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- Tasks: Ensure high-quality document checks and compliance with regulatory standards.
- Company: Join a forward-thinking company dedicated to quality and innovation.
- Benefits: Gain valuable experience, training opportunities, and a supportive work environment.
- Why this job: Make a real difference in research quality while developing your skills.
- Qualifications: Knowledge of GLP/GCP regulations and experience with QC processes.
- Other info: Dynamic team atmosphere with opportunities for personal growth.
The predicted salary is between 36000 - 60000 £ per year.
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 check 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.
Skills, Education & Qualifications
- Solid knowledge of reviewing QC documents, data and data tables.
- Solid knowledge of GLP/GCP regulations.
- Strong Watson/LIMS experience.
Document Quality Associate in Fordham employer: Resolian
Contact Detail:
Resolian Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Document Quality Associate in Fordham
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their values and how they align with yours. This will help you answer questions confidently and show that you're genuinely interested.
✨Tip Number 3
Practice your communication skills! Whether it's discussing your experience or explaining complex concepts, being clear and concise is key. Consider mock interviews with friends or using online resources to sharpen your skills.
✨Tip Number 4
Don't forget to apply through our website! We love seeing applications directly from candidates who are excited about joining us. Plus, it shows initiative and interest in being part of our team.
We think you need these skills to ace Document Quality Associate in Fordham
Some tips for your application 🫡
Know the Role Inside Out: Before you start writing your application, make sure you really understand what a Document Quality Associate does. Familiarise yourself with GLP/GCP standards and the specific responsibilities mentioned in the job description. This will help you tailor your application to show that you're the perfect fit for us!
Show Off Your Attention to Detail: Since this role is all about quality and meticulousness, make sure your application reflects that. Double-check for any typos or errors, and ensure your formatting is consistent. We want to see that you can QC your own work before you even get to us!
Be Specific About Your Experience: When detailing your past experiences, be specific about how they relate to the responsibilities of the role. Mention any relevant experience with QC checking, using Watson LIMS, or working under GLP/GCP regulations. The more we see how your background aligns with our needs, the better!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Resolian
✨Know Your Regulations
Make sure you brush up on GLP and GCP standards before the interview. Being able to discuss these regulations confidently will show that you understand the importance of compliance in the role of a Document Quality Associate.
✨Familiarise Yourself with SOPs
Take some time to review standard operating procedures (SOPs) related to document quality. This will not only help you answer questions more effectively but also demonstrate your proactive approach to understanding the company's processes.
✨Showcase Your Attention to Detail
Prepare examples from your past experiences where your attention to detail made a significant impact. Whether it was catching an error in a report or improving a process, being able to articulate these moments will highlight your suitability for the role.
✨Ask Insightful Questions
Come prepared with questions that show your interest in personal development and efficiency improvements. Asking about training opportunities or how the team collaborates on QC checks can set you apart as a candidate who is genuinely invested in growth.
