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Pharmaceutical Assistant Engineer Jobs (NOW HIRING)

PIVOT Workforce

Project Engineer

Indianapolis, IN

$80K - $90K/yr

Key Responsibilities: Assist the project team in planning, scheduling, and coordinating construction activities for pharmaceutical projects. Support the Project Engineer in managing day-to-day ...

Eliquent Life Sciences, Inc

Project Engineer

Montrose, CA · On-site

$90K - $100K/yr

... procedures. * Assist in troubleshooting and resolving engineering issues during commissioning and initial production phases. Skills: The required skills in Pharmaceutical Engineering and ...

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Pharmaceutical Assistant Engineer information

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$33K

$88.8K

$134.5K

How much do pharmaceutical assistant engineer jobs pay per year?

As of Sep 11, 2026, the average yearly pay for pharmaceutical assistant engineer in the United States is $88,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $104,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Pharmaceutical Assistant Engineer jobs?

For Pharmaceutical Assistant Engineer jobs, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Assistant Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 1% Temporary, and 3% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $88,754 per year, or $42.7 per hour.

Validation Engineer

Valley Falls, KS • On-site

Pioneer Data Systems
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Pioneer Data Systemsexternal

Contractor

Re-posted 6 days ago

Job description

Company Description
Job Description
Job Description: POSITION SUMMARY
• Validation engineer with experience in equipment, HVAC, utility and process qualification within a pharmaceutical industry. Previous plant experience is recommended. Background in aseptic processing, microbiology, environmental monitoring, chemistry, and production is recommended. The additional resources are requested for a total of fourteen (14) weeks starting in December 2017 and ending March 2018 to support Winter Shutdown changes. Hours can involve weekend or night shifts. Validation activities including writing system impact assessments, oversight of engineering during shutdown activities, execution of installation qualification, operational qualification, performance qualification, and summarizing qualification results/drafting qualification report summaries. The support staff must act in accordance with plant safety requirements, training and procedures.
POSITION RESPONSIBILITIES
• Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs) and regulatory guidelines.
• Coordinates and communicates all testing with affected functional groups and evaluates test results.
• Executes equipment, facility, utility and computer system, Automated Process Control validation studies to include protocol preparation, scheduling, protocol execution, analyze data and compose a final report.
• Oversee and assist Engineers and/or Technicians with their assigned projects.
• Provide technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGXP, CFR 21 Parts, 11, 210 and 211, EU Annex 11, ICH Q7, Q8 and Q9, and other applicable regulations, procedures and industry guidance.
• Thorough understanding of risk based validation, industry standards and best practices for validation.
ORGANIZATIONAL RELATIONSHIPS
• Will interact with Shutdown stakeholders: Engineering, Operations, Quality, Safety, Planning, Contractors, etc.
• Weekly/daily meeting attendance as required.
• Will participate in team led by Pfizer group leaders.
EDUCATION AND EXPERIENCE
• Education: BS/BA degree in science, engineering, manufacturing technology or closely related field or combination of education and work experience
• Experience: Recommended minimum of 4 years pharmaceutical validation experience
TECHNICAL SKILLS REQUIREMENTS
• Knowledge of ICH and other regulatory guidelines; demonstrated ability to interpret and apply these guidelines to document writing
PHYSICAL POSITION REQUIREMENTS
• Logistics: Requires contractor to be on-site weekly with travel home every other weekend
• Must be able and willing to work beyond office hours which may include weekends.
• Requires routine sitting, standing, walking, listening and talking
• Acute mental and visual attention at all times
• Handle multiple projects while managing frequent interruptions
• Requires moderate lifting or moving up to 25 pounds (lbs
Qualifications
Additional Information
Anuj Mehta
732-947-3452

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