QC Scientist III

QC Scientist III

Harrogate Full-Time 36000 - 60000 Β£ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead QC projects, perform technical appraisals, and ensure regulatory compliance.
  • Company: LabCorp is a global leader in drug development solutions, supporting innovative treatments.
  • Benefits: Enjoy competitive salaries, health cover, pension contributions, and flexible working options.
  • Why this job: Join a dynamic team, develop your skills, and make a real impact in healthcare.
  • Qualifications: A scientific degree (BSc/MSc/PhD) and expertise in relevant scientific disciplines are required.
  • Other info: Includes a 6-month onboarding period with both office and lab work.

The predicted salary is between 36000 - 60000 Β£ 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.

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: 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.

QC Scientist III employer: Digital Invaders

LabCorp Drug Development is an exceptional employer, offering a dynamic work environment in Harrogate where innovation meets collaboration. With a strong focus on employee growth, we provide comprehensive training and career development opportunities, alongside competitive salaries and a robust benefits package. Our culture promotes teamwork and scientific excellence, making it an ideal place for QC Scientists to thrive while contributing to life-changing treatments.
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Contact Detail:

Digital Invaders Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land QC Scientist III

✨Tip Number 1

Familiarise yourself with the specific techniques mentioned in the job description, such as CE, HPLC, and Bioassays. Being able to discuss your hands-on experience or knowledge of these methods during an interview will demonstrate your suitability for the role.

✨Tip Number 2

Network with professionals in the pharmaceutical and biotech industries, especially those who work in quality control or drug development. Engaging with them on platforms like LinkedIn can provide insights into the company culture and potentially lead to referrals.

✨Tip Number 3

Prepare to discuss your experience with regulatory compliance and GMP practices. Highlight any relevant projects where you ensured adherence to these standards, as this is crucial for the QC Scientist role.

✨Tip Number 4

Showcase your leadership skills by preparing examples of how you've trained or mentored others in a lab setting. This will align well with the responsibilities of training and coaching QC analysts in the position.

We think you need these skills to ace QC Scientist III

Technical Expertise in CE, HPLC, LC-MS, Bioassays, QPCR, RTqPCR, Digital PCR
Method Validation and Transfer
Batch Release Testing
Stability Studies
Regulatory Compliance Checks
Analytical Data Appraisal
Project Management
Training and Mentoring Skills
Interpersonal and Negotiation Skills
Commercial Awareness
Knowledge of GMP
Health and Safety Policies
Effective Communication Skills
Problem-Solving Skills
Attention to Detail

Some tips for your application 🫑

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the QC Scientist III position. Tailor your application to highlight relevant experiences and skills that align with the role.

Highlight Relevant Experience: Emphasise any previous experience you have in laboratory settings, particularly in techniques like CE, HPLC, or Bioassays. Use specific examples to demonstrate your technical expertise and how it relates to the job.

Craft a Strong Cover Letter: Write a compelling cover letter that not only introduces yourself but also explains why you are interested in LabCorp and how your background makes you a suitable candidate for the QC Scientist role.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in a QC role.

How to prepare for a job interview at Digital Invaders

✨Know Your Techniques

Familiarise yourself with the specific techniques mentioned in the job description, such as CE, HPLC, and Bioassays. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.

✨Demonstrate Regulatory Knowledge

Since the role involves regulatory compliance checks, brush up on GMP guidelines and any relevant regulations. Be ready to explain how you have ensured compliance in past projects.

✨Showcase Communication Skills

Effective communication is key in this role. Prepare examples of how you've successfully communicated complex scientific information to both internal teams and external clients, highlighting your ability to influence and negotiate.

✨Prepare for Technical Questions

Expect technical questions related to method validation, data appraisal, and stability studies. Review your past experiences and be ready to discuss specific challenges you faced and how you overcame them.

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