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Quality Manager Jobs in Puerto Rico (NOW HIRING)

PR · On-site

$62K - $80K/yr

Quality & CI Manager __ At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what ...

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

Quality & CI Manager At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you ...

Quality Engineer

Arecibo, PR · On-site

$80 - $100/hr

Quality & CI Manager__At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you ...

Quality Engineer

Arecibo, PR · On-site

$62K - $80K/yr

Quality & CI Manager At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you ...

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

Quality Systems & Change Control ... Regulatory Compliance & Manufacturing Change Management The Personality Part: * Our Next Piece is ...

Sr. Quality Engineer

Carolina, PR · On-site

$100 - $125/hr

For Senior Quality Engineering Specialist services in the Quality Assurance / QA Engineering (FUME ... Investigations, Root Cause Analysis (RCA), CAPA, change control, and risk management methodologies ...

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Associate Quality Analyst II Description: Responsible for implementing and maintaining the ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

Lead or support product lifecycle quality activities, including process quality, incoming materials, product evaluation, validation, change management, and continuous improvement. Responsibilities ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

Lead or support product lifecycle quality activities, including process quality, incoming materials, product evaluation, validation, change management, and continuous improvement. Responsibilities ...

Showing results 41-60

Quality Manager information

What does a quality manager do?

As a quality manager, your job is to oversee Quality Assurance (QA) and Quality Control (QC) for each product or service assigned to you. Your duties include guaranteeing products and services meet the standards of your organization, keeping management aware of any problems with production, and ensuring that the manufacturing process goes as smoothly as possible. This job has different aspects depending on where a product or service is in the development cycle. Products that are still being designed need QA to make creation as smooth as possible, while released products require QC to ensure the expected level of quality is maintained.

What are the key skills and qualifications needed to thrive as a quality manager, and why are they important?

To thrive as a Quality Manager, you need expertise in quality control processes, data analysis, and regulatory compliance, typically supported by a relevant degree and experience in quality management systems. Familiarity with ISO standards, Six Sigma, and software tools like Minitab or SAP is highly valued, along with certifications such as CQE or Six Sigma Green/Black Belt. Strong leadership, problem-solving abilities, and excellent communication are crucial soft skills for driving continuous improvement and facilitating cross-departmental collaboration. These skills ensure product and process excellence, regulatory adherence, and organizational efficiency.

What are some common challenges quality managers face when implementing new quality standards across teams?

Quality Managers often encounter resistance to change when introducing new quality standards, as team members may be accustomed to established processes. Ensuring consistent understanding and adoption across departments requires clear communication, comprehensive training, and ongoing support. Additionally, balancing the need for compliance with production deadlines can be challenging, so Quality Managers must collaborate closely with operations, engineering, and leadership teams to align goals and foster a culture of continuous improvement.

What is the difference between Quality Manager vs Quality Supervisor?

AspectQuality Manager

Required CredentialsTypically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE or Six Sigma are common.
Work EnvironmentOversees multiple teams or departments, strategic planning, and process improvement initiatives.
Employer & Industry UsageUsed across manufacturing, healthcare, and service industries to lead quality programs.
Common Search & ComparisonOften compared with Quality Supervisor due to overlapping responsibilities and career progression.

The main difference between a Quality Manager and a Quality Supervisor lies in their scope and responsibilities. A Quality Manager focuses on strategic quality initiatives, process improvements, and managing teams at a higher level, often requiring advanced certifications. In contrast, a Quality Supervisor typically oversees daily operations, supervises staff directly, and implements quality procedures. Both roles are essential in maintaining quality standards, but the manager role involves broader planning and leadership functions.

How much do quality managers earn?

Quality managers typically earn a median annual salary of around $70,000 to $100,000, depending on experience, industry, and location. Those with certifications like Six Sigma or ISO auditor credentials may command higher salaries, especially in manufacturing and healthcare sectors.

Is it hard to be a quality manager?

Being a quality manager involves overseeing quality assurance processes, which requires strong attention to detail, problem-solving skills, and knowledge of industry standards like ISO. The role can be demanding due to the need for continuous improvement, audits, and collaboration across departments, but it is manageable with relevant experience and certifications such as Six Sigma or ISO auditor training.

