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Full Time Operative Iq Jobs (NOW HIRING)

Senior Firmware Engineer

San Francisco, CA ยท On-site +1

$162K - $252K/yr

Senior Firmware Engineer Description - Who We Are HP IQ is HP's new AI innovation lab. Combining ... About The Role The System Software team is responsible for firmware, operating system software ...

Shift Leader

Port Orange, FL ยท On-site

$18 - $19/hr

Position Type: * Full-time Our Benefits Include: * A fun work environment where you can positively ... Learning first-hand from an experienced Operator and Restaurant Leaders * An in house leadership ...

... in operating mills, lathes, Swiss turning machines, and gundrills. This is a hands-on role in a ... Follow validated procedures (IQ/OQ/PQ) to ensure quality and consistency * Monitor and maintain ...

Team Leader

Phillipsburg, NJ ยท On-site

$16 - $24/hr

Self-Aware, Ownership, Productivity, Operational IQ & Adaptable Assistant Director: PT/FT 20-40 ... Most Chick-fil-A restaurants are locally owned and operated by independent, franchised Operators ...

US Operator

Alpharetta, GA ยท On-site

$24.04/hr

This is a full-time/hourly, onsite position. The payrate is $24.04 an hour. Key Responsibilities ... Support the Execution of our IQ/OQ/PQ validation process prior to go-live of our new manufacturing

Injection Molding Technician

Woodland, CA ยท On-site

$30 - $36/hr

Injection Molding Technician - Silicone Medical Device Manufacturing | Woodland, CA Full-Time | On ... Support validation activities including IQ, OQ, and PQ when required. Leadership & Operator Support

US Operator

Alpharetta, GA ยท On-site

$24.04/hr

This is a full-time/hourly, onsite position. The payrate is $24.04 an hour. Key Responsibilities ... Support the Execution of our IQ/OQ/PQ validation process prior to go-live of our new manufacturing

Self-Aware, Ownership, Productivity, Operational IQ & Adaptable Assistant Director: PT/FT 20-40 ... Most Chick-fil-A restaurants are locally owned and operated by independent, franchised Operators ...

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Showing results 1-20

Full Time Operative Iq information

See salary details

$15K

$241.3K

$387K

How much do full time operative iq jobs pay per year?

As of Jun 9, 2026, the average yearly pay for full time operative iq in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Operative Iq vs Full Time Operative?

AspectFull Time Operative IqFull Time Operative
CredentialsTypically requires basic certifications or training in industry-specific skillsSimilar certifications, often with additional specialized training
Work EnvironmentIndoor/outdoor settings depending on industry, often in manufacturing or logisticsSimilar environments, with hands-on tasks in industrial or warehouse settings
Employer UsageCommonly used in logistics, manufacturing, and warehousing sectorsWidely used across similar sectors, often interchangeable in job listings

Full Time Operative Iq and Full Time Operative roles share similar credentials and work environments, often within logistics and manufacturing industries. The main difference lies in specific job responsibilities and employer terminology, but both roles require comparable skills and certifications.

More about Full Time Operative Iq jobs
What cities are hiring for Full Time Operative Iq jobs? Cities with the most Full Time Operative Iq job openings:
What are the most commonly searched types of Operative Iq jobs? The most popular types of Operative Iq jobs are:
What states have the most Full Time Operative Iq jobs? States with the most job openings for Full Time Operative Iq jobs include:
What job categories do people searching Full Time Operative Iq jobs look for? The top searched job categories for Full Time Operative Iq jobs are:
Infographic showing various Full Time Operative Iq job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 90% Physical, 5% Hybrid, and 5% Remote job distribution, with an average salary of $241,295 per year, or $116 per hour.

Process Validation Engineer

LAPORTE L.C.C.

