Johnson & Johnson
Quality Engineer
Quality Engineer
Location: Turnhoutseweg, Beerse
Duration: End of the year initially
Hours: Full time, Hybrid (3 days on site, 2 days at home)
roles and responsibilities
Maintain a current knowledge of international regulations, guidelines and industry practices related to system qualification
Participate in system introduction and system change projects and assure quality and compliance aspects.
Assuring that the qualification status is maintained during assessment and execution of changes and projects
Ensuring that all system changes that may have impact on quality, compliance or registration, are evaluated and approved in order to execute adequate control, documentation and qualification.
Review and approval of qualification documents such as (system level) Impact Assessment (IA), critical aspect risk assessments, (General) User Requirements ((G)URS), DQ/IQ/OQ/PQ protocols & reports, QSR, Test- and traceability matrices, …for compliance to regulations, guidelines and J&J procedures.
Review and approval of Periodic System Quality Reviews (PSQR) and Area Validation Master Plans (VMPs)
Ensuring that deviations related to systems (qualification, maintenance, calibration and/or use) with possible impact on quality and/or compliance are evaluated thoroughly investigated and that adequate corrective and preventive actions are implemented
Responsible for review and approval of calibration/certification procedures, calibration rationales, calibration master forms and completed calibration records.
Responsible for review and approval of preventive maintenance procedures and master forms.
Responsible for review and approval of parameter lists, alarm lists and transmission lists and other documents in eSTREAM
Responsible for review and approval of qualification / system related procedures/work instruction.
Make sure that all deliverables out of qualification are implemented in the quality systems: SOPs, Work instructions, Calibration records, Maintenance plans, …
Prepare for regulatory and customer inspections and act as a spokesperson for QA qualification related matters during audits
Interact regularly with other functional groups/departments involved in qualification projects to assure that timelines for system qualifications are met and the cross-department objectives are realized
Pro-actively and continuously challenge the quality of the qualification processes to improve the performance of qualification and develop and implement improvements.
cGxP / ATMP
Always uses the appropriate cGxP and procedures.
Reports incidents and deviations.
Proposes solutions to improve compliance with cGMPs.
Safety, Health & Environment (SHE)
Always uses the appropriate prevention rules and procedures.
Uses the available personal and collective protection materials correctly.
Works neat and tidy.
Reports (near) accidents, incidents, deviations and risky situations.
Cooperates on and suggests solutions to improve safety, health and environment.
Participate actively on promotion campaigns, working on the safe behaviour program, prevention controls.
Addresses to other colleagues and third persons when prevention procedures are not followed or in case of unsafe behaviour
how to succeed
5 years experience in the Pharmaceutical industry
Master Engineering, Pharmacy or equivalent degree
Thorough knowledge of pharmaceutical legislation, cGMP regulations and guidelines in the area of system qualification
Knowledge of the different systems used during the manufacturing process
Strong analytical thinking, risk assessment and communication skills.
Collaboration and teaming skills
Mindset for innovation and optimization
Fluent in Dutch and English (written and spoken)
Other knowledge requirements:
Comet system for incident handling / control of change
eStream: computerized maintenance management system
TrüVault: document management system
Summit (training system)
Kneat
details
This role offers a very competitive hourly rate. This contract will run until the end of the year initially with possibility of extension.
This is a hybrid role (3 days on site, 2 days at home). Some more on-site time may be required at the beginning of the assignment.
you are welcome here
Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.
about Johnson & Johnson
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.
application process
We are looking to process the first round of applications within the next 2 working days.
We do not accept applications via email.
questions
If you would like some additional information about the role please contact: simone.strong@randstadsourceright.co.uk
Diversity, Equity & Inclusion
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.