Specialist - Extractables and Leachable - MSAT EM

Responsibilities:
- Work with internal and external laboratories to ensure E&L testing is completed in a scientific, compliant and cost effective manner.
- Conduct and document E&L risk assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices.
- Deliver key technical information to business partners to support business decisions and/or regulatory filings.
- Manage risk identification and escalation to GSK stakeholders.
- Ensure compliance with external and internal requirements (e.g., GSK QMS, GSK GQSOPs) through interaction with internal organization.

Basic Qualifications (required):
- Bachelor’s degree in Pharmaceutical Sciences, Engineering, Chemistry, Biology, or a related scientific field.
- 5+ years’ experience in leading E&L assessments.
- Experience with pharmaceutical best practices in analytical and manufacturing technologies, validation, and GMP compliance.

Preferred Qualifications:
- Advanced degree (Master’s or PhD) in a relevant scientific or engineering discipline.
- Experience working with contract manufacturing organizations (CMOs).
- Demonstrated ability to work effectively across a diverse customer base.
- Awareness of FDA/US Pharma and GMP requirements related to packaging.
- Ability to work effectively in a matrix organization across geographies and cultures.
- Strong verbal and written communication skills.
- Prioritization skills.

Compensation/Benefits:
- Belgium salary range (gross base): EUR 70,650 to EUR 117,750.
- May offer an annual bonus and eligibility for share-based long-term incentive program (details provided during recruitment process).