Validation Engineer

11 hours ago

Singapore No deviation Full time $80,000 - $120,000 per year


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.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.

Position Overview

We are looking for a Validation Engineer to manage and execute validation activities, including equipment, utilities, and facility qualifications. You will develop and support the creation of validation documentation, apply a science-based approach to validation, analyze data, and assist with investigating deviations. Collaboration with cross-functional teams and adherence to safety, quality, and regulatory standards are key aspects of this role to ensure the successful delivery of validation projects.

Key Responsibilities

  • Develop, execute, and document protocols (IQ, OQ, PQ) and reports for new qualification.
  • Coordinate the completion of cleaning performance qualification.
  • Investigate and resolve discrepancies/incidents arising from qualification activities.
  • Perform Periodic review Site Validation Maintenance Program, ensuring systems remain in a validated state throughout their lifecycle.
  • Support change control activities, ensuring proper validation assessments and documentation.
  • Support other day-to-day validation activities, ensuring adherence to approved Validation SOPs, Plans, and Policies.
  • Work closely with End-Users, Quality, and Engineering functions to ensure validation activities are completed as planned.

Required Qualifications

  • Fair knowledge and experience of the practical and theoretical requirement of validation program in a GMP facility.
  • Relevant experience in validation of facility, equipment, utility, cleaning, and/or sterilization.
  • Familiarity with Regulatory requirements and Standards (e.g., FDA, EMEA, GAMP and ICHQ7).
  • Ability to read and interpret technical documentation, system specifications, and validation protocols.
  • Strong analytical, problem-solving, and organizational skills.
  • Excellent communication skills and ability to work in a team-oriented environment.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
  • Willingness to learn and adapt in a fast-paced, regulated industry.

Why join us?

  • Generous Leave Policy including 3 days to care for aging family members, reflecting our commitment to family wellbeing.
  • 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.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team

Please submit your resume, outlining your qualifications and experience relevant to the role, here.


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