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Quality Control Investigator Jobs in Puerto Rico

Sr Quality Engineer

Juncos, PR · On-site

$86K - $116K/yr

The Senior Quality Engineer is responsible for driving product and process quality initiatives ... investigations. * Expertise with Minitab, Statistical Process Control (SPC), trend analysis, and ...

Sr Quality Engineer

Juncos, PR · On-site

$86K - $116K/yr

The Senior Quality Engineer is responsible for driving product and process quality initiatives ... investigations. * Expertise with Minitab, Statistical Process Control (SPC), trend analysis, and ...

For Manufacturing Services in the Quality Systems area. WHAT MAKES YOU A FIT: The Technical Part ... Responsible for authoring investigation reports. * Responsible for execution of corrective actions.

Quality Engineer

San Lorenzo, PR · On-site

$70K - $91K/yr

... Control, Process Validation, Test Method Validation, and Sampling Plan Development and Review. Generates quality indicators and supports nonconformance investigation and corrective action ...

Quality Engineer

San Lorenzo, PR · On-site

$70K - $91K/yr

... Control, Process Validation, Test Method Validation, and Sampling Plan Development and Review. Generates quality indicators and supports nonconformance investigation and corrective action ...

Quality Engineer

San Lorenzo, PR · On-site

$70K - $91K/yr

... Control, Process Validation, Test Method Validation, and Sampling Plan Development and Review. Generates quality indicators and supports nonconformance investigation and corrective action ...

Quality Engineer

San Lorenzo, PR · On-site

$52K - $67K/yr

... Control, Process Validation, Test Method Validation, and Sampling Plan Development and Review. Generates quality indicators and supports nonconformance investigation and corrective action ...

Ensures investigations of plant events are evaluated in a timely manner; completed thoroughly and ... and ensure material control until regulatory approval. Conform to EHS management system ...

For Manufacturing Services in the Quality Systems area. WHAT MAKES YOU A FIT: The Technical Part ... Responsible for authoring investigation reports. * Responsible for execution of corrective actions.

Investigate QC hold, quarantine and reject for materials not meeting standards, ensure the initiation of exception documentation and oversee the implementation of any corrective action * Responsible ...

Support Manufacturing and Quality Control investigations. * Evaluate production process failures and support Non-Conformance Reports and Corrective and Preventive Action Reports within expected ...

Change Control * Documentation Review * Validation * PPQ * Project management skills. * Strong ... Lead investigations. * Lead site audits. * Own site quality program procedures. * Designee for QA ...

Lead investigations. * Lead site audits. * Own site quality program procedures. * Designee for QA ... Change Control, Documentation Review, Validation, PPQ. SKILLS: * Project management skills.

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

Strong knowledge of Quality Management Systems (QMS), including change control, risk management, nonconformance investigations, and assessment of quality impact resulting from equipment, facility ...

Showing results 41-60

Quality Control Investigator information

What is a quality control investigator?

Quality Control Investigators are professionals responsible for ensuring that products or services meet established quality standards and regulatory requirements. They inspect processes, materials, and finished goods, investigate quality issues, and recommend corrective actions to prevent recurrence. Their work is crucial in maintaining product safety, consistency, and compliance across various industries, such as manufacturing, pharmaceuticals, and food processing.

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

To thrive as a Quality Control Investigator, you need expertise in quality assurance processes, attention to detail, and a background in science or engineering, often supported by relevant certifications such as Six Sigma or ISO compliance. Familiarity with laboratory equipment, statistical analysis software, and quality management systems is typically required. Strong analytical thinking, problem-solving abilities, and effective communication are essential soft skills in this role. These competencies ensure that products and processes consistently meet regulatory standards and company expectations, minimizing errors and maintaining organizational integrity.

