Quality Engineer

Quality Engineer

Nottingham Full-Time 36000 - 48000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality investigations and collaborate with teams to improve processes.
  • Company: Join a dynamic biotech company focused on innovation and quality.
  • Benefits: Enjoy a competitive salary, flexible hours, and opportunities for professional growth.
  • Why this job: Make a real impact in quality assurance while working with cutting-edge technology.
  • Qualifications: Degree in Business, Sciences, or Engineering; 5+ years in quality operations required.
  • Other info: Work Monday to Thursday with early finish on Fridays!

The predicted salary is between 36000 - 48000 £ per year.

Seeking a Quality Engineer to work closely with Operations, Manufacturing, R&D, and Quality teams to drive continuous improvement and ensure compliance with industry standards. The role involves managing quality processes, investigating non-conformances, and implementing corrective and preventive actions (CAPA).

Key Responsibilities:

  • Lead quality investigations for market defects, identifying root causes and implementing CAPA.
  • Collaborate with cross-functional teams on failure modes and impact assessments.
  • Interface with customers and suppliers to address manufacturing non-conformances.
  • Drive process improvement initiatives using SPC, Six Sigma, and Lean methodologies.
  • Ensure manufacturing processes meet operational and regulatory requirements (ISO 9001, 13485, 21 CFR Parts 210 & 211).
  • Support audits, change control, document control, and product validation.
  • Provide training and guidance on best practices and quality standards.

Requirements:

  • Degree in Business, Sciences, or Engineering.
  • 5+ years’ experience in quality operations within biotech or pharmaceutical manufacturing.
  • Strong knowledge of ISO 9001/13485 and regulatory compliance.
  • Proficiency in problem-solving tools (ASQ, Green Belt, Lean Six Sigma preferred).
  • Excellent communication, collaboration, and decision-making skills.
  • Advanced MS Office skills preferred.

Quality Engineer employer: Meriden Media

As a Quality Engineer at our company, you will be part of a dynamic team that values innovation and continuous improvement in the biotech and pharmaceutical sectors. We offer a supportive work culture that encourages professional growth through training and collaboration with cross-functional teams, all while enjoying a competitive salary and flexible working hours. Located in a thriving area, our company not only prioritises compliance with industry standards but also fosters an environment where your contributions directly impact product quality and customer satisfaction.
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Contact Detail:

Meriden Media Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Engineer

✨Tip Number 1

Familiarise yourself with the specific quality standards mentioned in the job description, such as ISO 9001 and 13485. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality compliance.

✨Tip Number 2

Brush up on your knowledge of problem-solving tools like Six Sigma and Lean methodologies. Being able to discuss how you've applied these techniques in past roles can set you apart from other candidates.

✨Tip Number 3

Network with professionals in the biotech and pharmaceutical industries. Engaging with others in your field can provide insights into the company culture at StudySmarter and may even lead to referrals.

✨Tip Number 4

Prepare examples of your experience with cross-functional collaboration. Since the role involves working closely with various teams, showcasing your ability to communicate and collaborate effectively will be crucial during the interview process.

We think you need these skills to ace Quality Engineer

Analytical Skills
Attention to Detail
Technical Aptitude
ISO 9001
ISO 13485
Regulatory Compliance
Six Sigma
Lean Methodologies
Problem-Solving Skills
Data Analysis
Communication Skills
Collaboration Skills
Project Management
Root Cause Analysis
CAPA Implementation
SPC
Change Control
Document Control
Product Validation
Training and Guidance

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in quality operations, particularly within biotech or pharmaceutical manufacturing. Emphasise your knowledge of ISO 9001/13485 and any problem-solving tools you are proficient in.

Craft a Strong Cover Letter: In your cover letter, explain why you are passionate about quality engineering and how your background aligns with the responsibilities outlined in the job description. Mention specific experiences where you've successfully implemented CAPA or driven process improvements.

Highlight Relevant Skills: Clearly list your skills that match the job requirements, such as your proficiency in Six Sigma, Lean methodologies, and advanced MS Office skills. Use examples to demonstrate how you've applied these skills in previous roles.

Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Quality Engineer role.

How to prepare for a job interview at Meriden Media

✨Know Your Quality Standards

Make sure you have a solid understanding of ISO 9001 and 13485, as well as other relevant regulations. Be prepared to discuss how you've applied these standards in your previous roles.

✨Showcase Your Problem-Solving Skills

Be ready to provide specific examples of how you've used problem-solving tools like Six Sigma or Lean methodologies to address quality issues. Highlight any successful CAPA implementations you've led.

✨Emphasise Collaboration

Since the role involves working with various teams, demonstrate your ability to collaborate effectively. Share experiences where you worked cross-functionally to resolve quality concerns or improve processes.

✨Prepare for Technical Questions

Expect technical questions related to quality engineering and manufacturing processes. Brush up on your knowledge of SPC and failure modes, and be ready to discuss how you've handled non-conformances in the past.

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