At a Glance
- Tasks: Ensure high-quality documentation and compliance with regulatory standards in a dynamic lab environment.
- Company: Join a forward-thinking company dedicated to quality and innovation.
- Benefits: Full-time role with opportunities for personal development and training.
- Other info: Flexible work environment with opportunities for growth and collaboration.
- Why this job: Make a real impact by ensuring the accuracy and quality of important studies.
- Qualifications: Attention to detail and a passion for quality control 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.
Document Quality Associate in Fordham employer: Kids for the Future
At our Fordham location, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. As a Team Lead in Immunoassay, you will benefit from extensive professional development opportunities, competitive compensation, and the chance to work with cutting-edge technology in a supportive environment. Join us to make a meaningful impact in the bioanalytical field while enjoying a balanced work-life dynamic.
We think you need these skills to ace Document Quality Associate in Fordham
Communication Skills
Problem-Solving Skills
Organizational Skills
Adaptability
Compassion
Flexibility
Teamwork
