Are you passionate about advancing medical breakthroughs and transforming patient care? Join us and play a pivotal role in shaping the future of innovative medicines. We are a leading company in gene editing, dedicated to revolutionizing treatments and improving lives. Our dynamic team thrives on collaboration, creativity, and a shared commitment to excellence. If you’re ready to bring your expertise to a company that’s at the forefront of medical science, we want to hear from you!
In this role, you’ll be at the heart of our clinical trials, ensuring that our supply chain is optimized to support cutting-edge research and development. You’ll lead the charge in managing global clinical supplies, from finished goods to critical components, while aligning supply chain activities with our mission.
Key Responsibilities
Supply Planning: Develop and maintain comprehensive clinical supply plans that drive manufacturing, labeling, and forecasting activities. Oversee supply planning for various clinical programs, including finished goods, drug products, and critical components.
Collaboration: Work closely with clinical teams, manufacturing sites, and external vendors to ensure consistent inventory levels and timely availability of supplies for clinical trials.
Packaging & Labeling: Plan and manage packaging and labeling operations to support clinical supply requirements.
Metrics & KPIs: Define and track key performance indicators related to supply and demand to ensure optimal operations.
Problem-Solving: Address and resolve any supply chain challenges or risks that could impact clinical trial timelines. Propose and implement solutions to mitigate issues.
Process Improvement: Continuously evaluate and enhance supply chain planning processes to optimize efficiency and effectiveness.
Regulatory Compliance: Ensure all activities comply with established SOPs and GXP regulations.
Qualifications
Education: Bachelor's degree in Biological Sciences or a related field.
Experience: 10-12+ years in a cGMP supply chain environment or with GCP regulations. Experience with clinical supply chain planning is essential.
Skills: Proficiency in Microsoft Office (Word, Excel, Outlook). Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment. Excellent analytical, problem-solving, and communication skills.
Collaborative: Proven ability to work effectively with internal teams, manufacturing partners, and external stakeholders.
Preferred Qualifications
Specialized Knowledge: Experience with cold chain management and cell and gene therapies. Certifications such as APICS CPIM or CSCP are highly desirable.
Interpersonal Skills: Excellent communication skills, both verbal and written, with a strong ability to influence and work independently or within a team.
What We Offer
Work Environment: Enjoy a balanced approach with flexibility for remote work while benefiting from in-person collaboration and mentorship opportunities.
Culture: Be part of a forward-thinking organization that values innovation, collaboration, and a shared mission to improve patient outcomes.
Compensation: Competitive salary ranging from \(197,800 to \)223,900 per year, with comprehensive benefits.
Ready to make an impact? APPLY NOW and help us drive the future of medical innovation!
Employment Type: Full-Time
Seniority level
Director
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Human Resources Services
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