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- Tasks: Review data to ensure quality standards and compliance with regulations.
- Company: Join Labcorp, a leading Contract Research Organisation dedicated to building a healthier world.
- Benefits: Enjoy competitive salary, health coverage, pension, flexible working, and career development opportunities.
- Why this job: Be part of a mission-driven team that impacts patient care and drug development.
- Qualifications: A-level education or equivalent; relevant experience in lab administration or data review preferred.
- Other info: Labcorp values diversity and encourages all qualified applicants to apply.
The predicted salary is between 30000 - 42000 £ per year.
Do you have attention to detail and enjoy administrative work?
Do you want to work for a company that helps build a healthier and safer world?
As one of the world’s premier Contract Research Organisations, our mission is to help build a healthier and safer world by providing research services for a multitude of organizations.
The Bioanalysis division at our site in Harrogate, North Yorkshire provides end-to-end analytical solutions and testing services to ensure quality control of our clients manufactured drug products. We work with leading pharmaceutical and biotech clients to ensure that their manufactured drug product or API (Active Pharmaceutical Ingredient) passes all quality testing. Once this testing is complete, it brings our clients one-step closer to successfully launching that drug product on the market; helping bring medicine to patients
As a Quality Control Reviewerat Labcorp Drug Development you will play an essential part in making this happen. This is a role that could offer a degree of flexible working.
Job responsibilities include:
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Assists co-workers and internal customers with interpretation and understanding of regulatory requirements e.g., GLPs (good laboratory practice), SOP (Standard Operating Procedure) requirements and other guidance documents
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Reviews data to ensure quality standards are met and to verify compliance to applicable SOP and regulatory requirements
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Maintains and seeks to expand a strong working knowledge of regulatory requirements (e.g. GLPs), SOP requirements, and other guidance documents. Applies existing knowledge to data review tasks
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Maintains a working knowledge of client SOPs and requirements. Applies knowledge to data review tasks
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Collects error tracking data for items reviewed
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Monitors citation trends in eQA (Quality Assurance) and performs follow-up actions with respondents, management, or others, if needed, to prevent recurring citations, problems, or errors
What Labcorp Drug Development can offer you:
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Competitive salary and a comprehensive benefits package, including health coverage and contributory pension.
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Ability to work with a variety of different clients on wide ranging projects.
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Flexible working and career development opportunities.
Education/Qualifications and experience:
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\”A\” level education or equivalent however relevant experience may be substituted for education
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Ideally laboratory administration, data review or other related work experience
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Ability to efficiently use basic software (e.g., Word, Excel, PowerPoint)
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Proof reading experience would be useful along with excellent written and verbal skills
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Attention to detail and used to working to tight deadlines within a regulated environment
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.
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Quality Control Reviewer employer: Laboratory Corporation
Contact Detail:
Laboratory Corporation Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Reviewer
✨Tip Number 1
Familiarise yourself with Good Laboratory Practices (GLPs) and Standard Operating Procedures (SOPs). Understanding these regulatory requirements will not only help you in the role but also demonstrate your commitment to quality control during any discussions.
✨Tip Number 2
Network with professionals in the pharmaceutical and biotech industries. Attend relevant conferences or webinars to connect with people who work in quality control roles, as they can provide insights and potentially refer you to opportunities at Labcorp.
✨Tip Number 3
Brush up on your data review skills. Practice reviewing sample data sets for accuracy and compliance, as this will prepare you for the tasks you'll encounter in the role and show your proactive approach to potential employers.
✨Tip Number 4
Highlight your attention to detail in conversations and interviews. Share specific examples from your past experiences where your meticulous nature led to successful outcomes, as this is a key trait for a Quality Control Reviewer.
We think you need these skills to ace Quality Control Reviewer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Quality Control Reviewer. Familiarise yourself with terms like GLPs and SOPs, as well as the importance of quality control in drug development.
Tailor Your CV: Highlight relevant experience in laboratory administration or data review. Emphasise your attention to detail and any experience you have with regulatory requirements or proof reading, as these are crucial for this role.
Craft a Strong Cover Letter: In your cover letter, express your passion for contributing to a healthier and safer world through quality control. Mention specific examples from your past experiences that demonstrate your skills and how they align with the job requirements.
Proofread Your Application: Ensure that your application is free from errors. Given the nature of the role, attention to detail is paramount. A well-proofread application reflects your commitment to quality and professionalism.
How to prepare for a job interview at Laboratory Corporation
✨Showcase Your Attention to Detail
As a Quality Control Reviewer, attention to detail is crucial. During the interview, provide examples of how you've demonstrated this skill in previous roles, especially in administrative or data review tasks.
✨Familiarise Yourself with Regulatory Requirements
Make sure you have a solid understanding of GLPs and SOPs. Be prepared to discuss how these regulations impact your work and how you ensure compliance in your previous experiences.
✨Demonstrate Your Software Proficiency
Since the role requires efficient use of software like Word, Excel, and PowerPoint, be ready to talk about your experience with these tools. You might even want to mention specific projects where you used them effectively.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle tight deadlines. Think of scenarios where you successfully managed challenges in a regulated environment and be ready to share those stories.
