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Director Validation Jobs (NOW HIRING)

Sr. Validation Engineer

Pepperell, MA · On-site

$43.27 - $53.49/hr

Candidates with an HSD/GED, technical training, or an Associate's degree combined with mechanical aptitude or relevant industry experience considered. * 5+ years of direct validation experience ...

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

PR · On-site

Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Proven experience as a Validation Engineer in a manufacturing environment. * Strong knowledge ...

Direct validation test plans from development through completion, including failure analysis, reporting, and coordination with customer joint qualification (JQ) requirements. * Perform hands-on ...

Position Overview The Director, DRG Validation is responsible for the strategic leadership, operational performance, innovation, and growth of the DRG Validation solution across both pre-pay and post ...

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Director Validation information

See salary details

$28.5K

$135.2K

$199K

How much do director validation jobs pay per year?

As of Jul 11, 2026, the average yearly pay for director validation in the United States is $135,161.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,500.00 and $186,500.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Director Validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What does a Director of Validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the key skills and qualifications needed to thrive in the Director Validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

More about Director Validation jobs
What cities are hiring for Director Validation jobs? Cities with the most Director Validation job openings:
What are the most commonly searched types of Validation jobs? The most popular types of Validation jobs are:
What states have the most Director Validation jobs? States with the most job openings for Director Validation jobs include:
Sr. Validation Engineer

Sr. Validation Engineer

Alcami Corporation

Pepperell, MA • On-site

$43.27 - $53.49/hr

Full-time

Posted 5 days ago


Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

The Senior Validation Engineer will plan, schedule, coordinate, and track all facets of assigned validation projects. Develop highly specific protocols and execute complex systems. The Sr. Validation Engineer will execute protocols for Installation, Operational and Performance Qualification testing on chambers and rooms including: autoclaves, cryo-freezers, cold rooms, refrigerators, incubators, sterilizers, depyrogenation ovens, stability chambers, and warehouses. Also, Steam in Place (SIP) validation using biological indicators and projects requiring specialized knowledge or expertise (GMP manufacturing facilities and equipment, computerized systems). Process, assemble and review data, generate documentation and reports. The Sr. Validation Engineer will be a source of technical knowledge for validation staff and customers and will deliver excellent customer service, resulting in long-term relationships.

On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 4:30pm.
  • This position is for day shift but may require some occasional off shift and/or weekend coverage to accommodate schedules and/or project timelines.
Responsibilities
  • Perform pre- and post-validation verification on test equipment.
  • Perform calibrations incidental to validation including controllers, gauges, recorders, etc.
  • Create and execute validation protocols, procedures, and final reports; perform validation projects.
  • Perform peer review of validation reports.
  • Learn and execute troubleshooting strategies in the field.
  • Independently manage technical writing and documentation aspects of validation reports.
  • Write and work with clients to resolve deviations.
  • Maintain records of pertinent information for the project including project costs reconciliation.
  • Relay opinions or interpretations of results to customer.
  • Train validation team members.
  • Other duties as assigned.
Qualifications
  • BA/BS in technical or science related field of study preferred. Candidates with an HSD/GED, technical training, or an Associate's degree combined with mechanical aptitude or relevant industry experience considered.
  • 5+ years of direct validation experience required.
Knowledge, Skills, and Abilities
  • Experience with autoclave qualification and processes.
  • Experience with validation of temperature-controlled units and temperature mapping.
  • Experience with validation of sterilization processes (steam sterilizers, SIP).
  • Experience with validation of GMP laboratory and manufacturing equipment and computerized systems.
  • Calibration expertise (temperature, humidity, CO2, pressure, timer) is a plus.
  • Ability to perform tasks with high standard of quality and accuracy.
  • Spreadsheet and word processing applications experience, computer literacy.
  • Strong written and verbal communication skills.
  • Proficient with test instruments.
  • ISO 9001, ISO 17025, GMP and GLP knowledge.
Travel Expectations
  • Up to 80% travel expected. This position includes travel during the day to client sites.
Physical Demands and Work Environment

The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee will regularly stand, walk, and use hands, frequently reach, stoop, kneel, crouch or crawl and talk or hear, and occasionally sit and climb or balance. In this role, the employee will frequently work in an office, lab or at customer sites and be exposed to extreme cold (non-weather). The employee will occasionally be exposed to wet or humid conditions, work near moving mechanical parts, work in high places, near toxic or caustic chemicals, in outdoor weather conditions and exposure to vibration. The noise level that is typical for this position is loud.

Pay Range The base hourly pay range for this position is $43.27 - $53.49 per hour. Disclosure Statement The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. Actual base salary will be based on a number of factors including, but not limited to, relevant skills, competencies, and experience, and upon joining Alcami will be reviewed periodically. Alcami may change the published salary range based on company and market factors. Employment Type: FULL_TIME

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