This position is responsible for directing all aspects of CMC (Chemistry, Manufacturing and Controls) for pharmaceutical drugs and agents as well as the analytical work associated with that CMC across all of the small molecule projects within Pharma Cinq and, potentially, gene therapy projects. The responsibilities span the range of CMC from sourcing starting materials to formulation development, planning and managing manufacturing of API (active pharmaceutical ingredient) and potential drug products, as well as directing the associated analytical work. This position will also be responsible for the CMC sections of relevant regulatory (FDA and other) documents from INDs to NDAs. This position will work closely with senior management and will supervise the work of others directly and/or across interdisciplinary teams.
Duties And Responsibilities
Identifies and works with the most suitable manufacturers of API’s
Oversees and directs the transfer of manufacturing processes and analytical methods from any current or past vendors to the most suitable CDMOs for each drug candidate
Identifies and works with the most suitable chemistry process development-improvement and scale-up laboratories
Identifies and works with the most suitable formulation development labs
Works within and/or leads project teams to accomplish project goals and manages/coordinates work of other team members
Ensures that manufacturing processes, analytical methods and new formulations are and will meet FDA (and other) regulatory requirements, including GLP and GMP
Acts as the primary interface with Quality Assurance on matters related to CMC and methods development and validation
Manages and works with subject matter experts and consultants as needed
Troubleshoots and optimizes manufacturing processes and analytical methods
Writes CMC sections of INDs, NDAs, Prior Approval Supplements (PAS), Annual Reports and other FDA (and other regulatory authorities) documents and submissions
Reviews CMC data and reports as well as other sections of INDs, NDAs, PAS, Annual Reports intended for submission to FDA and other regulatory agencies
Prepares and/or supports preparation of invention disclosures and patent applications
Presents progress, challenges, milestones, needs to senior management and makes recommendations
Works cross functionally with other business units on projects/products or associated deliverables.
Specific duties may vary depending upon prioritization of projects and programs
Experience And Qualifications
Ph.D. in Organic Chemistry, Chemical Engineering or related field
Bachelor’s degree in chemistry prior to Ph.D. preferred
A minimum of 12 years directly relevant industrial experience
A minimum of 5 years direct experience managing external CDMOs (contract drug manufacturing organizations) and participating in project teams composed of internal and external (CDMO, consultants) team members
Direct experience with and knowledge of the requirements for tech transfer of drug substance and drug product manufacturing processes and analytical method development and validation
Direct, hands-on experience with writing and reviewing CMC sections of INDs, NDAs and related regulatory documents
Direct experience in managing and directing formulation development
Direct experience in selecting and working with stage-appropriate CDMOs
Direct experience in selecting and working with process improvement and scale-up labs
Knowledge, Skills And Abilities
Thorough understanding of FDA requirements and guidelines for GMP manufacturing and analytical methods for clinical and commercial pharmaceuticals
Knowledge of viral vectors and gene therapy development and manufacturing is a plus
Problem solving skills and demonstrated ability to organize and move project tasks forward in an orderly and structured fashion.
Strong analytical skills with the demonstrated ability to gather and evaluate complex data and information and develop a recommendation and plan of action.
Excellent organizational, planning, and time management skills with the ability to manage multiple and often changing priorities and issues of varying complexity, while meeting time-sensitive deadlines and deliverables.
Solid leadership skills with demonstrated knowledge and understanding of staff management practices and processes. Ability to establish accountabilities and expectations and manage performance to achieve results.
Demonstrated propensity to be collaborative, proactive, and self-motivated in the prioritization, execution and completion of projects.
Strong communication (written and verbal) skills regardless of the format (e.g., documents, public speaking situations, presentations, etc.).
Attention to detail with demonstrated commitment to excellence and performance.
Proven proficiency in Microsoft Office (i.e., Word, Excel, PowerPoint, Outlook).
Expertise with data analysis programs, such as JMP and GraphPad Prism.
Physical Demands
While performing the duties of this job, the individual is frequently required to sit for long periods, use a computer and participate in telephone (or WebEx, etc.) calls. The individual is occasionally required to travel to contract manufacturers or laboratories.
Work Environment
Office environment.
Occasional travel to contract manufacturing or laboratory sites
Seniority level
Director
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Biotechnology Research
Referrals increase your chances of interviewing at MESO SCALE DIAGNOSTICS, LLC. by 2x