Jobs for validation engineer at South Dakota

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...

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...

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...

Roles & Responsibilities : Responsible to create and execute qualification protocols (IQ/OQ/PQ), including identification and resolution of non-conformances/deviations. Responsible to initiate the preparation and calibration of thermocouple for Kaye AVS/Ellab to monitor and record temperature, ensure that all validation functions and related capabilities...

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...

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...

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...

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...

Mechanical Engineers/ Chemical Engineers/ Pharmacy Graduates Good Pay and Quick Placements Please Reach us For Training and Placements in Validation Engineer/ QA/ Manufacturing Enginner Looking for MS in Engineering Graduates for Contracting/ Consulting Company. Drafting Installation Operational qualification protocols for Bioreactors. Responsible for...

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...

Job Title: Device Engineer Location: South San Francisco, CA (Onsite) Duration: 12 months contract with possible of extension Pay rate: $55-60/hr on W2 with benefits Description: The Device Engineer II will be responsible for providing design, development and implementation support to project teams developing combination drug delivery devices for parenteral...

Executive Summary The Device Engineer II will be responsible for providing design, development and implementation support to project teams developing combination drug delivery devices for parenteral pharmaceutical therapeutics at ***. The candidate has technical expertise in the development and commercialization of drug-device combination medical products,...

Industry: Medical Devices Position: Device Engineer II Location: South San Francisco, CA Duration: 12 months contract (+Possibility of extension)Executive Summary The Device Engineer II will be responsible for providing design, development and implementation support to project teams developing combination drug delivery devices for parenteral pharmaceutical...

Mechanical Engineer (Contract)RESPONSIBILITIESDeveloping, 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 process...

Mechanical Engineer (Contract)RESPONSIBILITIESDeveloping, 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 process...