QA Csv Contractor

il y a 2 jours


Geel, Belgique J&J Temps plein

**QA CSV Contractor / Quality Assurance Computer System Validation**

**Location**:Geel, Belgium - Hybrid working - 3 days a week on site

**Duration**: 12 months

**Hours**: 40 hours

Imagine your next project working as a QA CSV Contractor for Johnson & Johnson.

Support the QA Engineering department at J&J Geel in assuring that all CSV related regulatory and procedural requirements are fulfilled during the complete life cycle (concept, project, operational and retirement phase) for Geel manufacturing automation systems.

**roles and responsibilities**
- Review and approve CSV documents & CSV records such as SOPs, user requirements, impact/risks analysis’s, test plans, test scripts, change controls, CAPA’s etc ) in order to maintain compliance to regulations, guidelines, and J&J policies and standards.
- Be part of engineering teams and interact with other groups for the introduction of new/upgraded systems and processes. To give advice and support for the preparation of CSV related activities and guard the cGMP aspects.
- Address and follow-up of deviations occurred during execution of CSV activities.
- Communicate status (quality&compliance, planning, ) towards J&J QA Qualification team members.

**how to succeed**
- ** Fluent in English & Dutch (written and spoken)**
- Experience in chemical and/or pharmaceutical industry with respect to CSV of manufacturing automation systems.
- Knowledge of cGMP regulations and guidelines.
- Capacity to ‘translate’ technical information into information that can be understood at every level of the organization.
- Being able to correctly estimate the urgency, criticality and impact of decisions related to the function.
- Ability to multi-task and work on a variety of projects at one time.
- Ability to work independently and work in cross-functional team environment.
- Good communication skills.
- Manufacturing automation systems used within pharmaceutical or chemical industry (f.e. DeltaV).
- Problem report, change request systems. (f.e. Comet)
- Document Management systems (f.e. TruVault)
- Test tools (f.e. Kneat)

**benefits**

This role offers a very competitive hourly rate. This contract will run for **12 months.**

**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 Innovative Medicine**

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

**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”.


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