Principal Scientist R&D & cGMP Preparative Chromatography

Job Description

General Summary:

Vertex Pharmaceuticals is seeking a highly experienced and motivated Principal Scientist to join the Vertex Manufacturing Center (VMC) Kilo Lab in a dual-capability role that is central to our drug substance development mission. This is an exceptional opportunity for a seasoned pharmaceutical scientist with deep expertise in analytical and preparative chromatographic purification in both an R&D and cGMP environment including large-scale preparative HPLC supercritical fluid chromatography (SFC) Ion-pair reversed phase high-performance liquid chromatography (IP-RPHPLC) ion exchange chromatography (AEX/CEX) and size exclusion chromatography (SEC). This individual will play a pivotal role in jumpstarting Vertexs emerging kilo-scale cGMP purification capabilities and laboratory contributing also to new therapeutic modalities with significant pipeline impact.

Key Duties and Responsibilities:

• Lead Preparative Chromatography Method Development Spearhead the development optimization and scale-up of preparative HPLC and SFC purification methods across all scales from semi-preparative to kilogram for both R&D and cGMP selecting appropriate chromatographic modes (RP NP IEX SEC) based on compound class and impurity profile
• Execute & Troubleshoot Complex Purification Campaigns Lead hands-on execution of mass-directed and preparative purification campaigns for complex small molecule drug substances troubleshooting challenging separations and developing creative scientifically sound solutions
• Establish & Maintain Lab Infrastructure: Drive equipment procurement column packing system qualification and ongoing maintenance of large-scale chromatography platforms; influence technology selection and lab infrastructure investments to build a world-class separations capability
• Perform Kilo-Lab Scale Synthesis: Ability to flex into multi-step synthesis of drug substance intermediates and APIs at gram-to-kilogram scale including reactions in jacketed vessels and large-scale reactor systems with full accountability for safety quality and yield
• Support Scale-Up & Process Chemistry Collaboration: Partner with Process Chemistry Analytical DevelopmentD and project teams to implement and adapt synthetic routes for kilo-lab operations performing workups crystallizations filtrations and drying at scale and interpreting analytical data (NMR HPLC MS) to drive process decisions
• Build Peptide and Oligonucleotide Purification Capability: Define the strategic roadmap and lead the implementation of kilogram oligonucleotide synthesis (solid-phase phosphoramidite chemistry) and purification platforms (IP-RP HPLC AEX/CEX ultrafiltration/diafiltration) including equipment procurement qualification and SOP establishment
• Mentor & Develop Scientific Staff: Provide hands-on mentorship technical coaching and structured training to junior scientists associates and technicians equipping them to independently master preparative chromatography separations techniques and kilo-lab operations
• Author & Own GMP Documentation: Author review and approve SOPs master batch records validation protocols purification reports and technical documents in full compliance with cGMP standards and Vertex quality systems
• Lead Cross-Functional Technical Initiatives: Serve as the organizational SME for preparative purification and drug substance chemistry; lead cross-functional project teams and act as primary technical liaison with Analytical Development Process Chemistry Quality and Manufacturing groups
• Ensure GMP Compliance Quality & Safety: Ensure all lab operations adhere strictly to cGMP regulations EHS standards and Vertex quality requirements; maintain meticulous documentation (ELN batch records deviations change controls) and support internal/external audits as a subject matter expert

Knowledge and Skills:

• Expert-level proficiency in preparative chromatography (HPLC SFC IP-RP AEX CEX SMB and SEC) across all scales encompassing method development column selection mobile phase optimization mass-directed purification systems and chromatography data systems (e.g. Empower OpenLab)
• Demonstrated track record of technical leadership and cross-functional collaboration with the ability to influence stakeholders lead project teams and drive scientific decisions without direct authority.
• Strong written and verbal communication skills with proven ability to present complex technical findings to diverse audiences ranging from bench scientists to senior leadership
• Experience mentoring and developing junior scientists and technical staff fostering growth in separations techniques and kilo-lab operations
• Deep working knowledge of cGMP regulations documentation standards and quality systems as applied to drug substance manufacturing including authoring and reviewing batch records SOPs deviation reports and validation protocols
• Demonstrated commitment to laboratory safety environmental health standards and maintaining a culture of quality and compliance across all operations
• Ability to flex into hands-on synthetic organic chemistry at kilogram scale including jacketed reactor operations large-scale workups and the ability to interpret complex analytical data (HPLC LC-MS NMR Karl Fischer) to drive purification and synthetic decisions

Education and Experience:

• Ph.D. in Analytical Chemistry Organic Chemistry Medicinal Chemistry Chemical Engineering or a closely related discipline preferred; M.S. or B.S. with extensive relevant industry experience will be considered.
• Bachelors degree and 10 years Masters degree and 7 years or PhD and 4 years of hands-on industry experience in R&D and cGMP pharmaceutical analytical and preparative separations drug substance development manufacturing or the equivalent combination of education and experience

At Vertex we embrace continuous learning and encourage employees to stay informed on advances in AI technology automation and industry trends. We seek talent who bring an external perspective demonstrate curiosity and sound judgment and thoughtfully adopt new capabilities that improve decision-making drive innovation increase efficiency and help deliver better outcomes for patients.

Pay Range:

Disclosure Statement:

Flex Designation:

Flex Eligibility Status:

In this On-Site designated role you will work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at