Drug Product Operations Engineer
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| Job Type | Permanent |
| Location | Sligo |
| Area | Sligo, Ireland |
| Sector | Engineering |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1002960 |
| Job Views | 105 |
- Description
- Team Horizon is seeking a Drug Product Operations Engineer for our client who are a global leader in the biopharmaceutical industry, for their site in Sligo. In this role you will work support and facilitate safe and compliant operations within the Drug Product and Synthroid manufacturing areas and support in implementing and sustaining continuous improvement initiatives and to assist in Root Cause Analysis and Corrective/Preventative Action determination as part of investigation processes.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Play a central role in highlighting and implementing continuous improvement ideas and operational excellence opportunities identified through tracking and monitoring of production performance.
Assist with the development of lean and continuous improvement skills throughout the manufacturing organization.
Assist in the pre-campaign planning of Drug Products and APIs, in reviewing lessons learned from previous campaigns with operations personnel and supports post-campaign activities.
Act as a delegate for the DP and Synthroid Operations Leads for certain activities and tasks based on level of experience and competence.
Assist and lead Root Cause Analyses and identification of Corrective/Preventative actions as part of investigation processes.
Assist in following up and closing operations related CAPAs, safety actions and compliance suggestions.
Personally responsible for adhering to all SOPs related to Quality, Safety and Environmental Compliance. Should act as role model for the identification and implementation of Positive Compliance interventions.
Implement changes to Operating SOPs as required.
Represent operations on introductions and execution of NPI projects.
Assist in the identification, implementation and execution of key Manufacturing and Site Strategies
Adhere to and supports all EHS & E standards, procedures and policies.
Any other duties as assigned.
What you need to apply:
A minimum of 3 - 5 years manufacturing or Engineering experience in regulated pharmaceutical industry and / or a minimum Degree in Engineering or relevant technical discipline.
Technical working knowledge of API and/or Drug Product Processing and Unit Operations.
Working knowledge of continuous improvement and operational excellence techniques and tools.
Strong ability to evaluate, diagnose and troubleshoot problems.
Lean Six Sigma Qualifications or knowledge would be an advantage.
