Gamp jobs

Los Angeles, California

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Today

Position: Equipment EngineerLocation Northridge, CA-On SiteDuration: Long Term Contract Key ResponsibilitiesDevelop and execute Installation, Operational, and Performance Qualification (IQ/OQ/PQ) protocols specifically for blood glucose monitoring sensor manufacturing equipment.Define and document critical process parameters (CPPs) and equipment capabilities to ensure stable sensor performance within specification limits.Establish preventive maintenance plans, calibration schedules, and critical

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Third Party, Contract

$60+

Sr RBV and VM Technical Business System Analyst

Remote

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20d ago

Job Details: Position: Sr RBV and VM Technical Business System Analyst Location: Remote Type: Contract Required Qualifications Proven experience in CSA and GAMP 5 implementation. Strong knowledge of Veeva validation management and Veeva configurations. Excellent analytical and problem-solving skills. Demonstrated ability to work effectively with global, virtual teams. Experience working independently, guiding project teams, and making informed decisions. Prior hands-on experience with CSA and GA

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Contract, Third Party

$60 - $65

Senior CQV Engineer/Validation Engineer

No location provided

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Today

Direct hire /Full time On-site Boulder, CO Salary expectation: You povide Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The successful candidate will lead and execute CQV deliverables associated with GMP-regulated process equipment, utilities, automation systems, cleanrooms, and manufacturing operations. This role requires hands-on technical expertis

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Full-time

$DOE

Sr RBV and VM Technical Business System Analyst@ Remote Role

No location provided

•

Today

Job Role: Sr RBV and VM Technical Business System Analyst Location: 100% Remote Role Duration: Long Term Contract Key Responsibilities: Lead and execute system analysis and validation efforts following CSA and GAMP 5 methodologies. Handson experience performing Veeva configurations, creating reports and dashboard Develop and manage Veeva validation documentation including requirements, test scripts, traceability, and risk assessments. Collaborate with global and virtual teams to define syste

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Contract, Third Party

Information Systems Engineer 3

Sunnyvale, California

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Today

Detailed Job description: Position Overview: Person will be responsible for identifying, developing and implementing software solutions. This will include working with process owners to identify continuous improvement opportunities and develop software solutions to support process effectiveness and efficiencies. Individual will also be accountable for managing projects and software throughout their respective lifecycles. Roles and Responsibilities: Directly participate

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Contract, Third Party

$88 - $88

On Site MES IT Coordinator

Cincinnati, Ohio

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13d ago

Role: On Site MES IT Coordinator Location: Cincinnati, OH (Onsite) JD: The Site MES IT Coordinator serves as the primary site-level IT and MES liaison responsible for coordinating Manufacturing Execution System (MES) implementation, deployment, and ongoing operational support across manufacturing facilities. This role acts as the critical interface between site operations, Quality, MSAT, Validation, IT/OT teams, Global MES organizations, vendors, system integrators, and offshore development team

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Contract

Depends on Experience

CSV Engineer

Raleigh, North Carolina

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Today

Description: The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of complex computerized systems, custom-developed applications, enterprise databases, data platforms, and business intelligence solutions used within regulated GxP environments. This role partners with IT, Software Development, Data Engineering, Manufacturing, Quality, and business stakeholders to ensure that custom software applications, databases, reporting platforms, and system integrat

Full-time

Manufacturing IT / MES Site Lead Coordinator (Multiple Locations - USA)

Remote

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30+d ago

Manufacturing IT / MES Site Lead Coordinator (Multiple Locations - USA) We are looking to hire a candidate with the mentioned skill sets and experience for one of our clients within the pharmaceutical Industry. This is a 12+ month contracting role, with potential for extension. Multiple Locations in the USA. Role Summary: The Site MES IT Coordinator will support Manufacturing Execution System (MES) project implementation and post-go-live support at the manufacturing site level. This role will

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Contract

Depends on Experience

Computer Systems Validation Specialist III

Portsmouth, New Hampshire

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Today

Computer Systems Validation Specialist Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed. The Computer Systems Validation (CSV) Specialist leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. They conduct risk assessments, review change requests and test scripts, draft protocols, and oversee GMP documentation revisions. This role acts as the QA CSV represen

