Job matched to your search
F&F bioprocess engineer
agap2 Switzerland · Basel
Free · Join 5,000+ job seekers using Qarera
How well do you match this role?
Tap the skills you already have — then see your real match score, what’s missing, and your resume fixed for this job.
Job description
agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.
As a consultant , you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills.
You are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio.
Your main responsibilities
- Drive continuous improvement of the GMP quality system for Fill & Finish , ensuring inspection readiness
- Support batch release through rigorous review of batch records and manufacturing documentation
- Review and approve GMP documents ( SOPs, protocols, reports ) related to aseptic processes and equipment
- Act as SME for process validation and equipment qualification ( URS, FAT/SAT, IQ/OQ/PQ )
- Lead investigations ( deviations, CAPAs, OOS, complaints ) using a risk-based approach
- Manage change controls impacting processes and systems
- Ensure oversight of aseptic operations ( media fills, CCS )
- Oversee qualification and lifecycle of Fill & Finish equipment (filling lines, isolators, lyophilizers)
- Manage CMO quality oversight and external partner performance
- Contribute to APQR and support audits and inspections as SME
Your profile
- Master’s degree in Pharmacy, Engineering, Biotechnology, or Quality
- 3–8 years of GMP experience in pharma/biotech
- Strong expertise in Fill & Finish ( aseptic processing, sterile manufacturing, equipment qualification )
- Good understanding of USP, DSP, Fill & Finish
- Solid knowledge of cGMP ( EU GMP, FDA )
- Experience in aseptic environments ( isolators, cleanrooms, CCS )
- Background in validation/qualification activities
- Strong analytical, communication, and stakeholder management skills
- Comfortable in a cross-functional, international environment
- Fluent in English and German (mandatory)
Thank you for your interest in this opportunity, please note that only the selected candidates for a first exchange will be contacted.
More jobs in Basel
Browse related jobs
Don’t just read the job — see if you’ll get it.
Get your match score, a resume tailored to this exact role, and jobs like it — free.
Check my fit for this job