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Assessor Iqa Jobs (NOW HIRING)

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

Creating, modifying and finalizing Image Quality Assessment/Photograph Quality Assessment (IQA/PQA) Summaries * Creating, modifying and finalizing Quality Control (QC) Summaries * Creating, modifying ...

Corning

IQA Technician

Phoenix, AZ

Participate in technical training, skills assessments, and meet qualification requirements. 7. Improvement and Innovation: * Identify and propose job improvement projects. * Actively collaborate with ...

Corning

IQA Technician

Tolleson, AZ · On-site

Participate in technical training, skills assessments, and meet qualification requirements. 7. Improvement and Innovation: * Identify and propose job improvement projects. * Actively collaborate with ...

Corning

IQA Technician

Tolleson, AZ · On-site

Participate in technical training, skills assessments, and meet qualification requirements. 7. Improvement and Innovation: * Identify and propose job improvement projects. * Actively collaborate with ...

OSI Systems, Inc

Sr. Manager Quality

Snoqualmie, WA · On-site

$165K - $185K/yr

Manages conformity assessment audits of policies, procedures and quality systems to identify non ... Facilitate basic IQA training of all audit staff, including Checklist preparation, documenting ...

AMRI

Director, Quality Operations

Albuquerque, NM

They work closely with Quality Compliance to assess deviations related to production batches ... Direct the Incoming QA (IQA), Manufacturing QA (MQA), Aseptic Core Monitoring (ACM), Sterility ...

Clario Tech

Medical Oncologist

$204.75/hr

Perform Photo Image Quality Assessment (Photo IQA) and participate in the medical photography process * Review study protocols, charters, and associated clinical and technical documentation * Ensure ...

Bioclinica

OR · On-site

$199.75/hr

Perform Photo Image Quality Assessment (Photo IQA) and participate in the medical photography process * Review study protocols, charters, and associated clinical and technical documentation * Ensure ...

Flex Ltd.

Technical Program Manager

Milpitas, CA · On-site

$120K - $165K/yr

... assessment, and close alignment with Quality, Engineering, and Operations. Based on this, the role ... IQA (Incoming Quality): Perform inspections and enforce material control. * Production: Align build ...

Flex

Technical Program Manager

Milpitas, CA · On-site

$120K - $165K/yr

... assessment, and close alignment with Quality, Engineering, and Operations. Based on this, the role ... IQA (Incoming Quality): Perform inspections and enforce material control. * Production: Align build ...

Thermo Fisher Scientific

FSP QA Auditor I

Worcester, MA · On-site

$25.60 - $38/hr

What You'll Do: • Support IQA/SQA group as responsible for specification revisions of Commodities ... Very good problem solving, risk assessment and impact analysis abilities • Proficient at ...

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Assessor Iqa information

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$32.5K

$75.3K

$125.5K

How much do assessor iqa jobs pay per year?

As of Jun 9, 2026, the average yearly pay for assessor iqa in the United States is $75,259.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,000.00 and $97,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Assessor IQA, and why are they important?

To thrive as an Assessor IQA (Internal Quality Assurer), you need a solid understanding of assessment principles, sector-specific qualifications, and a recognized IQA qualification such as the Level 4 Certificate in Leading the Internal Quality Assurance of Assessment Processes and Practice. Familiarity with assessment management systems and digital portfolio tools is typically required, along with up-to-date knowledge of regulatory standards. Strong attention to detail, effective communication, and organizational skills help ensure accuracy and maintain high standards in assessment processes. These skills and qualities are essential to uphold assessment integrity, comply with regulatory requirements, and support learners and assessors effectively.

What are Assessor IQAs?

Assessor IQAs, or Internal Quality Assurers, are professionals responsible for ensuring that assessment processes within educational or vocational organizations are consistent, fair, and meet required standards. They typically review and monitor the work of assessors, provide feedback, and help maintain the quality and integrity of qualifications. Their role is crucial in maintaining compliance with awarding body regulations and supporting continuous improvement in assessment practices. Assessor IQAs may also contribute to staff training and standardization activities.

What is the difference between Assessor Iqa vs Quality Assurance Inspector?

AspectAssessor IqaQuality Assurance Inspector
Required CredentialsCertifications in assessment and quality standards, relevant industry trainingQuality assurance certifications, inspection training
Work EnvironmentOffice settings, assessment centers, client sitesManufacturing plants, inspection stations, warehouses
Employer & Industry UsageUsed in industries like manufacturing, construction, and service sectors for evaluating complianceCommonly employed in manufacturing, production, and quality control roles

While both roles focus on quality and compliance, Assessor Iqa primarily evaluates processes and standards through assessments, whereas Quality Assurance Inspectors perform physical inspections to ensure product quality. The roles often overlap but differ in their methods and focus areas within the quality management system.

