Deskripsi Pekerjaan
Join Adecco as a Senior Process Engineer in the dynamic biopharma and life science industry. This pivotal role combines technical expertise with strategic innovation to optimize manufacturing processes, ensuring compliance with stringent regulatory standards while driving efficiency and product quality. You'll lead cross-functional teams in developing, scaling, and validating bioprocessing workflows for life-saving therapeutics and diagnostics. Your work will directly impact patient outcomes by advancing manufacturing excellence and implementing continuous improvement initiatives in a cutting-edge environment. Adecco offers a collaborative culture where your process engineering skills will transform complex scientific challenges into scalable solutions.
This opportunity is ideal for a visionary engineer passionate about bridging laboratory innovation with industrial-scale production. You'll work with state-of-the-art bioreactors, chromatography systems, and purification technologies while maintaining rigorous cGMP compliance. The position includes comprehensive benefits and performance-based incentives, making it a compelling career move for professionals seeking to make measurable contributions to global healthcare advancement.
Tanggung Jawab
- Lead end-to-end process optimization and scale-up of biomanufacturing workflows
- Develop and execute process validation protocols for biologics and pharmaceutical products
- Drive continuous improvement initiatives through DOE and data-driven analysis
- Ensure compliance with cGMP, FDA, and EMA regulatory requirements
- Collaborate with R&D, quality, and production teams on technology transfer
- Implement robust PAT (Process Analytical Technology) systems
- Investigate process deviations and implement CAPA strategies
- Mentor junior engineers and lead cross-functional project teams
Kualifikasi
- Bachelor's degree in Chemical Engineering, Biotechnology, or related field (Master's/PhD preferred)
- Minimum 5+ years of biopharma process engineering experience
- Expertise in mammalian cell culture, fermentation, or downstream purification
- Strong knowledge of QbD, risk assessment, and process validation principles
- Proficiency with process simulation tools (e.g., SuperPro Designer, gPROMS)
- Experience with regulatory documentation (INDs, BLAs, CMC sections)
- Proven track record in technology transfer and scale-up activities
- Certifications (e.g., PMP, Six Sigma) highly desirable