Specialist, MSEO Manufacturing Systems Validation

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Roles & Responsibilities:Develop and execute comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly systems.Lead the validation of SEA Vision Yudoo and AVI systems, ensuring strict compliance with industry standards and regulatory requirements.Author, execute, and document Installation Qualification (IQ),...

Key Responsibilities Perform commissioning, qualification, validation, and maintenance activities within the facility. Oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors. Lead and support quality investigations, CAPAs, and process improvements to enhance compliance and efficiency. Develop and implement...

Key Responsibilities Perform commissioning, qualification, validation, and maintenance activities within the facility. Oversee multiple CQV projects, providing updates and coordinating with internal teams and external vendors. Lead and support quality investigations, CAPAs, and process improvements to enhance compliance and efficiency. Develop and implement...

Role name:Computer System ValidationPrinceton Junctio, NJRole Description:Develop and execute validation protocols for computer systemsEnsure compliance with regulatory requirements and industry standardsCreate detailed validation documentation including plans, reports, and scriptsConduct risk assessments and impact analyses related to computer...

Responsibilities: Support Client commissioning / validation for facility, utility, equipment, cleaning and process validation projects. Prepare and execute commissioning / validation lifecycle documents. Participate in any stage of clinical or commercial production including green field construction, facility renovation, new product development,...

ResponsibilitiesResponsible for validation programs in support of GMP manufacturingResponsible for facility, utility and equipment qualification programsResponsible for QA role in process and assay validation programsReview or author validation related documents such as design specification, URS, FAT, SAT, IQ, OQ, PQ for utility and equipmentAssume QA lead...

ResponsibilitiesResponsible for validation programs in support of GMP manufacturing Responsible for facility, utility and equipment qualification programs Responsible for QA role in process and assay validation programs Review or author validation related documents such as design specification, URS, FAT, SAT, IQ, OQ, PQ for utility and equipment Assume QA...

Piper Companies is currently seeking an experienced Validation Engineer (CSV/CQV) in Raritan, NJ to work for an industry leading Pharmaceutical company. Responsibilities for the Validation Engineer (CSV/CQV) Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance...

Are you looking for a challenging and rewarding career opportunity? We invite you to apply for the position of Manufacturing Mechanic Specialist at BlueTriton Brands.About UsAs a leading branded beverage company, BlueTriton Brands is committed to delivering high-quality products to our customers while minimizing our environmental footprint. Our...

JOB DESCRIPTION Job Description Our employees work on the world's most advanced electronics. At Electronic Systems, you'll be among the brightest minds, working on the aerospace and defense industry's most difficult problems. Drawing strength from our differences, we're innovating for the future. And you can, too. We put our customers first –...

Role: Data Validation SpecialistAbout Resource Informatics GroupWe are a premier provider of data validation services, dedicated to ensuring the accuracy and integrity of our clients' data. Our team of experts is committed to delivering high-quality results, on-time and within budget.Key Responsibilities:Validate large datasets to ensure data consistency and...

Work for a manufacturer in Henderson county as a Quality Systems Specialist: * This role supports process controls and process improvements, maintains document control system, including creating, reviewing, and revising documentation according to standard operating procedures, and cooperates in driving quality improvement within the organization. This is a...

Work for a manufacturer in Hunterdon county as a Quality Systems Specialist: * This role supports process controls and process improvements, maintains document control system, including creating, reviewing, and revising documentation according to standard operating procedures, and cooperates in driving quality improvement within the organization. This is a...

Work for a manufacturer in Hunterdon county as a Quality Systems Specialist: * This role supports process controls and process improvements, maintains document control system, including creating, reviewing, and revising documentation according to standard operating procedures, and cooperates in driving quality improvement within the organization. This is a...

JOB DESCRIPTION Job Description BAE Systems is hiring for a Senior PC Design Specialist in our Hudson, NH or Fort Wayne, IN location. See what you're missing. Our employees work on the world's most advanced electronics – from detecting threats for F-35 pilots to illuminating the night for soldiers. Spanning air, land, sea, and space, we are developing...

CQV engineer :Design Documentation: URS, FRS, DS, and other engineering specifications Validation Processes: IQ, OQ, PQ, Process Validation (PV), Computer Systems Validation (CSV), Master Validation Plan (MVP) Quality Systems: Change Control, Non-Conformances, Requalification protocols (IQ/OQ/PQ) in compliance with GMP, FDA, and other regulatory requirements...

MANUFACTURING ENGINEERSUMMARYThe company is seeking a Manufacturing Engineer with 5+ years of proven experience in a manufacturing environment to join our team. As Manufacturing Engineer, your main role will be to evaluate existing processes for improvement, reduce cost and develop best practices. Develop and implement innovative solutions while maintaining...

Job Title: Equipment Validation EngineerLocation: Jersey city, NJJob Description:We are seeking an experienced Equipment Validation Engineer for a long-term project with a leading pharmaceutical/biotech client. The ideal candidate will have a strong background in equipment validation within regulated environments and be capable of independently developing...