QC Analytical/Microbiology Lead

No deviation Pte Ltd; Singapore; On-site; SGD 180,000 - 240,000; Full time

Job summary

No deviation Pte Ltd is seeking a QC Analytical/Microbiology Lead to direct all QC analytical chemistry and microbiology activities across project execution and operational readiness. You will shape sampling strategies for process validation, utilities and water/WFI systems qualification, environmental monitoring, and cleaning validation.

As the SME for QC analytics, you will oversee method transfer and validation, equipment readiness, SOPs, and sampling plans, ensuring cGMP/data integrity and

Qualifications

• Bachelor's or master's degree in a related scientific discipline.
• Minimum 8+ years in pharma/biotech/biologics/sterile manufacturing.
• Experience across QC Analytical Chemistry and Microbiology functions.
• Experience supporting qualification, validation, PPQ, and commercial manufacturing.

Responsibilities

• Lead QC analytical and microbiology sampling to support project execution and readiness.
• Develop sampling strategies for process validation, utilities qualification, water/WFI systems, environmental monitoring, and cleaning validation.
• Coordinate lab activities across commissioning, qualification, PPQ, and manufacturing start-up.
• Oversee method transfer, verification, qualification, and validation programs.
• Lead quality investigations (OOS/OOT/deviations/CAPAs) and drive corrective actions.
• Collaborate with CQV, Manufacturing, Engineering, MSAT, Validation, and QA across projects.

Skills

QC Analytical Chemistry

Microbiology

Project Leadership

Regulatory Compliance

Education

Bachelor's or Master's Degree in Microbiology/ Biotechnology/ Pharmaceutical Sciences

Job description

Position Overview

The QC Analytical/Microbiology Lead will direct all QC analytical chemistry and microbiology activities supporting project execution and operational readiness. This role develops sampling strategies for process validation, utilities and water/WFI systems qualification, environmental monitoring, and cleaning validation, while coordinating lab activities across commissioning, qualification, PPQ, and manufacturing start-up. As the QC subject matter expert, the Lead oversees method transfer and validation, laboratory equipment and resource readiness, SOP and sampling plan development, and ensures compliance with cGMP and data integrity standards. The role also leads quality investigations (OOS/OOT/deviations/CAPAs) and serves as the primary QC representative across cross-functional teams including CQV, Manufacturing, Engineering, MSAT, Validation, and QA.

Key Responsibilities

Project Leadership & Operational Readiness

• Lead all QC analytical and microbiology sampling activities to support project execution, operational readiness, and successful milestone delivery.
• Develop and implement comprehensive sampling strategies for process validation, utilities qualification, water systems, WFI systems, environmental monitoring programs, and cleaning validation activities.
• Coordinate laboratory activities to support commissioning, qualification, validation, process performance qualification (PPQ), and manufacturing start-up activities.
• Identify project risks related to sampling, testing, laboratory capacity, and resource constraints, implementing mitigation plans to maintain project timelines.
• Ensure all testing activities align with project schedules, regulatory expectations, and business objectives.

Analytical & Microbiology Technical Leadership

• Provide technical leadership for analytical chemistry and microbiological testing activities.
• Support method transfer, method verification, method qualification, and analytical method validation programs.
• Serve as the subject matter expert (SME) for QC analytical and microbiology operations during project execution.
• Review and interpret analytical and microbiological data to support qualification, validation, and product release activities.
• Troubleshoot technical issues and provide scientific guidance for complex testing requirements.

Laboratory Readiness & Compliance

• Ensure laboratory readiness by overseeing:
  • Laboratory equipment qualification and readiness
  • Analytical and microbiological methods
  • Standard Operating Procedures (SOPs)
  • Sampling plans and protocols
  • Consumables and inventory management
  • Sample management systems
  • Laboratory resource and testing capacity planning
    
• Ensure all laboratory activities are performed in accordance with cGMP, Data Integrity, ALCOA+ principles, and applicable regulatory requirements.
• Support audit and inspection readiness activities, including regulatory, customer, and internal audits.

Quality Systems & Investigations

• Review and approve analytical and microbiological testing results and reports.
• Lead or support investigations related to:
  • Out-of-Specification (OOS) results
  • Out-of-Trend (OOT) results
  • Deviations
  • Laboratory investigations
  • CAPAs
    
• Perform root cause analysis and implement effective corrective and preventive actions.
• Support continuous improvement initiatives to enhance laboratory performance, compliance, and operational efficiency.

Cross-Functional Collaboration

• Collaborate closely with:
  • CQV (Commissioning, Qualification & Validation)
  • Manufacturing Operations
  • Engineering
  • MSAT
  • Validation
  • Quality Assurance
  • Regulatory Affairs
    
• Ensure timely communication and coordination of sampling and testing activities across project teams.
• Act as the primary QC representative for project meetings, readiness reviews, and technical discussions.

Required Qualifications

Education

• Bachelor's Degree or Master's Degree in Microbiology, Biotechnology, Pharmaceutical Sciences, Chemistry, Biochemistry, Life Sciences, or a related scientific discipline.

Experience

• Minimum 8+ years of experience within pharmaceutical, biotechnology, biologics, vaccine, or sterile manufacturing environments.
• Demonstrated experience across both QC Analytical Chemistry and Microbiology functions.
• Experience supporting major capital projects, facility start-ups, technology transfers, or new manufacturing facilities is highly preferred.
• Proven experience supporting qualification, validation, PPQ, and commercial manufacturing activities.
• Experience with GMP-regulated laboratory operations and quality systems.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.