UNIMED SDN. BHD. (UNIMED) is a pharmaceutical company incorporated in the year 1981. With close to 40 years of experience in the healthcare industry, our primary business is focused in importing, marketing and distributing quality generic pharmaceutical finished formulations, nutraceutical, medical devices and various herbal & supplement products at a cost-effective option for our valued partners and customers


Senior Executive - Analytical


Roles and Responsibilities

  1. Fundamental knowledge and minimum 2 years actual HPLC analysis experience in pharmaceutical formulation company
  2. Writing laboratory investigations such as OOS, OOT, analytical incidents.
  3. Exposure to current pharmacopoeia and ICH guidelines
  4. To test R & D samples
  5. Provide analytical support to In-process production samples, process validation samples, routine analysis of RM, finished products and compilation of report / CoA.
  6. Trouble shooting HPLC analysis and its remedies.
  7. Maintain cGLP levels in all activities of analysis.
  8. Preparation of analytical method validation protocol and report
  9. Maintain HPLC logbook, working standard consumption record
  10. To execute any instruction issued by plant head.

General Requirement


Qualification: B. Pharm / M. Pharm

Experience: 2 3 years experience

Gender: Male

Age: up to 35 years




Production Executive




Roles and Responsibilities


  1. Good experience in R & D product development and process production for eye drops, eye suspension, eye ointment related areas
  2. Conduct literature search for assigned projects.
  3. Procure RM, PM excipients and innovator samples for related products under development through seniors / purchase dept.
  4. Execute drug product scale up batches from lab scale / pilot scale / stability studies / exhibit batches.
  5. Record and report sufficient production data for development batches.
  6. Co-ordinate with QA, QC, production and engineering for process validation batches and compile BMR, process validation protocol and report.
  7. Finalize finished product specification in liaison with QA, QC, production and engineering.
  8. Perform pre-formulation and formulation trials for robust formulation.
  9. To compile technology transfer documents like Master Formula Record (MFR), Pharmaceutical Development Report (PDR) and facilitate its execution.
  10. Review analytical reports of raw materials and finished products and conclude with comments.
  11. Co-ordinate with analytical development lab, QA, QC, RA and production for product related activities.
  12. Prepare SOPs, BMR and system related documents like FP specification, stability specs.
  13. To schedule production activities for eye drops, eye suspension, eye ointment and ensure its smooth execution.
  14. To plan the manpower requirements for each section with HR and ensure its availability.
  15. To deliver the planned production quantity and / or to take corrective reschedule action to utilize the resources efficiently.
  16. To guide and direct junior staff to yield optimum batch wise output.
  17. To adopt online completion of production records and get it timely approved by QA.
  18. To execute any instruction issued by plant head.


General Requirement


Qualification: B. Pharm / M. Pharm

Experience: 1-2 years experience in formulation eye drops, eye suspension, eye ointment

with 2-3 years’ experience in production.

Gender: Male

Age: up to 35 years


Email: recruitment@unimed.com.my

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