Senior Pharma Manufacturing Specialist (cGMP)

Manpower Staffing Services (Singapore) Pte Ltd; Santo Niño 1st; On-site; PHP 6,869,000 - 9,814,000; Part time

Job summary

Manpower Staffing Services (Singapore) Pte Ltd seeks an experienced pharmaceutical manufacturing professional to operate equipment and execute drug product processes in a cGMP environment at the Tuas site. You will ensure real-time documentation, batch records, and compliance with production schedules.

The role requires 8+ years in pharmaceutical manufacturing, strong knowledge of cGMP, and hands-on experience with equipment. Fast-paced GMP setting experience and teamwork are essential.

Qualifications

• Diploma or Degree in Pharmaceutical Science, Chemical Engineering, Life Sciences, or related field.

Responsibilities

• Operates pharmaceutical manufacturing equipment and executes drug product manufacturing processes in compliance with cGMP requirements 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
• Participate in equipment qualification and cleaning validation activities
• Attend and apply GMP training programs

Skills

cGMP knowledge

Batch records

Deviation management

Communication

Attention to detail

Education

Pharmaceutical Science

Chemical Engineering

Life Sciences

Job description

Manpower Staffing Services (Singapore) Pte Ltd seeks an experienced pharmaceutical manufacturing professional to operate equipment and execute drug product processes in a cGMP environment at the Tuas site. You will ensure real-time documentation, batch records, and compliance with production schedules.

The role requires 8+ years in pharmaceutical manufacturing, strong knowledge of cGMP, and hands-on experience with equipment. Fast-paced GMP setting experience and teamwork are essential.