Social network you want to login/join with:
Lead Process Engineer - Pharma Projects - Cork City or Sandyford, Dublin
Office/Project Location: Cork City or Sandyford, Dublin
Employment Type: Contract
Work Location: Office Based / Hybrid
Pay: Negotiable hourly rate
Experience: 10+ years
Visa: EU passport or Stamp 4 visa required
Our client is an international engineering and PM consultancy with Life Science projects across Ireland.
The Lead Process Engineer will coordinate and supervise the development of process design providing guidance and technical leadership throughout the project development, with the right commitment on time, productivity, and quality in accordance with specific design criteria and client requirements.
They will manage, lead and motivate project teams by means of technical competence, interpersonal sensitivity and conflict management skills.
Responsibilities
1. Process Design Basis: Applies process design criteria, guidelines and contract requirements to process design work.
2. Flow Diagrams: Prepares flow diagrams and participates in flow diagram reviews, ensuring they correspond to the flow sequence, operability and safety of the unit/system.
3. Equipment Datasheets: Prepares process and utility equipment specification sheets and understands their importance as a communication tool.
4. Control Philosophy: Prepares instrumentation process data and assists in establishing control philosophy for control systems.
5. Calculations: Performs specifications/calculations and technical studies, ensuring they are well organized and correctly referenced.
6. Equip Selection/Review: Reviews and approves equipment bid tabulations and vendor data for conformance to specifications.
7. Operating Manual: Assists in the production of plant operating manuals, ensuring they are technically correct and clearly written.
8. Field Work: Assists in process fieldwork and performs plant checkouts to ensure designs have been correctly implemented.
Requirements
1. Honours degree in Chemical Engineering with a minimum of 7-10 years of experience in the design of process systems in Pharmaceutical/Nutritional/Medical devices.
2. Knowledge of relevant cGMP requirements and ISPE Baselines.
3. Software knowledge: Office; Super Pro(R) & Schedule Pro(R), PipeFlo, Flexsim, or other process engineering simulations software.
4. Fluency in English; Italian knowledge extremely fluent/mother tongue.
5. Willingness to work in an international company, to share and capitalize expertise with other offices.
#J-18808-Ljbffr