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Validation - Engineer I/II - Project Farma at PerkinElmer - ApplyBlast

Validation - Engineer I/II - Project Farma

PerkinElmer

4 months ago

2.9 on Glassdoor

Onsite

Full Time

Intern

0 applicants

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About this role

This full-time role involves executing technical tasks, developing CQV protocols, and authoring validation documents for pharmaceutical clients while ensuring compliance with FDA and GMP regulations. Engineers collaborate with cross-functional teams to deliver high-quality life sciences projects, contribute to business growth, and maintain professional relationships with clients. The position requires an individual to be willing to travel domestically up to 100% to meet client project requests and achieve billability targets.

Responsibilities

Execute specific technical tasks ensuring high-quality deliverables
Perform CQV tasks like protocol development and equipment testing
Author technical documents including SOPs and testing protocols
Execute system validation protocols using GxP best practices
Maintain billable targets by completing assigned project tasks

Skills

Qualifications

Bachelor's Degree in Life ScienceBachelor's Degree in EngineeringCapital Project Engineering Experience

About PerkinElmer

perkinelmer.com

Headquarters

Shelton, Connecticut, United States

Company Size

5001-10000 employees

Founded

1937

View Profile

PerkinElmer is a global leader in life sciences and analytical instrumentation, delivering hardware, software, and services that enable discovery, measurement, and testing across biopharma, food safety, environmental analysis, and industrial markets. The company’s portfolio includes mass spectrometry, chromatography, spectroscopy, thermal analysis, and lab IT solutions, serving customers worldwide to advance science and safety.