QC In-Process Control Expert

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

As our QC In-Process Control Expert you will be supporting our QC and manufacturing teams in Hungary. You will lead in-process testing strategy, ensure methods are robust and compliant, and partner with cross-functional teams to resolve technical issues.
We value practical problem solvers who communicate clearly, coach others, and drive improvements.

Responsibilities:

• Design, review and maintain in-process control testing methods and procedures to meet regulatory and GMP requirements.
• Support method verification and validation activities between development, QC and manufacturing.
• Lead investigations for atypical in-process results and support root cause analysis and corrective actions.
• Monitor in-process data trends and provide recommendations to improve process control and product quality.
• Provide technical guidance and training to operators on IPC methods and good laboratory practices.
• Act as a technical SME in cross-functional meetings, audits and inspections.
  
  This position is mostly on-site due to hands-on laboratory and manufacturing responsibilities, but occasional Home Office days are possible.

• Degree in Chemistry, Biochemistry, Chemical/Bioengineering, Pharmacy or related scientific discipline.
• Minimum 3 years’ experience in a GMP-regulated laboratory or manufacturing environment.
• Practical experience with in-process control testing, method validation or method verification.
• Experience supporting investigations, deviations and corrective actions in a regulated setting.
• Good knowledge of Good Manufacturing Practice (GMP) and data integrity expectations.
• Fluent in both English and Hungarian languages

• Advanced degree in a relevant scientific field.
• Experience with analytical techniques used for IPC (for basic microbiology and physical chemical methods,).
• Familiarity with laboratory information systems (LIMS/LES) and computerized system validation.

• Permanent contract
• Annual bonus and annual salary review
• Cafeteria (flexible benefits)
• Commuting support (company shuttle buses from Budapest and surrounding towns of Gödöllő, or fuel support if using your own car)
• Group life and accident insurance package
• Voluntary pension fund contribution
• Paid parental and caregiver leave
• Modern and clean working environment with an innovative culture