Pharmaceutical Technician (CCP for Biomedical Manufacturing Industry)

MSD INTERNATIONAL GMBH (Singapore Branch)

Singapore

On-site

SGD 36,000 - 58,000

Full time

14 days+
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Job summary

MSD INTERNATIONAL GMBH (Singapore Branch) is seeking a routine operations specialist to execute scheduled manufacturing tasks, ensure precise documentation, and meet performance metrics. You will participate in GMP walk downs and maintain up-to-date information on digital boards while upholding housekeeping standards.

The role requires 1–3 years of experience, a Diploma or Technical School education, and willingness to rotate day/night shifts.

Qualifications

  • Diploma or Technical School graduate with background in operations and maintenance environment.
  • Willing to work in 12 hours rotating shift (day/night).
  • 1 to 3 years of working experience.

Responsibilities

  • Complete all assigned operations with accurate documentation and meet performance metrics.
  • Participate in GMP walk downs when assigned and update digital boards accurately and timely.
  • Maintain good facility housekeeping and communicate effectively during shift handovers.
  • Complete batch sheet updates and reviews; back-validate batch sheets when assigned.

Skills

Attention to detail
Communication skills

Education

Diploma or Technical School

Job description

Routine Operation
  • Responsible for completing all assigned operations, ensuring accurate and timely documentation
  • Completion on modules.
  • Meet performance metrics of the assigned operations.
  • Participates in GMP walk down if assigned.
  • Provides accurate information to digital boards and ensures all digital boards are updated in a timely manner.
  • Responsible for maintaining and ensuring good facility housekeeping.
  • Effectively communicates during shift handover.
  • Completed batch sheet updates, completes batch sheet reviews and checks back batch sheets when assigned.
Non Routine Operation / Campaign turnaround Activities
  • Responsible to perform OQ/PQ and support IQ when assigned.
  • Be a backup for Production Lead & SIC after completing the required training.
  • Technical competence of a 02 and the additional SME knowledge in at least one of the modules.
Incident, Event, Atypical and Customer Complaint Investigations
  • Provides and raises effective notification for all events and atypical.
  • Facilitate problem solving from initiation to completion or rejection.
  • Provide technical support in the area of work.
  • Support in data collection to assist investigations.
  • Participates in investigation when assigned and provide inputs on preventive action.
Quality/ SHE Stewardship
Quality
  • Ensures manufacturing related activity is completed according to established procedures and all associated documentation is completed to a high standard.
Safety, Health & Environment
  • Ensures compliance to all Safety and cGMP requirements and participates as ERT team member when assigned.
  • Highlights "Near Miss" and other improvement ideas for work environment.
People Excellence
Self
  • Exhibit a positive attitude and provide constructive feedback & solutions to issues /opportunities in the work place. '
  • Responsible to participate in improvement projects and actively generate ideas.
  • Develops and updates on career path with manager, which is aligned with Performance Management Process.
  • Ensures both operational knowledge and technical skills are maintained and compliant against individual training requirements.
  • Use Tier process and other opportunities to engage positively with others to improve both communication + teamwork skills.
Qualification:
  • A Diploma or Technical School graduate with background in operations and maintenance environment.
  • Must be willing to work in 12 hours rotating shift (day/night).
Experience:
  • 1 to 3 years of working experience.
Leadership, Professional and Functional Competencies*
  • Refer to Career Framework Competency Model.
Other Personal Attributes*:
  • Understand and follow safety procedures/practices.
  • Willing to work in a cGMP working environment.
  • Has a good writing and communication skill.
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