Quality Control Analyst (Packaging) at Catalyx
Cork, County Cork, Ireland -
Full Time


Start Date

Immediate

Expiry Date

16 Jul, 25

Salary

0.0

Posted On

16 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Cglp

Industry

Information Technology/IT

Description

Catalyx are seeking an experienced candidate to join our team and work as a QC Analyst for our customer site in Cork.

WHO WE ARE :

Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services RD, production, packaging, and delivery processes—globally—with a sophisticated blend of products, technologies, and lifecycle services.
Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high- risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations.

SKILLS AND EXPERIENCE:

  • Degree in relevant field
  • Post-graduate studies as appropriate to augment primary degree.
  • Operational experience of quality laboratories in a fast moving manufacturing environment.
  • Detailed knowledge of quality management systems, pharmaceutical manufacturing operations, requirements for cGLP, pharmacopoeial methods and stability.
  • Understand relevant quality/compliance regulations.
  • Adaptable and flexible
  • Strong attention to detail.
Responsibilities
  • Review and release of Primary and secondary Packaging components.
  • Completion of the associated auxiliary tasks related to this analysis e.g. data review, archiving, liaising with Materials management etc
  • Quality investigation and root cause analysis.
  • Provide Services in a LEAN and 5S environment and adhere to the good lab practices.
  • Comply with safety and quality procedures and participate in internal and external audits as required.
  • Maintain laboratory housekeeping standards.
  • Demonstrate strong scientific and GMP documentation skills.
  • May be required to perform other duties as assigned.
Loading...