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Job Details

Quality Engineer

Company: Clinical Professionals Ltd
Location:
Reference: JO-1803-404934
Closing Date: 20 Aug 18
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

MedTech Professionals are working with a brand new partner located to the south-east of Bremen, who are looking to take on board an experienced Quality Engineer to supplement the existing Quality team

Requirements:

Quality Engineer

Location: South-east Germany

Salary: Competitive

Job type: Office-based, full-time

MedTech Professionals are working with a brand new partner located to the south-east of Bremen, who are looking to take on board an experienced Quality Engineer to supplement the existing Quality team. The client have been in operation for over 15 years and specialise primarily in Biodegradable devices.

This is an outstanding opportunity for a junior Quality Engineer to gain some excellent experience working with Quality Management Systems, in preparation perhaps for a career later on working in-depth with suppliers.

Responsibilities of the role

Participate in maintenance of the quality system to ISO13485 Standards

Help with implementation of changes to documents within the quality system, development and maintenance of quality system documents

Participate in cross-functional team projects

Conduct and coordinate hygiene/cleanroom validation tests and prepare relevant reports, as well as oversee sterilization validations at the sterilization vendors

Investigate internal quality issues and interface with other relevant parties to resolve those issues

Provision of day-to-day troubleshooting support and resolve immediate problems in manufacturing

Conduct internal and/or supplier audits

Help review and close out action plans

Implement production and/or quality process improvements and analyse outcomes

Interact with other functional departments to develop product/process validations, risk management

Liaison with suppliers and customers as required

Prepare reports to communicate involvement and results of quality activities

Analyse quality data to observe trends and develop corrective/preventive actions

Ensure all activities are in compliance with Quality System requirements

Perform other duties as assigned

Candidate requirements

A Bachelor’s Degree in science or engineering, or other related Life Science subject

At least 2-3 years’ proven experience in the medical device industry as a Quality Assurance engineer

Fluency in both German and English languages

Experience in implantable devices or catheter based technologies is a plus, as is experience with process validation, new product development process, internal auditing, CAPAs and Six Sigma

Key words

Quality, Qualitӓt, Engineer, Ingenieur, Ingenieurwissenschaft, Engineering, Quality Management Systems, QMS, Cardiovascular, Peripheral, Vascular, Hamburg, ISO 13485, 9001, audits, internal, external, Deutsch, Deutschland, German, Germany, Englisch, English, supplier, customer, close out, troubleshooting, interface, sterilization, hygiene, cleanroom, Life Sciences;

If you are interested in this role and would like to apply, please get in touch with Lucy Thurmott on +49 (0)711 2225 4403 or via email at lucy@medtechprofessionals.com

In the event you don’t feel quite ready to take on such responsibility we’d appreciate your contact anyway as we do have plenty of other roles currently available in Quality, Regulatory and Clinical. We also operate a generous bonus scheme for successful referrals so do pass these details on to relevant friends and colleagues.

Apply for this job: Quality Engineer

Contact Information:

Address:  Clinical Professionals Ltd
33 Blagrave Street,
Reading
RG1 1PW
England
Tel:  0118 959 4990
Fax:  0118 956 0607
Website:  Visit Our Web Site

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