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Quality Control Jobs in Puerto Rico (NOW HIRING)

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and ... Provides assessments to change control records, deviations, audit processes that need support form ...

QA Specialist- ProQN669

Juncos, PR · On-site

$60 - $80/hr

Serve as a designee for the QA Manager on the local Change Control Review Board (CCRB), as applicable. * Serve as a Quality contact for complex projects involving new products. * Provide quality and ...

Demonstrate validated expertise in Quality Systems such as deviations, CAPA, and change control. * Exhibit experience in computer systems validation or computer systems quality assurance ...

Customer Quality Engineer

Arecibo, PR · On-site

$125 - $150/hr

Create/implement & maintain company quality documentation: quality control plans, quality procedures & work instructions.Ensure timely resolution on internal and supplier related issues impacting the ...

Showing results 41-60

Quality Control information

What is quality control?

Quality control (QC) is a process by which businesses ensure that their products or services meet specific standards of quality. This typically involves systematic inspection, testing, and corrective actions to detect and address defects or inconsistencies. Quality control helps maintain customer satisfaction, comply with regulations, and reduce waste or costly errors. QC can be applied at various stages of production and is essential in industries such as manufacturing, food production, and pharmaceuticals.

What are the key skills and qualifications needed to thrive as a quality control professional?

To thrive as a Quality Control professional, you need keen attention to detail, analytical skills, and a background in science, engineering, or manufacturing, often supported by relevant certifications like Six Sigma or ISO standards. Familiarity with quality management systems (QMS), statistical process control (SPC) software, and inspection equipment is typically required. Strong problem-solving abilities, communication, and teamwork set top performers apart in this role. These skills are crucial to ensure product consistency, prevent defects, and maintain compliance with industry standards.

What are some common challenges faced by quality control professionals and how can they be addressed?

Quality Control professionals often encounter challenges such as maintaining consistency across production batches, adapting to new regulatory standards, and managing tight deadlines without compromising quality. Addressing these challenges requires strong attention to detail, effective communication with production and engineering teams, and continuous learning to stay updated on industry best practices. Many companies support their QC staff with regular training sessions, clear documentation protocols, and collaborative problem-solving meetings to ensure quality standards are upheld.

What is the difference between Quality Control vs Quality Assurance?

AspectQuality ControlQuality Assurance
FocusDetecting defects in products or servicesPreventing defects through process improvements
ActivitiesInspections, testing, samplingProcess audits, standards development
CredentialsOften requires technical training or certifications in testingCertifications like ISO, Six Sigma are common
Work EnvironmentLaboratory, production lines, manufacturingProcess development, documentation, audits

While Quality Control focuses on identifying defects after production, Quality Assurance aims to prevent defects through process improvements. Both roles are essential for maintaining product quality, but they differ in approach and activities.

Is a quality control job physically demanding?

A quality control job can involve physical tasks such as inspecting products, standing for extended periods, and handling materials. The physical demand varies depending on the industry and specific role, but many positions require good attention to detail and manual dexterity. Some roles may also involve lifting or moving objects, so physical fitness can be beneficial.

What do quality control workers do?

Quality control workers inspect products and materials to ensure they meet safety and quality standards. They use tools like measurement devices and follow procedures to identify defects, document issues, and ensure compliance with specifications, often working in manufacturing or production environments. Attention to detail and knowledge of quality standards are essential for this role.

What are the most commonly searched types of Quality Control jobs in Puerto Rico?

The most popular types of Quality Control jobs in Puerto Rico are:

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

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

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

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

What cities in Puerto Rico are hiring for Quality Control jobs?

Cities in Puerto Rico with the most Quality Control job openings:

Infographic showing various Quality Control job openings in Puerto Rico as of August 2026, with employment types broken down into 87% Full Time, 5% Part Time, and 8% Contract. Highlights an 98% In-person, and 2% Hybrid job distribution.
West Pharmaceutical Services
Pharmaceutical and Medicine Manufacturing • 10K+ employees

Full-time

PTO

Posted 29 days ago


Key responsibilities

  • Perform sampling, inspections, and testing of in-process and finished goods products per applicable procedures and AQL plans.

  • Review inspection records to ensure product conforms to specifications and proper documentation practices.

  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by site.


West Pharmaceutical Services rating

8.5

Company rating: 8.5 out of 10

Based on 32 frontline employees who took The Breakroom Quiz

13th of 122 rated packaging manufacturers


Job description

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  

There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.  

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.  

#LI-MQ1

Job Summary

The role is essential in ensuring in-process and finished products meet customer specifications. This role provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record keeping. Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

#LI-MQ1

Shift
  • 12-hour shift on 2, 2, 3 rotation.
Essential Duties and Responsibilities
  • Perform sampling, inspections, and testing of in-process and finished goods products per applicable procedures and AQL plans, utilizing both visual means as well as calibrated test equipment to include laser micrometer, optical comparator and other equipment as applicable.
  • Release acceptable in-process and finished goods product for further processing and/or shipping as applicable per site.
  • Understand and follow applicable ISO standards requirements.
  • Perform review of inspection records to assure product conforms to specifications and proper documentation practices.
  • Retains sample of finished products and maintains all applicable documents to form batch records and ensures appropriate batch records disposition (i.e. filing, scanning etc.) as necessary.
  • Print documents from Master Control, shopfloor or other software program and manages documents related to the Quality System.
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by site.
  • Generate rejection and deviation reports as directed by site.
  • Perform trace back investigation of nonconforming raw material and product as directed by site.
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Other duties as assigned.
Education
  • High school diploma or GED required.
  • Associate degree in Science, Math, or related field preferred.
Work Experience
  • No minimum required.
  • 1+ year in a cGMP environment or related field preferred.
Preferred Knowledge, Skills and Abilities
  • ANSI, AQL, ShopFloor experience preferred.
  • Basic computer skills.
  • Ability to speak, read, and write in English preferred.
Travel Requirements
None: No travel required
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
What We Offer
Generous Paid Time Off (PTO): Flexible vacation, personal, and holiday leave ensures employees can maintain a healthy work-life balance and recharge effectively.
Recognition & Rewards: Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.
Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion-where all voices are heard and respected in a supportive environment.
Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives.
Global Career Opportunities: With facilities across North America, Europe, and Asia-Pacific, employees have opportunities for international exposure and cross-functional collaboration.
Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities.

West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening. 


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