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Quality Specialist (FOR SUPPLY CHAIN DEPT)

00777, PR
  • Expired: over a month ago. Applications are no longer accepted.
Job Description


PharmaLex is a highly successful and growing consulting company for the Healthcare industry. PharmaLex offers professional development, training, competitive compensation, plus a stimulating and collaborative work environment. We are committed in providing exciting career opportunities in an atmosphere that values trust, respect, teamwork, creative talent, enthusiasm and diligence.

General Description:

We are looking for resources to provide services in Juncos, Puerto Rico


  • Under minimal supervision provides Supply Chain work group supervision and technical expertise in support of successfully completing daily operations within scope of responsibility.
  • Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines and company procedures.
  • Direct and coordinate daily activities of personnel responsible for material receipt, storage and transport.
  • Ensures materials are received, stored and transported according to established performance standards and all applicable procedures and regulations.
  • Interacts with internal and external regulatory agencies to ensure compliance with cGMP, DOT, OSHA requirements.
  • Collaborate with other sites to maintain optimal flexibility for the storage of all materials and product.
  • Identify and oversee implementation of new and improved business and compliance systems and tools.
  • Partner with key internal customer groups and/or external suppliers to ensure successful operations and performance targets are achieved.
  • Responsible for business continuity programs for assigned areas.
  • Participate on global functional teams to coordinate and improve the transportation and Logistics of material movement and storage across the company's Supply Chain.
  • Direct and coordinate daily activities of personnel responsible for developing and managing Product demand and forecasts.
  • Organize and communicate on a regular basis the total demand and supply requirements to senior management.
  • Coordinate the Master Production Schedule for Finished Goods and effectively communicate any impact created by, and to the supply plan.
  • Manage the process of gathering, evaluating and feedback of global demand requirements.
  • Provide and coordinate the development of business case scenarios that demonstrate the impact of current or proposed operations plans.
  • Manage the preparation and communication of the Company wide Inventory Distribution Plan to achieve corporate goals of customer satisfaction and risk management.
  • Develop and coordinate the long-range production requirements based on Marketing forecasts, product approval and release timelines, clinical requirements, SKU put-up information and business planning timelines estimates.


  • Doctorate degree
  • OR Master’s degree and 2 years of experience
  • OR Bachelor’s degree and 4 years of experience
  • OR Associate’s degree and 10 years of experience
  • OR High school diploma / GED and 12 years of experience
  • Preferred in Sciences
  • Previous proven experience in Quality and Compliance areas.
  • Experience investigating deviation (non-conformance) from simple to complex investigation.
  • Knowledge in Computer and Technology
  • TrackWise system is a must
  • Proficiency in written and Oral Communication
  • Technical writing is a must
  • Critical thinker and problem solver
  • Have attention to detail
  • Research skills
  • Interviewing skills
  • Professionalism
  • Integrity
  • Persistence
  • Self-driven
  • Have organization skills, to plan investigation and meet deadlines

PharmaLex is an Equal Opportunity Employer.

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00777, PR
00777 USA



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