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This is a 12-month contract, with an immediate start. The role offers hybrid working, with 3 days on site in Paddington.
Looking for opportunities with purpose, impact and possibilities? Our client, Vertex, is a global biotechnology company that invests in scientific innovation. As they grow their pipeline at pace, they are strengthening their reputation for creating transformative medicines for people with serious diseases.
In June 2019, Vertex announced the establishment of a new research site in the Boston area where research, development, and clinical manufacturing for cell and genetic therapies will be primarily based. Cell and genetic therapies represent two rapidly emerging therapeutic modalities with the potential to treat—and even cure—several of the diseases Vertex is focused on, including sickle cell disease, Duchenne muscular dystrophy and type 1 diabetes.
Further investment in a research site specifically designed to advance these programs will be key to Vertex’s continued and sustained leadership in these exciting approaches.
At Vertex Cell and Genetic Therapies (VCGT) our research teams will bring together the best biology, technologies and enhanced manufacturing capabilities to ensure we bring these cutting-edge transformative therapies to patients as quickly as possible.
VCGT is seeking a Supply Chain Senior Planner to establish raw material plans and supply plans for all direct and indirect materials and manufacturing sites, supporting all VCGT programs.
This position will support Vertex’s cell and gene programs.
The Supply Chain Senior Planner will join the fast-growing supply chain team and report to the Associate Director of Supply Planning, VCGT.
The position will be supporting multiple manufacturing sites and programs as well as from process development to manufacturing.
This role will support planning needs for sites located in Providence, RI and Cambridge, MA and Boston, MA.
Key Duties and Responsibilities:
* Represents Supply Chain department on assigned project sub-teams and/or task forces and, with general guidance, executes supply chain production activities.
* Analyses the Material Requirement Plan to calculate raw material needed to support both internal and external demands.
* Delivers inventory plans with general guidance based on material requirements analysis in support of projects.
* Works with various cross-functional groups (such as Quality, Tech Ops, Regulatory, suppliers, etc.) to proactively and collaboratively resolve issues that may block the timely flow of materials or projects.
* Monitors a raw material risk management strategy and process that addresses any potential disruption to each of the programs within VCGT. This includes materials needed for the cell, gene and device manufacturing.
* Collaborate with internal stakeholders in the development and execution of product strategies.
* Communicate progress to management and key stake holders on material plan changes.
* Identify and mitigate risks related to supply chain disruption and delays, sup?plier product and / or manufacturing changes and supplier inability to support current or future demands.
* Analyse raw material consumption across the global supply chain. Identify ar?eas of risk and cost savings opportunities.
* Partner with Strategic Sourcing and CMC to ensure the supplier and material selection process is aligned with the overall product strategy.
* Execute all actions in accordance with established procedures and processes. Recommend improvements to such processes and system needs.
* Collaborate with key stakeholders to help solve supplier and material related is?sues (backorders, product quality concerns).
* Initiate and document planned/unplanned material deviations, NCMRs, and supplier CAPAs as necessary.
* Utilize business systems (Oracle ERP, Rapid Response) to understand data.
* Research past and expected spend levels to understand and action areas of cost savings opportunities and potential risk.
* Maintain strong cross functional relationships to bolster communication with internal and external stakeholders.
Knowledge and Skills:
* Ability to contribute to complex contract negotiations.
* Proven ability to manage multiple projects with high degree of effectiveness.
* Possesses a distinguished record of delivering on critical project goals and moving projects forward.
* Exhibits robust knowledge across supply chain disciplines.
* Strong knowledge in overall drug development.
* Demonstrates strong aptitude for managing and motivating others and building team unity.
* Proven ability to communicate clearly and concisely (written/oral) with all levels of the company.
* Good understanding of the medical device and biotech industry and market.
* High level understanding of GMP processes and regulatory requirements.
* Ability to effectively plan, prioritize, execute, follow up and anticipate challenges.
* Results orientated with strong sense of urgency to mitigate risk and close issues.
* Knowledge of ERP setups with skills and proficiency to include MRP and ability to download and analyze data.
* Experience with quality management systems (change controls, deviations, etc).
* Ability to communicate complex problems and necessary decision points both visually and verbally.
* Excellent interpersonal, verbal, and written communication skills.
* Advanced Degree Preferred.
* Experience working in a cGMP environment.
* Experience working in a start-up environment
Education and Experience:
* Bachelor’s Degree in Supply Chain/Manufacturing Operations-related disciplines
* 4+ year of Biotech, Pharmaceutical or CRO company related work experience
Vertex is partnering with Talent Works to manage their international temporary job openings. If you are successful in your application, you will be employed by Talent Works to work on a temporary assignment at Vertex.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Contract
Job function
* Job function
Supply Chain
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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