Sr. Tech, Operations

Caraway Therapeutics, Inc.; Ireland; On-site; EUR 55,000 - 75,000; Full time

Job summary

Caraway Therapeutics, Inc. is seeking a Senior Manufacturing Bioprocess Associate to provide on-site support for shop floor operations in a 24/7 facility in Dunboyne, Ireland.

The role requires hands-on operation of Fed Batch and Continuous Manufacturing with strict adherence to safety and GMP standards. You will work with cross-functional teams, author electronic batch records, sampling plans, and SOPs, and troubleshoot issues to drive continuous improvement in a state-of-the-art single-use

Qualifications

• Level 7 qualification in a science or engineering discipline.
• Level 6 with a minimum of 2+ years’ GMP Manufacturing experience.
• Competent in troubleshooting and show practical problem-solving capabilities.
• Ability to work independently and within a cross-functional team.
• Familiarity with contamination control and batch release requirements.
• Understanding of Upstream or Downstream Unit Operations for mAb manufacturing.
• Understanding of both continuous and batch fed manufacturing processes.
• Experience with Emerson DeltaV, PAS-X, and the use of Automation in a manufacturing Process.
• Experience in various Single-Use techniques and experiences in the area of an end to end Single Use facility.
• Commissioning and Qualification experience.

Responsibilities

• Will support end to end production operations for both Fed Batch and Continuous Manufacturing.
• Operate equipment according to electronic batch records, sampling plans and standard operating procedures.
• Ability to solve problems with a desire to continuously learn, improve and develop.
• Conduct all work activities with a strict adherence to the safety and compliance culture on site.
• Supporting the Authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.

Skills

Biopharmaceutical Manufacturing

Troubleshooting

Upstream Operations

Downstream Operations

DeltaV

PAS-X

SOPs

Education

Level 7 qualification in science/engineering

Level 6 with 2+ years GMP experience

Tools

DeltaV DCS

PAS-X

SAP Systems

Job description

Job Description

A fantastic opportunity has arisen for a Senior Manufacturing Bioprocess Associate.

The role for Senior Manufacturing Bioprocess Associate to provide operational support for shop floor operations of the Late Stage and Launch Pipeline at our new state of the art single use biotechnology facility in Dunboyne.

This role is a site-based role.

The role will be a 24/7 shift role.

Bring energy, knowledge, innovation to carry out the following:

The Senior Manufacturing Bioprocess Associate, is responsible for:

• - Will support end-to end production operations for both Fed Batch and Continuous Manufacturing.
• - Operate equipment according to electronic batch records, sampling plans and standard operating procedures.
• - Ability to solve problems with a desire to continuously learn, improve and develop.
• - Conduct all work activities with a strict adherence to the safety and compliance culture on site.
• - Supporting the Authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.

What skills you will need:

In order to excel in this role, you will more than likely have:

• - Level 7 qualification in a science or engineering discipline desired.
• - Level 6 with a minimum of 2+ years’ experience in a GMP Manufacturing requirement, shall be deemed equivalent.
• - Competent in troubleshooting and show practical problem-solving capabilities.
• - Ability to work independently and within a cross-functional team.
• - Familiarity with contamination control and batch release requirements.
• - Understanding of Upstream or Downstream Unit Operations for mAb manufacturing.
• - Understanding of both continuous and batch fed manufacturing processes.
• - Experience with Emerson DeltaV, Pas X, and the use of Automation in a manufacturing Process.
• - Experience in various Single-Use techniques and experiences in the area of an end to end Single Use facility.
• - Commissioning and Qualification experience.

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Required Skills:

Biopharmaceutical Manufacturing, DeltaV DCS, Downstream Operations, Good Manufacturing Practices (GMP), PAS-X, SAP Systems, Single Use Technology, Troubleshooting, Upstream Operations

Employee Status:
Regular

Relocation:
No relocation

VISA Sponsorship:
Yes

Travel Requirements:
No Travel Required

Flexible Work Arrangements:
Not Applicable

Shift:
1st - Day

Valid Driving License:
No

Hazardous Material(s):
NA

Job Posting End Date:
10/13/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.