Innovitusa

Full Time

Hiring:W2 Candidates OnlyVisa:Open to any visa type with valid work authorization in the USA Key Responsibilities Process Automation Analyze business processes and identify opportunities for automation. Design and develop automation workflows using RPA tools. Bot Development Bu

Hiring:W2 Candidates OnlyVisa:Open to any visa type with valid work authorization in the USA Key Responsibilities Process Automation Analyze business processes and identify opportunities for automation. Design and develop automation workflows using RPA tools. Bot Development Bu

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Full Time

This position works out of our Alameda CA location in the Abbott Diabetes Care Division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. Were revolutionizing the way peop

This position works out of our Alameda CA location in the Abbott Diabetes Care Division where we are focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. Were revolutionizing the way peop

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Full Time

Hiring:W2 Candidates OnlyVisa:Open to any visa type with valid work authorization in the USA Summary A QA Automation Engineer is responsible for designing developing and executing automated testing solutions to ensure the quality reliability and performance of software applications.

Hiring:W2 Candidates OnlyVisa:Open to any visa type with valid work authorization in the USA Summary A QA Automation Engineer is responsible for designing developing and executing automated testing solutions to ensure the quality reliability and performance of software applications.

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Roles & Responsibilities1. Implementation and continuous improvement of the Medical Device Quality2. Management Systems and associated CE requirements in order to meet customer3. and regulatory requirements 4. Preparation implementation and Maintenance of Manual policies work instruct

Roles & Responsibilities1. Implementation and continuous improvement of the Medical Device Quality2. Management Systems and associated CE requirements in order to meet customer3. and regulatory requirements 4. Preparation implementation and Maintenance of Manual policies work instruct

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The Regulatory and Quality Assurance Special II is responsible for reviewing and implementing the applicable regulatory aspects and quality systems of the company while maintaining compliance with all regulatory agencies (FDA State Local and AABB).We have an immediate opening for a Re

The Regulatory and Quality Assurance Special II is responsible for reviewing and implementing the applicable regulatory aspects and quality systems of the company while maintaining compliance with all regulatory agencies (FDA State Local and AABB).We have an immediate opening for a Re

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Full Time

Position SummaryThe Clinical Data Manager will integrate with both the data science and clinical operations teams to ensure the accuracy reliability security and usability of clinical data collected during clinical research. This position will play a critical role in ensuring collecti

Position SummaryThe Clinical Data Manager will integrate with both the data science and clinical operations teams to ensure the accuracy reliability security and usability of clinical data collected during clinical research. This position will play a critical role in ensuring collecti

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Full Time

Overview: Seeking a Biopharmaceutical Validation Engineer to support commissioning qualification and validation (CQV) activities for GMP manufacturing equipment and integrated systems. The role requires a self-driven professional capable of authoring and executing validation documenta

Overview: Seeking a Biopharmaceutical Validation Engineer to support commissioning qualification and validation (CQV) activities for GMP manufacturing equipment and integrated systems. The role requires a self-driven professional capable of authoring and executing validation documenta

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Full Time

Overview We are supporting a prominent medical device manufacturer in expanding their engineering team for high-visibility mammography product lines. This position plays a key role in enhancing manufacturing validation processes reinforcing quality systems and ensuring compliance thr

Overview We are supporting a prominent medical device manufacturer in expanding their engineering team for high-visibility mammography product lines. This position plays a key role in enhancing manufacturing validation processes reinforcing quality systems and ensuring compliance thr

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Full Time

Local Atlanta Candidates only Job Duty 1: Provide ongoing user support including troubleshooting and resolution of more complex Salesforce issues.Job Duty 2: Strengthen Salesforce reporting capabilities by creating advanced reports and dashboards including use of crossfilters and cus

Local Atlanta Candidates only Job Duty 1: Provide ongoing user support including troubleshooting and resolution of more complex Salesforce issues.Job Duty 2: Strengthen Salesforce reporting capabilities by creating advanced reports and dashboards including use of crossfilters and cus

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Full Time

Hiring: W2 Candidates Only Visa: Open to any visa type with valid work authorization in the USA Key Responsibilities Install configure and maintain Windows Server environments including: Windows Server () Manage and maintain: Active Directory Group Policy DNS and DHCP s

Hiring: W2 Candidates Only Visa: Open to any visa type with valid work authorization in the USA Key Responsibilities Install configure and maintain Windows Server environments including: Windows Server () Manage and maintain: Active Directory Group Policy DNS and DHCP s

