Process Development Engineer - Drug Product - Dublin


Location: Ireland

EUR 50,000 - 75,000

Job Type: Perm

Industry: Biotech-Pharma-Medical-Device-Jobs

Job ID: JO-1901-12465

Consultant: Karen McHugh






Do you have process development experience in Pharma Manufacturing including drug product development or technical transfer in the biopharmaceutical / bioprocessing field?

Would you like to work for a multinational Biopharmaceutical company based in Dublin? 

If interested in this role, please forward your CV to karen@jobcontax.com or call Karen on +353 1 7978720


Process Development Engineer - Drug Product - Dublin


Employer

JobContax is a preferred supplier to one of the world's leading BioPharma companies. 

With major capital investment happening in their plant, this is an exciting time to join the team. 


Job Description

Reporting directly to the Manufacturing Operations Manager, the Process Development Engineer will

- lead the technology transfer of new product introductions

- Support operational readiness for Drug Product manufacturing

- will provide technical support for all manufacturing activities associated with the facility with an effort to control costs while also improving process efficiency.


Responsibilities

Plant Operational Readiness

Lead the Drug Product Technical Transfer “Project”

Scope includes DP and Packaging

Delegate tasks and communicate priorities to team members

Own the DP Tech Transfer Schedule

Liaise with QC, QA, PD Lab, CAPEX Team, Logistics, Supply Chain and Manufacturing to ensure adherence to schedule and efficient troubleshooting

Understand regulatory requirements and communicate them to the project team

Lead the process validation

Provide technical support and direction to manufacturing personnel in order to ensure that the manufacturing and ancillary facilities can be operated to optimum efficiency and that Plant Turnarounds are executed in an efficient manner.

Support Plant operations team with achieving manufacturing schedule adherence.

Actively participate in problem identification, problem solving and change initiatives in cooperation with other teams and services. 

Continuous improvement with a cross functional focus is a core activity.

Investigate quality events as they arise and prepare deviation reports using site Trackwise system.

Participate in CAPEX projects associated with the facility, providing process knowledge input.

Complete required documentation relating to development and manufacturing activities in an accurate and timely manner.

Such documentation would include (but not be limited to) BMRs, SOP, Logbooks and EOPs.


Requirements

Minimum 5 years experience in Pharma Manufacturing including Technical Transfer

Experience of OSD Drug Product Processes essential

Experience of Capsule Filling, Blending and Primary Packaging desirable

Experience of High Containment Operation desirable

Excellent written and verbal communication skills

Flexible, willing and positive attitude / mind-set

Excellent planning, scheduling and prioritisation ability

Excellent documentation skills and attention to detail.

Excellent knowledge of Microsoft products and systems skills.

Strong Quality orientation.

Ability to work under pressure & managing conflicting tasks at the same time.

Attention to detail is critical.

Ability to work well with others to achieve organisational goals.

Safety focused.


Package

Total Package €50k - €75k

Excellent benefits package

Performance Related Bonus

Health Insurance

Pension

Flexibility 

Paid Maternity/Paternity Leave

Educational Assistance Programme

Zero Absence Award

Talent & Development Programme

Occupational Health & Wellness Programme


Contact

Karen McHugh is the consultant managing this position.

If you have any queries about this role, you can contact Karen by e-mail karen@jobcontax.com or phone +353-1-7978720

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