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Validation Engineer II

Rockville, MD · On-site

Our Validation Engineers will be involved with the qualification and requalification of equipment ... * 2 - 5 years of experience in at least one of the following areas: equipment/utility ...

CYNET SYSTEMS

Validation Engineer 2

Austin, TX · On-site

$55 - $60/hr

Bachelor's in Electrical Engineering or Computer Engineering with 2+ years of related experience ... Writes comprehensive electrical & functional test plans for the processor interface validation of ...

SUNCO

Validation Engineer II

Boston, MA · On-site

$90 - $100/hr

Overview As a Validation Engineer II in the lighting industry, you will be responsible for developing, validating, and supporting innovative lighting products from concept through production. You ...

New

Tolmar Inc.

Validation Engineer II

Windsor, CO

$90K - $100K/yr

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

Tolmar

Validation Engineer II

Windsor, CO · On-site

$90K - $100K/yr

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

CYNET SYSTEMS

Validation Engineer 2

Austin, TX · On-site

$56 - $59/hr

... validation and 2-8 years experience in semiconductor industry. * Demonstrated ability to grasp new technical concepts quickly. * Hardware description languages (e.g. Verilog). * Strong programming ...

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Validation Engineer 2

Bend, OR · On-site

$100 - $110/hr

Validation Engineer 2 Location: Bend OR 97703 United States Duration: 6-9 Months Job Summary: CQV Validation Specialist Contractor, CSV/CQV Specialist Schedule: Full-time, onsite Interview Process

New

Empower Pharmacy

Validation Engineer II

Houston, TX · On-site

POSITION SUMMARY Validation Engineer II drives compliance and manufacturing readiness across Empower's 503A and 503B operations through validation activities supporting sterile and non-sterile ...

Cadence Inc

Validation Engineer II

Staunton, VA · On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Tolmar

Validation Engineer II

Windsor, CO · On-site

$90K - $100K/yr

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

Cadence Inc

Validation Engineer II

Suffield, CT · On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Cadence Inc

Validation Engineer II

Cranberry Township, PA · On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Empower Pharmacy

Validation Engineer II

Houston, TX · On-site

Validation Engineer II drives compliance and manufacturing readiness across Empower's 503A and 503B operations through validation activities supporting sterile and non-sterile manufacturing. This ...

E2i Inc.

Validation Engineer II

Indianapolis, IN · On-site

E2i is a small systems integrator that has specialized in automation, validation, informatics ... Bachelor's degree in a related engineering field * 2 - 5 Years of relevant work-related experience

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How much do validation engineer ii jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for validation engineer ii 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 is a Validation Engineer II?

A Validation Engineer II is responsible for ensuring that processes, systems, and products meet regulatory and quality standards. They develop and execute validation protocols, perform testing, analyze data, and document results to maintain compliance with industry regulations. This role typically requires experience in validation methods, technical problem-solving, and collaboration with cross-functional teams. Validation Engineers II work in industries such as pharmaceuticals, medical devices, and manufacturing to ensure product reliability and safety.

What are the typical responsibilities of a Validation Engineer II?

A Validation Engineer II is responsible for planning, executing, and documenting validation activities for equipment, systems, and processes to ensure compliance with industry and regulatory standards. This includes developing and reviewing protocols, analyzing test data, troubleshooting issues, and supporting audits or inspections. You can expect to work closely with cross-functional teams such as quality assurance, manufacturing, and R&D to coordinate validation efforts and implement continuous improvements. The role offers opportunities to expand both technical expertise and project management skills, making it a strong stepping stone for career advancement in engineering and quality fields.

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

To thrive as a Validation Engineer II, you need a strong background in engineering principles, quality assurance methodologies, and experience with validation protocols, typically supported by a bachelor's degree in engineering or a related field. Proficiency with industry-specific tools such as statistical analysis software, ERP systems, and knowledge of regulatory standards like GMP or ISO is highly valued, and certifications like ASQ are advantageous. Excellent problem-solving, attention to detail, and effective communication are key soft skills for this role. These competencies are essential to ensure products and processes meet rigorous compliance and quality standards, minimizing risks and ensuring project success.

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Validation Engineer II jobs near you
Infographic showing various Validation Engineer Ii job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer II

Medvacon Life Sciences LLC

East Windsor, NJ • On-site

Full-time

Re-posted 6 days ago

Job description

POSITION OVERVIEW:
The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications.
ESSENTIAL JOB FUNCTIONS:
  • Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site Acceptance Testing, Installation Qualification, Operational Qualification, Performance Qualification, and Process Qualification for sterile and non-sterile manufacturing.
  • Oversees multiple validation projects, ensuring timely budget-compliant completion while driving continuous improvement to boost manufacturing efficiency.
  • Prepares, reviews, and approves technical documents, including Standard Operating Procedures and current Good Manufacturing Practice (cGMP) records, while managing change control, Corrective and Preventive Action, and quality investigations.
  • Operates and manages critical equipment, executing cleaning, sterilization, and lyophilization cycles.
  • Provides training, supports Research and Development and product development, manages contractors for Commissioning, Qualification, and Validation (CQV) activities, and assists with audits to ensure compliance.

QUALIFICATIONS:
  • Bachelor of Science degree in a scientific or engineering discipline.
  • 7 years Validation experience in the pharmaceutical or biotechnology industries.
  • Advanced knowledge of cGMP, CQV, sterilization process validation, and regulatory compliance, including Good Automated Manufacturing Practice and 21 Code of Federal Regulations Part 11.
  • Strong problem-solving, project management, and attention to detail, with proficiency in Microsoft Office Suite, Quality Management Systems, and experience in Computer System Validation and Cleaning Validation preferred.

KEY COMPETENCIES:
  • Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.
  • Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.
  • Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.
  • Resourcefulness: Secures and deploys resources effectively and efficiently.
  • Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.
  • Ensures Accountability: Holds self and other accountable to meet commitment.
  • Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.
  • Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.

VALUES:
  • People: Our people define who we are as a company, and we believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth.
  • Quality: Quality stands at the core of our mission, reflecting our commitment to excellence in every medication we produce.
  • Service: We are here to serve others. Every interaction with our patients, providers, employees, and other stakeholders comes from a place of service.
  • Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care.

SUPERVISORY RESPONSIBILITIES:
This position does not have supervisory responsibilities.
CERTIFICATES, LICENSES, REGISTRATIONS:
Certified Quality Engineer Preferred.
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com.

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