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- Tasks: Lead quality assurance processes and implement effective control systems for product development.
- Company: Join a forward-thinking company committed to quality and innovation.
- Benefits: Competitive pay, overtime opportunities, and a supportive work environment.
- Why this job: Make a real difference in product quality and process improvement.
- Qualifications: 3-5 years of experience and a relevant degree required.
- Other info: Collaborative culture with opportunities for professional growth.
The predicted salary is between 36000 - 60000 £ per year.
Overview
This position is Non-Exempt. Hours over 40 will be paid at Time and a Half.
Responsibilities
- Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements.
- Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements.
- Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues.
- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
- Design and conduct experiments for process optimization and/or improvement.
- Appropriately document experiment plans and results, including protocol writing and reports.
- Lead process control and monitoring of CTQ parameters and specifications.
- Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing).
- Lead the investigation, resolution and prevention of product and process non-conformances.
- Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member).
- Lead in the completion and maintenance of risk analysis.
- Work with design engineering in the completion of product verification and validation.
- Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
- Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Qualifications
- 3-5 years experience.
- Degree Required.
Quality Engineer II in Plymouth employer: Mindlance
Contact Detail:
Mindlance Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Engineer II in Plymouth
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by practising common questions and showcasing your problem-solving skills. Think about how you can demonstrate your experience with process controls and quality assurance during the chat.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your skills, especially in quality engineering.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their team.
We think you need these skills to ace Quality Engineer II in Plymouth
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in quality engineering. Use keywords from the job description, like 'process control systems' and 'CAPA systems', to show we’re on the same page.
Showcase Your Problem-Solving Skills: We love a good problem-solver! In your application, share specific examples of how you've applied systematic methodologies to tackle quality issues. This will help us see your analytical side in action.
Highlight Relevant Experience: Don’t forget to mention your experience with Six Sigma and Lean Manufacturing. If you’ve led teams or projects in these areas, let us know! It’s all about showing us how you can contribute to our quality initiatives.
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 don’t miss out on any important updates from us!
How to prepare for a job interview at Mindlance
✨Know Your Quality Standards
Familiarise yourself with FDA regulations and other relevant compliance standards. Be ready to discuss how your experience aligns with these requirements, as this will show that you understand the importance of quality in manufacturing.
✨Showcase Problem-Solving Skills
Prepare examples of how you've applied systematic problem-solving methodologies in past roles. Highlight specific instances where you identified and resolved quality issues, as this is crucial for a Quality Engineer II position.
✨Demonstrate Process Improvement Knowledge
Brush up on Six Sigma and Lean Manufacturing principles. Be prepared to discuss how you've led or participated in process improvement initiatives, as this will demonstrate your ability to contribute to ongoing product and process enhancements.
✨Communicate Effectively
Practice articulating your thoughts clearly and confidently. Since collaboration is key in this role, be ready to discuss how you've maintained positive communication with various stakeholders, including design engineering and microbiology teams.
