Quality Engineer
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Job Location:
Cambridgeshire - UK
Hourly Salary:
£ £ 20 - 26
Posted on:
9 days ago
Vacancies:
1 Vacancy
Job Summary
Our client a leading Pharmaceutical Company in Cambridgeshire is seeking a Quality Engineer to join their team on an initial 12 month contract. As the Quality Engineer you will be responsible for providing subject matter expertise to medical device and combination product development programmes throughout the product lifecycle. This role offers hybrid working (50% onsite).
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Engineerwill be varied however the key duties and responsibilities are as follows:
1. As the Quality Engineer you willlead design control and risk management activities for combination product development programmes ensuring deliverables are appropriately authored approved and maintained to support clinical trials and commercial licensures.
2. As the Quality Engineer you willsupport and facilitate effective risk management activities at external design companies and manufacturing facilities related to assigned projects.
3. As the Quality Engineer you willensure combination product development activities are compliant with quality and regulatory standards both internal and external.
4. As the Quality Engineer you willprovide input and support to design validation including but not limited to human factors engineering assessments.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Engineerwe are looking to identify the following on your profile and past history:
1. Relevant degree in a science or engineering discipline such as chemistry biology biomedical sciences mechanical engineering materials sciences or chemical engineering.
2. Proven industry experience in the pharmaceutical combination product and/or device industries.
3. A working knowledge and practical experience with ISO 13485 ISOCFR 820 21 CFR 4 and the EU Medical Devices Regulation.
Key Words:
Design Control / Risk Management / Medical Device / Combination Product / Pharmaceutical / Cambridge / Quality Standards / Regulatory Compliance / Human Factors Engineering
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors combining recruitment expertise with scientific knowledge to help you advance your career.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Engineerwill be varied however the key duties and responsibilities are as follows:
1. As the Quality Engineer you willlead design control and risk management activities for combination product development programmes ensuring deliverables are appropriately authored approved and maintained to support clinical trials and commercial licensures.
2. As the Quality Engineer you willsupport and facilitate effective risk management activities at external design companies and manufacturing facilities related to assigned projects.
3. As the Quality Engineer you willensure combination product development activities are compliant with quality and regulatory standards both internal and external.
4. As the Quality Engineer you willprovide input and support to design validation including but not limited to human factors engineering assessments.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Engineerwe are looking to identify the following on your profile and past history:
1. Relevant degree in a science or engineering discipline such as chemistry biology biomedical sciences mechanical engineering materials sciences or chemical engineering.
2. Proven industry experience in the pharmaceutical combination product and/or device industries.
3. A working knowledge and practical experience with ISO 13485 ISOCFR 820 21 CFR 4 and the EU Medical Devices Regulation.
Key Words:
Design Control / Risk Management / Medical Device / Combination Product / Pharmaceutical / Cambridge / Quality Standards / Regulatory Compliance / Human Factors Engineering
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors combining recruitment expertise with scientific knowledge to help you advance your career.
Company Industry
Pharmaceuticals
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
