Base: not specified; bonus/equity: annual bonus ba...
Hybrid
Oral solid dose and respiratory products
Product lifecycle management
Continuous product improvement
This role supports oral solid dose and respiratory products, providing scientific understanding of product performance and resolving technical issues across Global Supply and New Product Introduction
Job Summary
This role supports oral solid dose and respiratory products, providing scientific understanding of product performance and resolving technical issues across Global Supply and New Product Introduction.
Key responsibilities include delivering Product Lifecycle Management, monitoring Global Supply product performance, managing technical activities like NPI trials and RCAs, and providing expert product troubleshooting.
GSK offers a competitive base salary, annual bonus, opportunities for on-the-job training, industry conferences, professional development support, healthcare and wellbeing programs, and employee recognition programs.
Matching Summary
This role supports oral solid dose and respiratory products, providing scientific understanding of product performance and resolving technical issues across Global Supply and New Product Introduction.
Salary
Base: Not specified; Bonus/Equity: Annual bonus based on company performance; Benefits: Competitive base Salary, Opportunities to partake in on the job training courses, Opportunities to attend and partake in industry conferences, Opportunities for support for professional development/chartership, Access to healthcare and wellbeing programmes, Employee recognition programmes, Hybrid (onsite/remote) working within GSK policies (post training period)
Skills & Requirements
Must-have
Oral Solid Dose and Respiratory Products
Product Lifecycle Management
Continuous Product Improvement
Root Cause Analyses (RCAs)
cGMP aligned pharmaceutical environment
Nice-to-have
Self-motivated and resilient
Calm under pressure
Good people skills and influence
Strong continuous improvement mindset
Agile working culture
Key Requirements
Relevant qualifications in Scientific, Technical, or Engineering discipline
Relevant experience in a highly regulated technical industry
Experience in product development and transfer
Experience working in a cGMP aligned pharmaceutical environment