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

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

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

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

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

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

Infographic showing various Quality Manager job openings in Puerto Rico as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Manager, Value Stream Leader

Anasco, PR • On-site

$100 - $125/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago


Job description

Senior Manager, Value Stream Leader is responsible for end‑to‑end performance of a Tissue Technology medical device production value stream platform. The role includes acceptance of design transfers, lifecycle management, and final device shipment, ensuring safety, quality, customer service, and productivity.

Key Responsibilities
  • Ensure the safety of colleagues through an effective and continuously improving environmental, health, and safety program.
  • Provide training and maintain team knowledge of safety procedures, policies, permits, practices, PPE, housekeeping, and awareness.
  • Initiate and lead accident, near‑miss, and incident event notifications.
  • Lead, coach, and develop a team of technicians, operators, managers, supervisors, and process engineers.
  • Manage staffing, training, daily maintenance operations across shifts, attendance, overtime, operational issues, talent management, performance management, development planning, and reporting of results.
  • Conduct interviews, complete performance reviews, and justify promotions or disciplinary actions.
  • Serve on the site leadership team for strategic and tactical planning & execution to meet site objectives.
  • Align value stream objectives with overall site objectives and foster a culture of engagement through recognition, accountability, feedback, continuous improvement, and participation.
  • Ensure compliance with quality standards defined by SOPs, GMPs, global quality standards, and local procedures.
  • Partner with Quality Assurance and Regulatory Affairs to meet FDA QSR, GMP, ISO 13485, and other applicable standards.
  • Initiate, develop, and implement engineering studies and IQ/OQ/PQ/TMV validations for equipment and processes.
  • Coordinate specific efforts for development of manufacturing process requirements, specifications, FMEA, validations, ECR/ECO, and engineering drawings.
  • Investigate CAPAs, nonconformances, and root‑cause analyses, implementing sustainable corrective actions.
  • Maintain training and process documentation requirements.
  • Collaborate with supplier quality and procurement to address supplier issues and changes within the quality management system.
  • Coach and mentor lean Six‑Sigma initiatives (5S, Kaizen, VSM, Kanban, Standard Work, OEE) to reduce waste and improve flow.
  • Deliver measurable improvements in yield, throughput, and cycle time in line with KPI targets.
  • Lead process optimization, yield improvement, Six‑Sigma process excellence, and lean projects in partnership with cross‑functional teams.
  • Monitor process capability and performance metrics (CoPQ, Cpk, yield, run time, downtime, scrap).
  • Develop and manage all financial budgets within the value stream, including headcount, expenses, capital, and inventory.
  • Ensure cost of goods sold results align with financial targets.
  • Solve operational issues collaboratively and interact with senior management on cross‑departmental projects.
  • Complete other job‑related duties as assigned.
Qualifications & Competencies
  • Engineering or Technical degree with 8+ years of experience leading a team or equivalent management experience; or master’s degree with 5+ years of leadership experience.
  • Excellent organizational and written and oral English communication skills.
  • Financial acumen related to operations profit & loss management.
  • Proficiency in MS Office Suite and statistical analysis software.
  • Experience in a regulated environment (medical device or pharmaceutical preferred).
  • Familiarity with health, safety, and environmental regulations.
  • Self‑motivated team player capable of working independently and collaboratively at all levels.
Tools & Equipment Used
  • General office equipment: computers, printers, copiers, fax machines, telephone systems.
  • Software and systems: ERP (e.g., Oracle), CRM platforms, statistical analysis tools, project management software (e.g., MS Project, Jira), QMS platforms.
Physical Requirements

Employment requires sitting, talking, and moving throughout various areas of the building, travelling across company locations, periodically lifting or moving items up to 25 pounds, and travelling domestically and internationally by car, train, or airplane as required.

Salary & Benefits

Salary Pay Range: $87,000 – $122,000 USD. In addition to base pay, compensation may include bonus, commission, equity, or other variable components. Employees are eligible for medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, group legal insurance, and a 401(k) savings plan.

EEO Statement

Integra LifeSciences is an equal opportunity employer, committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations. For more information on your rights, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans. Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA.

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