Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.
Johnson & Johnson
BE - Analyst 2, Quality Assurance
Job is closed
Posted
Oct 26, 2022
Job ID:
JJJP00012873
Location
Courcelles
Hours/week
40 hrs/week
Timeline
1 year
Starts: Nov 7, 2022
Ends: Nov 6, 2023
Payrate range
Unknown
Quality Engineer
CQ HMD EMEA, Quality & compliance
Medical Devices, Med Tech
Location
Courcelles (Belgium) FTE% 100 %
Job Description
You will join an effective and open team. Together we support the Quality & Compliance of an operational distribution site. We value communication, clear sense of purpose, supporting on another and good understanding of customer's expectations.
The function is based within European distribution center at Courcelles, allowing to be exposed to the operational environment and develop QA operational activities such as shop-floor investigation & inspections. Every team member acts as a single-point of contact for an operational area and supports the area for all quality related topics (eg. gemba-walk, auditing, ..). As quality team we develop and deploy of effective and efficient quality processes that meet customer needs and applicable J&J & Health Authority compliance requirements.
Within the role you will be responsible for the following process:
· RIC ? Restricted Inventory CageProcess improvement! (shape lead)
· EDC traceability & Expiry support
Key Responsibilities
As a member of our team, you will:
Drive a culture of continuous improvement, where team members can identify areas for improvement on daily operational processes to drive data accuracy and global compliance and provide support to implement these initiatives by highlighting and discussing key changes/improvement programs with leadership and the appropriate partners.
Get encouraged and activated by supporting project team activities and guiding them towards compliant project execution
Broaden your network by the involvement in interaction with Franchise Supply Chain and EDC internal Operation.
Expand your knowledge by supporting and/or executing internal and external audits.
Elaborate Key Report on weekly basis and lead monthly franchise call.
Develop a detailed understanding of the distribution processes by being a zone owner and supporting daily operations within that zone (e.g. shop floor quality decision and investigations, root cause analysis, CAPA plans, GEMBA Walk...).
Get challenged by exposure to different type of process and human interactions.
Share your expertise by training & qualifying relevant partners and operators
Evaluate and ensure accurate documentation of applicable quality records and approve accordingly
Strengthen the team by driving process improvements, prioritization, and digitalization
Collaborate with peers in other parts of the EMEA commercial quality organization to improve process excellence, simplification and standardization across distribution sites
Qualification and experience:
3-4 years? experience in the medical device (or relevant) industry
Experience & interest in data analytics and reporting (R/Excell/Tableau/PowerQuery/Sharepoint)
Shown basis in QMS system process (document management, change control, non-conformance, CAPA, standards assessments)
Knowledge of GMP/GDP/ISO regulations
Competences: Strive for optimization, critical thinking, agility & invested in good collaborations with multiple partners
French & English
CQ HMD EMEA, Quality & compliance
Medical Devices, Med Tech
Location
Courcelles (Belgium) FTE% 100 %
Job Description
You will join an effective and open team. Together we support the Quality & Compliance of an operational distribution site. We value communication, clear sense of purpose, supporting on another and good understanding of customer's expectations.
The function is based within European distribution center at Courcelles, allowing to be exposed to the operational environment and develop QA operational activities such as shop-floor investigation & inspections. Every team member acts as a single-point of contact for an operational area and supports the area for all quality related topics (eg. gemba-walk, auditing, ..). As quality team we develop and deploy of effective and efficient quality processes that meet customer needs and applicable J&J & Health Authority compliance requirements.
Within the role you will be responsible for the following process:
· RIC ? Restricted Inventory CageProcess improvement! (shape lead)
· EDC traceability & Expiry support
Key Responsibilities
As a member of our team, you will:
Drive a culture of continuous improvement, where team members can identify areas for improvement on daily operational processes to drive data accuracy and global compliance and provide support to implement these initiatives by highlighting and discussing key changes/improvement programs with leadership and the appropriate partners.
Get encouraged and activated by supporting project team activities and guiding them towards compliant project execution
Broaden your network by the involvement in interaction with Franchise Supply Chain and EDC internal Operation.
Expand your knowledge by supporting and/or executing internal and external audits.
Elaborate Key Report on weekly basis and lead monthly franchise call.
Develop a detailed understanding of the distribution processes by being a zone owner and supporting daily operations within that zone (e.g. shop floor quality decision and investigations, root cause analysis, CAPA plans, GEMBA Walk...).
Get challenged by exposure to different type of process and human interactions.
Share your expertise by training & qualifying relevant partners and operators
Evaluate and ensure accurate documentation of applicable quality records and approve accordingly
Strengthen the team by driving process improvements, prioritization, and digitalization
Collaborate with peers in other parts of the EMEA commercial quality organization to improve process excellence, simplification and standardization across distribution sites
Qualification and experience:
3-4 years? experience in the medical device (or relevant) industry
Experience & interest in data analytics and reporting (R/Excell/Tableau/PowerQuery/Sharepoint)
Shown basis in QMS system process (document management, change control, non-conformance, CAPA, standards assessments)
Knowledge of GMP/GDP/ISO regulations
Competences: Strive for optimization, critical thinking, agility & invested in good collaborations with multiple partners
French & English
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