King Of Prussia, PA โ€ข On-site

Full-time

PTO

Posted 8 days ago


Job description

Process Validation Engineer (a minimum of 5 years of experience required)
Location: King of Prussia, PA
Employment Type: Full-time, mostly onsite
About Us
Are you ready to take the next step in your career? LAPORTE, a consulting engineering firm with 25 years of experience and a strong presence in North America and Europe, is seeking an Process Validation Engineer to join our growing team. With 25 offices and over 480 employees worldwide, we specialize in delivering innovative solutions for the pharmaceutical and food & beverage industries.
The Process & Validation Engineer is responsible for supporting the validation of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing sectors. The Process & Validation Engineer will ensure equipment, systems, and validation programs are compliant with a client's global/site standards and industry practices.
The Process & Validation Engineer will live near King of Prussia, PA. They will be motivated to grow and excel with the support and direction from an interdisciplinary team of engineers. Become part of a supportive work environment that emphasizes team culture and empowering engineers with more responsibility, professional growth, and a work-life balance.
At LAPORTE, we offer:
  • Competitive Salary
  • Comprehensive Benefits
  • Compensatory Paid Time Off (PTO)
  • Paid Parental Leave
  • A Flexible Work Environment that values work-life balance
  • Opportunities for Professional Growth

Responsibilities and Duties:
  • Carry out all aspects of a validation project for our clients including: authoring and/or executing Validation Master Plans (VMP), User Requirements Specifications (URS), Risk Assessments (RA), Design Qualification (DQ), Factory Acceptance Tests (FAT), Site Acceptance Tests (SAT), Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Process Validation (PV) protocols/reports in accordance with corporate and departmental procedures.
  • Validation Planning: Develop Validation Master Plans outlining the validation strategy, scope, and timelines for the project.
  • Documentation Management: Oversee the creation, review, and approval of validation protocols, reports, and other documentation required for validation activities.
  • Risk Assessment: Conduct Risk Assessments to identify potential validation issues and develop mitigation strategies to address them.
  • Protocol Execution: Oversee the execution of validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for equipment and systems within the QC building.
  • Commissioning Support: Collaborate with the commissioning team to ensure a seamless transition from construction to operation, verifying that systems and equipment are installed correctly and function as intended.
  • Standard Operating Procedure: Provide technical input with respect to Standard Operating Procedures (SOP) development. Revise or develop SOPs in compliance with industry standards and cGMP.
  • Support client Quality Assurance (QA) compliance teams by initiating change controls, documenting deviations, and contributing to the implementation of CAPA (Corrective and Preventive Actions) within validation activities.
  • Perform Periodic Review for various validated systems including computerized systems, laboratory equipment, manufacturing equipment, and infrastructure systems. Analyze information, draw the right conclusions based upon technical knowledge of the systems, and work effectively with different groups across site to determine status, gaps, and corrective actions.
  • Maintain up-to-date knowledge of validation requirements, practices, and procedures and coach other members of the team participating in validation activities.
  • Maintain up-to-date knowledge of current GP (Good Practices, e.g. GMP/GLP) regulations, guidelines within North America (Health Canada, US Food & Drug Administration) and EU Eudralex.
  • Maintain effective client relationships and act as a primary point of contact.
  • Ensure that projects are implemented in accordance within the agreed scope, timelines and budget.

Qualifications:
  • Bachelors degree in engineering field or relevant equivalent.
  • Minimum 5 years of prior experience preparing and executing equipment qualification documents (IQ/OQ/PQ) required.
  • Excellent knowledge of the Current Good Manufacturing Practices.
  • Excellent communication skills - verbal, written, listening and interpersonal with the ability to transfer knowledge to others.
  • Strong technical knowledge, relationship management, organizational planning, and project management skills.
  • Ability to demonstrate a sense of urgency, flexibility, and accountability.
  • Flexibility to travel to the client site as required.

Preferred Qualifications
  • Prior experience performing GxP risk assessments such as Functional Risk Assessments (FRA) or Failure Mode and Effect Analysis (FMEA).
  • Experience in Aseptic Processing.
  • Familiarity with Computerized Systems Validation and ISPE GAMP5 and 21 CFR Part 11.

Send us your application today. We look forward to meeting you!
The LAPORTE team