QC Analytical Support Officer-Pharma

EFOR (formerly Process Engineering Specialists)

Singapore

On-site

SGD 40,000 - 60,000

Full time

17 hours ago
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Job summary

PES International, a global services provider in Life Sciences, is seeking a QC Analyst in Singapore to support calibration, maintenance, and qualification of laboratory instruments.

The role emphasizes GMP compliance, data integrity, documentation, SOPs, audits, and continuous improvement within the QC department.

Qualifications

  • Experience with GMP and data integrity.
  • Ability to maintain equipment logs and documentation.
  • Support SOP development and revisions.

Responsibilities

  • Support routine calibration, maintenance, and qualification of laboratory instruments.
  • Maintain equipment logbooks and documentation.
  • Assist in coordinating equipment servicing and vendor maintenance activities.
  • Ensure laboratory documentation is completed accurately and timely.
  • Assist in preparation and revision of SOPs, forms, and records.
  • Support investigations, deviations, CAPA, and change control activities.
  • Comply with GMP, data integrity, EHS, and quality requirements.
  • Participate in laboratory audits and inspection readiness activities.
  • Support process improvement initiatives within the QC department.

Skills

Equipment management
GMP compliance
Documentation
Lab instrument calibration

Job description

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.

With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.

We are currently looking for QC Analyst to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities
Equipment Management
  • Support routine calibration, maintenance, and qualification activities for laboratory instruments.
  • Maintain equipment logbooks and associated documentation.
  • Assist in coordinating equipment servicing and vendor maintenance activities.
Documentation and Compliance
  • Ensure laboratory documentation is completed accurately and in a timely manner.
  • Assist in the preparation and revision of Standard Operating Procedures (SOPs), forms, and laboratory records.
  • Support investigations, deviations, CAPA, and change control activities when required.
  • Comply with GMP, data integrity, EHS, and company quality requirements.
  • Participate in laboratory audits and inspection readiness activities.
  • Support process improvement initiatives within the QC department.
  • Assist in implementation of laboratory best practices and operational excellence initiatives.

We are currently looking for candidates in Singapore.

To know more about the latest Jobs and Projects we are involved in, please follow us on LinkedIn at https://www.linkedin.com/company/processengineeringspecialists/mycompany/

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

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