We’re Hiring Application Scientist – Pharma Analytics / Purification (Downstream Processing)

Work Schedule Standard (Mon-Fri)Environmental Conditions Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job DescriptionRole OverviewWe’re not just looking for a lab executor here—this role sits at the intersection of process development, analytics, and scale-up.As an Application Scientist – DSP, you will lead the design, development, and optimization of downstream purification processes for biologics in a single-use bioprocessing environment. You’ll play a key role in enabling robust, scalable, and compliant purification workflows while collaborating across upstream, analytics, quality, and manufacturing teams.Key Responsibilities1. Downstream Process Development & Optimization

• Design and optimize purification processes including:

• Chromatography (affinity, ion exchange, etc.)
• Filtration (TFF, depth filtration)
• Viral clearance strategies
• Perform lab-scale studies to evaluate process parameters for yield, purity, and robustness
• Implement and optimize single-use technologies in DSP workflows
• Integrate downstream processes with upstream and analytical workflows

2. Pharma Analytics & Characterization

• Execute and support analytical workflows including:

• qPCR (minimum 3–4 years hands-on)
• Sanger Sequencing
• Support impurity profiling and adventitious agent testing strategies
• Interpret analytical data to guide purification and process decisions
• Collaborate with analytical teams for method development and validation

3. Technology Transfer & Scale-Up

• Lead transfer of DSP processes from lab to pilot and commercial scale
• Develop and review:

• SOPs
• Batch records
• Technology transfer documents
• Troubleshoot scale-up challenges in single-use manufacturing environments
• Work closely with engineering and manufacturing teams

4. Data Analysis & Documentation

• Analyze experimental data for process performance and optimization opportunities
• Ensure compliance with Good Documentation Practices (GDP)
• Prepare:

• Technical reports
• Protocols
• Client/stakeholder presentations

5. Cross-Functional Collaboration

• Partner with:

• Upstream Processing
• Analytical Development
• Quality & Regulatory
• Provide technical expertise in DSP during:

• Project reviews
• Troubleshooting discussions
• Act as a subject matter expert (SME) for purification and analytics

6. Continuous Improvement & Innovation

• Track advancements in:

• Downstream processing technologies
• Single-use systems
• Process Analytical Technology (PAT)
• Drive improvements in process efficiency, scalability, and cost-effectiveness
• Contribute to innovation initiatives within BDC

QualificationsEducation

• Ph.D. / M.S. / B.S./Post Graduation in:

• Chemical Engineering
• Biotechnology
• Biochemistry
• Or related field

Experience

• 8+ years in downstream process development in biopharma
• Strong expertise in:

• Chromatography
• TFF / filtration
• Viral clearance
• Hands-on lab experience with DSP equipment
• 3–4+ years hands-on experience in:

• qPCR
• Sanger Sequencing
• Experience in:

• Impurity testing
• Adventitious agent testing
• Exposure to:

• Pharma analytics
• Regulated environments (cGMP)
• Customer-facing or application roles (preferred)

Skills & Competencies

• Strong process development and troubleshooting capability
• Data-driven mindset with solid analytical skills
• Effective communication and presentation skills
• Ability to manage multiple projects and timelines
• Collaborative, team-oriented approach

Preferred / Desired Attributes

• Familiarity with:

• cGMP, ICH guidelines
• Regulatory expectations for biologics
• Knowledge of:

• PAT (Process Analytical Technology)
• Automation in DSP