Analytical Chemist (Lab Chemist)

About the Company

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Job Scope

Conduct specific chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials to finished goods and Stability study.

Job Details

• Conduct critical chemical and physical analyses such as raw materials, initial, in-process, final products, stability study.
• Conduct the incoming inspection (visual, dimensional and functional), review the result and release as per timeline.
• Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS system).
• Perform assays requiring precise analytical skills and understanding of chemistry principles.
• Complete all testing, including special project/ protocol testing in a timely and appropriate manner.
• Review the testing result of API, in process, finished product and Stability including result of incoming inspection.
• Maintain data integrity and ensure compliance with company SOPs and USP specifications, FDA, GLP and cGMP regulations.
• Ensure that the test results generated within the Chemistry lab are precise, accurate and completed on time.
• Be responsible for writing validation/Qualification protocols, reports and relevant test methods, new equipment and SOPs.
• Ensure that the test equipment is calibrated and in good condition before use.
• Keep tidiness in laboratory and ensure that the laboratory is properly and safely equipped to the international standard.
• Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
• May perform equipment maintenance and calibrations as required.
• To review the final analysis result of raw materials, finished product, stability result and document which related within chemical Laboratory.

Qualifications

• Bachelor’s degree in chemistry, or related science.
• 3 years’ experience in Analytical Laboratory in a pharmaceutical manufacturing with experience in handling key instruments like HPLC, AAS, UV, FTIR, or any related.
• Having knowledge in method validation, GMP, PIC/S, ISO 9001, ISO13485, Good Laboratory Practices, and ISO 17025 will be an advantage.
• Workable command of English and Computer literacy.
• Flexibility in working hours. (Able to work as shift - Day & Night (50/50) and Overtime).
• Mature with good interpersonal.

Benefit & Welfare

• Base Salary + Fixed Bonus
• Housing Allowance
• Transportation Allowance or Shuttle Van Provided
• OT & Nightshift Allowance
• Canteen
• Variable Bonus
• Group Life & Health Insurance
• Working Mon-Fri 8-5
• Etc.