Pharma QC Analyst

PROCESS ENGINEERING SPECIALISTS PTE. LTD.; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

An international services company is seeking a QC Analyst to manage analytical testing and ensure compliance with cGxP regulations in Singapore. The role involves conducting tests for various pharmaceutical products and requires strong documentation skills. This is a permanent position offering a chance to work on diverse projects in the Life Sciences Industry.

Qualifications

• Experience in conducting analytical testing for pharmaceuticals.
• Knowledge of data integrity requirements.
• Experience with stability testing and sample storage management is a plus.

Responsibilities

• Conduct analytical testing and document results for pharmaceuticals.
• Ensure adherence to cGxP regulations.
• Perform stability testing and manage sample storage.

Skills

Analytical testing

Documentation of results

Understanding of cGxP regulations

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 a QC Analyst to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities

• Conducting analytical testing and documenting results for API, drug substance, drug product, finished product, complaints, stability, and packaging materials
• Ensuring all activities adhere to cGxP regulations, including data integrity requirements
• Stability testing (when not conducted centrally):
  • Performing stability testing and sample storage management
  • Documenting analytical data for stability samples in accordance with cGxP standards

We are currently looking for candidates in Singapore.

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Sruthi Srikanth ([e-mail]).

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