Project Manager in Harrogate

Project Manager in Harrogate

Harrogate Temporary 36000 - 60000 £ / year (est.) No working from home possible
Labcorp

At a Glance

  • Tasks: Lead projects in In Vitro Toxicology and ensure compliance with industry standards.
  • Company: Join Labcorp, a global leader in Life Sciences and drug development.
  • Benefits: 12-month contract with opportunities for professional growth and development.
  • Other info: Inclusive workplace that values diversity and encourages all to apply.
  • Why this job: Make a real impact in healthcare by bringing essential medicines to market.
  • Qualifications: Experience in project management and In Vitro Toxicology is preferred.

The predicted salary is between 36000 - 60000 £ per year.

Are you looking to develop your In Vitro Toxicology career further? Do you have demonstrated experience in providing scientific and technical expertise and support to ensure compliance with laws, regulatory agency guidelines, Good Laboratory Practice (GLP), Standard Operating Procedures (SOP's) and Study Protocols? Are you passionate about developing yourself and others?

We are currently recruiting for a Project Manager/Technical Specialist at our site in Harrogate, North Yorkshire. Labcorp is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical, crop protection and chemical industries. We strive to make a difference to people's everyday lives by bringing essential medicines to the market.

This role is to provide scientific and operational leadership across assay development, validation, and study delivery to achieve ISO 17025 compliance for designated methods. The role will be a project and technical manager and will ensure valid, reliable results, robust data integrity; and an effective management system aligned with ISO 17025 and applicable GxP regulations (e.g., GLP, GCP) to support accreditation and client confidence. Please note, this is a 12 month fixed term contract.

ISO/IEC 17025 Technical Management:
  • Serve as Technical Manager for assigned methods with overall responsibility for technical operations, competence, and method performance monitoring; define competence requirements, authorisations, and ongoing training.
  • Maintain the laboratory's management system in alignment with ISO/IEC 17025 Clause 8 (documentation, document control, records, risk & opportunities, improvement, corrective action, internal audits, and management review).
  • Oversee participation in proficiency testing/interlaboratory comparisons (as applicable), trending of quality control data, and timely investigation of out‑of‑trend/nonconforming results.
  • Define, apply, and document decision rules when issuing pass/fail statements against specifications.
Project Management:
  • Demonstrates organisation skills – ability to work to agreed timelines; to prioritise own work and that of individuals working on the project, providing direction where required.
  • Assess resource requirements, communicate requirements to management/resourcing, develops awareness of project cost vs gain.
  • Initiates problem solving of adverse events during method development, validation, study and non-study work, encourages others to assist in providing solutions.
  • Works with the Project Lead/Study Director to ensure that any issues/obstacles are documented correctly.
  • Identifies process improvements and new/further method developments and shares with appropriate individual(s).
  • Provides regular updates on projects delivery, highlights any potential issues which may affect timelines, quality and/or cost to Project Lead.
Associated Documentation:
  • Reviews/writes laboratory SOPs and lab sheets in line with process improvements for study related work.
  • Prepares new SOPs and lab sheets in relation to new assay types/product lines.
  • Prepares/assists with the development of training guides/records in relation to new assay types/product lines.
  • Prepares reports prior to QA audit and dispatch to the client as audited draft within chosen scientific discipline (10%).
  • Produces a summary report of any method development/validation process undertaken and completed.
  • Addresses eQA comments regarding procedures, raw data, and reports.
  • Assists Project Lead to prepare protocol and report templates for new product lines.
  • Assists in the preparation of validation protocols for new study types and or method developments.
Education/Qualifications:
  • Degree in Biomedical / Forensics / Biological Sciences or equivalent is preferred but not essential.
Experience:
  • Must have recognised project management and invitro toxicology experience.
  • Technical competence of routine and specialised aerosol generation techniques across a wide range of industrial applications.
  • Experience of cross-site collaboration helping to drive harmonization.

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, colour, 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 our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Project Manager in Harrogate employer: Labcorp

Labcorp is an exceptional employer located in Harrogate, North Yorkshire, offering a dynamic work culture that prioritises employee development and collaboration. With a commitment to scientific excellence and compliance, employees benefit from comprehensive training opportunities and the chance to contribute to meaningful projects that impact global health. Join us to be part of a diverse team dedicated to innovation and making a difference in people's lives.

Labcorp

Contact Details:

Labcorp Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Project Manager in Harrogate

Join Biotechnology Meetups

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Apply Directly on Our Website

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We think you need these skills to ace Project Manager in Harrogate

In Vitro Toxicology
Scientific Expertise
Technical Support
Good Laboratory Practice (GLP)
Standard Operating Procedures (SOPs)
ISO 17025 Compliance
Project Management

Some tips for your application 🫡

Showcase Relevant Lab Skills:In the biotech world, your lab skills are paramount. Make sure your CV highlights specific techniques and equipment you’ve used, such as PCR, gel electrophoresis, or cell culture. This will give us a clear picture of what you can bring to Labcorp as a temporary teammate.

Highlight Your Research Experience:If you’ve worked on any research projects — whether during your studies or in previous positions — make sure to detail these in your application. Include the objective, your role, and what you achieved. This will help us see your potential and fit for the temporary position at Labcorp.

Keep It Concise and Relevant:Especially for a temporary role, we want to see a clear and focused application. Tailor your CV and cover letter to emphasise the qualifications and experiences that are most relevant to the biotech field and the specific role at Labcorp. This shows us you’re genuinely interested and capable.

Be Clear About Your Availability:Since it’s a temporary role, let us know right away when you’re available to start and how long you can commit. Include this in your cover letter — this kind of transparency saves us all time and helps us find the right fit quickly at Labcorp.

How to prepare for a job interview at Labcorp

Brush Up on Your Biotech Basics

Understanding the fundamental concepts in biotechnology is crucial. Be ready to discuss core topics like genetics, molecular biology, or bioinformatics, especially if you're asked technical questions. We suggest revisiting your coursework or recent projects to refresh your memory.

Demonstrate Your Adaptability

Since this is a temporary role, they’re likely looking for someone who can jump in and get up to speed quickly. Share experiences where you’ve adapted to new environments, tools, or teams in a short space of time. It shows you're ready to tackle the challenge head-on!

Emphasise Your Lab Experience

If you’ve got hands-on experience in lab settings, now’s the time to showcase it. Talk about specific techniques you’ve mastered, like PCR or chromatography, and any relevant safety protocols you’ve followed. These details help paint you as an effective team member from day one.

Be Prepared to Explain Your Passion

Hiring managers want to see your motivation, especially for a temporary position in a fast-paced field like biotechnology. Be ready to discuss what excites you about the industry, your career goals, and how this role at Labcorp aligns with them. It’s all about showing that you’re not just looking for a job, but a stepping stone in your biotech journey.