Environmental Monitoring (EM) Sampler

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

The Environmental Monitoring (EM) Sampler is responsible for performing routine environmental monitoring activities within GMP-regulated manufacturing and laboratory environments to ensure compliance with quality and regulatory standards. This role supports aseptic manufacturing operations by collecting viable and non-viable environmental samples, maintaining accurate documentation, and ensuring data integrity. The EM Sampler plays a key role in monitoring controlled environments, supporting investigations, and upholding contamination control practices.

Key Responsibilities

• Perform routine environmental monitoring in classified cleanroom areas (Grade A/B/C/D), including active air, passive air, surface, and personnel sampling.
• Execute sampling activities in accordance with approved SOPs, GMP requirements, and safety procedures while applying proper aseptic techniques.
• Label, handle, transport, and document samples accurately to ensure traceability and data integrity.
• Prepare, clean, disinfect, and perform calibration checks on sampling equipment before and after use.
• Support documentation review, trend analysis, deviation investigations, and follow-up actions related to environmental monitoring excursions.
• Maintain housekeeping standards in sampling and storage areas and ensure compliance with GMP, EHS, and data integrity requirements.
• Participate in internal and external audits or regulatory inspections as required.

Required Qualifications

• Diploma or Degree in Life Sciences, Microbiology, Biotechnology, or a related discipline.
• 1–3 years of experience in pharmaceutical or biotechnology manufacturing, preferably within aseptic or cleanroom environments.
• Fresh graduates with relevant internship or industrial attachment experience are encouraged to apply.
• Familiarity with GMP principles, environmental monitoring practices, and aseptic techniques.
• Strong attention to detail with the ability to maintain accurate documentation and follow established procedures.
• Good communication and teamwork skills, with the ability to work effectively in a regulated manufacturing environment.

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.

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.