Pharmaceutical Technologist

ANTAES ASIA PTE. LTD.; Singapore; On-site; SGD 36,000 - 47,000; Full time

Job summary

ANTAES ASIA PTE. LTD. is seeking a batch manufacturing professional to support life science projects. You will execute batch instructions, verify recipes in POMS/DeltaV, and ensure compliance with predefined procedures while actively pursuing process improvements.

The role requires a Nitec or Diploma in Chemistry or related field and 2+ years in a GxP environment, with a 12-hour rotating shift. Strong English communication and teamwork are essential.

Qualifications

• Diploma or Nitec in Chemistry/Chemical Engineering/Science or equivalent.
• 2+ years pharmaceutical/biopharmaceutical experience in Quality and/or Compliance (GxP).
• Able to work a 12-hour rotating shift (Day/Night).
• Strong organizational, written and spoken English skills.

Responsibilities

• Contribute to Life Science projects for Antaes Asia clients.
• Execute batch manufacturing instructions per defined procedures and training.
• Ensure batch execution adheres to critical process steps and flawless execution.
• Provide input on process improvements to meet targets and manufacturing excellence.
• Perform technical verification of batch-related recipes and documents.
• Participate in design of manufacturing recipes in DCS and support digitalization projects.
• Maintain a safe work environment per EHS policies and participate in risk assessments.

Skills

Batch manufacturing

Education

Nitec/Diploma in Chemistry or related

Job description

Job Description:

-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 asper 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:

Nitec/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