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Quality Process Improvement Manager Jobs in Puerto Rico

JC Automation Corp

PR · On-site

... product quality. * Investigations & CAPA Management: Lead and manage complex investigations ... Continuous process improvement and optimization methodologies * Technical writing -- protocols ...

Abbott

Associate Quality Engineer

Barceloneta, PR · On-site

$45K - $89K/yr

Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new ...

Inteldot

MES Business Analyst

Barceloneta, PR · On-site

$51K - $69K/yr

Knowledge of Quality Management Systems (QMS), document management systems, and controlled ... quality transformation initiatives. * Lean, Six Sigma, or process improvement experience.

Ferrovial

Quality Manager

San Juan, PR · On-site

Benefit from global and cross-business unit mobility, with development processes designed to ensure ... continuous improvement of the Project Quality Management System in alignment with USACE ...

JLL

Quality Manager

Juncos, PR

Develop and deploy quality awareness, training, and continuous improvement programs. Support and ... processes. Lead and facilitate quality review meetings, governance forums, and escalation ...

JC Automation Corp

PR · On-site

$74K - $101K/yr

Identify and lead process improvement initiatives related to inspection systems. Manage inspection-related capital or operational projects to maximize efficiency, quality, and compliance.

West Pharmaceutical Services

Sr. Quality Engineer

Cidra, PR · On-site

$84K - $114K/yr

Lead and manage QMS activities including CAPA, Failure Investigation, Non-Conformance assessment ... May support quality assurance improvement activities by evaluating products, processes or materials ...

West Pharmaceutical Services

Sr. Quality Engineer

Cidra, PR · On-site

$84K - $114K/yr

Lead and manage QMS activities including CAPA, Failure Investigation, Non-Conformance assessment ... May support quality assurance improvement activities by evaluating products, processes or materials ...

Boston Scientific

Process Eng - P4

Dorado, PR · On-site

Assesses process capabilities, prioritizes process improvement opportunities, and innovates and ... Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality ...

Boston Scientific

Process Eng - P4

Dorado, PR

Assesses process capabilities, prioritizes process improvement opportunities, and innovates and ... Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality ...

Boston Scientific

Process Eng - P4

Dorado, PR

Assesses process capabilities, prioritizes process improvement opportunities, and innovates and ... Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality ...

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Quality Process Improvement Manager information

What are the 5 components of quality improvement?

For a Quality Process Improvement Manager, the five components of quality improvement typically include defining the problem, analyzing current processes, designing and implementing solutions, monitoring results, and standardizing successful changes. These components help ensure continuous improvement and high-quality outcomes in organizational processes. Familiarity with tools like PDCA (Plan-Do-Check-Act) and data analysis is essential for effective quality management.

How much do process improvement managers make in the US?

Process improvement managers in the US typically earn between $70,000 and $120,000 annually, with the median salary around $90,000. Salaries vary based on experience, industry, location, and certifications such as Six Sigma or Lean management.

What are the key skills and qualifications needed to thrive as a Quality Process Improvement Manager, and why are they important?

To thrive as a Quality Process Improvement Manager, you need expertise in process analysis, project management, and quality assurance, often supported by a degree in engineering, business, or a related field. Familiarity with Lean, Six Sigma methodologies, and tools such as statistical analysis software or quality management systems is typically required, with certifications like Six Sigma Green or Black Belt being advantageous. Strong leadership, problem-solving, and communication skills enable you to drive change and motivate cross-functional teams. These competencies are vital for identifying inefficiencies, implementing effective solutions, and fostering a culture of continuous improvement within an organization.

What is the salary for a quality manager?

The salary for a Quality Process Improvement Manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. Certifications like Six Sigma or Lean can influence compensation, and the role often requires strong analytical and process improvement skills.

What is the difference between Quality Process Improvement Manager vs Quality Analyst?

AspectQuality Process Improvement ManagerQuality Analyst
CertificationsSix Sigma, Lean, CQEISO, Six Sigma Green Belt
Work EnvironmentLeadership, cross-departmental projectsData analysis, testing, inspection
Industry UsageManufacturing, healthcare, techManufacturing, software, healthcare

The Quality Process Improvement Manager focuses on leading initiatives to enhance processes and efficiency across departments, often requiring project management skills and strategic planning. In contrast, the Quality Analyst primarily conducts data analysis and inspections to ensure product or service quality. Both roles are vital in quality management but differ in scope, responsibilities, and focus areas.

What does a Quality Process Improvement Manager do?

A Quality Process Improvement Manager is responsible for analyzing existing business processes and identifying opportunities to enhance efficiency, quality, and productivity. They use methodologies such as Six Sigma, Lean, or Total Quality Management to design and implement improvements across various departments. Their role often involves collaborating with teams, monitoring key performance indicators, and ensuring compliance with industry standards to maintain high levels of quality and customer satisfaction.

What are some common challenges faced by Quality Process Improvement Managers when implementing new processes, and how can they be addressed?

