Contribute to Life Science projects for Antaes Asia clients
Responsible for execution of batch manufacturing instructions in accordance with pre-defined procedures and training.
Ensures batch execution is performed with adherence process critical steps and ensures flawless execution
Provides inputs on operational and process related improvements to achieve site business targets and manufacturing excellence.
Performs technical verification of batch related recipes (POMS and DeltaV), manual operations and adhoc manufacturing documentations
Provides input in design of manufacturing recipe in DCS
Participate in digitalization projects and identify areas for process and operational streamlining
Adheres to safe work environment in accordance with regulatory and global/local EHS policies
Participates in safety risks assessments or participates in process hazard analysis as an operations representative (PHA)
Actively resolve batch related document errors in a timely manner
Communicates all events/issues effectively with relevant stakeholders
Provide inputs for investigation - impact assessment and appropriate CAPA
Ensures overall plant upkeep during the shift and ensuring plant is always in audit ready mode
Oversees deliverables ahead, anticipates complexities and prevents potential
Ensures processes are running as per planned schedule with minimal delays. Highlights effectively to shift supervisor if delays are expected.
Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
Diploma in Chemistry, Chemical Engineering, Science or equivalent
Minimum 2+ years of pharmaceutical, biopharmaceutical experience in Quality and/ or Compliance (GxP) environment
This role would require 12 hour rotating shift (Day/ Night)
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
Excellent communication skills, both written and verbal, in English