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

Quality Control Investigators often encounter challenges such as managing tight deadlines for investigating quality deviations, ensuring thorough documentation, and coordinating with multiple departments to collect necessary information. To address these, it's important to develop strong organizational skills, maintain clear communication channels, and stay current with regulatory requirements. Proactively collaborating with production, QA, and regulatory teams can help streamline investigations and lead to more effective root cause analysis and corrective actions.

What is the difference between Quality Control Investigator vs Quality Assurance Specialist?

AspectQuality Control InvestigatorQuality Assurance Specialist
CertificationsOften requires GMP, GLP, or ISO certificationsSimilar certifications, with additional focus on auditing
Work EnvironmentLaboratory, manufacturing, or production settingsOffice, laboratory, or production environments
Primary FocusInvestigating quality issues, deviations, and non-conformancesDeveloping and implementing quality systems and procedures
Employer & Industry UsagePharmaceutical, biotech, manufacturingPharmaceutical, biotech, manufacturing

Both roles are vital in quality management, but the Quality Control Investigator primarily focuses on identifying and resolving quality issues through investigations, while the Quality Assurance Specialist develops systems to prevent issues. They often work together to ensure product quality and compliance.

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

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

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

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

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

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

Sr Quality Engineer

Juncos, PR • On-site

$86K - $116K/yr

Full-time

Posted 6 days ago


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

155th of 547 rated manufacturers


Job description

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the LifeThe Quality function partners across engineering, manufacturing, and operations to ensure products and processes meet regulatory, quality, and customer requirements throughout the product lifecycle. This team drives product and process quality through quality system oversight, continuous improvement, statistical analysis, and cross-functional collaboration.
This position is based in Juncos, Puerto Rico and follows an onsite work model.
The Senior Quality Engineer is responsible for driving product and process quality initiatives within a regulated manufacturing environment. This role partners closely with engineering and manufacturing teams to implement quality standards, lead complex investigations, analyze quality data, and support continuous improvement efforts that enhance compliance, reliability, and operational performance.
Primary Responsibilities
  • Lead complex Corrective and Preventive Action (CAPA), Nonconforming Material Report (NCMR), and root cause investigations to identify systemic issues and implement sustainable corrective actions.
  • Partner with engineering and manufacturing teams to establish, maintain, and improve product and process quality standards.
  • Develop, implement, and maintain quality protocols, procedures, and inspection strategies for manufacturing processes and products.
  • Design and execute inspection, testing, and evaluation methods to verify product quality and process effectiveness.
  • Apply statistical analysis techniques, including Statistical Process Control (SPC), trend analysis, and Minitab tools, to identify risks, monitor performance, and drive data-based decisions.
  • Assess product and process nonconformances, determine root causes, and ensure corrective actions meet reliability, compliance, and quality requirements.
  • Support quality system compliance with Good Manufacturing Practices (GMP), U.S. Food and Drug Administration (FDA) regulations, ISO 13485 requirements, and internal procedures.
  • Mentor and coach junior Quality Engineers while promoting a culture of quality and continuous improvement across the site.
Required Qualifications
  • Bachelor's Degree in Engineering and a minimum of 4 years of relevant experience; OR Master's Degree and a minimum of 2 years of relevant experience; OR PhD.
  • Experience supporting quality engineering activities within a regulated manufacturing environment.
  • Experience conducting investigations, assessing nonconformances, and implementing corrective actions.
  • Experience using statistical methods and data analysis to evaluate product or process performance.
  • Ability to collaborate effectively with cross-functional teams including engineering, manufacturing, and quality organizations.
Preferred Qualifications
  • Advanced knowledge of Good Manufacturing Practices (GMP), U.S. Food and Drug Administration (FDA) regulations, ISO 13485, and Quality System Regulations.
  • Experience leading complex CAPA, NCMR, and root cause investigations.
  • Expertise with Minitab, Statistical Process Control (SPC), trend analysis, and process capability assessments.
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Experience with manufacturing process controls, inspection optimization, digital quality systems, and quality data analytics tools.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.


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