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ABEC has been a leading supplier to the biopharmaceutical manufacturing industry for over 50 years. ABEC's unique value is based on combining long experience with the ability to engineer, design, manufacture, commission, qualify, and service the entire bioprocess to reduce overall cost, shorten time to market, and maximise productivity. ABEC's products include process and equipment engineering/consulting services, comprehensive site services, bioreactors and fermenters, filtration and chromatography systems, prep and hold systems, and cleaning/sterilisation systems.
Position Summary:
This position reports to the Project Engineer Team Lead or Engineering Manager. The Project Engineer designs, specifies, and commissions new and renovated biopharmaceutical process and clean utility equipment, provides engineering support, and leads deviation investigations for equipment and manufacturing processes. As Project Engineer, you will be responsible for assisting the Project Manager in achieving or exceeding the project operating income, project execution plan, and customer satisfaction goals.
Responsibilities:
1. Work effectively in a professional, team-based office environment to meet customer-focused, date-driven commitments.
2. Keep Project Manager(s), team members, and management informed about workload progress, needs, and updates regularly.
3. Identify scope of supply changes that affect project cost.
4. Serve as a direct technical contact with customers for assigned projects.
5. Support Project Manager activities on an as-needed basis or when the Project Manager is unavailable.
6. Contribute to departmental goals, objectives, and improvement initiatives.
7. Review, generate, and understand customer specifications, requirements, and proposals.
8. Analyze customer specifications concerning company offerings, scope, and commercial terms.
9. Maintain contract files according to company procedures.
10. Support engineering-related deliverables to meet customer expectations for equipment form, fit, and function.
11. Assist in creating and approving engineering/design documentation such as P&IDs, GA drawings, detailed design drawings, BOMs, etc.
12. Perform calculations for equipment verification and system sizing.
13. Prepare specifications and equipment data sheets.
14. Support design verification activities and participate in design reviews.
15. Review and approve Engineering Change Notices (ECNs) ensuring accuracy before release.
16. Collaborate with automation and electrical engineering teams on related deliverables.
17. Work with automation teams to review customer requirements and generate related documentation like FRS and DDS.
18. Support manufacturing and quality resources in fabrication, assembly, and qualification of engineering deliverables.
19. Act as a technical contact for projects under fabrication and quality verification.
20. Supervise or conduct pre-FAT, FAT, and SAT activities domestically and internationally.
21. Create test plans and coordinate customer approvals.
22. Generate IQ/OQ documentation as needed.
23. Support the development of engineering standards and procedures.
24. Participate in continuous improvement initiatives to enhance performance and reduce operational costs.
25. Travel to customer sites as required.
26. Perform other tasks as assigned.
Qualifications:
* Honours BSc or BEng in Mechanical, Biological, Chemical Engineering, or equivalent experience.
* At least 3 years of post-graduate engineering experience in related industries.
* Preferred 5 years of experience supporting biopharma or piping systems markets, or supporting manufacture and testing of custom equipment per customer specs.
* Optional: 2 years of experience in automation and control systems engineering related to bioprocesses.
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