Bayside Solutions ยท 1 day ago
Quality Director
Bayside Solutions, Inc. is seeking a Quality Director to oversee small molecule development and pharmaceutical manufacturing. The role involves managing CMO/CDMO/CRO oversight and supporting regulatory submissions while ensuring quality standards are met.
Information TechnologyStaffing AgencyTelecommunicationsVirtual Reality
Responsibilities
Open to relocating candidates, but can also work remotely. If remote, would travel on-site to Chicago 2-4 times a year for board meetings. (full relo package)
Open to starting on a contract basis to get onboarded asap, but intent is to have this as a permanent position
Comp is still being finalized, but we have targeted $200-250k in the past with flexibility for the right candidate
Prefer ~10+ years of industry experience
Small Molecule experience required
Highly prefer a background in Manufacturing
Oversight of CMO/CDMO/CROs (EU / Japan / US)
Experience with Neurological / Neurodegenerative products preferred
CMC experience is a plus
Highly prefer candidates who have had experience bringing a product from discovery to clinical and commercialization
Experience supporting regulatory submissions is highly preferred
Auditing/CAPA/Supplier/vendor review required
Able to work independently
Can present ideas/suggestions with data to support reasoning
Willingness to push/escalate ideas when needed
Can handle a broad range of personalities
Able to work in an environment without all SOPs in place
Comfortable wearing multiple hats and working outside of job description if/when needed
Qualification
Required
Small Molecule experience required
Oversight of CMO/CDMO/CROs (EU / Japan / US)
Auditing/CAPA/Supplier/vendor review required
Able to work independently
Can present ideas/suggestions with data to support reasoning
Willingness to push/escalate ideas when needed
Can handle a broad range of personalities
Able to work in an environment without all SOPs in place
Comfortable wearing multiple hats and working outside of job description if/when needed
Preferred
Prefer ~10+ years of industry experience
Experience with Neurological / Neurodegenerative products preferred
CMC experience is a plus
Highly prefer candidates who have had experience bringing a product from discovery to clinical and commercialization
Experience supporting regulatory submissions is highly preferred
Benefits
Full relo package