Job Title

Global Giant in the Life Science SpaceRegulated Industry (Pharmaceutical / Medical Device)6-week Contract / Temp Opportunity with potential to extendWe are currently seeking the services of an experienced Validation Specialist / Document Writer to join a global pharmaceutical company to prepare, review and execute validation protocols within cross functional teams.Key responsibilities include:Review, prepare and write validation protocols for variety of equipment such as filling lines, case packers and palletisers.Review of qualification documentation using QMS and Document Management Systems.Prepare & update GMP SOPs.Collaborate effectively within cross functional project teams to meet strict deadlines.Skills & ExperienceTertiary qualifications in Engineering or Science related discipline.Minimum of 3 years'' Validation / Documentation experience in GMP environment.Sound experience in the pharmaceutical / medical device industry.Solid technical writing skills and attention to detail.Excellent organisational and time management skills.Confident communicator with a demonstrated history of meeting timelines with accuracy.This is an exciting temp / contract opportunity for a pharmaceutical professional to join a major player on a project that requires an immediate start!Working Holiday Visa holders are encouraged to apply!To submit your application in strict confidence, click the ''apply'' button. If you require further information, please contact Voula Triantafillou on0437 853 201. #J-18808-Ljbffr