Job Description

Job Outline: 1. To manage clinical affair matters within Xepa-Soul Pattinson (Malaysia) Sdn Bhd 2. To perform trial monitor during the conduct of bioequivalence (BE) / clinical studies 3. To perform Research and Development work leading to formulation development of new products and/or reformulation projects. 4. To coordinate stability study arrangement for new products and/or reformulation projects. 5. To liaise with internal clients including Innovation & Development (I&D), Technical Services, Regulatory Affairs, QA/ QC and Material/ Procurement Departments and sometimes part-take in meeting with external clients, including clinical research organizations (CROs) as well as raw material vendors for activities relevant to new product development (NPD). 6. To support Regulatory Affairs in dossier preparation. 7. To assist in management of analytical section within I&D. Minimum Requirements: 1. Bachelor\'s degree in pharmacy; preferably with at least two years of experience in pharmaceutical manufacturing, formulation and/or quality control. 2. Good presentation and communication skill. 3. Able to work well in a team environment.
Founded in 1967 in Singapore, Xepa has grown and evolved at the cutting edge of the industry. From our modest first years when Xepa Laboratories Pte. Ltd. produced a limited range of pharmaceutical products in a small flatted factory, we have relocated twice to larger manufacturing plants in Melaka, Malaysia. Today, Xepa is the leading manufacturer of off-patent pharmaceuticals in Malaysia.
Bachelor\'s or Equivalent