glp jobs in remote

Tucson, Arizona

•

Today

Aptask Global Workforce (AGW) is seeking a Quality Control Associate - Reagent Manufacturing for a 12 month contract position with a major healthcare company located in Tucson, AZ. Responsibilities: Perform inspection and testing of raw materials, in-process materials and finished goods in a compliant manner Document test results, complete batch records, document observations and generate reports for qualification testing Conduct data analysis of raw material, in-process and finished goods test

Full-time

USD 30.02 per hour

Junior/QC Quality Analyst (Onsite)

Boulder, Colorado

•

Yesterday

Please note that this is a 12-18 months contract position, onsite. Please note this is an entry-level position for fresh college graduates with Bachelor's Degrees. Qualifications: Bachelor's degree or equivalentGenerally requires minimal to no prior relevant work experienceDemonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpfulProven skills in coordinating and leading day-to-day tasks and working in collaboration to accomplish deadlines and

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Contract

Depends on Experience

Junior/QC Quality Analyst (Onsite)

Boulder, Colorado

•

Yesterday

Please note that this is a 12-18 months contract position, onsite. Only candidates local to Boulder, CO should apply. All other candidates will be rejected. Please note this is an entry-level position for fresh college graduates with Bachelor's Degrees. Qualifications: Bachelor's degree or equivalentGenerally requires minimal to no prior relevant work experienceDemonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpfulProven skills in coordina

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Contract

Depends on Experience

Quality Control Associate - Reagent Manufacturing

Tucson, Arizona

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Today

Software Guidance & Assistance, Inc., (SGA), is searching for a Quality Control Associate - Reagent Manufacturing for a contract assignment with one of our premier Pharmaceutical Services clients in Tucson, AZ. Responsibilities : The Quality Control Associate - Reagent Manufacturing will be an integral part of a team that performs raw material and finished goods testing. The individual will be responsible for review, generation and sign-off of quality documentation. The ideal candidate wil

Contract

USD 25.75 - 25.75 per hour

Principal Hair Color Chemist

New York, New York

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Today

Description: Who We Are John Paul Mitchell Systems ("JPMS") is recognized worldwide for developing and marketing innovative hair and skin care products since 1980. We've been serving the professional beauty industry with salon-quality hair care products, styling tools and professional hair color through our family of brands including Paul Mitchell, MITCH, Awapuhi Wild Ginger, Tea Tree, Paul Mitchell Tools, Neuro, The Demi, Paul Mitchell the Color, Blonde, and Color XG. We were the first profes

Full-time

USD 150,000.00 - 165,000.00 per year

Director, R&D for Assay Services

Waltham, Massachusetts

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Today

Description: We are seeking a highly experienced and hands-on scientific leader to serve as Director of R&D for the SeQure portfolio, leading an interdisciplinary team in the development and deployment of off-target assessment assays supporting that support cell and gene therapy programs. This role will drive strategy and execution for innovative assay platforms designed to characterize genome editing outcomes and support therapeutic development programs across partner and internal pipelines.

Full-time

USD 220,000.00 - 230,000.00 per year

SAP GRC (Governance, Risk & Compliance) Consultant - Onsite (Oakland, CA) | Fulltime

Oakland, California

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Today

SAP GRC (Governance, Risk & Compliance) Consultant Onsite - Oakland, CA Fulltime Role Overview This role will be responsible for managing IT compliance frameworks, ensuring adherence to SOX (ITGC) and GxP regulations, and working closely with Finance, QA, and Audit teams to maintain audit readiness and operational excellence. Key Responsibilities Manage and oversee SAP GRC (Governance, Risk & Compliance) frameworkDrive SOX ITcompliance, including evidence collection, testing, and auditsPerform S

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Full-time

Depends on Experience

Laboratory Technologist I

La Verne, California

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3d ago

Job Title: Laboratory Technologist I Location: La Verne, CA (Fully On-Site) Schedule: 44/36 Work Week (MondayThursday, every Friday off) Pay Rate: $37.39 $40.59/hour (DOE) Employment Type: Contract / Temp-to-Hire (if applicable) Position Overview We are seeking a detail-oriented Laboratory Technologist I to support a water treatment facilitys Chemistry Compliance Team. This is an entry-level laboratory role focused on routine wet chemistry analysis, sample handling, and regulatory compliance s

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Contract

37 - 40

Scientist II (HPLC Method Validation)

Lebanon, New Jersey

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Today

Shift: Monday through Friday, 8:30 AM - 5:00 PM Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives. This is an onsite full-time Raw Materials Scientist II position located in Lebanon, NJ The primary focus of this position will be performing HPLC method validations in a GMP environment. Monday - Friday, from 8:30

