Are you looking for...
an exciting professional challenge?
We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
NextPharma Tampere has several decades of extensive experience in pharmaceutical development, commercial manufacturing and packaging of ophthalmic products.
As a Validation Engineer, you will work in a pharmaceutical manufacturing environment with a focus on sterilization validations, equipment qualification, and quality system compliance.
Your responsibilities will include:Sterilization validations
Steam-In-Place (SIP) process validations for Blow-Fill-Seal (BFS) machines and tanks
Validation of heat sterilization processes for polymer components
Maintenance of production equipment and utility qualifications
Small equipment qualifications
Risk assessments and technical change management
Participation in projects as the validation representative
We hope you bring:Bachelor's or Master's degree in Engineering
Independent and proactive working style
Experience in the pharmaceutical industry, validation and qualification activities
Knowledge of quality systems and standards (ISO 9000, GMP)
Customer-oriented mindset
Fluent written and spoken English and Finnish
What we offer:An opportunity to work and grow your skills in a highly regulated pharmaceutical environment and develop your expertise in GMP-regulated manufacturing and validation activities
Diverse and meaningful validation projects
Collaboration with experienced industry professionals in a team of 12 supportive colleagues at Tampere site