Johnson & Johnson
Jobid=A.0.049
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com.
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
NL020-GATT Headquarters
Job Description:
Key Responsibilities:
- Ensures workload and priorities of the role are aligned with business need.
- Is accountable for Base Business Activities & engineering projects, including remedial actions when applicable.
- Serves as the engineering reviewer/approver for process development studies and validation documentation in alignment with the Engineering Manager (including CSV).
- Represents engineering department for internal and external communication/reporting/meeting either as a standalone responsibility if applicable or as the Engineering Manager’s delegate.
- Maintains connection with other departments as appropriate.
- Provide input into annual budgets and manage project spending.
- Responsible for communicating business related issues or opportunities to next management level.
- For those who supervise/lead or manage a staff, responsible for ensuring that subordinates follow all company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
- Performs other duties assigned as needed.
Qualifications
- University / Bachelor’s Degree, Engineering degree or Equivalent in a Life Science, Process Engineering, or Physical Science. An advanced degree, such as Master degree in a Technical or Science field is preferred.
- Generally requires (4-6) years related experience.
- Statistical and analytical problem solving.
- Strong written and oral communication in English required.
- Experience in the Medical Device industry and GMP.
- Demonstrated knowledge of manufacturing principles and practices, and procedures.
Required Knowledge
- Equipment and Process Validation / Establish Equipment requirements (URS, FAT, SAT)
- Mechanical and automation background with 4 to 6 years in industry, preferred in medical field.
- Capable to interpret the process flow sheets.
- Capable to interpret the vendor maintenance/calibration/qualification reports to verify the effectiveness of the vendor’s work and adopt the outcomes into the process.
- Project management.
- Manufacturing processes improvements
- Lean and/or Six Sigma belt
- Troubleshooting and machine design review
- Proper communication skills; making complex issues easy for others to understand when acting as a core team member in projects.
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