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Associate Raw Material Supply - Biopharma (JP8126)

Cambridge, MA · Biotech/Pharmaceutical
Job Title: Associate Raw Material Supply (JP8126)
Location: Cambridge, MA (Remote then onsite after Covid-19 restrictions are lifted)
Employment Type: Contract
Business Unit: Raw Materials - Specifications 
Duration: 12 months with likely extensions
Job posting date: 1/19/2021
Note: Remote until COVID-19 restrictions are lifted.
 
3 Key Consulting is hiring Associate Raw Material Supply for a consulting engagement with our client, a leading global bio-pharmaceutical company.
 
Job Summary:
Will support raw material specification management process by performing all tasks associated with master data management required to onboard new raw materials or complete revisions to existing materials. The position requires the ability to work in a fast paced dynamic environment and the ability to communicate with cross-functional teams.
 
Responsibilities include:
  • SAP master data management, adherence to timelines to support clinical and commercial production.
  • Change control, CAPA, and Deviation ownership to support the external supply specification management team.
  • Provide project support for specification management initiatives.
  • Consistently follow Standard Operating Procedures (SOPs).
 
Qualifications: 1+ year of experience within quality systems, track wise, CAPA, owning change control records, procurement, SAP, supply chain, a self-starter and independent worker
(This is not warehouse, this is all computer based)

Skills:
  • Technical writing; SAP experience.
  • Quality System record ownership (change control, CAPA, NC)
  • Project Management
  • Degree in Life Science (Biochemistry, Analytical Chemistry, Bio-Manufacturing, Process development, Chemistry, Biology) or Engineering is preferred.
 

Top Must have Skill Sets:
  • Good Written and Verbal Communication
  • Ability to work cross-functionally with technical and non-technical functions
  • Strong ability to organize and complete deliverables on time
 
Day-To-Day Responsibilities:
Author and own change controls to revise or create master data to support material onboarding.
Coordinate with specification owners to ensure master date timelines are maintained.
On occasion own CAPA or Nonconformance records to support the specification management team
 
Employee Value Proposition:
Newly formed role that will gain you exposure to the company’s process
 
Red Flags:
Someone who cannot work independently (with some support)
Someone who cannot be flexible with changing priorities
 
Interview Process: 
Phone & Video WebEx 
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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