Jobs Referso Partner API

Free job alerts

FDA Quality System Regulation jobs

Job titleLocation

Popular:United States Canada Viet Nam

All filtersRefine by skill, company, date, job type, industry and more

Company

Skillsjobs that use all of them

FDA Quality System Regulation

Popular

Date posted

Any timePast hourPast 24 hoursPast week

Workplace

RemoteHybridOn-site

Job type

Full-timePart-timeContractInternshipTemporary

Experienceyears required

0–2 years2–5 years5–10 years10+ years

Salary

Salary listed

Education

High schoolAssociate degreeBachelor's degreeProfessional certificatePostgraduate degree

Industryfield of work

Software & InternetHardware & ElectronicsEngineeringHealthcareLife Sciences & ResearchFinance & AccountingSales & Business DevelopmentMarketing & CommunicationsCreative & DesignCustomer Service & SupportAdministrative & OfficeHuman Resources & RecruitingLegal & ComplianceManagement & OperationsEducation & TrainingRetailHospitality & Food ServiceManufacturing & ProductionSkilled Trades & ConstructionTransportation & LogisticsFacilities, Cleaning & SecuritySocial Services & Public SectorEnergy, Environment & Agriculture

1 selected

Skill:FDA Quality System Regulation

Referso Jobs

Fresh jobs from employer career sites in the US and Europe. Search free, get alerts free, and let Referso apply when you're ready.

Job seekersSearch jobs Free job alerts Remote jobs

RefersoAuto-apply How it works Pricing Log in

For companiesPartner API (beta)API docs Contact sales

CompanyAbout Contact Privacy Terms

© 2026 Referso. Jobs link to the original posting; Referso is not affiliated with the employers listed.Privacy Terms Request a removal

1–2 jobs· newest first

Microbiology Technician 3New
Viant · Heredia, Costa Rica
On-site · Full-time · Mid
Manager, Quality Systems
Baxter International Inc. · Tijuana, Mexico
Full-time · Manager

+10K new in the last hour

Microbiology Technician 3

Viant · Posted Nov 9, 2026

Heredia, Heredia, Costa Rica
On-site
Full-time · Mid
4+ years

Apply with Referso

AI

Apply on careers page

Support environmental control activities, executing environmental routine testing for viable and non-viable particles for air and product contact surfaces follow quality system and in compliance with Good manufacturing practices.

Responsibilities

Perform investigation process for out of tolerance equipment
Include new equipment at the calibration and maintenance system
Review and approve cleanroom intrusion plans
Get involved in various stages of equipment and processes validations: run or write protocols and reports for IQ, OQ, PQ and TMV; as well as any other document relating to validation
Performs or coordinate microbiology testing as offered by the Microbiology Lab, including LAL, Bioburden, Environmental monitoring

Requirements

Microbiology or Quality Technician
Biotechnology, Microbiology and Biology Bachelor degree
Nice to have: sterilization
Nice to have: Minitab

Skills

Microsoft office Bilingual English/Spanish – Intermediate FDA Quality System Regulation Medical Device Directive ISO 13485 process validation requirements GMPs ISO USP FDA regulations statistical techniques root cause analysis tools Minitab

See full job description

Manager, Quality Systems

Baxter International Inc. · Posted Nov 6, 2026

Tijuana, Baja California, Mexico
Full-time · Manager
8+ years

Apply with RefersoAI Apply on careers page

Lead strategic quality systems and compliance for a manufacturing site, driving continuous improvement, audits, and regulatory readiness.

Responsibilities

Lead continuous improvement of the Quality Management System
Drive quality objectives and KPIs
Champion quality culture and coaching
Oversee CAPA, audits, document control, training
Serve as primary quality systems expert during audits

Requirements

Bachelor's degree in Engineering or related technical discipline
Nice to have: Certified Lead Auditor training
Nice to have: CAPA programs
Nice to have: risk management methodologies
Nice to have: process validation

Skills

Quality Management Systems FDA Quality System Regulation (21 CFR Part 820)ISO 13485 CAPA internal audits document control training programs

nonconformance management

quality governance

regulatory audits

process validation

quality remediation

risk management methodologies

cross-functional stakeholder influence

continuous improvement initiatives

See full job description