ZipRecruiter

Log In

1

Qc Jobs in Puerto Rico (NOW HIRING)

Quality Consulting Group

SPECIALIST QA

Juncos, PR · On-site

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 ...

Frey Consulting Group

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 ...

Inteldot

Specialist QA 35669

Juncos, PR · On-site

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

BlackBerry Inc.

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 ...

previous page

Showing results 41-60

All JobsQc JobsQc Jobs in Puerto Rico

Qc information

What is a quality control (QC) specialist?

QC, or Quality Control professionals, are responsible for ensuring that products and processes meet established quality standards and regulations. They inspect, test, and monitor outputs at various stages of production to identify defects or deviations from specifications. QC professionals play a critical role in maintaining product consistency, safety, and customer satisfaction across industries such as manufacturing, pharmaceuticals, and food processing. Their work helps prevent defective products from reaching consumers and supports continuous improvement within organizations.

What skills and qualifications are needed to thrive as a quality control (QC) specialist?

To thrive as a Quality Control (QC) Specialist, you need a strong understanding of quality assurance processes, attention to detail, and often a background in science or engineering. Familiarity with quality management systems (such as ISO 9001), statistical process control tools, and inspection equipment is typically required. Analytical thinking, teamwork, and effective communication are crucial soft skills that help in identifying issues and collaborating with production teams. These skills and qualifications ensure that products consistently meet standards, reduce defects, and maintain customer satisfaction.

What challenges do quality control (QC) specialists face in fast-paced manufacturing environments?

QC professionals in fast-paced manufacturing settings often encounter challenges related to balancing speed with accuracy. They must ensure that products consistently meet quality standards while keeping up with tight production deadlines. This can involve quickly identifying defects, implementing corrective actions, and effectively communicating with production teams to minimize downtime. Adaptability and strong attention to detail are essential for managing these pressures and maintaining product integrity.

What is the difference between Qc vs Quality Inspector?

AspectQcQuality Inspector
CertificationsOften requires certifications like ASQ CQE or CQAMay also hold similar certifications, but less frequently required
Work EnvironmentTypically in manufacturing, production, or quality control labsPrimarily in manufacturing plants, assembly lines, or inspection stations
Employer & Industry UsageUsed across various industries including automotive, aerospace, and electronicsCommonly found in manufacturing and production sectors
Job FocusFocuses on quality control processes, data analysis, and complianceFocuses on inspecting products, identifying defects, and ensuring standards

Both Qc and Quality Inspector roles are vital in quality management, often overlapping in manufacturing environments. Qc generally encompasses broader quality control responsibilities, including data analysis and process improvement, while Quality Inspectors focus more on product inspection and defect detection. The choice between roles depends on the specific industry and company structure.

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

The most popular types of Qc jobs in Puerto Rico are:

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

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

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

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

What cities in Puerto Rico are hiring for Qc jobs?

Cities in Puerto Rico with the most Qc job openings:

Qc jobs near you
Infographic showing various Qc job openings in Puerto Rico as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 7% Part Time, 2% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Quality Auditor

Cidra, PR

West Pharmaceutical Services
Pharmaceutical and Medicine Manufacturing • 10K+ employees
Learn more about West Pharmaceutical Servicesexternal

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. 

What West Pharmaceutical Services employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply