Advisor / Csv Quality

**Job Specification**:
We offer:

- **Vibrant and dynamic employment - **we are a highly specialised, growth company operating in a critical sector of the economy - our future is strong and exciting
- **Opportunities to develop your skills and yourself - **our rapid growth brings greater opportunities for you to learn and grow faster
- **A great team where we all support each other - **enjoy your work - after all you spend about a third of your time here

**Our Company**:“We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.

We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.

The role is based in Northamptonshire, near the town of Rushden. The Rushden site is a centre of excellence for Radiolabelled Sciences incorporating both Metabolism and Chemistry. At our Rushden site, the Chemistry QA team are responsible for assuring compliance with cGMP with the Metabolism QA team being responsible for assuring compliance with the Principles of GLP and GCP with both QA sections providing advice and support to ensure compliance is maintained.

We offer our employees a supportive teamwork environment, enabling them to develop and liberate their true potential.

The position we are seeking to fill is for an **Advisor, CSV Quality **to act as a quality assurance contact for Computerised System Validation (CSV) and Data Integrity (DI) enquires and advise staff of the specific regulatory requirements. With excellent attention-to-detail, you will bring a methodical approach to following written procedures and evaluating systems and records with an ability to work accurately to deadlines. Ideally you will have existing auditing experience although addition training can be provided. You will be a strong team-player with exceptional interpersonal and communication skills.
- We offer a competitive salary and a progressive and comprehensive suite of employee benefits
- We offer a state of the art working environment in our modern Hoddesdon site
- We offer the opportunity for growth and development and will support funding for relevant training and development programmes

**Qualification**:
**Requirements**:

- Experience of auditing and reporting
- Demonstrable ability to follow written procedures and to evaluate systems and records
- Ability to work to written systems and a methodical approach to performing duties
- Excellent attention to detail and a methodical approach
- Effective organizational and time management skills
- Appreciative of the need to comply with regulatory requirements
- Willingness to share information and help others
- Excellent communication and interpersonal skills with the ability to provide support to other teams

**Key roles and responsibilities**:

- Conduct timely and effective audits for Computer System Validation (CSV) and Data Integrity (DI) according to company Standard Operating Procedures and to promptly report findings to the responsible person and management
- Conduct reviews of CSV Acceptance Test Plans and Amendments for completeness and compliance with regulatory requirements and to approve the final documentation
- Investigate deviations from CSV Acceptance Test Plans or SOPs to advise scientific staff accordingly
- Audit and approve CSV Test Reports confirming that methods, procedures and results accurately and completely reflect the raw data
- Conduct reviews of the spreadsheets to enable a validated status

**Why Should You Apply?**
- This is an opportunity for you to gain valuable auditing and CSV experience, to make a real impact in a highly scientific and regulated environment, demonstrate teamwork, ambition and the desire to grow with the department
- Build and shape your career in an environment that sets and commits to the highest standards of Quality
- To be part of a team who support each other, embrace and solve technical challenges and put excellence at the heart of all that we do
- Pharmaron is a premier R&D service company supporting the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities having established diverse drug R&D service capabilities, ranging from synthetic, medicinal, process and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development. With operations in China, US and UK staffed by over 19,000 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan, and China._