This position reports into the Production Lead and is based in our Cape Town, South Africa location.
Who We Are
At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, were the house of iconic brands - including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSONS 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 futureand yours. For more information, click here .
Support production (dispensary, manufacturing, packaging and distribution) processes to ensure these that these processes are optimised, reliable and efficient under the direct supervision of a senior engineer.
- 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.
- 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
- Understand process flow
- Understand process controls as well as risks
- Understand technically the equipment and optimisation requirements
- Understand process/product cost structure
- Support training to operators
- Ensure GMP, EHS and Quality compliance during the execution of the Plan and all related tasks. Ensures compliance with work instructions according to the relevant SOP's
- Perform in process audits both planned and ad hoc accordingly to ensure that GMP standards are met and maintained.
- Support regulatory with technical documents
- Good planning and administrative competencies
- Good verbal and written communication
- Logical approach to problem solving and trouble shooting
- High work standards and business ethics
- Must be available to work shifts if required
Primary Location
Europe/Middle East/Africa-South Africa-Western Cape-Cape Town
Job Function
Administration
Organization
Johnson & Johnson (Proprietary) Limited
Job Qualifications
- In process Btech/B Eng (Industrial/Chemical Engineering)
