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Senior Manager, Supply Chain Systems

unlimited holidays - fully flexible
Remote: 
Full Remote
Experience: 
Senior (5-10 years)

Offer summary

Qualifications:

BS degree in related field, 6-8 years of Supply Chain experience, 2 years in GMP manufacturing environment, Proficient in Excel and ERP systems.

Key responsabilities:

  • Oversee timelines for internal activities and CMOs
  • Support data gathering for Sales Operations Planning
Nuvalent, Inc. logo
Nuvalent, Inc. Biotech: Biology + Technology Startup https://www.nuvalent.com/
11 - 50 Employees
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Job description

The Company:
With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.  Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. 

The Role:
Reporting to the Associate Director, Supply Chain Packaging, the Senior Manager, Supply Chain Systems will have full exposure across the different areas of the supply chain team. Nuvalent outsources all cGMP manufacturing activities to Contract Manufacturing Organizations (CMOs) to support all Clinical and Commercial production. This role will be responsible for supporting the Supply Chain department across systems, planning and operations and ensure the efficient and effective management of supply chain activities, contributing to the organization's overall success. Our fast-paced environment and hands-on opportunity will challenge you to innovate and learn while having fun with supportive and passionate colleagues.  
Responsibilities:


•    As a member of cross functional teams that includes CMC, QA, and Regulatory; execute activities for Supply Chain team on assigned projects.
•    With support from Supply Chain Management, oversee timelines for both internal activities and external production activities at Contract Manufacturing Organizations (CMOs) to ensure continuous supply of Commercial and Clinical materials through the supply chain.
•    Implement and maintain serialization for commercial products.
•    Maintain accurate inventory including production, data entry and reporting.
•    Support data gathering and reporting for Sales & Operations Planning (S&OP).
•    Execute supply chain system tests as required.
•    Issue financial inventory reports including Lot Genealogy reports to Accounting Department. 
•    Project management department projects including product launch activities to ensure that action items are identified and tracked against a project plan.
•    Support supply planning for both clinical supply chain and commercial supply chain (as needed).

Competencies:
•    Excellent problem solving, communication and organization skills 
•    Flexibility with changing priorities, strong attention to detail, ability to work well under pressure and take on unfamiliar tasks 
•    Ability to work in a collaborative environment, drive to learn and improve skills 
•    Ability to strategically plan, organize and manage multiple projects simultaneously. 
•    Ability to prioritize tasks/issues and identify risks in the future, raising awareness of potential issues in a proactive manner. 
•    Strong work ethic, ability to meet deadlines and flexibility on potential occasions you may need to work outside of immediate job role or normal job hours to get the task done and meet the deadline. 

Qualifications: 
•    BS degree in Business, Supply Chain/Material Management or life science field or related experience.
•    6-8 years of Supply Chain experience.
•    Minimum 2 years of direct experience in a GMP manufacturing environment.
•    Demonstrated knowledge and comprehensive understanding of supply chain planning, such as S&OP planning, demand planning, supply planning, inventory management.
•    Demonstrated knowledge of GMP, quality and supply chain and regulatory requirements.
•    Proficient in Excel and Microsoft productivity suite
•    Prior experience using ERP/Oracle/SAP as a platform is a plus

Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.


Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.

Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.

If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Excel
  • Problem Solving
  • Collaboration
  • Communication
  • Strong Work Ethic
  • Physical Flexibility
  • Strategic Planning
  • Detail Oriented

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