Wales

Critical Needs. Immediate Action.

SERB is a fast-growing global specialty pharma company designed to address rare and urgent conditions by delivering life-saving medicines when time and complexity leave no room for failure.

We operate end-to-end across 100+ countries, ensuring 70+ essential medicines for rare diseases, emergency care, and medical countermeasures reach patients and clinicians with urgency – wherever and whenever they are needed.Shaped over the past 25 years by an entrepreneurial, disruptive spirit, SERB combines the focus and agility of a biotech with the scale, reach, and reliability of a global pharmaceutical company — always grounded in medical purpose, not corporate convention.

Our 600+ employees are driven by three core values:

• Patients first, always
  Patients are not a concept — they are why we act, especially when time matters most.
  
• Impact focused
  We are agile, entrepreneurial, and disciplined - working smart and learning continuously to deliver results that matter, with the consistency, quality, and trust that critical care demands.
  
• Team powered
  We go the extra mile - together - because our shared commitment drives extraordinary outcomes.

Guided by a clear ambition and a relentless focus on patients, SERB continues to expand through selective, innovative acquisitions, launching new treatments and entering new geographies. Across every step — from integration to delivery — our people act with passion, ownership, and determination to ensure life-saving medicines become available to patients who need them, worldwide.

Broad Function

Responsible for the management of CMC process development of biological manufacturing processes to support new and existing biological products.

Principle Responsibilities
1. Lead process development activities for therapeutic antibodies.
2. Manage team of scientists in development and small-scale manufacturing.
3. Develop innovative manufacturing solutions for new and existing biological products.
4. Maintain good LCM of the current approved products
5. Perform process characterizations studies (e.g. viral and impurity clearance studies, chromatography resin reuse, process limit evaluations).
6. Support the scale up and transfer of manufacturing processes from CMC to GMP production.
7. Provide specialized technical CMC input to project teams and support the Operations group on with significant manufacturing investigations and CAPAs
8. Compile and/or assist Regulatory in compilation of CMC sections of all regulatory filings. Provide expert advice with agency interactions, as required. Support setting of CMC budgets and ensure adherence to this budget throughout the financial year.
9. Provide due diligence support for in- and out-licensing products as required.
10. Ensure projects are delivered on time, in-line with all relevant guidelines, to budget, and in line with business needs.
11. Complete additional tasks considered necessary to meet business and customer requirements as indicated by the Line Manager.
12. To adhere to SERB’s polices on health, safety and workplace policies.
13. Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with SERB values.
14. Carry out other reasonable tasks as required by the Line Manager.
The above duties and responsibilities are not an exhaustive list and you may be required to undertake any other reasonable duties compatible with your experience and competencies. This description may be varied from time to time to reflect changing business requirements.

Serb Pharmaceuticals is an equal opportunity employer. We offer competitive compensation & benefit packages, challenging opportunities and a culture of working together in a supportive way built on our strong foundation of values.