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- Tasks: Lead QC projects, write protocols, and ensure regulatory compliance in a lab environment.
- Company: Join LabCorp, a global leader in drug development and innovative treatment solutions.
- Benefits: Enjoy competitive salaries, comprehensive benefits, and flexible work options between home and the lab.
- Why this job: Be part of groundbreaking projects that impact lives while developing your skills in a supportive culture.
- Qualifications: A scientific degree is required; experience in QC or related fields is preferred.
- Other info: Includes a 6-month onboarding period with training in laboratory and regulatory practices.
The predicted salary is between 36000 - 60000 £ per year.
About LabCorp Drug Development As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully. The Role Our largest UK site in Harrogate, is currently recruiting for a QC Scientist to join our CE and Compendials section within the BioPharmCMC business unit. Within the CMC business unit; the department is dedicated to the development, validation and execution of many techniques across several sections such as CE, HPLC, Bioassay, Molecular Biology and Virology. Techniques include CE, HPLC, LC-MS, Bioassays, QPCR, RTqPCR and Digital PCR to support many Bio Pharmaceutical products. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role, although based in the CE section may cover all of the different sections of the BioPharmaceutical CMC department in a molecule lead capacity. As part of this role you will provide technical oversight for clinical and pre-clinical studies; stability studies, batch release testing of commercial product and product development studies executed by the sections in a GMP environment. In more detail, you will be… • Acting as the molecule lead in supporting client projects • Writing method validation/transfer, batch release and stability protocols. • Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. • Perform regulatory compliance checks and maintain regulatory oversight during study execution. • Lead technical or regulatory investigations when required throughout the conduct of a project. • Training, mentoring and coaching of QC analysts and other team members. What Labcorp Drug Development can offer you • A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. • Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. • Ability to work with a variety of different clients on wide ranging projects. • Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information • Position includes a 6-month onboarding & probationary period during which working hours are 8:45am – 5pm, based at our site in Harrogate. • The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. What we’re looking for QC Scientists are the most successful at Labcorp with: • Scientific degree (BSc / MSc / PhD or equivalent) required • Ability to communicate effectively at all levels with internal employees and external clients, with the ability to get things done by influencing others. • Commercial awareness, interpersonal and negotiating skills and ability to learn and maintain knowledge of process excellence processes. • Either: Technical expertise in at least one of the following scientific disciplines: CE, ICE, Moistures, Osmolality, Colorimetry, UV analysis, Particulates using HIAC, pH & Appearance testing. • Either: Experience within industry or similar, with study management and client management. • Preferred: An in-depth understanding of health and safety policies and a good understanding of GMP Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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 our or contact us at For more information about how we collect and store your personal data, please see our .
QC Scientist III employer: Labcorp
Contact Detail:
Labcorp Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Scientist III
✨Tip Number 1
Familiarize yourself with the specific techniques mentioned in the job description, such as CE, HPLC, and Bioassays. Having hands-on experience or knowledge in these areas will make you stand out as a candidate.
✨Tip Number 2
Highlight any previous experience you have in a GMP environment. Understanding regulatory compliance is crucial for this role, so be prepared to discuss how you've navigated these processes in past positions.
✨Tip Number 3
Demonstrate your ability to communicate effectively with both internal teams and external clients. Prepare examples of how you've influenced others or managed client relationships in your previous roles.
✨Tip Number 4
Showcase your leadership skills by discussing any mentoring or training experiences you've had. This role involves coaching QC analysts, so illustrating your ability to guide others will be beneficial.
We think you need these skills to ace QC Scientist III
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the QC Scientist III position. Understand the key responsibilities and required qualifications, as this will help you tailor your application to highlight relevant experiences.
Highlight Relevant Experience: In your CV and cover letter, emphasize any experience you have with techniques mentioned in the job description, such as CE, HPLC, or Bioassays. Provide specific examples of how you've applied these skills in previous roles.
Showcase Communication Skills: Since effective communication is crucial for this role, include examples in your application that demonstrate your ability to communicate complex scientific information clearly to both internal teams and external clients.
Tailor Your Cover Letter: Write a personalized cover letter that addresses why you are interested in working at LabCorp and how your background aligns with their mission of supporting innovative drug development. Mention your understanding of GMP and regulatory compliance if applicable.
How to prepare for a job interview at Labcorp
✨Showcase Your Technical Expertise
Be prepared to discuss your technical skills in detail, especially in areas like CE, HPLC, and Bioassays. Highlight any relevant experience you have with these techniques and how you've applied them in previous roles.
✨Demonstrate Effective Communication Skills
Since the role requires collaboration with clients and team members, practice articulating your thoughts clearly. Prepare examples of how you've successfully influenced others or resolved conflicts in a professional setting.
✨Understand Regulatory Compliance
Familiarize yourself with GMP guidelines and regulatory compliance standards relevant to the pharmaceutical industry. Be ready to discuss how you've ensured compliance in past projects or studies.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities and decision-making skills. Think of specific instances where you led a project or overcame challenges, particularly in a laboratory or client-facing environment.
