At a Glance
- Tasks: Ensure quality control of documents and reports while adhering to regulatory standards.
- Company: Join a forward-thinking company dedicated to excellence in research and development.
- Benefits: Enjoy a full-time role with opportunities for personal growth and development.
- Other info: Flexible work culture with opportunities to collaborate and learn from experienced professionals.
- Why this job: Be part of a team that values quality and innovation in a dynamic environment.
- Qualifications: Attention to detail and a passion for quality assurance are essential.
The predicted salary is between 44595 - 54505 £ per year.
Location: Newmarket Road, Fordham, CB7 5WW, United Kingdom
Employee Type: Regular Full Time
Responsibilities:
- Have a good knowledge of, and perform regulated studies to the appropriate GLP/GCP standards and latest regulatory guidelines.
- Be familiar with, and work in accordance with, SOPs and Study Documents.
- Complete all paperwork in compliance with good record keeping principles; correctly and on time with GLP/GCP.
- QC check the reports to a consistent and high standard including reviewing of study files against standard checklists.
- Be able to accurately communicate findings identified during the QC check.
- Make suggestions as to how processes can be improved, and efficiency maximised.
- Take an interest in your own personal development, seek out training, and look for opportunities to grow.
- Embrace Resolian values and be respectful to colleagues.
- Be flexible; realise that timelines, priorities and requirements will change regularly and respond to these challenges positively.
- Take responsibility for knowing what needs to be done each day, and doing it promptly.
- Familiarise yourself with, and work to, the Health and Safety Policy relevant to your role, paying particular attention to COSHH in the lab.
- Complete any Mandatory Training appropriate for your role.
- Have a good knowledge of QC checking reports including documents, data and data tables produced within the IA and LCMS Bioanalysis departments.
- Understand how to QC check sample management documentation.
- Use Watson LIMS and ResoLIMS to QC check report text, tables and figures.
- Focus on quality and attention to detail with an ability to perform QC checks in a meticulous manner.
- Communicate with Report Writers and SD/PI/APMs to provide updates on QC check progress. Update SharePoint and the Team forum appropriately.
- Liaise with the relevant SD/PI/APM and/or Report Writer for any matters that require further discussion.
- Work with QA to discuss audit findings and develop a clearer understanding of what is required, ultimately leading to enhanced efficiency and effectiveness.
- Communicate workload to the line manager and make sure that the day-to-day workload is manageable.
- Work with the QC team to provide cover for other team members as required.
- Look for opportunities outside of your core role. Contribute and participate without affecting your day-to-day responsibilities.
Requirements:
Skills, Education & Qualifications
Document Quality Associate in Fordham employer: Kids for the Future
At JPA Health, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our commitment to employee growth is evident through tailored development opportunities and a supportive environment that encourages professional advancement. Located in a vibrant area, we offer unique advantages such as flexible working arrangements and a focus on work-life balance, making us an ideal choice for those seeking meaningful and rewarding careers in the healthcare and life sciences sector.
We think you need these skills to ace Document Quality Associate in Fordham
Communication Skills
Problem-Solving Skills
Organizational Skills
Adaptability
Compassion
Flexibility
Teamwork
