Quality Specialist - II (Associate)

Primary Talent Partners
  • Rahway, NJ
  • $45.86 Per Hour
  • Instant Apply
1 day ago

Job Description

Primary Talent Partners has a new contract opening for a Quality Specialist - II (Associate) to join our pharmaceutical client in Rahway, NJ. This is a 23-month contract to start with the potential for extensions. 


Pay:$45.86/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.


Description
Responsibilities:
  • This position reports to the Associate Director, Global Clinical Complaints, Global Development Quality, and supports the clinical complaint process for clinical supplies used in worldwide clinical trials.
  • The primary focus of this role is the intake, processing, documentation, coordination, and follow-up of distribution-related clinical complaints, including issues associated with shipment, delivery, transportation and handling of clinical supplies
  • The individual will communicate with clinical sites and internal stakeholders to obtain required information, ensure complaints are accurately documented and routed to the appropriate investigating function, and monitor activities through completion.


Primary Responsibilities:
  • Receive and process distribution-related clinical complaints in accordance with established procedures and work instructions.
  • Communicate with clinical sites and internal stakeholders to obtain required complaint information and supporting documentation to ensure they meet establish criteria for processing
  • Review complaint information for completeness and perform initial categorization using established criteria and decision tools.
  • Enter, maintain, and update complaint information within applicable complaint management systems.
  • Route complaints to the appropriate functional area for investigation and follow up in accordance with established procedures and to support timely completion and on-time closure of reported distribution complaint.
  • Support coordination of clinical supply activities associated with distribution-related complaints, including usability assessment of supplies impacted by temperature excursions during shipping, shipment issues/errors, shipments to incorrect destinations, temperature device malfunctions, etc.


Education Minimum Requirement:
  • Bachelor degree, technical emphasis in an appropriate scientific or engineering field preferred;
  • Required Experience and Skills
  • Minimum of 3 to 6 years of relevant post-degree experience in the Pharmaceutical or equivalent industry (Good Manufacturing Practice (GMP) related field) including Technical, Engineering, Quality or Operations.
  • Ability to follow established procedures, work instructions, and defined decision criteria.
  • Strong attention to detail and ability to maintain accurate documentation.
  • Effective written and verbal communication skills, particularly when obtaining information and following up with internal stakeholders or clinical sites.
  • Ability to manage assigned activities and meet established timelines.
  • Ability to recognize issues requiring escalation and seek guidance when appropriate.
  • Effectiveness and creativity in approaching and solving technical problems.
  • Basic understanding of the use and maintenance of Microsoft applications (such as MS Excel, Outlook, and/or MS Access).
  • Demonstrated teamwork skills and the ability to work independently.
  • Willingness and ability to learn complaint-management and clinical-supply systems and processes.


Preferred Experience and Skills:
  • Previous experience in clinical supply, distribution, logistics, customer service, complaint intake, or quality-related operations.
  • Previous experience in quality control, quality assurance, auditing or regulatory affairs.
  • Ability to independently manage multiple priorities.
  • Familiarity with clinical trials or the clinical supply chain.
  • Experience with systems such as Veeva, SAP, TrackWise, or other quality/supply-chain systems is preferred but not required.


Note:
  • Hybrid(3 days onsite flexible)
  • Rahway,NJ


Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com


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Numbers & Facts

LocationRahway, NJ
Salary$45.86 Per Hour

Skills

  • Auditingunmatched
  • Biotech and Pharmaceuticalunmatched
  • Clinical Information Systemsunmatched
  • Clinical Supportunmatched
  • Clinical Trialunmatched
  • Communication Skillsunmatched
  • Customer Support/Serviceunmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Logisticsunmatched
  • Medical Productsunmatched
  • Microsoft Access Databaseunmatched
  • Microsoft Excelunmatched
  • Microsoft Outlookunmatched
  • Microsoft Product Familyunmatched
  • Multitaskingunmatched
  • Presentation/Verbal Skillsunmatched
  • Problem Solving Skillsunmatched
  • Procedure Developmentunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Regulationsunmatched
  • SAPunmatched
  • Software Administrationunmatched
  • Supply Chainunmatched
  • Team Playerunmatched
  • Time Managementunmatched
  • Usability Engineeringunmatched
  • Writing Skillsunmatched

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