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Process engineer

Bitsch
g2 Recruitment
Prozessingenieur
Inserat online seit: 19 Mai
Aufgaben der Stelle

Job Title: Process Engineer – Pharmaceutical Project

Contract Type: Freelance / Contract

Duration: 5 months

Start Date: ASAP

Role Overview

We are seeking an experienced Process Engineer to support a major pharmaceutical project in Visp, Switzerland. This is a hands‑on, multidisciplinary role requiring strong technical capability across process design, calculations, and engineering review.

The successful candidate will play a key role in ensuring process systems are technically sound, compliant, and validated, supporting both engineering delivery and project execution.

Key Responsibilities

  • Develop and review process design documentation, including:
  • Process Flow Diagrams (PFDs)
  • Piping & Instrumentation Diagrams (P&IDs)
  • Perform and validate process calculations, including:
  • Flow rates, mass and energy balances
  • Equipment sizing and performance verification
  • Conduct plausibility checks on engineering deliverables and design assumptions
  • Define and support User Requirement Specifications (URS)
  • Size and specify key process equipment, including:
  • Pumps
  • Vessels and tanks
  • Process systems and utilities
  • Interface with multidisciplinary teams (mechanical, automation, electrical, validation)
  • Support design reviews, HAZOPs, and project engineering activities
  • Ensure compliance with pharmaceutical and GMP standards
  • Provide technical input throughout design, construction, and commissioning phases

Requirements

  • Proven experience as a Process Engineer within pharmaceutical or life sciences projects
  • Strong knowledge of:
  • Process engineering fundamentals
  • Equipment sizing and system calculations
  • Pharmaceutical production processes (API, sterile, or biotech preferred)
  • Experience producing or reviewing:
  • PFDs, P&IDs
  • URS and engineering specifications
  • Demonstrated ability to perform plausibility checks and validate design outputs
  • Experience working in a multidisciplinary engineering environment
  • Knowledge of GMP regulations and compliance standards
  • Strong analytical and problem‑solving abilities

Language & Location Requirements

  • German: Preferred (for site coordination and documentation)
  • Willingness to work on‑site in Visp, Switzerland

Why This Role

  • High‑profile pharmaceutical project in a leading European hub
  • Long‑term freelance contract with strong project pipeline
  • Opportunity to work within a multidisciplinary, international team
  • Exposure to complex, high‑value engineering solutions
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