OQ jobs in Dallas, TX

Plano, Texas

•

11d ago

Minimum experience of 10 years in Medical devices - Manufacturing Engineering. Good Experience working on Process Validations (IQ, OQ, PQ) Experience developing manufacturing processes and technologies, which includes process characterization Experience working on PFMEAs Experience performing Data analysis (Minitab) Evaluate process and design alternatives based on Design for Manufacturability principles. Ability to work within a team and as an individual contributor in a fast-paced, changing en

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Third Party, Contract

$40 - $45

Senior CSV Engineer

Remote or Massachusetts

•

Yesterday

Job Description: We are looking for a Senior Computer System Validation (CSV) Engineer to perform validation of computerized systems associated with Client's facilities, utilities, and equipment for the qc lab validation project. This role will focus on EMS, Client, and laboratory informatics/software platforms (e.g., HPLC/qPCR control software, Sicknotes, Blue Mountain), ensuring compliance with 21 CFR Part 11, Annex 11, and data integrity requirements. The CSV Engineer will obtain documentatio

Full-time

Field Service Engineer II

Remote or Raleigh, North Carolina

•

Yesterday

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biolog

Full-time

CSV and Validation Engineer

Remote or New Jersey

•

Yesterday

Job Description: We are seeking a hands-on CSV and Validation Engineer to validate software used with laboratory instruments and lab informatics platforms. The role owns risk-based validation planning and execution aligned to EMA Annex 11 and 21 CFR Part 11, authors audit-ready documentation, and partners with QA/IT/Lab to transition systems to standardized SOPs. Responsibilities: Plan and execute computer system validation using a risk-based CSA approach aligned to GAMP 5. Validate instrument

Full-time

Senior Supplier Engineer

Remote or Danvers, Massachusetts

•

Yesterday

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 91,000.00 - 147,200.00 per year

Supplier Engineer, Electrical Systems

Remote or Danvers, Massachusetts

•

Yesterday

Full-time

USD 77,000.00 - 124,200.00 per year

Principal Engineer, Tooling

Remote or Connecticut

•

Yesterday

Job Description Position Summary The primary function of this job is to lead the execution of plastic components strategies and initiatives for ICU Medical Device products. These strategies will be defined by the Operations team with inputs from the stakeholders. Stakeholders include: PMOs, R&D, Operations, Procurement, and Supplier Quality. This position will lead the execution of tooling, equipment, and manufacturing processes relative to plastics. Represents the Advanced Manufacturing Engin

Full-time

Computer System Validation (CSV) Engineer

Remote or Massachusetts

•

Yesterday

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. uthor and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's degree

Full-time

Biovia Discoverant System Administrator

Remote

•

30+d ago

Biovia Discoverant System Administrator Remote - Nearshore/Offshore (Must Work in PST hours) Long-Term Rolling Contract Job Description: The BIOVIA Discoverant System Administrator is responsible for the deployment, configuration, maintenance, and performance optimization of the Discoverant platform. This role ensures system reliability, data integrity, and regulatory compliance across manufacturing and quality operations. The administrator collaborates with cross-functional teams to support l

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Contract

$30 - $40

SDMS Validation Engineer

Remote

•

30+d ago

Role: Scientific Data Management System (SDMS) Validation Engineer Location: NEAR SHORE - South America/Canada Length: Long term rolling contract CSV engineers and for the applications: Discoverant, BIOVIA ELN, SDMS, Empower, LabX, SoftMax Pro. Job Description: Job Overview: The SDMS (Scientific Data Management System) Validation Engineer is responsible for the qualification, validation, and compliance of scientific data management systems within laboratory environments, particularly in regula

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Contract

$30 - $35

LIMS and QC Applications Consultant

Remote or Hybrid in Bridgewater, New Jersey

•

Today

Solution Architecture and Design: Lead the design and development of LabVantage LIMS solutions tailored to business and laboratory needs. Develop system workflows, configurations, and integrations with other enterprise systems (e.g., S4 Hana ERP, MES, ELN, SDMS). Define data models, interface designs, and system configurations. Implementation and Deployment: Oversee installation, configuration, and validation of LabVantage LIMS applications. Develop and execute project plans, ensuring timely an

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Full-time, Contract

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OQ jobs in Dallas, TX, USA