Qc Jobs in Puerto Rico (NOW HIRING)

This is whereyour work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

As the QC Manager, you will lead and organize the operations of the Microbiology and Chemistry Laboratories. You will work closely with Manufacturing, Supply Chain, Quality, Regulatory, and R&D teams to ensure laboratory testing activities are executed in compliance with FDA regulations, USP standards, company policies, and current Good Manufacturing Practices (cGMPs).

This role is responsible for the development and implementation of laboratory policies, systems, procedures, specifications, and testing programs for Raw Materials, In-Process Materials, Finished Products, Stability Programs, and Method Transfers. You will also oversee laboratory validation activities, quality monitoring programs, and change control processes to support business priorities, quality objectives, and operational excellence.

• Direct and manage all Microbiology and Chemistry Laboratory operations.
• Coordinate laboratory activities with Manufacturing and Supply Chain teams.
• Lead, supervise, train, and develop exempt and non-exempt laboratory personnel.
• Ensure laboratory services are delivered efficiently, cost-effectively, and in compliance with applicable regulations and standards.
• Perform weekly, monthly, and annual reporting as required by site leadership and company procedures.

• Ensure compliance with all applicable FDA, USP, OSHA, EPA, cGMP, corporate, federal, and state requirements.
• Establish, implement, and maintain laboratory standard operating procedures and policies.
• Conduct and approve laboratory investigations, including root cause analysis activities.
• Conduct trend analysis, including Annual Product Review data evaluations.
• Ensure all laboratory changes are appropriately managed through the change control system.
• Maintain accountability for the Product Stability Program.

• Manage the laboratory validation program, including equipment, processes, test methods, software, and related systems.
• Lead and support method transfer activities where applicable.
• Participate in process validation and revalidation programs.
• Oversee testing and analysis of validation samples.
• Support continuous improvement initiatives through laboratory automation and testing method enhancements.

• Ensure laboratory analysts are properly trained and qualified to perform testing activities.
• Verify adherence to Good Laboratory Practices, company standards, and regulatory requirements.
• Routinely audit analyst performance, testing accuracy, and documentation practices to assess training effectiveness and compliance.

• Develop and manage departmental operating and capital budgets.
• Maintain laboratory technologies, software, and equipment in an updated state.
• Prepare and submit capital expenditure requests as needed.
• Ensure all laboratory service contracts are maintained and current.
• Evaluate and manage laboratory maintenance service suppliers.

• Bachelor's degree in Chemistry, Microbiology, or a related scientific discipline.
• Minimum of 8 years of experience in Quality Systems within a regulated environment.
• Minimum of 3 years of management or supervisory experience in a laboratory setting.
• Experience with wet chemistry and/or microbiology laboratory procedures.
• Root Cause Analysis training and practical experience.
• Working knowledge of applied statistics and statistical tools.
• Strong understanding of FDA regulations, USP standards, cGMPs, laboratory operations, and quality systems.
• Experience with laboratory validation programs, method transfers, and stabil
• Proven ability to train, motivate, coach, and develop employees.
• Strong presentation and communication skills.
• Demonstrated success in change management and leading organizational change.
• Demonstrated commitment to integrity, accountability, teamwork, collaboration, and performance excellence.
• Strong facilitation and conflict resolution skills.

• Fully bilingual in English and Spanish.
• Ability to effectively communicate and present information to management, customers, and regulatory auditors.

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

PO Box 518 Road 144 Km 20.6|Jayuya, PR 00664|United States of America