Director, Supply Chain Quality

Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world’s premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others.

Position Summary

The Director Supply Chain Quality will be a Quality Assurance professional primarily responsible for the day-to-day quality functions of Crinetic’s global supply chain for clinical and commercial products and assuring compliance with FDA, European, and other country-specific regulations. This position will be responsible for developing collaborative and productive partnerships internally, as well as externally with global contract organizations and strategic partners. This individual will be an integral part of the company’s effort to develop small molecule therapeutics for rare endocrine disorders and endocrine-related tumors through support of GMP operations.

Essential Job Functions And Responsibilities

These may include but are not limited to:

• Directly support the Senior Director GMP QA with day-to-day quality functions of the global supply chain for clinical and commercial products and assuring compliance with FDA, European, and other country-specific regulations
• Focus on immediate and short-term (<2 years) strategic planning horizon
• Identify compliance gaps and improvement opportunities to inform Quality and CMC business partners and/or Inspection Readiness plans with respect to global supply chain processes and vendors
• Oversight for GMP Quality Events (Product Quality Complaints, Temperature Excursions, Deviations, CAPAs) processes with appropriate escalation of Major and Critical events with potential to impact patient safely, product quality or supply delays
• QA Lead for market actions, such as stock recovery, recall and field alert reporting processes, including notifications to regulatory authorities, partners, and Responsible and Qualified Persons (QPs) as appropriate
• GMP oversight for both commercial and clinical activities related to labeling, serialization (DSCSA), randomization, and blinding
• QA Lead for supply chain compliance requirements for clinical (direct to patient, just-in-time and depot models) and commercial distribution
• Serve as Project Manager for assigned process improvement initiatives, participate on projects and teams representing Supply Chain Quality, including Change Control Review Board, review of GMP QMR sections and others to be defined
• Responsibility for identifying global Supply Chain Quality related risks and develop or assist in developing mitigation plans with business partners
• Represent QA in internal and external team meetings
• Perform, review and/or approve impact assessments and risk assessments
• Write and review Standard Operating Procedures
• Perform vendor audits as assigned and support vendor lifecycle activities
• Actively manage and coach direct reports by encouraging professional and personal development, leading by example and nurturing individual growth to optimize team performance
• Other duties as assigned

Education and Experience:

Required

• Bachelor’s degree or Master’s degree with scientific or technical discipline
• A minimum of 12 years of relevant Quality Assurance GMP experience in a biotech/pharmaceutical setting with 8 years of supervisory leadership, continuous improvement and/or project management experience. An equivalent combination of experience and education may be considered
• Demonstrated knowledge of FDA/EMA/ICH standards and regulations
• Experience working with Contract Management Organizations and/or auditing CMOs
• Experience with large stakeholder management, QMR, and reporting out to senior management teams
• Demonstrated knowledge of commercial serialization requirements (DSCSA) as well as clinical blinding (randomization)
• Previous history of coordinating a Qualified Persons (QP) release processes to streamline efficiency within global clinical supply chain
• Experience implementing a just-in-time (JIT) or Pooled Material Supplies (PMS) clinical supply chain
• Experience at a global level with product complaint, stock recovery, recall and field alert report processes
• Demonstrate ability to effectively organize, prioritize and work in a fast-paced environment
• Demonstrate ability to function individually and in a team environment
• Strong project management skills with ability to manage multiple projects and execute in adherence to timelines
• Must be able to communicate effectively with all levels of personnel as well as with Contract Manufacturing Organizations
• Software knowledge: MS Office, DocuSign, electronic QMS systems

Preferred

• Solid dosage or drug substance experience is preferred, however, experience in other dosage forms with relevant experience is acceptable
• Prior experience with Veeva QMS systems (Quality vault)

Physical Demands And Work Environment

Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities.

Laboratory Activities (if applicable): Biology and chemical laboratory environment experience needed. Environmental health and safety requirements also apply.

Travel

You may be required to travel for up to 15% of your time.

The Anticipated Base Salary Range: $156,000 - $195,000

In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience and education. Crinetics Pharmaceuticals is a multi-state employer, and this salary range may not reflect positions that work in other states. Your recruiter can share more about the specific salary range during the hiring process.

Equal Opportunity Employer

Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender (including gender identity and/or expression), pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws.

Vaccination Requirement

Following extensive monitoring, research, consideration of business implications, and advice from internal and external experts, Crinetics requires that all employees and contractors be fully vaccinated and have received the COVID-19 vaccines as a condition of employment. “Full vaccination” is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation.