Process Engineer
Workplace: Malmö, Sweden
Expires: June 19, 2025
Join APL as a Process Engineer where you will develop and maintain efficient, robust, and GMP-compliant manufacturing processes impacting human health directly. Work in a regulated environment with a focus on quality, problem-solving, and continuous improvement in pharmaceutical production.
Main requirements:
- Academic degree in engineering, chemistry, biotechnology, or relevant natural science
- Experience in a similar role within process or pharmaceutical manufacturing
- Experience working in regulated environments, preferably with GMP requirements
- Structured and solution-oriented with genuine quality focus
- Fluent in Swedish and English, both spoken and written
Responsibilities:
- Develop, document, and implement manufacturing methods and instructions
- Troubleshoot, analyze, and resolve manufacturing process issues
- Assess and follow up on cost effects of process changes
- Handle deviations, complaints, and lead CAPA work
- Lead change requests (CR/CC) and improvement initiatives
- Design and update protocols, formulas, articles, and workflows
- Perform risk assessments according to current regulations
- Train personnel on changes in processes and documentation
Required hard skills:
- Process development and manufacturing documentation
- Problem-solving within manufacturing processes
- Knowledge of GMP and regulated environments
- Risk assessment and CAPA management
- Change management in production processes
Recommended hard skills:
- Experience with pharmaceutical contract manufacturing
- Cost analysis of process changes
Soft skills:
- Change willingness
- Helpful attitude
- Stress tolerance
- Responsible and accountable
Natural languages:
- Swedish (Proficient)
- English (Proficient)
Cultural skills:
- Work within regulated pharmaceutical production environment
- Collaboration in quality-focused teams