Validation Engineer
$50 - $55 per hourjob summary:
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical company is seeking a Validation Specialist to support critical qualification activities for manufacturing equipment, facilities, and utilities during a high-priority site startup. location: Piscataway, New Jersey
job type: Contract
salary: $50 - 55 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
skills: Good Manufacturing Practices (GMP), Equipment Validation
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Are you a driven validation professional looking to make an immediate impact on a major GMP facility expansion? A leading global pharmaceutical company is seeking a Validation Specialist to support critical qualification activities for manufacturing equipment, facilities, and utilities during a high-priority site startup. location: Piscataway, New Jersey
job type: Contract
salary: $50 - 55 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Design, review, and execute FAT, IQ, OQ, and PQ protocols for GMP equipment, utilities, and facilities.
- Act with a project management mindset to schedule vendors, manage tight timelines, and track validation deliverables.
- Perform re-qualification activities and write detailed technical investigation reports for non-conformances.
- Partner closely with Maintenance, Engineering, Quality, and external vendors to ensure seamless installation and commissioning.
- Generate weekly and monthly validation progress reports to keep project schedules on track.
qualifications:
- Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related field.
- 2+ years of validation/qualification experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment.
- Strong working knowledge of GDP, FDA regulations, and risk-based validation principles.
- Proven ability to draft/execute protocols, analyze test data, document discrepancies, and manage vendor schedules.
- Flexibility to work occasional weekend hours as required by project and vendor schedules.
skills: Good Manufacturing Practices (GMP), Equipment Validation
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on us.fitly.work.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Vacancy posted 1 day ago
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