Job Title: Quality Engineer
Location: Cambridge, UK
Duration: 12 Months
Work Type : Hybrid
Overview:
TekWissen is a global workforce management provider throughout the UK, Europe and many other countries in the world. The below client is an American multinational pharmaceutical and biotechnology corporation.
Job Description:
* This position is in the Biotherapeutics Pharmaceutical Research and Development Devices Centre of Excellence located in client location.
* The incumbent will provide design control and risk management subject matter expertise to medical device and combination product development programmes throughout the product lifecycle.
* This will involve generation and review of design history file and risk management file components whilst interacting with cross functional development teams at all levels of the organisation.
POSITION RESPONSIBILITIES
* Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures.
* Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects.
* Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external.
* Provide input and support to design validation including, but not limited to, human factors engineering assessments.
* Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply.
* Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture.
* Support the generation of all regulatory submission data and content for assigned device projects.
* Support internal and external audits of the DCoE Quality Management System.
EDUCATION, SKILLS AND EXPERIENCE
* BSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries
* OR MSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries OR PhD in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline).
* History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
* Experience in design controls and risk management for combination products.
* Familiar with Human Factors Engineering - Usability Engineering.
* Familiar with device assembling manufacturing processes.
TECHNICAL SKILLS REQUIREMENTS.
* Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
* Familiarity with EN 62366, EN 60601, and EN 62304.
* Able to learn and apply established procedures in a reliable and consistent manner.
* Capable of working independently with minimal supervision.
* High level of attention to technical details and accuracy.
* Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
* Able to work collaboratively in cross functional teams.
* Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills.
* Proficiency in general computer software such as word processing, spreadsheets, presentations.
* Understand Good Manufacturing Practices (GMP).
TekWissen® Group is an equal opportunity employer supporting workforce diversity.