Overview
We are seeking a Process Engineer to support Safety Instrumented Systems (SIS) projects in pharmaceutical or high-containment environments. Lead SIL assessments, Safety Requirement Specification development, and overall SIS lifecycle management to ensure process safety and regulatory compliance.
Responsibilities
* Lead and execute SIL assessments for Safety Instrumented Systems.
* Develop Safety Requirement Specifications (SRS) and support the full SIS lifecycle, including design, verification, validation, and commissioning.
* Conduct HAZOP, LOPA, and risk analysis workshops to identify and mitigate process hazards.
* Collaborate with engineering, operations, and QA teams to ensure compliance with process safety standards and regulatory requirements.
Required Skills & Experience
* Proven experience with ISA 61511 / functional safety standards.
* Hands-on experience performing SIL assessments, risk analyses, and SRS development.
* Experience in pharmaceutical or high-containment manufacturing environments.
* Knowledge of HAZOP, LOPA, and process hazard analysis techniques.
* Understanding of process safety, regulatory compliance, and GMP requirements.
This is a hybrid working model: 1 day onsite, 4 days remote.
Details
* Seniority level: Entry level
* Employment type: Contract
* Industries: Pharmaceutical Manufacturing and Biotechnology Research
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