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Entry Level Pharma Validation Engineer Jobs (NOW HIRING)

FITS LLC

Process Validation Engineer - 134

Villalba, PR · On-site

No sterile package design or pharma design The Personality Part: * Our Next Piece is someone who ... Guide engineers regarding design concepts and specification requirements to best utilize equipment ...

PSC Biotech

Validation Engineer I

Bodega Bay, CA · On-site +1

$20 - $23/hr

Your Role We are hiring a Validation Engineer I to join our team! This position will support system ... This is an entry-level, remote position. Successful candidates have a bachelor's degree within an ...

PSC Biotech

Validation Engineer I

Bodega Bay, CA · On-site +1

$20 - $23/hr

Your Role We are hiring a Validation Engineer I to join our team. This position will support system ... This is an entry-level, remote position. Successful candidates have a bachelor's degree within an ...

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Entry Level Pharma Validation Engineer information

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How much do entry level pharma validation engineer jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for entry level pharma validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Pharma Validation Engineer jobs? The most popular types of Pharma Validation Engineer jobs are:
Entry Level Pharma Validation Engineer jobs near you
Validation Engineer-Portsmouth, New Hampshire(Hybrid)

Validation Engineer-Portsmouth, New Hampshire(Hybrid)

Sailotech

Portsmouth, NH • On-site

Contractor

Posted 21 days ago

Job description

Position: Validation Engineer II

Location: Portsmouth, New Hampshire(Hybrid)


The CSV Engineer will, as an individual contributor, identify and implement industry best practices through an extensive industry network and detailed knowledge of applicable regulations. During the scoping portion of these improvement projects the person in this role will work with other experienced members of the CSV team to identify roadblocks and additional efficiencies. Additional day to day tasks will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions.
Execute all responsibilities as the CSV owner for significant site and process improvement projects, to ensure compliance to appropriate regulatory requirements and industry standards while maximizing efficiency.
Perform all aspects of QMS process’ – Change Control (particularly associated with DCS ( DeltaV) and MES ( Syncade) systems, Deviations, CAPAs. Perform other duties as assigned.
Key requirements include:
1) Substantial experience in in equipment and/or computer validations. Must have Working experience with Controls Automation, Process Control Systems, Distributed Systems, Manufacturing Execution Systems (MES) required, DeltaV preferred.
2) Prior experience leading projects in a Biotech/Pharma or biologics industry.
3) Strong attention to detail and ability to work independently and meet deadlines successfully.