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Niche GMP commissioning and project execution skills create moderate applicant density.
Role requires pharma GMP commissioning and validation experience, limiting transferability across industries.
Mandatory engineering degree, explicit 3-5 years requirement and GMP/qualification expectations raise filtering.
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Provide technical support across all phases of engineering projects including design, procurement, construction, commissioning, and handover to ensure smooth execution and compliance.
Coordinate with internal teams and external stakeholders including contractors and vendors to align project activities and ensure timely, quality-driven project delivery.
Prepare and review technical documentation, monitor project progress, perform inspections and tests, and report deviations to maintain adherence to quality standards and regulatory compliance.
Graduation in Mechanical, Electrical, Chemical, Biotechnology Engineering or related field is mandatory.
3-5+ years of relevant work experience in project execution within engineering.
Experience or exposure to installation, commissioning, and qualification (IQ, OQ, PQ) of plant equipment and systems in a GMP environment.
Not explicitly mentioned: Notice period requirement.
Experienced in managing multi-phase engineering project execution including cost estimation, scheduling, and vendor coordination within regulated environments such as GMP.
Skilled in technical documentation, compliance management, and using project management tools (e.g., MS Project) and design software (e.g., AutoCAD).
Demonstrates strong execution focus, problem-solving agility, and quality and compliance mindset essential for handling complex engineering projects in pharmaceutical/biotech settings.