Clinical Supply Chain Planning Director
hace 4 semanas
Company Overview: CRISPR Therapeutics is a leading biotechnology company that has transformed from a research-stage company to a diverse portfolio of product candidates across various disease areas. The company has established strategic partnerships with leading companies and has a presence in Zug, Switzerland, and the US.
Position Summary: We are seeking an experienced Clinical Supply Chain Planning Director to manage and optimize global supplies to ensure timely availability of clinical supplies for clinical trials. The successful candidate will lead the establishment of a robust clinical supply planning model, develop and maintain strong collaborative relationships with team members, and ensure alignment with company goals.
Responsibilities:
- Generate and maintain a clinical supply plan to drive manufacturing, labeling, and forecasting supply activities across internal and external stakeholders.
- Lead and manage the supply planning for finished goods, drug product, drug substance, and critical components across multiple clinical programs.
- Collaborate with clinical teams and other internal/external stakeholders to forecast demand based on trial protocols and timelines.
- Coordinate with manufacturing sites, clinical sites, and label/storage/distribution vendors and other internal stakeholders to ensure consistent inventory is available at each node to sustain the clinical trial(s).
- Plan and oversee packaging and labeling operations both internally and with CMOs as required to support the clinical supply plan.
- Define and implement KPIs/metrics related to supply and demand.
- Work closely and proactively with internal/external stakeholders to ensure seamless operation of clinical trials and address any challenges.
- Participate/lead investigations in close collaboration with Quality, as applicable.
- Identify issues and/or risks with meeting clinical supply requirements and suggest solutions to meet timelines.
- Continuously evaluate and improve supply chain planning business processes to optimize operations.
Requirements:
- Bachelor's degree in Biological Sciences or related fields.
- 10-12+ years' experience working within a cGMP supply chain environment and/or with GCP regulations.
- Excellent computer skills (Microsoft Office Word, Excel, Outlook) required.
- Experience with clinical supply chain planning.
- Willingness to work in a flexible environment.
- Excellent organizational skills, enough to multi-task in an extremely fast-paced environment with changing priorities while maintaining attention to detail.
- Clear and succinct verbal and written communication skills.
- Strong analytical, problem-solving, and critical thinking skills.
- Ability to influence others and work independently and in a team environment.
- Experience working closely with Manufacturing, Project Management, functional team leaders, clinical teams, contract manufacturing partners, and/or cold chain shippers and logistics providers.
Preferred Qualifications:
- Experience with cold chain, and cell and gene therapies highly preferred.
- Additional specific qualifications in the area of clinical supply chain planning including APICS CPIM or CSCP, and related professional certifications.
Competencies:
- Collaborative – Openness, One Team.
- Undaunted – Fearless, Can-do attitude.
- Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
- Entrepreneurial Spirit – Proactive. Ownership mindset.
CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication, and offer opportunities for our employees to connect.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law.
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