Contamination Control Specialist (6 months contract)

No deviation; Singapore; On-site; SGD 90,000 - 150,000; Full time

Benefits offered by this job

Generous leave policy

Health & wellness coverage

Professional development

Inclusive culture

Job summary

No Deviation seeks a dedicated contamination control professional to support sterile product quality and GMP compliance. The role involves monitoring microbiological data, leading investigations, and driving CAPAs within a cross-functional team.

You will contribute to validation activities and trend analysis to strengthen the contamination control program. The incumbent will engage shop-floor leadership, review monitoring data, and propose improvements to uphold product quality and inspection

Qualifications

• Sterility assurance and microbiological/contamination control experience in pharma/biotech.
• Ability to review documentation and ensure compliance with SOPs and quality standards.
• Knowledge of GMP and regulatory requirements for sterility and microbiological control.
• Strong communication with multiple functions and management.
• Ability to lead investigations with a cross-disciplinary team.

Responsibilities

• Lead as SME for contamination control subject area and SOPs.
• Conduct risk assessments related to contamination control.
• Oversee site activities and performance for contamination control systems.
• Lead investigations, CAPA proposals, and effectiveness checks.
• Collaborate with cross-functional teams to ensure product quality.
• Ensure presence on the shop floor to monitor practices vs SOPs.

Skills

Sterility assurance

Microbiological control

GMP compliance

CAPA investigations

Data analysis

Communication

Job description

About No Deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

Position Overview

This role is responsible for supporting the site's contamination control and sterility assurance programme by monitoring microbiological and environmental data, leading investigations and CAPAs, conducting risk assessments, and ensuring GMP compliance. Working closely with cross-functional teams, the incumbent drives contamination control improvements, supports validation activities, and helps maintain product quality and inspection readiness.

Key Responsibilities

• Leading as SME for specific subjects as part of the Contamination Control SOP in her/his area of expertise
• Conducting risk assessments related to contamination control
• Overseeing site activities and performance for contamination control systems in her/his scope of responsibilities
• Leading investigation following contamination control failures and proposing corrective and preventive actions (CAPA)
• Collaborating with cross-functional teams to ensure product quality
• Ensuring presence on the shop floor to oversee practices, identify gaps vs SOP for contamination control
• Reviewing data from contamination control monitoring to propose improvements as necessary (from monitoring and trends)
• Supporting the preparation of validation protocol and supporting projects related to her/his area of expertise
• Perform microbiological trend analysis for environmental monitoring (EM), utilities, personnel monitoring, and contamination control programme
• Analyze microbiological investigation data to identify trends, recurring issues, and potential contamination risks
• Prepare and present contamination control trend reports, providing meaningful insights and recommendations
• Lead or support microbiological investigations, including root cause analysis (RCA), CAPAs, and effectiveness checks

Required Qualifications

• Experience in sterility assurance and microbiological or contamination control within a pharmaceutical or biotechnology environment
• Ability to meticulously review and analyze documentation, processes, and products to ensure compliance with the global operating procedures and Quality standards
• In-depth knowledge of regulatory requirements and Good Manufacturing Practices (GMP) relevant to sterility assurance and microbiological control
• Communication skills to communicate with a large number of functions (from shopfloor to management) and to present complex subjects
• Ability to organize and lead routine investigations with a multi-disciplinary team

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.