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Senior Recruitment Consultant @Fastnet | Total Talent Partner | Market leader in the Life Sciences sector | Recruitment & Staffing, Contract…
Overview:
We are seeking an experienced Senior Downstream Scientist to lead bioprocess development projects supporting pharmaceutical and biotech clients across Ireland and globally. This role is central to the design, optimization, and scale-up of downstream processes for a diverse range of biotherapeutics, including monoclonal antibodies, viral vectors, and advanced therapies.
You will play a key role in delivering high-impact process solutions to clients through data-driven development, collaboration, and technical leadership within a multidisciplinary team.
Key Responsibilities:
* Lead the development and optimization of downstream processes (e.g. chromatography, tangential flow filtration, depth filtration) for global and local pharma clients.
* Design and execute experimental plans to support purification strategies from bench scale through to tech transfer.
* Act as a technical lead for client projects, providing scientific direction and project updates in a client-facing role.
* Collaborate closely with internal teams including analytical, engineering, and quality to ensure robust, scalable processes.
* Mentor and guide junior scientists, fostering technical growth within the team.
* Prepare and review protocols, development reports, and regulatory-supporting documentation.
* Support technology transfer and scale-up activities for clinical and commercial readiness.
* Contribute to the continuous improvement of downstream capabilities, methods, and workflows.
Qualifications & Experience:
* PhD in Biotechnology, Biochemistry, or related field with 5+ years of relevant industry experience; or MSc with 7+ years; or BSc with 10+ years.
* Extensive experience in downstream process development for biopharmaceuticals, with a strong track record of client-facing project delivery.
* In-depth knowledge of chromatography (affinity, ion exchange, HIC), tangential flow filtration, and related purification techniques.
* Familiarity with regulatory expectations and tech transfer into GMP environments.
* Strong problem-solving, communication, and technical writing skills.
* Proven ability to manage timelines and technical scope across multiple projects.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Research and Science
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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