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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in oligonucleotide manufacturing processes and GMP compliance, with a strong focus on project leadership and cross-functional collaboration. Proven ability to drive innovation and improve production capacity while mentoring and guiding team members.
Highest-signal resume keywords
Oligonucleotide Process DevelopmentGMP ManufacturingTechnical Expertise in Bioconjugate ManufacturingProject LeadershipCross-Functional Team Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Oligonucleotide ManufacturingProcess UnderstandingModeling and CharacterizationRegulatory Document PreparationTechnology TransferScientific ResearchPublicationsPatentsPresentationsProcess Improvement
Soft Skills
People-Centered LeadershipTeam BuildingCoachingInterdisciplinary CollaborationCommunication
Certifications & Qualifications
PhDPharmDMD
Industry Keywords
Pharmaceutical IndustryCGMPCMCPDTDynamic Environment
About the role
Key responsibilities & impact- Lead a multidisciplinary project team in the development of sustainable and cost-effective processes for oligonucleotide manufacturing
- Work with cross-functional teams to develop strategies and implementation plans to expand production capacity and improve yield
- Drive oligonucleotide technology innovation
- Support cGMP manufacturing and technology transfer to GMP production facilities
- Develop strategies to ensure process performance through process understanding, modeling and characterization
- Guide successful completion of project deliverables and ensure timelines are met
- Work cross-functionally to deliver regulatory documents and support regulatory filings
- Serve as a technical expert and keep current in the field of bioconjugate manufacturing
- Coach and provide career and scientific / technical advice to colleagues within the organization
Requirements
What you’ll need- Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of Scientific experience
- OR Master’s degree and 5 years of Scientific experience
- OR Bachelor’s degree and 7 years of Scientific experience
- Doctoral degree and 4+ years in the pharmaceutical industry with expertise in oligonucleotide process development
- GMP manufacturing and technology transfer to CMOs
- Demonstrated functional representation on a CMC or PDT team
- Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results
- People-centered leadership skills in building strong teams through mutual trust and respect
- Proven track record of publications, patents and presentations
Benefits
Comp & perks- Comprehensive employee benefits package
- Retirement and Savings Plan with generous company contributions
- Group medical, dental and vision coverage
- Life and disability insurance
- Flexible spending accounts
- Discretionary annual bonus program
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible
- Career development opportunities
- Work/life balance
- Financial plans with opportunities to save towards retirement or other goals