Quality Investigator I: GMP Sterile Investigations
Quality Investigator I: GMP Sterile Investigations

Quality Investigator I: GMP Sterile Investigations

Full-Time 30000 - 42000 £ / year (est.) No home office possible
Go Premium
R

At a Glance

  • Tasks: Conduct investigations into non-compliances while ensuring adherence to cGMP regulations.
  • Company: Join a world-leading cell and gene therapy organisation in Edinburgh.
  • Benefits: Enjoy a competitive salary, generous annual leave, and pension plans.
  • Why this job: Make a real difference in the life sciences field with a focus on quality.
  • Qualifications: Degree in Life Science and 2 years of experience in sterile manufacture or quality roles.
  • Other info: Inclusive workplace with opportunities for personal and professional growth.

The predicted salary is between 30000 - 42000 £ per year.

A world-leading cell and gene therapy organization in Edinburgh is seeking a Quality Investigator I to perform investigations of non-compliances in compliance with cGMP regulations.

The ideal candidate will have:

  • A degree in Life Science
  • At least 2 years of experience in sterile manufacture or quality roles
  • Strong technical writing skills

The position offers a competitive salary, comprehensive benefits including generous annual leave and pension plans, and a commitment to inclusivity in the workplace.

Quality Investigator I: GMP Sterile Investigations employer: RoslinCT

Join a world-leading cell and gene therapy organisation in Edinburgh, where you will be part of a dynamic team dedicated to innovation and excellence in the field of quality investigations. With a strong commitment to employee growth, comprehensive benefits including generous annual leave and pension plans, and a vibrant, inclusive work culture, this is an excellent opportunity for those looking to make a meaningful impact in their careers.
R

Contact Detail:

RoslinCT Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Investigator I: GMP Sterile Investigations

✨Tip Number 1

Network like a pro! Reach out to professionals in the cell and gene therapy field on LinkedIn. Join relevant groups and engage in discussions to get your name out there.

✨Tip Number 2

Prepare for interviews by researching the company’s recent projects and values. This shows you’re genuinely interested and helps you tailor your answers to what they care about.

✨Tip Number 3

Practice your technical writing skills! Since this role requires strong writing abilities, consider drafting mock reports or summaries of investigations to showcase your expertise.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed and shows you’re serious about joining our team.

We think you need these skills to ace Quality Investigator I: GMP Sterile Investigations

cGMP Regulations
Technical Writing Skills
Investigation Skills
Quality Assurance
Sterile Manufacture Experience
Life Science Degree
Attention to Detail
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in sterile manufacture or quality roles. We want to see how your background aligns with the Quality Investigator I position, so don’t be shy about showcasing relevant skills and achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about cell and gene therapy and how your technical writing skills can contribute to our team. Keep it engaging and personal – we love to see your personality!

Showcase Your Compliance Knowledge: Since this role involves investigations of non-compliances, make sure to mention any experience you have with cGMP regulations. We’re looking for candidates who understand the importance of compliance in the industry, so let us know what you know!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and you’ll be on your way!

How to prepare for a job interview at RoslinCT

✨Know Your cGMP Regulations

Make sure you brush up on current Good Manufacturing Practices (cGMP) before your interview. Being able to discuss specific regulations and how they apply to sterile manufacturing will show that you’re not just familiar with the theory, but that you can apply it in practice.

✨Highlight Your Technical Writing Skills

Since strong technical writing skills are a must for this role, prepare examples of reports or documentation you've created in previous positions. Be ready to discuss how your writing has contributed to compliance and quality assurance in your past work.

✨Prepare for Scenario-Based Questions

Expect to face scenario-based questions that assess your problem-solving abilities in non-compliance situations. Think of specific instances where you identified issues and how you resolved them, as this will demonstrate your practical experience and critical thinking skills.

✨Show Your Commitment to Inclusivity

This organisation values inclusivity, so be prepared to discuss how you’ve contributed to a positive team environment in the past. Share experiences that highlight your ability to work collaboratively with diverse teams and how you support an inclusive workplace culture.

Quality Investigator I: GMP Sterile Investigations
RoslinCT
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

R
  • Quality Investigator I: GMP Sterile Investigations

    Full-Time
    30000 - 42000 £ / year (est.)
  • R

    RoslinCT

    50-100
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>