Demo

Program Manager, Quality Control

Varite
Lenexa, KS Full Time
POSTED ON 2/4/2025
AVAILABLE BEFORE 5/4/2025

Job Description :

Work Schedule - Standard (Mon-Fri) 8am to 5pm

Environmental Conditions - Office

How will you make an impact?

The role supports manufacturing by collaborating with various functional teams to enhance operations and optimize processes.

Key Responsibilities :

  • Documentation Review & Updates -

Ensure batch manufacturing records and SOPs are accurate and meet ISO standards.

  • Identify discrepancies in the manufacturing process system versus records and update accordingly.
  • Evaluate and update documentation to ensure compliance with cGMPs and alignment with regulations.
  • Employee Support - Assist employees with documentation corrections and batch management processes through daily interactions.
  • Education / Experience

  • Bachelor's degree or 3-5 years of experience with previous experience in operations / Manufacturing or quality assurance in a medical device or pharmaceutical facility.
  • Project Management is a plus
  • Knowledge, Skill, and Requirements

  • bility to understand and analyze process manufacturing systems
  • Highly autonomous and able to identify and resolve opportunities through multiple functional groups.
  • Working Knowledge of BSI and ISO standards and regulations - ISO 17034
  • Excellent organizational skills and analytical and problem-solving abilities,
  • Possesses exceptional time management and multi-tasking abilities to meet commitments and deadlines.
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