Full-time

Technical Business Analyst ( Life Science )

Remote

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14d ago

Title: Sr RBV and VM Technical Business System Analyst Location: CA/Remote Type: Contract JD: Sr RBV and VM Technical Business System Analyst Key Responsibilities: Lead and execute system analysis and validation efforts following CSA and GAMP 5 methodologies. Handson experience performing Veeva configurations, creating reports and dashboard Develop and manage Veeva validation documentation including requirements, test scripts, traceability, and risk assessments. Collaborate with globa

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Contract, Third Party

$50 - $52

System Test and Validation Lead

Remote or Arlington Heights, Illinois

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4d ago

Drive validation and compliance activities for complex GxP systems as a Senior Consultant, Regulatory, Risk, and Compliance. This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address emerging validation considerations for AI/ML-enabled systems and automation frameworks. If this sounds exciting, then this team may be the right fit for you! Work you'll do As a Senio

Full-time

USD 95,000.00 - 145,000.00 per year

Process Automation Engineer (DeltaV)

Calabasas, California

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Today

Wunderlich-Malec Engineering (WM) is a 100% employee-owned ESOP and one of the largest and most well-established engineering companies in the United States. When you join WM you become part of a company that is: 100% employee-owned with 40+ years of industry historyENR (Engineering News Record) Top 500 firmRated as a top System Integrator Giant We have a Process Automation Engineer position open in Calabasas, CA. This position is responsible for designs, implements, and maintains process automat

Full-time

USD 120,000.00 - 180,000.00 per year

Controls Engineer II, Operational Technology

Silver Spring, Maryland

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Today

California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs. United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop

Full-time

USD 84,000.00 - 120,000.00 per year

Validation Engineer II

Plainville, Massachusetts

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Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goal

Full-time

USD 66,000.00 - 99,000.00 per year

Engineer, Automation

Maryland

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Today

Automation Engineer Position Summary: Work Schedule: Monday - Friday, 8am - 5pm. 100% on-site Catalent's Baltimore and Harmans, Maryland sites provide industry-leading GMP development and manufacturing services for advanced biopharmaceuticals, including viral vectors, next-generation vaccines, and oncolytic viruses. Our FDA-licensed, state-of-the-art Gene Therapy manufacturing campus in Harmans/BWI features two facilities located just five miles from BWI Airport and 13 miles from downtown Balt

Full-time

USD 80,000.00 - 110,000.00 per year

Automation Engineer III

San Diego, California

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Today

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Summary: This role is responsible for designing, specifying, and maintaining control systems supporting biopharmaceutical manufacturing facilities and processes, including aseptic fillin

Full-time

USD 93,360.00 - 107,280.00 per year

Senior Automation Systems Administrator - Manufacturing & Lab Support

Menands, New York

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Today

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Systems Administrator to join our IOPS team, providing expertise in the configuration and administration of automated and computerized system software and firmware across our manufacturing and laboratory operations. In this role, you will ensure systems remain in a compliant and validated state - leading projects, driving

Full-time

USD 78,700.00 - 128,700.00 per year

Lead Technology Compliance

Raritan, New Jersey

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Today

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 94,000.00 - 151,800.00 per year

Senior Engineer Facilities

Redwood City, California

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Today

Reporting to the Director Facilities & Engineering, the Senior Engineer Facilities is responsible leading the equipment reliability program, championing continuous improvement, running capital projects (up to and above $250k), and being the site authority on facility and utility systems. The role combines the benefit of small site (agile and broad responsibilities) with the structure, knowledge, and resources of a leading global pharmaceutical company. This is a senior level role where the engin

Full-time

USD 101,643.00 - 152,464.00 per year

Senior Manager, IT Applications - Laboratory Informatics

Troy, New York

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Today

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Manager (Manager or Senior Manager) to join our IOPS IT team, overseeing the day-to-day maintenance, support, and development of Regeneron's IT Applications portfolio - including Empower CDS, SDMS, and other business-critical systems. In this role, you will lead a team of analysts, drive audit readiness and compliance, and

Full-time

USD 108,000.00 - 206,100.00 per year

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