What are some common challenges faced by an Assessor IQA, and how can they be addressed?

Assessor IQAs (Internal Quality Assurers) often face challenges such as balancing a large caseload of assessments with ensuring each learner receives thorough feedback and support. Navigating changes in assessment standards or regulations can also be demanding. Effective time management, regular communication with assessors and learners, and staying updated with industry standards are key strategies for overcoming these challenges. Collaborating closely with team members and attending ongoing professional development sessions can further enhance effectiveness in the role.
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What cities are hiring for Assessor Iqa jobs? Cities with the most Assessor Iqa job openings:
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Assessor Iqa jobs near you
Infographic showing various Assessor Iqa job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 94% Full Time, and 5% Part Time. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $75,259 per year, or $36.2 per hour.
Associate Medical Writer

Associate Medical Writer

Bioclinica

Princeton, NJ • On-site

Full-time

Posted 5 days ago

Job description

Company Description
Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials. We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia. We are headquartered in Doylestown, PA. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device organizations
Job Description
The Medical Writer will be responsible for the creation and development of all study start-up documents such as the Site Manual and associated forms, as well any required Protocol Amendment Impact forms and Compliance Reports for the life of each study. The Medical Writer is also expected to provide guidance and support to the Clinical Project Management Team, including the review of Project-Specific Work Instructions and attending document-related Sponsor calls.
Primary Responsibilities
Performs study start up responsibilities by:
  • Creating, modifying and finalizing Site Manuals, associated fillable forms, Quick Reference Guides and labels
  • Creating, modifying and finalizing Image Quality Assessment/Photograph Quality Assessment (IQA/PQA) Summaries
  • Creating, modifying and finalizing Quality Control (QC) Summaries
  • Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Notes to File (NTFs), Corrections and Deviation Reports
  • Creating, modifying, and finalizing Key Points Documents (KPDs) from CRs
  • Creating, modifying and finalizing paper Source Documents based on ToOs
  • Creating, reviewing, modifying and finalizing MedComm Meeting Minutes
  • Attending internal and external meetings relating to the Site Manuals, IQA/PQA/QC Summaries, CRs/KPDs, Source Documents and any other MedComm-related study start-up documents
  • Running Scheduled Tasks for generating MedComm webpages
  • Maintaining MedComm document webpages
  • Checking MedComm webpages for errors
  • Performing Project Close-outs as they occur based on receipt of Study Closure forms
  • Reviewing and updating Charter Training Slides (CTS) and CTS quiz(zes) as needed
  • Documenting study-specific Protocol Training (Kick-off Meeting Slides, Protocol Overview Presentations, etc.) by filling out and collecting signatures on group training forms as required

Manages the clinical study document development process by:
  • Creating, modifying, finalizing and attaching signed final Compliance Reports (CRs) to Final MedComm documents or review Project Team-created CRs
  • Updating the MedComm database every time a document is created, sent out for internal or Sponsor review, finalized, deemed inactive/on-hold, or cancelled
  • Providing guidance to assigned Project Teams and Project Team members
  • Providing language updates, as required, for all MedComm document templates as needed
  • Creating Final Effective documents

Secondary Responsibilities
Maintains Quality Service and Departmental Standards by:
  • Reading, understanding and adhering to organizational Standard Operating Procedures ("SOP")
  • Updating department SOPs and Work Instructions as needed
  • Assisting in establishing and enforcing departmental standards

Contributes to team effort by:
  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Participate in internal training activities
  • Helping others to achieve results
  • Performing other duties as assigned

Maintains Technical and Industry Knowledge by:
  • Staying up-to-date on response criteria publications posted by Medical Communications
  • Participating in Medical Writing Training activities, including creating/reviewing training modules
  • Participating in Clinical Project Management Training activities, including creating/reviewing training modules
  • Attending and participating in applicable company-sponsored training

Qualifications
Education:
  • Bachelor's Degree in either the Life or Physical Sciences (e.g., Biology, Chemistry, Physics, Pharmaceutics, etc.) preferred

Experience:
  • 1+ years medical writing experience required
  • 2+ years of experience in pharmaceutical/clinical/imaging research preferred
  • Demonstrated proficiency in medical, pharmaceutical, regulatory, clinical writing
  • Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint, Access)
  • Understanding and knowledge of medical and/or clinical trial terminology desired

Additional skill set:
  • Ability to work in a group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Organization and time management skills for managing multiple projects concurrently

Additional Information
Working conditions:
  • Travel: 0-5%
  • Lifting: 0-10lbs
  • Other: Computer work for long periods of time

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

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