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Pharmaceutical Validation Jobs (NOW HIRING)

Arthur Lawrence

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CSV/CQV Validation Lead - Pharmaceutical Industry

San Juan, PR · On-site

$50 - $60/hr

At least two years of experience leading or managing validation projects. * Extensive CSV and/or CQV experience within pharmaceutical, biotechnology, medical-device, or another regulated life ...

Alcami Corporation

Sr. Validations Specialist

Morrisville, NC · On-site

$77K - $106K/yr

... pharmaceutical validation of equipment and GxP computerized systems. Specific responsibilities include reviewing SOP's, composing/revising SOP's and validation master plans; supporting facility ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

New

Netpace

Registered Pharmacist

Sinking Spring, PA · On-site

... pharmaceutical practice. Performing other administrative tasks when needed. Pharmacist Requirements Proven experience as a pharmacist. Valid license to practice as a pharmacist. Excellent verbal and ...

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

New

Validation & Engineering Group, Inc

PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

New

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

New

Actalent

Microbiology Validation

East Troy, WI

Apply working knowledge of 21 CFR Parts 210 and 211, data integrity principles, and pharmaceutical laboratory cGMP requirements to all validation activities. * Collaborate closely with Operations ...

New

Validation & Engineering Group, Inc

PR

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

New

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Pharmaceutical Validation information

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How much do pharmaceutical validation jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for pharmaceutical validation 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 some of the main challenges encountered in a pharmaceutical validation role?

One of the main challenges in Pharmaceutical Validation is staying updated with constantly evolving regulatory requirements and ensuring that all validation activities meet stringent compliance standards. Professionals often manage multiple concurrent projects, which requires effective prioritization, organization, and close coordination with cross-functional teams such as quality assurance, manufacturing, and engineering. Thorough documentation and meticulous attention to detail are essential, as even minor oversights can lead to compliance issues. However, overcoming these challenges provides valuable problem-solving experience and opportunities for advancement within quality assurance, regulatory affairs, or project management.

What is a pharmaceutical validation?

A Pharmaceutical Validation job involves ensuring that systems, equipment, and processes in the pharmaceutical industry meet regulatory and quality standards. Professionals in this role develop protocols, conduct testing, and document validation activities to ensure compliance with regulations like FDA, EU GMP, and ISO standards. They work with manufacturing processes, laboratory instruments, and software to verify that products are consistently produced and controlled according to required quality standards. This role is critical in maintaining drug safety, efficacy, and regulatory approval.

What are the key skills and qualifications needed to thrive in pharmaceutical validation, and why are they important?

To thrive in Pharmaceutical Validation, you need a strong background in pharmaceutical sciences or engineering, familiarity with regulatory guidelines (such as FDA, GMP, and ICH), and hands-on experience in validation protocols. Proficiency with validation lifecycle documentation tools, quality management systems (QMS), and specialized software like TrackWise or ValGenesis is essential. Attention to detail, analytical thinking, and excellent collaboration and communication skills are highly valued in this role. These competencies ensure that pharmaceutical processes, equipment, and systems meet strict quality standards, supporting product safety and regulatory compliance.

More about Pharmaceutical Validation jobs
What cities are hiring for Pharmaceutical Validation jobs? Cities with the most Pharmaceutical Validation job openings:
What are the most commonly searched types of Pharmaceutical Validation jobs? The most popular types of Pharmaceutical Validation jobs are:
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Pharmaceutical Validation jobs near you
Infographic showing various Pharmaceutical Validation job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 3% Part Time, and 7% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer II

Sun Pharmaceutical Industries

Billerica, MA • On-site

$104K - $115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Job description

Job Summary
Validation Engineer II is expected to execute validation and qualification activities for pharmaceutical manufacturing systems in compliance with cGMP requirements, industry standards, and standard operating procedures under guidance from Manager.
Area Of Responsibility
  • Supports the execution of equipment validation and maintenance as required
  • Execute, under supervision, equipment qualification and requalification for manufacturing
  • Participates in the operation of process equipment as well as associated documentation
  • Support execution of preventative maintenance of pharmaceutical process equipment and utilities
  • Supports equipment readiness to support the production schedule and is in proper condition/calibration
  • Provide operational coverage for manufacturing equipment and utilities
  • Support production personnel on equipment and utility operation
  • Support re-qualification of process equipment, testing & certifications of manufacturing process
  • Support area manufacturing and new product/process transfer activities
  • Participates in equipment/utility related CAPAs, Deviations, and Investigations
  • Review, under supervision, process utilities and equipment logs
  • Support loading / lyophylization cycle and coordination of equipment
  • Participates in the troubleshoot and remediate exceptions found during FAT/SAT/IQ/OQ/PQ
  • Supports timely closure of equipment/utility related CAPAs and/or Change Controls
  • Support Validation of equipment/utilities/process transfers and re-qualifications
  • Support URS/FS/DS engineering documents of process related systems
  • Other duties as assigned

Work Conditions:
  • Office
  • Lab
  • Manufacturing area/clean room area
  • Maintenance Shop
  • Exposure to noise, hot and cold, outside elements, some radiation

Physical Requirements:
  • Stand, sit, walk, use hands and fingers to handle or feel, reach with hands and arms
  • Climb or balance, stoop, kneel, crouch or crawl, talk, hear, taste, smell
  • Close vision; ability to adjust focus
  • Operate computer/office machines, autoclave, depyrogenation oven, vial filler, freeze dryer, steam generators, power tools
  • Wear proper gowning and safety equipment as needed
  • Lift up to 50 lbs.

Travel Estimate
Up to 0%
Education and Job Qualification
  • Bachelor's in Science, Engineering or related field preferred or equivalent experience

Experience
  • Minimum 4+ years related experience preferred
  • Ability to oversee cGMP validation compliance efforts
  • Ability to operate and maintain process equipment and utilizes (Sterilizers, Depyrogenation Ovens, Lyophilers, Incubators, CTU's)
  • Familiarity with FDA cGMP, SOPs and ISO standards
  • Knowledge of pharmaceutical manufacturing equipment and utilities
  • Familiarity/Knowledge of aseptic techniques
  • Excellent organizational skills

The presently-anticipated base compensation pay range for this position is $104,000 to $115,500. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.

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