Jobs for validation engineer at South Carolina

Job DescriptionJob DescriptionJob Title: Validation Engineer Location: Remote Duration: 12 monthsCompany Overview: Pulivarthi Group is a premier global provider of staffing and IT technology solutions, renowned for delivering exceptional services tailored to each client's unique needs. With a steadfast commitment to excellence, we merge expertise with...

Responsibilities: Validation Strategy: Develop validation strategies aligned with regulatory standards. Protocol Generation: Author and review validation protocols for processes and equipment. Execution: Lead validation studies and analyze data, ensuring adherence to timelines. Reporting: Prepare comprehensive validation reports with findings and...

For Equipment Validation services in the Manufacturing area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree in Life Science or Engineering and five (5) years of experience in Validation Life Cycle within the Medical Device Industry.Bilingual (English and Spanish)Administrative and according to business needsExperience in: Process...

Multiple Positions and systems are available: SDMS/Labx/Veeva RIM/SDMS/ValGenesis/Labware LIMS Perform "Data Integrity” related- risk assessments, Deviation investigations suggest implementing remediations in CGMP operations. Performs Data Integrity compliance/impact assessments, risk assessments, and create short executive summary reports. ...

Roles&Responsibilities: Pack Bay 3 will be repurposed to be a dedicated line for the packaging of autoinjector devices for client WCS-081. The new packaging line will be utilizing equipment from the existing line as well as bringing in new equipment. The existing equipment that will be modified include the Dividella Cartoner, Pester Case Packer, Pester...

Process Validation Engineer (Contract)RESPONSIBILITIESOverseeing and reviewing design and construction work related to process improvements in a cGMP manufacturing facility.Supporting startup, Commissioning, Qualification, and Validation (CQV) of process equipment, and developing process technical transfer documents.Collaborating with senior leadership to...

Process Validation Engineer (Contract)RESPONSIBILITIESOverseeing and reviewing design and construction work related to process improvements in a cGMP manufacturing facility.Supporting startup, Commissioning, Qualification, and Validation (CQV) of process equipment, and developing process technical transfer documents.Collaborating with senior leadership to...

For Equipment Validation services in the Manufacturing area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree in Engineering and five years of experience in Validation Life Cycle within the Medical Device Industry.Bilingual (English and Spanish)Administrative and according to business needsExperience in: Equipment troubleshooting.Validation Life...

ResponsibilitiesPerforms validation document generation, program management, and protocol execution activities. Interface with Engineering, and end user groups to support development of life cycle documents and system requirements. Design the validation approach with technical oversight, provide the scientific rationale and acceptance criteria, and...

For Equipment Validation services in the Manufacturing area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree inEngineering and five years of experience in Validation Life Cycle within theMedical Device Industry.Bilingual (English and Spanish)Administrativeand according to business needsExperience in: Troubleshooting of equipment.ValidationLife...

Responsibilities: Client is looking for a Senior Process Validation consultant who has some TMV experience. They are good on the process engineering side and the consultant will be responsible for writing/executing process validation protocols. Wants to see a strong documentation and writing background, core of the job. Will run some PQs and...

Job DescriptionWe are seeking a Growth and Improvement minded Validation Specialist that can help drive our Strategic Operating Priorities.Invent | Pursue the Most Promising Internal and External Science to Address Significant Unmet Medical NeedsExecute | Prioritize Resources Behind Our Key Growth Drivers (Oncology, Vaccines, Select Specialty Areas, Animal...

Validation Engineer > > Location: South San Francisco, CA Onsite > > Contract Duration: 5 Months > > Visa: Any (Except OPT & CPTs) > > C2C > > JOB DESCRIPTION::Duties > > * Important: Genentech has mandated COVID-19 vaccination for their > workforce, effective > * October 1st, 2021. All external personnel...

Responsible for Resolves competing constraints between interrelated functions (engineering purchasing manufacturing regulatory marketing etc.) required to deliver the product to market. Defines protocols and conduct the necessary testing required to validate the safety and effectiveness of the design(s). Develops and maintains an effective and corroborative...

Our client is looking to bring on a Design Quality Engineer. With 5-8 years of experience. 75% of the project is document review and providing guidance. It is less hands on production. There is still deliverables but will be one of the reviewers. Will need to understand reviewing documentation. Looking for Risk Management – Designing FMEAs(not the process...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...

Responsibilities: Generation and execution of validation plans, validation protocols (IQ/OQ/PQ), and completion reports, with a major focus on sterilization and microbiology of medical devices. Provide statistical analysis of the date to support the reports. Generation and implementation of change controls and engineering notices (ECO). ...

Mechanical Engineer (Contract) RESPONSIBILITIES Developing, implementing, and continuously improving manufacturing processes to enhance yield, reduce costs, and improve productivity. Representing Process Engineering in R&D and Project Team meetings, providing technical expertise in technology transfers, analytical method development, validation, and...

Design Quality Engineer Environment: Our client is a large medical device manufacturer that develops a number of Medical Device products. They are currently in need of an experienced Design Quality Engineer to support remediation activities surrounding risk management and design FMEAs as well as SFMEAs.Responsibilities:This role's emphasis is for supporting...

Design Quality Engineer Environment: Our client is a large medical device manufacturer that develops a number of Medical Device products. They are currently in need of an experienced Design Quality Engineer to support remediation activities surrounding risk management and design FMEAs as well as SFMEAs. Responsibilities: This role's emphasis is for...