Senior Pharma Manufacturing Technologist — 12-Month Contract

Manpower Staffing Services (Singapore) Pte Ltd; Singapore; On-site; SGD 90,000 - 120,000; Full time

Benefits offered by this job

12 months contract

On-site Tuas

Job summary

Manpower Staffing Services (Singapore) Pte Ltd is seeking an experienced pharmaceutical manufacturing professional to operate equipment and execute processes in a cGMP environment. The role requires hands-on operation of manufacturing lines, documentation, and adherence to production schedules.

You will manage batch records, qualify equipment, and maintain GMP standards in a fast-paced facility located in Tuas, Singapore. 12-month contract with a focus on quality, accuracy, and teamwork.

Qualifications

• Diploma or degree in Pharmaceutical Science, Chemical Engineering, Life Sciences, or related field.
• Minimum 8+ years in pharmaceutical manufacturing operations.
• Solid knowledge of cGMP, batch record documentation, and deviation management.

Responsibilities

• Operate pharmaceutical manufacturing equipment and execute drug product manufacturing processes in compliance with cGMP and production schedules.
• Execute drug product manufacturing operations including dispensing, blending, granulation, compression, coating, and filling.
• Operate and perform basic maintenance on pharmaceutical manufacturing equipment.
• Complete batch records, logbooks, and GMP documentation accurately and in real-time.
• Perform in-process controls, sampling, and checks as specified in batch records.
• Maintain cleanliness and GMP compliance in production areas.
• Identify and report process deviations, equipment malfunctions, and safety concerns.
• Attend and apply GMP training programs.

Skills

cGMP knowledge

Batch records

Deviation management

Drug product manufacturing

Education

Diploma or Degree in Pharmaceutical Science

Chemical Engineering

Life Sciences

Tools

Pharma manufacturing equipment

Job description

Manpower Staffing Services (Singapore) Pte Ltd is seeking an experienced pharmaceutical manufacturing professional to operate equipment and execute processes in a cGMP environment. The role requires hands-on operation of manufacturing lines, documentation, and adherence to production schedules.

You will manage batch records, qualify equipment, and maintain GMP standards in a fast-paced facility located in Tuas, Singapore. 12-month contract with a focus on quality, accuracy, and teamwork.