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?
Innovative Environment: Work in a cutting-edge facility committed to continuous improvement and operational excellence.
Career Growth: Access comprehensive training and development opportunities, especially as the company expands.
Meaningful Work: Help produce life-changing biologic medicines for patients around the world.
Key Responsibilities:
Lead SME in cleanroom operations: drug substance pooling, aseptic filling, and related activities.
Write, review, and approve SOPs, BMRs, and other cGMP documentation.
Support technical execution of validation protocols.
Manage and investigate deviations; implement corrective actions.
Maintain QMS records within defined KPIs.
Support tech transfer of processes to commercial scale.
Supervise operations and ensure compliance with cGMP.
Mentor new hires and support team capability building.
Participate in audits, PAIs, and regulatory inspections.
What We’re Looking For:
5+ years of experience in biopharmaceutical manufacturing (biosimilars preferred).
Degree in Biotechnology, Chemistry, or Bio/Chemical Engineering.
Sterile filling and gowning certification required.
Hands-on experience with syringe/vial filling and visual inspection in a start-up or scale-up environment is a plus.
Experience supporting regulatory inspections (e.g., FDA, EMA) is highly desirable.
What’s on Offer:
Full relocation support, including temporary accommodation.
Competitive salary based on experience and seniority.
Shift allowance.
Comprehensive training and leadership development.
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.