Daily new jobs

 

Software Quality Assurance Engineer

Share on social media:

Apply Save this job

1 person also applied on this job


The company

Our client is a professional organisation, based in Netherlands. The company you will be working for is based in Noord-Brabant, The Netherlands. It is one of the major players in the field of medical devices, and well-known throughout The Netherlands and abroad.

Role description

The Software Quality Assurance Engineer role is a vital organizational component ensuring regulated automated tools used in the Quality System are appropriately validated and controlled through their life cycle from development, deployment, change control and retirement. This includes ensuring project teams adhere to processes and control mechanisms for software, hardware, data and relevant security to meet regulatory requirements.

This role provides subject matter expertise with respect to the compliance and control of regulated tools used in the Quality Systems. The scope of this role extends from PH Q&R specific tools to those tools controlled by the PH business units that have implications in their respective quality systems. Support in this manner is determined by organizational demand and location of the tool with regards to the particular quality system(s) it is supporting.

Responsibilities

Enforce policies and procedures for System Life Cycle control for use in Healthcare across all automated processes that drive, interface with, and provide data for the Quality System.

Support development of the validation strategy and the validation effort from planning to retirement of Q& R systems and tools including interfaces to and from the system.

Support regulatory and internal audits. Provide subject matter expertise during regulatory and partner inspection.

Provide software quality assurance support in design and development of software solutions, and facilitate the application of controls and risk management by reviewing and approving IT change-control requests submitted by cross-functional project teams to assess potential quality system impact.

Ensure that system development projects and changes to existing systems are conducted in compliance with the FDA Quality System Regulation and Medical Device Directives.

Work alongside other validation professionals to gather data, plan activities, and obtain reviews and approvals of documentation including approving documentation with respect to software development lifecycle policies and procedures.

Assist in developing user, functional and technical requirements for IT systems.

Provide guidance and support to personnel in their validation efforts, to ensure compliance.

Provide GxP-related quality assurance oversight, with an emphasis on software validation.

Track system life cycle deliverables and activities to ensure that regulations, protocols, procedures, and methodologies are followed, and that appropriate and complete documentation is captured and reported to support validation activities.

Represent Quality & Regulatory Compliance and Control on cross-functional teams in support of SDLM activities.

Advise technical personnel and management on regulatory compliance and interpretation and recommend appropriate corrective actions where needed.

Requirements

Minimum 7-10 years’ experience in validation of computer systems and systems security and control including supervision of a technical professional staff

Experience working in disciplined regulated industry in the application of automated technology particularly 21 CFR, ISO 13485, GAMP 5

Minimum of 7 computerized systems implementations, comprised of multiple application types, in a regulated environment

Demonstrated ability to interact and communicate (both oral and written) with junior project team/ organizational members, business leaders and senior executives.

Expertise in IT protocols related to software/hardware validation, information security, data lifecycle management

Understanding of current inspectional practices of FDA, notified bodies and other regulatory agencies including previous interface with such bodies during regulatory assessments or inspections

Ability to apply current inspectional techniques to project documentation during the system lifecycle and prior to FDA inspection to ensure a comprehensive documentation package is created and maintained.

Effective judgment and decision making skills, typically made under stressful situations

Competency in project management and the execution of multiple projects

Other information

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim de Jong.


Job alert

  • No registration required
  • Stay up-to-date on the latest jobs

SIRE Information Technology®

Ref. number: 48523
Listed by: SIRE Information Technology®
Listed on: 21-08-2019
Country: The Netherlands
Employment: Freelance
Expertise: 6 - 10 years
Location Type: On location
Education: Bachelor
Language: English
Sector: Medical Devices
Specialisation: Quality

Search again

Related jobs

Steven Kruis
(Junior) C# .NET Developer - Interessante Bonus!

The Netherlands
Freelance
Quality

Steven Kruis
Freelance .NET Development opdracht

The Netherlands
Freelance
Quality

SIRE Life Sciences®
Sales Manager (Technical Ingredients)

The Netherlands
Freelance
Quality

SIRE Life Sciences®
Regulatory Affairs Officer

The Netherlands
Freelance
Quality

SIRE Life Sciences®
Team Leader Quality Assurance

The Netherlands
Freelance
Quality

Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Belgium BVBA

Science 14 Atrium
14b, Rue de la Science
1040 Bruxelles
+32 (0) 2 588 1277

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences UK

702 Howard House Dolphin Square
SW1V3PQ London
+44 7307 179882

SIRE Life Sciences Maastricht

ROOOMS Maastricht
Boschstraat 21
6211 AS Maastricht


SIRE Group GmbH

Platz 3
6039 Root
Luzern
+41 (0)43 508 1743

SIRE Staffing Solutions

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE Information Technology

Calypso Building
Kruisplein 480
3012 CC Rotterdam
+31 (0) 10 316 1066

SIRE Healthcare

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 85 044 4640

SIRE Finance

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 85 044 4630

SIRE Engineering

Calypso Building
Kruisplein 480
3012 CC Rotterdam
+31 (0) 10 316 6626

SIRE Human Resources

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 85 044 4620

SIRE Staffing

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 85 044 4650

Product Price