Quality Control Associate Specialist — Hybrid/Pharma QC

MSD Malaysia; Carlow; Hybrid; EUR 60,000 - 80,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

MSD Carlow is seeking an Associate Specialist in Quality Control to support QC operations, documentation, deviations, investigations, and cGMP compliance across the manufacturing site. The role emphasizes data integrity, Right First Time, and effective document lifecycle management.

You will contribute to NPI, tech transfers, and lifecycle activities from a QC perspective, review testing documentation, and mentor colleagues in compliant documentation and continuous improvement.

Qualifications

• Bachelor's degree in Analytical Chemistry/ Biochemistry or closely related field.
• 4+ years of cGMP Quality Control experience in pharma/biopharma.
• Experience with HPLC and ELISA systems and related software.

Responsibilities

• Perform and support QC activities with data integrity and QMS alignment.
• Review testing documentation and ensure regulatory compliance and QA readiness.
• Support deviation investigations using root cause analysis and CAPA.
• Assist with NPI, tech transfers, and lifecycle QC activities.
• Mentor peers to prepare compliant, high‑quality documentation.

Skills

ELISA

GMP

HPLC

Regulatory compliance

Quality systems

Education

Bachelor's degree in Analytical Chemistry/ Biochemistry

Tools

LIMS

ELN systems

Job description

MSD Carlow is seeking an Associate Specialist in Quality Control to support QC operations, documentation, deviations, investigations, and cGMP compliance across the manufacturing site. The role emphasizes data integrity, Right First Time, and effective document lifecycle management.

You will contribute to NPI, tech transfers, and lifecycle activities from a QC perspective, review testing documentation, and mentor colleagues in compliant documentation and continuous improvement.