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Job Function:
Supply Chain EngineeringJob Sub Function:
Chemical EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Geel Antwerp BelgiumJob Description:
Johnson & Johnson Innovative Medicine Supply Chain Manufacturing Science and Technology (MSAT) Geel is recruiting a Cleaning Science Engineer. This role is focusing on the cleaning processes in our small molecule drug substance Geel site and is located in Geel Belgium. Janssen Geel is the largest internal chemical manufacturing site of Active pharmaceutical ingredients (API) and spray dried powders (SDP) in the internal Johnson & Johnson network
The cleaning science engineer supports our cleaning processes. Performing robust cleaning processes according to the latest standards introducing process optimizations supporting new product and technology introductions supporting issue management from a science perspective and overall performance management are key objectives in this role.
This position strongly contributes to the global Small Molecule Drug Substance (SM DS) MSAT strategy and the productivity performance of the Geel site. The Cleaning science engineer is a team member of the Geel site MSAT team and is expected to have a strong cross functional collaboration mindset.
The key responsibilities are as follows:
Own cleaning processes to meet Safety quality environmental and cost standards
Life cycle management of cleaning processes for execution in production systems (MES SAP (future Transcend))
SPOC to the business owners QA during audits for cleaning recipes protocols and reports but also leading root cause problem solving for cleaning process related issues
Support of the Cleaning Science Lab for rapid investigational support and continued process improvements
Use innovation and PAT technologies for continuous improvement of cleaning processes
support the CIP/Cost avoidance targets focusing on cleaning processes
Maintain Gantts of cleaning processes
Assess CCs/define actions for process/equipment changes
Support equipment specific studies as input for cleaning validation e.g. Impact assessment cleaning (FMEA) Equivalency studies cleaning Cleaning boundary studies.
Review cleaning VMP / protocols / reports / trend reports / cleaning quality reviews delivered by validation team
Closely collaborate with the site-based validation team the global cleaning community of practice and site-based stakeholders (Operations QA Planning MAM Development)
Reviewing of Cleaning Quality Reviews (CQR)
Support equipment specific studies as input for cleaning validation e.g. Impact assessment cleaning (FMEA) Equivalency studies cleaning Cleaning boundary studies.
Qualifications:
Masters Degree or PhD preferably in Chemical engineering or process technology (bioengineering industrial engineering or chemistry) or proven record in an industrial operational environment.
Solid understanding of API manufacturing.
Affinity and pronounced interest with data analytical tools and proven understanding in chemical synthesis.
Ability to lead and encourage teams strong interpersonal skills e.g. influencing and handling conflicting interests.
Able to take decisions autonomously. Strong skills in communication and a result driven personality.
Strong analytical skills high level of accuracy good acumen on cost improvements.
Owns good project management organizing planning and coordination skills. Experience in process excellence lean production concepts and tools (certification is a plus).
Develops strong collaborations with internal and external business partners.
Big picture orientation with attention to detail able to operate in two worlds at one time sees the why as well as the what; can zoom in or out as needed.
Working knowledge of English (both verbally and written) and Dutch (or willing to develop proficiency in Dutch)
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Required Skills:
Preferred Skills:
Required Experience:
IC
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