an excellent eye for detail, the ability to successfully manage multiple tasks simultaneously and previous laboratory experience with a good solid understanding of awide range of analytical techniques.

Working as an Analytical Data Verification Officer you will provide an in-depth review of analytical data produced from a range of analytical instrumentation, to ensure that it has been generated and recorded in compliance with cGMP, Data integrity (ALCOA)and local SOP/IOPs.

As an Analytical Data Verification Officer your role includes but is not limited to a review of raw, Request for Analysis forms, Analytical worksheets, validation, and stability reports, COAs, reference standards and electronic systems such as Empower.

**DUTIES**

Your role as an Analytical Data Verification Officer will include:

- Read and understand the procedures that are being reviewed, and that any regulatory, GMP and company procedure requirement updated are being adhered to
- Reviewing calculations data transcriptions and analysts’ analysis for accuracy, legibility, contemporaneous, original, and attributable (ALCOA) Verify the traceability and integrity of all data generated to support an analysis
- Review of Empower Audit trails to ensure compliance and accuracy
- Ensure that the experimentation has been performed as per the appropriate procedure and or testing protocol. Identify anomalies, out of precisions/trends/specifications and to inform the relevant supervisor or QC section manager through a consultation todetermine the course of action
- Work together with QC analysts to ensure any corrections are made and discuss improvements if applicable
- Review of Validation, Stability reports or other documentation required and assist in data entry and/or report writing for regulatory submission as required
- Report into the Data verification supervisor to update on the status of given of tasks, to ensure completion within the agreed deadlines, and to discuss any issues that may have occurred
- Adhere to Company and Regulatory requirements; and to ensure that confidential information is always protected
- Complete all Departmental and Site cGMP and safety training assignments as required in a timely manner
- Completion of any other tasks as required by the QC department

**ABOUT THE COMPANY**

The company provides integrated Chemistry, Manufacturing and Control capabilities to fully support drug substance development and GMP manufacturing on both laboratory and commercial scales for Active Pharmaceutical Ingredients.

**CANDIDATE REQUIREMENTS**
- A minimum of a degree (BSc) in a scientific discipline or equivalent
- Previous cGMP laboratory experience with a good solid understanding of a wide range of analytical techniques such as HPLC, GC, NMR, FT-IR and Karl Fischer etc, coupled with experience in the review of analytical data/documentation
- Knowledge of GMP and other regulatory requirements relevant to an analytical environment required
- Experienced with Empower CDS software
- Understanding of method validation and stability studies
- An excellent eye for detail
- Excellent time management skills and the understanding of prioritization of tasks based on department/client requirements
- Ability to successfully manage multiple tasks simultaneously
- Excellent written and verbal communication skills
- Analytical and good problem-solving skills
- Being Pro-active with objectives, liaising with relevant teams within the department, and fulfilling the tasks set to completion
- A friendly, positive attitude and a great team player

**APPLY TODAY**

JOB REF: AWDO-P9071

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