Quality Process Improvement Managers often encounter resistance to change from staff, difficulty in aligning cross-functional teams, and challenges in quantifying the impact of new processes. Addressing these challenges involves clear communication about the benefits of proposed changes, involving key stakeholders early in the process, and utilizing data-driven metrics to track progress. Building strong relationships across departments and fostering a culture of continuous improvement can also smooth the transition and ensure long-term success.

What does a quality improvement manager do?

A quality improvement manager oversees processes to enhance product or service quality within an organization. They analyze data, implement process changes, and monitor outcomes to ensure compliance with standards and improve efficiency, often using tools like Six Sigma or Lean methodologies.
What are popular job titles related to Quality Process Improvement Manager jobs in Puerto Rico? For Quality Process Improvement Manager jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Quality Process Improvement Manager jobs in Puerto Rico look for? The top searched job categories for Quality Process Improvement Manager jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Quality Process Improvement Manager jobs? Cities in Puerto Rico with the most Quality Process Improvement Manager job openings:
Quality Process Improvement Manager jobs near you

Principal Process Scientist

JC Automation Corp

PR • On-site

Full-time

Posted 26 days ago

Job description

About Company:

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

ABOUT THE ROLE

We are seeking a Principal Process Scientist to serve as the Subject Matter Expert (SME) for sterile manufacturing processes, with specialized focus on liquid and lyophilized parenteral products. This senior-level role combines deep scientific expertise with hands-on operational support, driving process optimization, compliance, and technology transfer in a cGMP pharmaceutical environment.

The ideal candidate brings extensive experience in manufacturing operations, complex investigations, process validation, and cross-functional leadership, ensuring strategic alignment with site priorities and regulatory requirements.


RESPONSIBILITIES

  • Subject Matter Expertise (SME): Serve as the primary technical authority for sterile manufacturing processes, including liquid and lyophilized parenteral products, providing guidance to manufacturing, engineering, quality, and validation teams.
  • Daily Manufacturing Support: Support daily manufacturing operations with advanced technical expertise, ensuring processes operate within validated parameters and in compliance with cGMP and site procedures.
  • Troubleshooting & Process Optimization: Lead technical troubleshooting efforts for manufacturing deviations and process-related issues. Drive continuous process optimization to improve yield, efficiency, and product quality.
  • Investigations & CAPA Management: Lead and manage complex investigations, including root cause analysis for deviations. Develop and implement effective Corrective and Preventive Actions (CAPAs) to prevent recurrence.
  • Process Validation: Plan and execute process validation activities, ensuring all protocols, reports, and supporting documentation meet regulatory and internal standards.
  • Technology Transfer: Lead technology transfer efforts for new or existing products, coordinating with cross-functional teams to ensure successful scale-up and site integration.
  • Regulatory Compliance: Ensure strict adherence to cGMP regulations, FDA guidelines, and internal site procedures. Support regulatory inspections and audits as the technical SME for sterile manufacturing processes.


REQUIREMENTS & QUALIFICATIONS

Required

  • Bachelor's, Master's, or Ph.D. in Life Sciences, Chemical Engineering, Pharmacy, Bioengineering, or a closely related scientific discipline.
  • Extensive background in sterile manufacturing processes with specialized focus on liquid and lyophilized parenteral products.
  • Proven experience supporting daily manufacturing operations and providing advanced technical troubleshooting.
  • Demonstrated capability in managing complex investigations, root cause analysis, and CAPA implementation.
  • Hands-on experience executing process validation activities and leading technology transfer efforts.
  • Deep understanding of cGMP regulations, FDA guidelines, and compliance requirements in a highly regulated pharmaceutical environment.
  • Exceptional cross-functional collaboration skills with manufacturing, engineering, quality, and validation teams.


Preferred

  • Ph.D. or advanced degree with focus on sterile pharmaceutical manufacturing or bioprocessing.
  • Experience supporting FDA or EMA regulatory inspections as a process SME.
  • Familiarity with lyophilization process development and scale-up.
  • Experience with statistical tools for process monitoring and data analysis (e.g., JMP, Minitab).


SKILLS

Technical Skills

  • Sterile manufacturing processes — liquid and lyophilized parenteral products
  • Process validation (IQ/OQ/PQ/PPQ) and technology transfer
  • Deviation management, root cause analysis, and CAPA systems
  • cGMP regulations, FDA guidelines, and regulatory documentation
  • Continuous process improvement and optimization methodologies
  • Technical writing — protocols, reports, SOPs, and investigation summaries
  • Microsoft Office 365


Soft Skills

  • Senior-level technical leadership and SME authority
  • Strong cross-functional collaboration and stakeholder alignment
  • Analytical mindset with structured problem-solving capabilities
  • Ability to manage multiple priorities in a fast-paced regulated environment
  • Clear scientific communication across technical and non-technical audiences
  • Adaptability and availability to support other shifts as business needs require