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- Tasks: Lead validation of medical device manufacturing processes and ensure compliance with regulatory standards.
- Company: Join a dynamic Medical Device company known for innovation and high-quality production.
- Benefits: Enjoy competitive pay, career growth opportunities, and a collaborative work environment.
- Why this job: Make a real impact on product safety and quality while working with cutting-edge technology.
- Qualifications: Bachelor's degree in engineering or life sciences and 5 years of relevant experience required.
- Other info: Ideal for those passionate about healthcare and eager to contribute to meaningful projects.
The predicted salary is between 43200 - 72000 £ per year.
This is an exciting opportunity to join a Medical Device company with the manufacturing expertise to take new products through initial design and development through to high volume manufacture.
Due to expansion, a new role has been created for a highly skilled& experiencedValidation Engineer to jointhe Operationsteam inSuffolk.You will play a key role in ensuring the quality, safety, and compliance ofthemedical devicesproducedthrough the validation of manufacturing processes, equipment, and systems.
Key Responsibilities
Develop, execute, and document validation protocols and reports for manufacturing processes, equipment, cleaning, and sterilisation processes.
Ensure compliance with relevant regulatory standards such as ISO 13485,FDA andEU MDR.
Collaborate with cross-functional teams including Quality Assurance,R&D, Regulatoryand Manufacturing to support process improvements.
Conduct risk assessments and validation lifecycle activities to ensure product quality and manufacturing consistency.
Participate in audit preparations and support regulatory inspections related to validation activities.
Maintain validation documentation in accordance with regulatory and company requirements.
Qualifications & Experience:
Bachelors degree in engineering,life sciencesor a related field(Chemical, Mechanical Engineering)
Minimum of 5years\’ experience inprocessvalidation within the medical device manufacturing industry.
Strong understanding of validation methodologies (IQ/OQ/PQ) and validation lifecycle.
Knowledge of regulatory standards (ISO 13485, FDA regulations, EU MDR).
Experience with risk management tools and techniques.
Data driven, comfortable using statistical software.
Excellent problem-solving, communication, and organisational skills.
Ability to work independently and as part of a multidisciplinary team.
Preferred Qualifications:
Previous experience in a Process Validation role in a CMDO or medical device manufacturer working at volume
Knowledge of the operation and constraints associated with high volume automation systems
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Lead Validation Engineer employer: Halian Technology Limited
Contact Detail:
Halian Technology Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Validation Engineer
✨Tip Number 1
Network with professionals in the medical device industry, especially those who have experience in validation engineering. Attend industry conferences or local meetups to connect with potential colleagues and learn about the latest trends and challenges in the field.
✨Tip Number 2
Familiarise yourself with the specific regulatory standards mentioned in the job description, such as ISO 13485 and FDA regulations. Being able to discuss these standards confidently during an interview will demonstrate your expertise and commitment to compliance.
✨Tip Number 3
Prepare to showcase your experience with validation methodologies like IQ/OQ/PQ. Think of specific examples from your past roles where you successfully implemented these processes, as this will help you stand out during discussions with our hiring team.
✨Tip Number 4
Brush up on your knowledge of risk management tools and techniques. Be ready to discuss how you've applied these in previous roles, as this is crucial for ensuring product quality and manufacturing consistency in our operations.
We think you need these skills to ace Lead Validation Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in process validation, particularly within the medical device manufacturing industry. Emphasise your understanding of regulatory standards like ISO 13485 and FDA regulations.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality and compliance in medical devices. Mention specific examples of how you've successfully developed and executed validation protocols in previous roles.
Highlight Key Skills: In your application, clearly outline your skills in risk management, problem-solving, and collaboration with cross-functional teams. These are crucial for the role and should be evident in your written materials.
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 essential for a Validation Engineer.
How to prepare for a job interview at Halian Technology Limited
✨Know Your Regulations
Familiarise yourself with ISO 13485, FDA regulations, and EU MDR. Be prepared to discuss how your experience aligns with these standards and how you can ensure compliance in the role.
✨Demonstrate Validation Methodologies
Be ready to explain your understanding of validation methodologies such as IQ/OQ/PQ. Share specific examples from your past work where you successfully implemented these processes.
✨Showcase Cross-Functional Collaboration
Highlight your experience working with cross-functional teams. Prepare examples that demonstrate your ability to collaborate effectively with Quality Assurance, R&D, and Manufacturing to drive process improvements.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving skills. Think of scenarios where you faced challenges in validation processes and how you overcame them, showcasing your analytical and organisational abilities.
