Process Validation Scientist

Process Validation Scientist

Full-Time 26000 - 30000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a Process Validation Scientist, focusing on DNA synthesis and validation operations.
  • Company: Be part of an innovative biotech company revolutionising gene therapy near Cambridge.
  • Benefits: Enjoy a competitive salary, comprehensive benefits, and a full-time permanent role.
  • Why this job: This role offers hands-on experience in cutting-edge biotechnology with a collaborative team culture.
  • Qualifications: A BSc in a Biological discipline and experience in a quality-driven lab environment are essential.
  • Other info: Perfect for those looking to advance their career in a dynamic and impactful field.

The predicted salary is between 26000 - 30000 £ per year.

Contract: Full-Time and Permanent (Monday – Friday)

Sector: Biotechnology

Salary: £26,000 – £30,000 (depending on experience and interview performance)

Our client is an innovative biotechnology company based outside of the centre of Cambridge. They run their own gene therapy portfolio and have built a GMP platform to synthesise gene constructs which provides exciting possibilities for ensuring cheaper, faster and more accurate DNA / gene constructs than traditional plasmid-based methods. In a key phase of their growth, our client is looking to onboard a Scientist join their team which focuses on process validation, supporting tech transfer, MSAT and manufacturing processes for DNA synthesis.

The Opportunity

This is an opportunity for an individual who holds a BSc in a Biological discipline who has experience working in a controlled environment (GMP, GLP, GCP, ISO17025, ISO9001 etc). If you are looking for the next step in their career then this opportunity could be for you. The key responsibilities of the role include:

  • Performing process validation operations around a range of areas: DNA synthesis, DSP / downstream purification, molecular biology, consumable management, experimental documentation handling.
  • Work in collaboration with R&D and manufacturing teams to ensure the smooth transition of products to manufacturing.
  • Analysis of experimental data and updating of the QMS documentation where necessary.
  • Working independently on validation projects, completing them to a high standard.
  • Troubleshooting of laboratory processes and contributing to continuous improvement initiatives.

Skills and Experience Needed

The ideal candidate will have the following:

  • BSc/MSc or equivalent in biochemistry, molecular biology, or a related life science field (essential)
  • Experience working in a quality driven environment (GMP, GLP, GCP, ISO9001 / ISO17025) (essential)
  • Previous laboratory experience, using techniques such as western blotting, DNA/RNA/protein extraction, qPCR, chromatography, electrophoresis (essential)
  • Prior experimental validation experience or design of experiments (DoE) (desirable)
  • Great attention to detail (essential)
  • Organisational and planning skills (essential)

The Package

Our client is offering this opportunity on a full-time, permanent basis. A competitive salary and comprehensive benefits package is offered.

To Apply

If you would like to learn more about the vacancy, or to apply, please contact Charlie Cox on or 07903 204577

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Compulsory fields are in bold .

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Process Validation Scientist employer: taylorollinson Ltd

Our client is an innovative biotechnology company located just outside the vibrant centre of Cambridge, offering a dynamic work environment that fosters collaboration and creativity. With a strong focus on employee growth, they provide comprehensive training and development opportunities, alongside a competitive salary and benefits package. Joining this team means being part of a pioneering organisation at the forefront of gene therapy, where your contributions will directly impact the future of biotechnology.
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Contact Detail:

taylorollinson Ltd Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Process Validation Scientist

✨Tip Number 1

Familiarise yourself with the specific GMP and GLP regulations relevant to the biotechnology sector. Understanding these guidelines will not only help you in interviews but also demonstrate your commitment to quality and compliance, which is crucial for a Process Validation Scientist.

✨Tip Number 2

Network with professionals in the biotechnology field, especially those who work in process validation or related areas. Attend industry conferences or local meetups to make connections that could lead to job opportunities or valuable insights about the role.

✨Tip Number 3

Brush up on your laboratory techniques, particularly those mentioned in the job description like western blotting and qPCR. Being able to discuss your hands-on experience with these methods during an interview can set you apart from other candidates.

✨Tip Number 4

Prepare to discuss your previous experiences with experimental validation and design of experiments (DoE). Be ready to provide examples of how you've successfully managed projects and contributed to continuous improvement initiatives in past roles.

We think you need these skills to ace Process Validation Scientist

BSc/MSc in Biochemistry or Molecular Biology
Experience in GMP, GLP, GCP, ISO9001, ISO17025
Laboratory Techniques (Western Blotting, DNA/RNA/Protein Extraction, qPCR, Chromatography, Electrophoresis)
Experimental Validation Experience
Design of Experiments (DoE)
Attention to Detail
Organisational Skills
Planning Skills
Data Analysis
Troubleshooting Skills
Collaboration Skills
Quality Management System (QMS) Documentation Handling
Continuous Improvement Initiatives

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in biotechnology and any specific skills related to process validation, such as working in GMP environments or using laboratory techniques like qPCR and chromatography.

Craft a Strong Cover Letter: Write a cover letter that clearly explains why you are interested in the Process Validation Scientist role. Mention your educational background, relevant experience, and how your skills align with the company's goals in gene therapy and DNA synthesis.

Highlight Relevant Experience: In your application, emphasise any previous laboratory experience and your familiarity with quality-driven environments. Be specific about your roles in experimental validation and any contributions to continuous improvement initiatives.

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

How to prepare for a job interview at taylorollinson Ltd

✨Know Your Science

Brush up on your knowledge of biochemistry and molecular biology, especially the techniques mentioned in the job description like western blotting and qPCR. Being able to discuss these topics confidently will show your expertise and passion for the field.

✨Understand GMP and Quality Standards

Familiarise yourself with Good Manufacturing Practices (GMP) and other quality standards like GLP and GCP. Be prepared to discuss how you've applied these principles in your previous roles, as this is crucial for the position.

✨Demonstrate Problem-Solving Skills

Think of examples where you've successfully troubleshot laboratory processes or contributed to continuous improvement initiatives. Highlighting your analytical skills and attention to detail will impress the interviewers.

✨Prepare Questions

Have a few thoughtful questions ready about the company's gene therapy portfolio or their approach to process validation. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Process Validation Scientist
taylorollinson Ltd
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  • Process Validation Scientist

    Full-Time
    26000 - 30000 £ / year (est.)

    Application deadline: 2027-08-24

  • T

    taylorollinson Ltd

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