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Incoming Quality Control Inspector Jobs in Puerto Rico

Amspec LLC.

PR

Responsible for inspection and sampling work performed in the field, completion of all necessary paperwork, correct distribution of samples and timely communications with office staff. Primary Duties ...

Intertek

Inspector I, Caleb Brett

Bayamon, PR

Bringing quality, safety, and sustainability to life. What are we looking for? The Petroleum Inspector is responsible for performing volume measurement, temperature measurement and sampling of ...

Lufthansa Technik

PR · On-site

Quality Support Team Inspector Organization: Lufthansa Technik Puerto Rico (LTPR) Department ... Document noted discrepancies on company control forms and follow-up to ensure all the noted ...

Lufthansa Technik

PR · On-site

Quality Support Team Inspector Organization: Lufthansa Technik Puerto Rico (LTPR) * Description of ... Document noted discrepancies on company control forms and follow-up to ensure all the noted ...

JLL

QA Specialist

Gurabo, PR · On-site

... quality control programs that ensure products and services meet established specifications and customer requirements. Inspection & Testing * Conducts in-process inspections and final product ...

New

PHARMALOGIC HOLDINGS

PR · On-site

... FDA inspections at the site and is listed on the FDA filing and associated permits as applicable. Ideally, there will be separation of QA functions from production and QC functions. However ...

Medtronic

Sr Quality Engineer

Humacao, PR

$89K - $121K/yr

Develop and implement inspection, testing, validation, and process evaluation methods to ensure ... May specialize in the areas of design, incoming material, production control, product evaluation ...

Medtronic

Sr Quality Engineer

Humacao, PR

$89K - $121K/yr

Develop and implement inspection, testing, validation, and process evaluation methods to ensure ... May specialize in the areas of design, incoming material, production control, product evaluation ...

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Incoming Quality Control Inspector information

What is an incoming quality control inspector?

An Incoming Quality Control (IQC) Inspector is responsible for inspecting raw materials, components, and products received from suppliers to ensure they meet quality standards and specifications. They perform visual and dimensional inspections, review documentation, and identify any defects or deviations. IQC Inspectors work closely with suppliers and internal teams to resolve quality issues and prevent defective materials from entering production. Their role helps maintain product reliability, compliance, and overall manufacturing efficiency.

What are the typical daily responsibilities of an incoming quality control inspector?

As an Incoming Quality Control Inspector, your day usually involves examining and testing raw materials or components upon arrival to ensure they meet required specifications and company standards. You will use various measurement tools, review shipping documents, record inspection findings, and report any discrepancies to the quality or production teams. Collaborating closely with purchasing, warehouse, and production staff is common to resolve issues quickly and keep production running smoothly. Staying organized and detail-oriented is important, as your work helps maintain the overall quality and integrity of the finished products.

What are the key skills and qualifications needed to thrive as an incoming quality control inspector?

To thrive as an Incoming Quality Control Inspector, you need a solid understanding of quality assurance principles, inspection techniques, and attention to detail, typically backed by a high school diploma or technical certification. Familiarity with measurement tools like calipers, micrometers, and quality management systems (such as ISO 9001) is commonly required, along with experience documenting and reporting inspection results. Strong observational skills, effective communication, and a methodical approach help inspectors navigate potential quality concerns and collaborate across departments. These skills and qualities are vital to ensure that all incoming materials and products meet company standards and regulatory requirements, thereby protecting the organization's reputation and production quality.

Are incoming quality control inspectors in demand?

Incoming quality control inspectors are in demand in manufacturing and production industries due to the need for ensuring product quality and compliance. Employment opportunities often depend on industry growth, technological advancements, and the requirement for certifications such as ASQ CQI certifications. The role typically requires attention to detail, inspection skills, and familiarity with measurement tools and standards.

How can I become an incoming quality control inspector?

To become an incoming quality control inspector, candidates typically need a high school diploma or equivalent and should develop skills in inspection techniques, measurement tools, and quality standards. Relevant certifications, such as ASQ Certified Quality Inspector (CQI), can improve job prospects, and experience in manufacturing or production environments is often preferred.

Is incoming quality control inspector a good career?

An incoming quality control inspector plays a key role in ensuring products meet quality standards, often requiring attention to detail and knowledge of inspection tools. The career can offer stable employment with opportunities for advancement and certification, such as ASQ certifications, depending on the industry and company size.

What are popular job titles related to Incoming Quality Control Inspector jobs in Puerto Rico?

For Incoming Quality Control Inspector jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Incoming Quality Control Inspector jobs in Puerto Rico look for?

The top searched job categories for Incoming Quality Control Inspector jobs in Puerto Rico are:

Incoming Quality Control Inspector jobs near you
Infographic showing various Incoming Quality Control Inspector job openings in Puerto Rico as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

ZL01-120925 - Specialist Quality Control

Validation & Engineering Group, Inc.

Juncos, PR • On-site

Full-time

Posted 19 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Specialist Quality Control

SUMMARY
Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.
FUNCTIONS
  • Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.
  • Resolve technical issues and troubleshoot for assays as necessary
  • Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety.
  • Manage existing and/or develop and implement new programs, processes and methodologies.
  • Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.
  • Approve lab investigations, Lead audit teams
  • May serve as subject matter expert to develop technical training.
  • May perform routine work in a specific area of responsibility as necessary.
  • Represents the department/organization on various teams, independently responsible for following through on multi-site action items.
  • May interact with regulatory agencies regarding area(s) of responsibility including written responses.
  • May resolve issues with outside resources.
  • Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements.

EDUCATION
  • Doctorate OR
  • Masters + 2 years of directly related experience OR
  • Bachelors + 4 years of directly related experience OR

COMPETENCIES/SKILLS
  • Excellent communication skills, facilitation and presentation skills.
  • Excellent technical writing skills.
  • Strong computer operation skills including work processing, presentation, database and spreadsheet application skills.
  • Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion.
  • Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities.
  • Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution.
  • Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility.
  • Knowledge of pharmaceutical processes.
  • Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products.
  • Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products.
  • Extensive knowledge and application of GMPs/CFRs.
  • Ability to evaluate compliance issues.
  • Skill in evaluating and documenting according to Company and various guidelines.
  • Proficient at maintenance, troubleshooting and operation of equipment in area of expertise.
  • Advanced scientific data analysis and interpretation skills.
  • Advanced skills in solving complex problems.
  • Advanced data trending and evaluation.
  • Strong skill in working independently and to effectively interact with various levels.
  • Ability to interact with regulatory agencies both orally and in writing.
  • Initiate, coordinate and lead cross functional teams.
  • Excellent skill in leading, motivating, influencing, and negotiating.

ATRIBUTES:
  • Scientific Data Analysis.
  • Strong Technical Writing (English and Spanish) mainly focuses.
  • Strong knowledge in Microsoft Excel as a Tool for Data Analysis.
  • Good Communication skills.
  • Project Management.
  • Knowledge in Computer System and Method Validation (Experience preferable).
  • Strong knowledge and experience with quality process management.
  • Basic Knowledge on equipment preventive maintenance and troubleshooting.
  • Agile on prioritization of critical tasks.
  • Ability to develop inspection or qualification protocols in a short timeframe period.
  • Strong negotiation skills.

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