About No deviation
At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.
We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.
Position Overview
We are looking for an experienced MSAT Process Development Senior Scientist to lead the development and verification of downstream processes, including ultrafiltration and chromatography. This role involves collaborating with global teams, overseeing small-scale studies, and driving process optimization and troubleshooting. The ideal candidate will have 3-5 years of experience in process development or manufacturing within the biopharmaceutical industry.
Key Responsibilities
- Lead and execute studies to evaluate and develop processes, including Proof of Concept (POC) and scale-down model verification for downstream operations like ultrafiltration and chromatography.
- Work closely with global R&D teams to exchange data, ensuring alignment and progress on project milestones.
- Oversee small-scale experimental activities, including drafting protocols and reports, managing samples, and coordinating efforts across various departments for seamless execution.
- Investigate and assess alternative methods for in-process testing to improve operational efficiency and accuracy.
- Facilitate the transfer of analytical methods to production teams, ensuring standardization and adherence to compliance requirements.
- Collaborate with cross-functional teams to identify optimization opportunities and resolve issues in manufacturing processes.
Required Qualifications
- Bachelor’s or master’s degree in biotechnology, Chemical Engineering, Biochemistry, or a related field.
- 3-5 years’ experience in MSAT, process development, or manufacturing within the biopharmaceutical industry.
- Hands-on experience in downstream processes, including ultrafiltration and chromatography.
- Strong understanding of scale-down model verification studies and analytical method development.
- Familiarity with data analysis tools and techniques.
- Excellent collaboration and communication skills to work effectively with global teams.
- Ability to manage multiple priorities and deliver results within tight deadlines.
Why join us?
- Generous Leave Policy including 3 days to care for aging family members, reflecting our commitment to family wellbeing.
- Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
- Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
- Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
- Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.
How to apply
Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!
Please submit your resume, outlining your qualifications and experience relevant to the role, here.