Full-time

Systems Engineer

Ambler, Pennsylvania

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22d ago

Job DescriptionCatalyx is seeking an experienced Systems Engineer to support / upgrade laboratory systems operating within regulated GLP and GMP environments.Key Responsibilities Execute Windows 11 upgrades on business-critical laboratory and manufacturing PCs Perform system assessments to determine compatibility and upgrade readiness Support validation activities in GLP/GMP-regulated environments Develop and execute test protocols (IQ/OQ support as required) Coordinate with Lab IT, QA, Automati

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Full-time

Depends on Experience

Technician 3 - Product Development Engineering

Brea, California

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Today

Job Description Summary We are seeking a Product Development Technician for our Brea, CA facility. This person contributes to the completion of routine technical tasks and develops solutions to routine technical problems of specified scope. Their contacts are primarily with immediate supervisor, project leaders, and other professionals in the unit. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of hea

Full-time

USD 30.70 - 47.60 per hour

Reliability Engineer - Device Assembly and Packaging

Concord, North Carolina

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 66,000.00 - 96,800.00 per year

Validation Engineer

Suffield, Connecticut

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Today

At Cadence, we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical, life sciences, automotive, and other advanced industries. We're an engineering company at heart-with over 75 engineers across our organization-and have built a legacy of over three decades of manufacturing excellence by doing what others consider impossible. Position Overview: We are seeking a highly motivated Validation

Full-time

Data Management Associate

West Point, Pennsylvania

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Today

Job Description PDMB provides data-driven operations and automation support to regulated bioanalytical laboratories. We combine laboratory domain knowledge, robotic work cells, and modern data platforms to ensure reliable, compliant, and continuously improving lab operations. You'll join a multidisciplinary team partnering with lab scientists, automation engineers, IT, Clinical, and QA, to turn operational and scientific data into trusted insights. The PDMB Regulated Bioanalytics Department is

Full-time

USD 87,300.00 - 137,400.00 per year

Data integrity Specialist

Edison, New Jersey

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Today

Job Description: Implement and maintain data integrity controls for HPLC systems (Empower, Chromeleon) in compliance with ALCOA+ principles and regulatory standards (21 CFR Part 11, Annex 11). Review audit trails, monitor user access, and perform periodic data reviews. Lead and coordinate Out-of-Specification (OOS) investigations (Phase I & II), including root cause analysis, hypothesis testing, and CAPA implementation. Perform titration-based content uniformity tests as per SOPs and pharma

Full-time

Data integrity Specialist

Edison, New Jersey

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Today

Job Summary: The Data Integrity Specialist is responsible for implementing and maintaining data integrity controls for HPLC systems (Empower, Chromeleon) in compliance with ALCOA+ principles and regulatory standards such as 21 CFR Part 11 and Annex 11. The role ensures compliance with GLP, GMP, and good documentation practices while supporting validated systems, audit readiness, and laboratory data accuracy. Roles & Responsibilities: Implement and maintain data integrity controls for HPLC s

Full-time

Veeva QMS Consultant

Remote

•

Today

Veeva QMS ConsultantJob Description: Veeva QMS consultant to support the implementation, optimization, and ongoing management of Quality Management Systems (QMS) within a regulated scientific environment. This role will focus on leveraging Veeva Vault QMS solutions to ensure compliance, streamline processes, and enhance operational efficiency across quality and regulatory functions. The ideal candidate combines strong scientific domain knowledge with technical expertise in QMS platforms and Veev

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Full-time

Depends on Experience

Industrial Hygienist

Davie, Florida

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Today

Stefanini Group is hiring! Stefanini is looking for Industrial Hygienist in Davie, FL (Onsite) For quick Apply, please reach out to Vipul Bhardwaj - call: / email: Work Hours: M-F (40 hours) Work Location: Davie, FL (Onsite) Shift: M-F (8:00 AM - 5:00 PM) but will need to support off shifts as needed for sampling events. Ensure compliance with health, safety, and environmental regulations.Conduct quantitative and qualitative monitoring of workplace conditions, including air sampling and biologic

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Contract

$60 /hr

Technical Writer

Washington, District of Columbia

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Yesterday

Job Role: Technical Writer Work Authorization: CitizenLocation: Onsite, Washington, DC Project Description: The technical writer positions are responsible to prepare technical documents for global use within Operational Controls including: Qualification & Validation, Facilities Design & Maintenance, Vendor & Materials Management, Production & Disposition, and Product Distribution, and Governance Controls: Management Responsibilities, Training & Qualification, Event Management, Document & Change

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Contract

Depends on Experience

Test Automation Lead / Consultant

Indianapolis, Indiana

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8d ago

We are seeking a Test Automation Lead / Consultant with strong hands-on expertise in Test Complete and MABL, capable of guiding, mentoring, and resolving complex automation challenges for distributed QA teams. This role requires deep technical automation skills, test strategy ownership, client-facing consulting experience, and strong domain knowledge in clinical and pharmaceutical systems. Key Responsibilities Automation Leadership & Delivery: Act as an Automation SME for Test Complete and MABL,

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Full-time

$100,000 - $120,000

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glp jobs in remote