We are working with a purpose-driven biopharmaceutical company focused on increasing global access to high-quality, cost-effective biologic medicines. This is a unique opportunity to join a rapidly growing organisation committed to innovation, collaboration, and patient impact.
As part of our partnership, Impel Talent is supporting the expansion of the company’s manufacturing team to staff a brand new, state-of-the-art facility. This new site will significantly increase production capacity and house development labs, drug product refills, offices, and warehouse space.
You’ll be joining a dynamic Drug Product / Fill Finish team, where your role will be key in maintaining the highest standards of compliance and safety. You’ll act as a subject matter expert, supporting aseptic operations including recombination and pooling of drug substance, sterile filling, equipment changeovers, and sampling—prior to visual inspection.
Why Join?
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Innovative Environment: Work in a cutting-edge facility committed to continuous improvement and operational excellence.
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Career Growth: Access comprehensive training and development opportunities, especially as the company expands.
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Meaningful Work: Help produce life-changing biologic medicines for patients around the world.
Key Responsibilities:
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Lead SME in cleanroom operations: drug substance pooling, aseptic filling, and related activities.
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Write, review, and approve SOPs, BMRs, and other cGMP documentation.
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Support technical execution of validation protocols.
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Manage and investigate deviations; implement corrective actions.
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Maintain QMS records within defined KPIs.
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Support tech transfer of processes to commercial scale.
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Supervise operations and ensure compliance with cGMP.
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Mentor new hires and support team capability building.
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Participate in audits, PAIs, and regulatory inspections.
What We’re Looking For:
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5+ years of experience in biopharmaceutical manufacturing (biosimilars preferred).
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Degree in Biotechnology, Chemistry, or Bio/Chemical Engineering.
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Sterile filling and gowning certification required.
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Hands-on experience with syringe/vial filling and visual inspection in a start-up or scale-up environment is a plus.
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Experience supporting regulatory inspections (e.g., FDA, EMA) is highly desirable.
What’s on Offer:
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Full relocation support, including temporary accommodation.
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Competitive salary based on experience and seniority.
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Shift allowance.
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Comprehensive training and leadership development.
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Support for wellbeing and work-life balance.
Next Steps:
To explore this opportunity confidentially, please contact Impel Talent’s Uri Lasker Lourenco at uri.lourenco@impeltalent.com or apply directly. Let’s create impact together—by helping deliver affordable, high-quality biologic medicines to the patients who need them most.
