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Posted 6 days ago

Temp-QA AssociateAlkermes · Wilmington

Temp-QA Associate

WilmingtonOn-siteFull-time

AI Summary

Supports daily manufacturing operations and quality systems in a pharmaceutical GMP setting, handling GxP documentation, document management, SOP development and evaluation of executed records. Temporary, 0-2 years of pharmaceutical QA experience required.

About this role

This is a temporary position.

This role is responsible for supporting the daily activities related to manufacturing operations and quality systems.

Qualifications

Education:

  • Requires a Bachelor’s degree in a scientific discipline or equivalent experience.

Experience:

  • 0-2 years’ experience in a Quality Assurance role in the pharmaceutical industry.

Responsibilities

Key Duties:

  • Issuance of GxP documentation.
  • Document Management System Support.
  • Support documentation lifecycle (Document Scanning, Verification, Retention, and Destruction).
  • Develop Standard Operating Procedures and other quality related documents.
  • Evaluation of executed documentation (logbooks, controlled forms, and other documentation).
  • Support area initiatives and projects.

Skills / Abilities:

  • Experience in Pharmaceutical Quality Assurance, including the ability to identify and resolve compliance issues.
  • Ability to increase others knowledge of US end European GMP regulations and guidance.
  • Strong written and oral communication skills.
  • Experience in support of quality systems for drug product manufacturing and quality control operations.
  • Working knowledge of US Drug Product GMP requirements and associated guidelines.

Personal Attributes:

  • Team Player committed to quality; motivated self-starter; detail and results oriented; Well organized, efficient worker with good communication skills; innovative thinker and problem solver; flexible and can embrace change; can manage multiple duties and tasks.
  • Ability to utilize knowledge and interpersonal skills to provide leadership, direction and development of others.
  • Good computer skills.
  • Good work ethic, dependable, punctual, and flexible.
  • Good motivator of personnel.
  • Good team player with a can-do attitude.
  • Can get things done on the basis of influence.
  • Can work in a fast-paced environment with multiple issues open simultaneously.
  • Highly organized.
  • Attention to detail.
  • Identifies opportunities to improve and contributes to problem solving.

Skills

ComplianceDocument Management SystemDrug Product ManufacturingEuropean GMPGMPGxP DocumentationQuality AssuranceQuality Control OperationsQuality SystemsStandard Operating ProceduresUS Drug Product GMP

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