Industrial Engineer Intern
at Johnson Johnson
Cape Town, Western Cape, South Africa -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 15 Sep, 2024 | Not Specified | 17 Jun, 2024 | N/A | Business Ethics,Process Flow,Logical Approach,Operators,Written Communication | No | No |
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Description:
WHO WE ARE
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, BENYLIN®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.
PROCESS KNOWLEDGE
- Understand process flow
- Understand process controls as well as risks
- Understand technically the equipment and optimization requirements
- Understand process/product cost structure
- Support training to operators
Responsibilities:
Support production (dispensary, manufacturing, packaging and distribution) processes to ensure these that these processes are optimized, reliable and efficient under the direct supervision of a senior engineer.
Four different pillars to achieve the above goal:
- Day-to-Day Support: The Industrial Engineer Intern (IE) is responsible to properly support the production area to ensure optimized performance and processes.
- Process Knowledge: The IE must understand the production processes for which he/she is responsible. This scopes scientific understanding of the process, knowhow on production equipment within the process and identifying risks to ensure execution in compliance.
- Product Stewardship: This pillar scopes basically the ownership of the product as well as the GMP documentation in responsibility. The IE will monitor the processes to ensure they are capable and in control, will lead or coordinate any changes (change controls, transfers, etc) and will lead or participate in root cause investigations in case deviations occur.
- Continuous Improvement: The IE should lead actions to improve the production processes and achieve leaner and more efficient practices. For this, the IE will identify improvement areas, evaluate risks and execute following Good Documentation Practices e.g., Change Control.
Key Responsibilities
Based on the four pillars;
Day-to-Day Support:
- Ensure that procedures and process within area of responsibility are performed in accordance with relevant Standard Operating Procedures, Work Instructions and current Good Manufacturing Practices.
- Drive and support close out of all relevant compliance related audit findings.
- Responsible for performing line-openings and in process checks according to legislative and company requirements.
- Update GMP documents (SOP, WI, PPI and PI etc), as required and train accordingly.
- Ensure effective communication to all relevant parties.
- Ensure all production documentation and processes are completed as per cGMP guidelines.
- Drive operator asset care with effectiveness checks.
- Drive root cause analysis.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Proficient
1
Cape Town, Western Cape, South Africa