Process Assistant (Compression)

About us Novugen is a wholly owned subsidiary company of a UAE-based group, SciTech International. With over 30 years of experience in the healthcare industry, the company is equipped with vast experience in venturing into strategic healthcare businesses and development of world-class healthcare facilities around the globe. We bring hard-to-source and technology intensive products to the market. Our manufacturing facility in Bandar Enstek, Negeri Sembilan is the FIRST USFDA approved pharmaceutical manufacturing facility in Malaysia and the only in Southeast Asia. We are also the first pharmaceutical company in the region to be vertically integrated from API to Finished Products R&D and manufacturing. The people behind Novugen are professionals coming from diverse backgrounds and nationalities from all over the world, working together to achieve one common goal. We strive to innovate new concepts to accelerate the launch of pharmaceuticals that lack robust generic alternatives due to their complexity. Our vision is to be the largest and fastest growing pharmaceutical company in Southeast Asia by 2025, competing in global markets. Through our passionate teams and continuous investment in R&D, we aim to provide early access to affordable medicine of the highest quality. This is our commitment to change lives worldwide. About the role The Process Assistant is responsible for operating and maintaining production machinery, ensuring compliance with SOPs, GMP, and safety guidelines. The incumbent must be able to perform in-process tests, document records, troubleshoot issues, and meet production schedules. The role also involves assisting with minor machine repairs and adapting to other production activities as required. Key Responsibilities: - Control o To strictly adhere to SOP, GMP and Safety procedures. In any event of any accident, ensure it is reported to the superior and Safety Officer. Training o To ensure relevant training both theoretically and practically (on-the-job) on GMP and SOP procedures are adhered to. Planning/Productivity o To ensure production work floor able to meet the monthly/weekly/daily schedule and given production productivity target. At same time quality assurance guideline must be followed adequately. o To operate, handle and clean the OSD machineries. o To ensure line clearance is completed before starting any process. o To carry out the in-process tests and record the data into BMR. o To troubleshoot the problematic products in given section as instructed by Line Leader or Supervisor. o To perform minor repair of machine under supervision of Line Leader. o To inform Line Leader if encountered machine breakdown event. Documentation o To ensure all the documents under his/her responsibilities are filled up correctly and in timely manner (e.g. BMR, Line Clearance, Logbook) Job Requirements: o Technical Certificates or Diploma in Pharmaceutical, Engineering or equivalent. o Minimum 1-3 years of experience in a manufacturing environment, preferably in pharmaceuticals or a related industry. o Knowledge and experience in adhering to GMP and SOP guidelines in a production setting. o Experience in completing and maintaining accurate production documentation o Applicants must be willing to do shift work