Validation Engineer
Vacaville, CA
Validation Engineer
Onsite Monday-Friday, 8:00 AM-4:00 PM, with weekly pay and healthcare benefits; 12+ month contract with potential extension or permanent placement. Requires a BS/BA, pharmaceutical/biopharmaceutical or equivalent experience, cGMP knowledge, and 2+ years in validation or equipment qualification.
Role: Validation Engineer - Onsite
Location: 1000 New Horizons Way, Vacaville, CA 95688
Contract: 12+ months contract with potential for extension and/or permanent placement
Schedule: Monday – Friday, 8:00 AM – 4:00 PM (includes a 30-minute unpaid lunch)
Pay Rate: $52/hour, based on experience
Benefits: Weekly pay and healthcare benefits offered!
Job Summary:
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's 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:
Perform qualification of 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 client's 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 trustful 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.
#TMCA
Location: 1000 New Horizons Way, Vacaville, CA 95688
Contract: 12+ months contract with potential for extension and/or permanent placement
Schedule: Monday – Friday, 8:00 AM – 4:00 PM (includes a 30-minute unpaid lunch)
Pay Rate: $52/hour, based on experience
Benefits: Weekly pay and healthcare benefits offered!
Job Summary:
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's 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:
Perform qualification of 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 client's 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 trustful 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.
#TMCA