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Senior bioprocess scientist

Shannon
Sigmar Recruitment
Scientist
€60,000 - €80,000 a year
Posted: 3 November
Offer description

Direct message the job poster from Sigmar Recruitment

Innovative Biopharmaceutical company specializing in gene therapy and plasmid DNA production.

Work with state‑of‑the‑art bioprocessing equipment and methodologies.

Opportunities for professional development and advancement within a dynamic and growing industry.

About Your New Job as Senior Bioprocessing Scientist:

* Act as the Subject Matter Expert (SME) for a designated bioprocessing stage, ensuring technical, safety, quality, compliance, and continuous improvement.
* Coordinate and supervise Bioprocessing Scientists during shifts, deputizing for the Team Leader when required.
* Define and oversee training approaches for technical and support activities, ensuring high‑quality execution.
* Perform advanced manufacturing activities in line with cGMP, leading quality issue rapid responses and root cause analysis investigations.
* Lead and prioritize initiatives to address recurring deviations, improve process yield, and enhance quality and safety.
* Ensure compliance with GMP, Data Integrity, and Good Documentation Practice (GDP), maintaining a safe and clean working environment.

What Skills You Need for Senior Bioprocessing Scientist:

* Minimum 5 years of hands‑on experience in biopharmaceutical manufacturing, with a focus on gene therapy, plasmid DNA, or viral vector production.
* Comprehensive understanding of upstream and downstream bioprocessing operations, including fermentation, purification, and aseptic techniques.
* Proven ability to handle quality events, including root cause analysis, CAPAs, change controls, and quality improvement initiatives.
* Demonstrated experience in leading and mentoring a team, providing guidance, task allocation, and performance feedback.
* Strong analytical mindset with the capability to troubleshoot process issues and implement effective solutions under GMP‑compliant conditions.
* Familiarity with GMP regulations and guidelines.
* Ability to effectively collaborate with QA, QC, Technical Transfer, and other teams.
* Strong written and verbal communication skills.
* A proactive approach to driving process optimization and continuous improvement.

What’s on Offer:

* Attractive compensation package.
* Comprehensive benefits including health insurance, retirement plans, and more.
* Opportunities for training and career advancement.
* Be part of a collaborative and innovative team.


Seniority level

* Mid‑Senior level


Employment type

* Full‑time


Job function

* Science


Industries

* Pharmaceutical Manufacturing
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