- Date Listed
- 11 Apr 2016
- Experience Level
- Entry Level / Junior Executive
- Job Period
- Flexible Start, For At Least 3 Months
- Profession
- Engineering
- Industry
- Others
- Location Name
- West Region
- Company Profile
Kimberly-Clark and its well-known global brands are an indispensable part of life for people in more than 175 countries. Every day, 1.3 billion people - nearly a quarter of the world's population - trust K-C brands and the solutions they provide to enhance their health, hygiene, and well-being. With brands such as Kleenex, Scott, Huggies, Pull-Ups, Kotex, and Depend, Kimberly-Clark holds No.1 or No. 2 share positions in more than 80 countries. With more than 140 years of history of innovation, we believe in recruiting the best people and empowering them do their best work. If fresh thinking and a passion to win inspire you, come Unleash Your Power at Kimberly-Clark.
Kimberly-Clark is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity or any other characteristic protected by law.
- Job Description
- Job OverviewIn Kimberly Clark Singapore, our goal is to provide a well-rounded program around the Product and Engineering Activities which supports the ASEAN region. The Process Engineer (Validation) intern’s core competency revolves around the support of a new Process Plant upgrade qualification and the functional support around this system. This role will be based in Kimberly Clark Manufacturing Plant at Tuas.Key ResponsibilitiesPlan, Prepare, Coordinate and Monitor Engineering ProjectsAssist with development of validation protocols, SOP and methodology in accordance to regulatory guidelinesCoordinate and Collaborate with various Vendors and Engineering team membersEssential RequirementsEngineering Undergraduate majoring in Pharmaceutical, Bio-medical or ChemicalAble to interpret Process drawings, Mechanical drawings and P&IDGeneral understanding of GMP, ISO 9001, ISO 22716, U.S.Pharmacopeial Standards #61 or of similar nature
FDA Validation Protocol Standard or of its equivalence
Relevant Industrial Experience will be advantageous
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