Validation Engineer

Katalyst HealthCares and Life Sciences

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA degree in a relevant scientific discipline
  • Experience in the pharmaceutical/biopharmaceutical industry
  • Minimum of two years' experience in Validation or equipment qualification
  • Knowledge of cGMP regulations
  • Strong decision-making and priority management abilities
  • Flexibility in problem-solving and work hours

Responsibilities

  • Support QC laboratory equipment qualification activities
  • Perform qualification of laboratory equipment per EQ policies
  • Coordinate qualification requirements with laboratory staff
  • Author, review, and execute equipment qualification protocols
  • Identify gaps in business, quality, and compliance
  • Sign documents as authorized by Client policies
  • Assist Senior Management with additional QC tasks

Benefits

  • Participation in continuous improvement projects
  • Full compliance with quality policies and standards
  • Support for right to operate and supply to patients
  • Engagement with a collaborative and supportive team
  • Opportunity for professional development and skill enhancement
Full Job Description
Job Description:
With direct supervision, the candidate is responsible for the support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Client principles, quality policies, standards, and core values. Maintains the company's right to operate, supply to patients, and cost-effectiveness by actively participating in continuous improvement projects.
Technical Responsibilities:
  • Perform qualification of laboratory equipment in accordance with EQ policies, plans, and procedures.
  • Coordinate with laboratory personnel to define qualification requirements.
  • uthor, review, and execute equipment qualification protocols.
  • Coordinate equipment qualification activities with vendors and other support groups.
  • Identify business, quality, and compliance gaps.
  • Sign documents for activities as authorized and described by Client policies, procedures, and job descriptions.
  • Perform any other tasks as requested by Senior Management to support QC laboratory operations.

Requirements:
Education:

  • BS/BA degree (preferably in a relevant scientific discipline).

Experience (may vary depending on site size/scope):
  • Experience in the pharmaceutical/biopharmaceutical industry, or an equivalent combination of education and experience.
  • Knowledge of cGMP or equivalent regulations.
  • Minimum of two years' experience in Validation or equipment qualification is desired.
  • bility to make sound decisions about scheduling and managing priorities.
  • Flexibility in problem-solving, providing direction, and work hours to meet business objectives.

Knowledge / Skills / Competencies:
  • Possesses strong verbal and written communication skills and the ability to influence at all levels.
  • Capable of building trustful and effective relationships.
  • ble to think strategically and translate strategies into actionable plans.
  • Takes responsibility, drives results, and achieves expected outcomes.

Work Environment / Physical Demands / Safety Considerations:
  • Standard office environment.

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