A
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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