Job Description
Job Summary
We hire W2 only - No C2C
With direct supervision, the candidate supports and executes QC laboratory equipment qualification activities in full compliance with current cGMP regulations and Lonza corporate 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.
Duties
Technical Responsibilities
Qualify laboratory equipment in accordance with EQ policies, plans, and procedures.
Coordinate with laboratory personnel to define qualification requirements.
Author, 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 Lonza policies, procedures, and job descriptions.
Perform any other tasks as requested by Senior Management to support QC laboratory operations.
Job 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.
Ability 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 trusting and effective relationships.
Able 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