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- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory...Suggested
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory...SuggestedFull time
- ...Job Summary We are seeking a Validation Specialist I for a contract opportunity supporting laboratory equipment validation within a regulated pharmaceutical manufacturing environment in Jayuya, Puerto Rico. This on-site role is ideal for an early-career validation...SuggestedContract workTemporary workWork at officeShift work
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory...Suggested
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory...Suggested
- ...communication skills and a positive attitude. Shift: 1st and according to business needs. Experience in: Executing process validation (IQ/OQ/PQ) NPI/NPD The Personality Part: ~ Our Next Piece is someone who treats everyone they meet like family,...SuggestedContract workFlexible hoursShift work
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory...SuggestedNight shiftAfternoon shift
- ...Job Description Job Description ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical... ...for planning, executing, and documenting computer system validation activities for GxP-regulated computerized systems within a pharmaceutical...SuggestedWork at officeLocal area
- ...Job Description Job Description ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical... ...of Role: We are seeking Commissioning, Qualification, and Validation (CQV) professionals to support validation activities in a...SuggestedLocal areaShift work
- ...Job Description Job Description ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical... ...development. Summary of Role: Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning...SuggestedLocal areaShift workNight shiftDay shiftAfternoon shift
- ...Baxter seeks a Senior Engineer Validation Specialist to lead process engineering, validation, and maintenance projects in a pharmaceutical manufacturing environment in Puerto Rico. The role involves managing technical upgrades, ensuring regulatory compliance, and mentoring...SuggestedShift work
$170k
Abbott Laboratories is seeking a Senior Operational Excellence Engineer to drive continuous improvement across biotech and pharmaceutical operations. In this role, you will lead Lean Six Sigma initiatives to optimize manufacturing, quality, and supply chain processes, using...Suggested$34.62 per hour
As an Associate Manufacturing or Quality Engineer in a regulated healthcare manufacturing environment, you support daily production by troubleshooting process and quality issues, implementing improvements, and maintaining compliance. Working with supervisors, engineers,...Suggested- ...obtain approvals and construct tooling as needed Develop processes, methods, and controls for new programs; supervise assembly and validation Set up new equipment, ensure proper operation, and train staff on usage and procedures Implement process improvements using...Suggested
- ...Job Description Job Description Job Title: Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico, providing flexible cGMP facilities and integrated services to accelerate the development, manufacturing, and...SuggestedContract workLocal areaFlexible hoursWeekend work
- ...cause investigations, corrective actions, and structured problem-solving methodologies Support equipment qualifications, process validations, and engineering documentation updates Requirements Completed freshman year at accredited university; pursuing bachelor's...Permanent employmentFull timeWork at officeVisa sponsorship
- Job Description Job Description Design and improve the production system end to end — layout, flow, capacity, and standard work — as we scale toward 1 GW. What you'll do Design line layout, material flow, and station balancing for throughput. Develop standard...
- ...and provide troubleshooting guidance. Work with Manufacturing, Maintenance, Process Development, Utilities, Facilities, QA and Validation to define requirements and recommendations for process and system modifications. Support deviations, equipment qualification,...Contract workShift workNight shift
- ...and maintain engineering procedures and compliance documentation Mentor junior team members and provide training on process and validation requirements Requirements Bachelor's degree in Engineering Minimum 4 years manufacturing, maintenance, R&D, or process...Work at office
- ...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented... ...by assisting with IT system upgrades, computer system validation activities, and controlled documentation updates related to manufacturing...Temporary work
$45k - $89.8k
Abbott seeks an Associate Manufacturing Engineer to support cardiac rhythm management manufacturing operations in Arecibo, Puerto Rico. The role involves optimizing line performance across quality, safety, yield, and output while collaborating with supervisors, quality...$13.18 - $25.02 per hour
Abbott seeks an Associate Manufacturing or Quality Engineer for its Puerto Rico facilities to support manufacturing operations and drive continuous improvement. This pipeline requisition targets future openings in 2026–2027, with the role focusing on quality, safety, compliance...- Job Description Job Description Job Summary We are seeking an experienced Industrial Engineer for a direct hire opportunity supporting manufacturing process improvement and operational efficiency initiatives in Jayuya, Puerto Rico. This role is ideal for an engineering...Temporary work
- ...ABOUT THE ROLE Plan, lead, and control the delivery of JCA validation, qualification, and procedural documentation services for the... ...or laboratory systems). -Experience managing client-facing consulting engagements with multidisciplinary teams. -Experience managing...Contract workWork at officeRemote work
- ...maintain process parameters, work instructions, SOPs, and technical documentation. Support new product introductions, process validations, and manufacturing line setups. Analyze yield, scrap, cycle time, and other manufacturing KPIs to improve operational performance...Work at office
- ...Job Description Job Description ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology,... ...in Engineering Preferred Qualifications: Experience in validations in a medical device environment. Collaborate closely with...Local areaImmediate startShift workDay shift
- ...Senior Process Engineer at Medtronic in Humacao, Puerto Rico, responsible for leading process development, optimization, and validation in regulated medical device manufacturing. Drives continuous improvement initiatives while ensuring compliance with quality and regulatory...
$51k - $71k
...role focused on optimizing manufacturing processes for collagen and lyophilization products. Responsible for process development, validation, continuous improvement, and cross-functional project leadership while ensuring regulatory compliance and operational efficiency....- Johnson & Johnson seeks process engineering co-op students for a twelve-month full-time position in Añasco, Puerto Rico. The role involves working on diverse engineering projects, assisting with design and development of materials and processes, and collaborating with ...Permanent employmentFull timeVisa sponsorship
- ...equipment, tooling, automation, and process enhancements to support operational objectives. Lead equipment qualification and validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Partner...Full timeTemporary workH1bWork at officeLocal areaImmediate startWorldwideFlexible hours

