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Online Remote Pharmaceutical Validation Engineer Jobs

Senior Device Validation Engineer

Atlanta, GA ยท Remote

$150K - $190K/yr

You will serve as the technical authority for our validation engineering efforts, bridge cross ... This isn't a remote position; you will be on-site at our Atlanta area facilities to lead physical ...

Remote Pharmacist

Birmingham, AL ยท Remote

$54.50 - $65.50/hr

If you're passionate about leveraging pharmaceutical knowledge for positive impacts and ... Uses appropriate online resources to research and respond to drug information questions. * Reviews ...

Remote Pharmacist

Columbia, SC ยท Remote

$54 - $64.75/hr

If you're passionate about leveraging pharmaceutical knowledge for positive impacts and ... Uses appropriate online resources to research and respond to drug information questions. * Reviews ...

Finalize the Automation Validation Plan Work with a team of Engineers and System Integration (SI ... Windows operating systems Windows Terminal Services/Remote Desktop VMWare Dell VRTX familiarity is ...

As a System Validation Manager at Cornelis Networks, you will build and lead our System Validation ... engineering environment. Location:This is a remote position for employees residing within the ...

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... If you are unable to use our online application process due to an impairment or disability, please ...

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Online Remote Pharmaceutical Validation Engineer information

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$22

$51

$78

How much do online remote pharmaceutical validation engineer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for online remote pharmaceutical 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.

How does an online remote pharmaceutical validation engineer typically collaborate with cross-functional teams while working remotely?

As an Online Remote Pharmaceutical Validation Engineer, collaboration with cross-functional teams such as quality assurance, production, and IT is crucial. Most communication and document reviews are conducted through video conferences, project management platforms, and secure document sharing tools. Regular virtual meetings help ensure alignment on validation protocols, timelines, and regulatory compliance. Building strong relationships and maintaining clear, proactive communication are essential for overcoming the challenges of remote work and ensuring project success.

What does an online remote pharmaceutical validation engineer do?

An Online Remote Pharmaceutical Validation Engineer is responsible for ensuring that pharmaceutical manufacturing processes, equipment, and systems comply with industry regulations and quality standards, all while working remotely. They develop and execute validation protocols, analyze data, and prepare documentation to demonstrate compliance with Good Manufacturing Practices (GMP). By working online, they use digital tools to monitor processes, collaborate with teams, and provide validation support from any location. Their role is essential in maintaining product safety and efficacy, even when not physically present on-site.

What is the difference between Online Remote Pharmaceutical Validation Engineer vs On-site Pharmaceutical Validation Engineer?

AspectOnline Remote Pharmaceutical Validation EngineerOn-site Pharmaceutical Validation Engineer
Work EnvironmentPerforms validation tasks remotely, often from home or a remote officeWorks on-site at manufacturing or laboratory facilities
Required CredentialsTypically holds a degree in life sciences, engineering, or related field; certifications like GxP or validation trainingSimilar credentials; often requires hands-on validation experience and industry certifications
Industry UsageCommon in companies adopting remote validation processes, especially during COVID-19Traditional validation roles in pharmaceutical manufacturing facilities

The Online Remote Pharmaceutical Validation Engineer and On-site Pharmaceutical Validation Engineer roles share similar credentials and industry applications. The main difference lies in the work environment, with remote engineers performing validation tasks virtually, while on-site engineers work directly at manufacturing sites. Both roles are essential for ensuring compliance and quality in pharmaceutical production, but remote roles offer greater flexibility and often require strong digital communication skills.

What skills and qualifications are needed to thrive as an online remote pharmaceutical validation engineer?

To excel as an Online Remote Pharmaceutical Validation Engineer, you need a solid background in pharmaceutical engineering, regulatory compliance (such as FDA or EMA guidelines), and process validation, typically supported by a relevant degree in engineering or life sciences. Familiarity with validation management software, data integrity systems, and industry standards like GAMP 5 is essential, and certifications such as Six Sigma or CQV can be advantageous. Strong analytical thinking, attention to detail, effective communication, and the ability to collaborate virtually are crucial soft skills in this remote environment. These skills ensure that all pharmaceutical systems and processes meet regulatory requirements, maintain product quality, and support efficient project delivery from a remote setting.
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Infographic showing various Online Remote Pharmaceutical Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 63% Full Time, 34% Part Time, 1% Temporary, and 2% Contract. Highlights an 80% Physical, 1% Hybrid, and 19% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Business Development Manager- Commissioning, Qualification, Validation (CQV) - Remote from home

Wood Plc

West, TX โ€ข On-site, Remote

Full-time

Re-posted 19 days ago


Job description

Overview / Responsibilities

Wood PLC, on a global scale, serves the Pharma-Bio, Oil & Gas, Federal, Infrastructure, Manufacturing, Mining, and Power Industries. Our Philadelphia office has become the center of excellence for our global Life Sciences network. It provides process engineering, process design, and commissioning - qualification - validation (CQV) services to pharmaceutical/biotechnology clients worldwide. For projects of every scale, we provide services that support a facility's entire life cycle to bring life-saving therapeutics from concept through fruition. Learning from our team of industry-leading experts in facility design, regulatory standards, and project management will pay dividends toward your future career.

Our CQV group at Wood is seeking a regional Director of CQV, open to various locations in the United States. The position will be responsible for the regional development, maintenance, and growth of the CQV business.

Primary responsibilities include CQV business development, building a local CQV group (recruiting, interviewing, hiring, team performance), identifying commissioning, qualification and/or validation opportunities, proposal development, project execution, and full responsibility for the profit and loss regional CQV business. This is a seller-doer position. As a candidate you must have the ability to identify opportunities, develop the team, and assist in project execution.

Previous experience as an Engineering/CQV service provider preferred.ย  Must be thoroughly knowledgeable in pharmaceutical industry cGMPs, commissioning, qualification, validation, and CQV project management.ย  Must have proven capability in leading project teams, scheduling, coordinating the efforts of a multidisciplinary team and identifying and building client relationships.

Ability to effectively interface directly with clients in representing Wood is essential.

****This position offers a competitive salary, opportunty for growth, and a signing bonus.

Skills / Qualifications

Essential Job Functions/Skills:

  • Effectively lead project teams managing scope, budget, and schedule to ensure project success is required
  • Fostering Wood's relationships with clients, business development
  • Ability to travel to client sites
  • Business development including identifying potential growth areas and development of CQV proposals
  • Hiring of CQV personnel
  • Extensive experience in commissioning/qualification/validation and a thorough understanding of cGMPs
  • Knowledge of the local pharma market
  • Ability to lead and or assist in project execution

Education and Experience Requirements:

  • BS Engineering (Chemical Engineering preferred); Other life sciences may be acceptable; Educational requirements may be relaxed for suitable experience
  • Minimum of 12 years of experience in engineering, commissioning, qualification, and validation primarily in the field of pharmaceuticals
Company Overview

Wood is a global leader in engineering and consultancy across energy and the built environment, helping to unlock solutions to some of the world's most critical challenges. We provide consulting, projects and operations solutions in more than 60 countries, employing around 40,000 people. www.woodplc.com

Diversity Statement

We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.

Employment Type: OTHER