Buyer, Strategic Sourcing Specialist

Adare Pharma

$80K — $95K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Business, Finance, Engineering, or Life Sciences; or extensive experience with a high school diploma.
  • 5+ years of experience in Pharmaceutical Manufacturing or other GMP-regulated industries.
  • Proficiency in Microsoft Word, Excel, PowerPoint, and Microsoft AX Enterprise.
  • Strong planning and coordination skills with adaptability to changing priorities.
  • Attention to detail in documentation and reporting.
  • Strong written communication skills with creativity and enthusiasm.
  • Ability to work collaboratively in team settings across multiple projects.

Responsibilities

  • Drive new project sourcing and material ordering for Packaging Operations.
  • Administer the Procure-to-Pay process effectively.
  • Manage delivery schedules and resolve supplier quality issues as necessary.
  • Identify and source new suppliers to support product development while ensuring cGMP compliance.
  • Collaborate with suppliers and finance to establish product costs.
  • Develop and maintain sourcing activity reports to communicate project statuses.
  • Provide sourcing support for scale-up, technology transfers, and commercial projects when needed.

Benefits

  • Support for professional development and training opportunities.
  • Collaborative work environment within cross-functional teams.
  • Opportunity to participate in innovative projects in the pharmaceutical sector.
Full Job Description
Position

Buyer, Strategic Sourcing Specialist

Location

Philadelphia, Pennsylvania

Summary

The Buyer, Strategic Sourcing Specialist will perform Direct Materials Sourcing and other Procurement activities including Supplier relationship management, Procure-to-Pay activities, process improvement, management of delivery schedules, and reporting activities as mandated by cGMP's policies/procedures. The Buyer is also an active team member of Packaging Operations Team, Customer Project Development Teams and leads Supplier sourcing and Direct Materials category reviews.

Responsibilities
  • Responsible for driving all aspects of new project sourcing and new material ordering for Packaging Operations involving primary & secondary packaging of OSD (oral solid dose) Therapeutics encompassing bottles, caps, desiccants, excipients, cartooning, labeling, as well as the Quality Control Lab.
  • Administrator of the Procure-to-Pay process
  • Manage delivery schedule(s) certificates of analysis, and supplier quality issues; resolve or escalate as appropriate
  • Identify and source new sources of supply to support new products and alternate sourcing activities that best meet the development and commercial requirements of Adare, including supplier sustainability, cGMP and capacity needs.
  • Work with suppliers, product development and finance to help establish costs of new products.
  • Develop and maintain reports on all sourcing activities as needed to communicate the status of all direct materials needed for development and alternate sourcing projects.
  • Provide sourcing support for scale-up, technology transfer and commercial projects when needed
  • Follow cGMPs, safety procedures, DEA procedures, department SOPs and company policies
  • Assist department in other assigned functions as required
  • Must participate and successfully complete all training as required by the company


Experience, Education, and Skills Required
  • B.S. or B.A. preferably in Business, Finance, Engineering, or Life Sciences with some direct procurement knowledge, or minimum High School diploma with extensive experience sourcing direct materials for chemistry labs and/or packaging lines
  • 5+ years Pharmaceutical Manufacturing or other GMP regulated industry experience
  • Computer skills and Microsoft Word, Excel, PowerPoint, Microsoft AX Enterprise
  • Good planning and coordination skills and able to adapt to changes in priorities and project schedules
  • Quality and attention to detail in documentation work and reports
  • Strong written communication skills, creativity, and enthusiasm
  • Ability to work well in a team setting and work on multiple projects
  • Good knowledge of cGMP requirements and current industry practices
  • Ability to effectively present information

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