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Innovitusa

Full Time

Key Responsibilities Design System Development: Build document and maintain a scalable design system and reusable component library using the U.S. Web Design System (USWDS) framework or similar enterprise systems. Accessible Component Development: Develop high-level wrapper component

Key Responsibilities Design System Development: Build document and maintain a scalable design system and reusable component library using the U.S. Web Design System (USWDS) framework or similar enterprise systems. Accessible Component Development: Develop high-level wrapper component

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Full Time

Hiring: W2 Candidates OnlyVisa: Open to any visa type with valid work authorization in the USA SummaryA Site Reliability Engineer (SRE) is responsible for ensuring the reliability scalability and performance of software systems and infrastructure. This role bridges the gap between de

Hiring: W2 Candidates OnlyVisa: Open to any visa type with valid work authorization in the USA SummaryA Site Reliability Engineer (SRE) is responsible for ensuring the reliability scalability and performance of software systems and infrastructure. This role bridges the gap between de

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Pennsylvania United States Position Overview We are looking for an experienced CSV Engineer to support the validation and lifecycle management of computerized systems in GMP-regulated manufacturing environments. The role bridges automation IT and quality compliance ensuring validated

Pennsylvania United States Position Overview We are looking for an experienced CSV Engineer to support the validation and lifecycle management of computerized systems in GMP-regulated manufacturing environments. The role bridges automation IT and quality compliance ensuring validated

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Full Time

Responsible for providing senior support in planning organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance policy planning and development ongoing quality improvement through clinica

Responsible for providing senior support in planning organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance policy planning and development ongoing quality improvement through clinica

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Innovitusa

Full Time

We are supporting a prominent medical device manufacturer in expanding their engineering team for high-visibility mammography product lines. This position plays a key role in enhancing manufacturing validation processes reinforcing quality systems and ensuring compliance through stron

We are supporting a prominent medical device manufacturer in expanding their engineering team for high-visibility mammography product lines. This position plays a key role in enhancing manufacturing validation processes reinforcing quality systems and ensuring compliance through stron

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About the job Experience/Knowledge/Technical Skills Required: 1. Around 2 to 5 years of experience in implementation in the QA domain preferably with some experience in working in the Medical Devices industry2. Internal/Lead Auditor of Quality Management Systems3. Knowledge and applic

About the job Experience/Knowledge/Technical Skills Required: 1. Around 2 to 5 years of experience in implementation in the QA domain preferably with some experience in working in the Medical Devices industry2. Internal/Lead Auditor of Quality Management Systems3. Knowledge and applic

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We are looking for an experienced CSV Engineer to support the validation and lifecycle management of computerized systems in GMP-regulated manufacturing environments. The role bridges automation IT and quality compliance ensuring validated systems maintain data integrity regulatory co

We are looking for an experienced CSV Engineer to support the validation and lifecycle management of computerized systems in GMP-regulated manufacturing environments. The role bridges automation IT and quality compliance ensuring validated systems maintain data integrity regulatory co

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Overview: Seeking a Biopharmaceutical Validation Engineer to support commissioning qualification and validation (CQV) activities for GMP manufacturing equipment and integrated systems. The role requires a self-driven professional capable of authoring and executing validation documenta

Overview: Seeking a Biopharmaceutical Validation Engineer to support commissioning qualification and validation (CQV) activities for GMP manufacturing equipment and integrated systems. The role requires a self-driven professional capable of authoring and executing validation documenta

Apply Now

Innovitusa

Full Time

Hiring: W2 Candidates OnlyVisa: Open to any visa type with valid work authorization in the USA Summary A .NET Developer is responsible for designing developing testing and maintaining applications using Microsoft technologies. This role focuses on delivering secure scalable and high-

Hiring: W2 Candidates OnlyVisa: Open to any visa type with valid work authorization in the USA Summary A .NET Developer is responsible for designing developing testing and maintaining applications using Microsoft technologies. This role focuses on delivering secure scalable and high-

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Innovitusa

Full Time

8 or more years of experience relies on experience and judgment to plan and accomplish goals independently performs a variety of complicated tasks may lead and direct the work of others a wide degree of creativity and latitude is expected. Develops software solutions by studying info

8 or more years of experience relies on experience and judgment to plan and accomplish goals independently performs a variety of complicated tasks may lead and direct the work of others a wide degree of creativity and latitude is expected. Develops software solutions by studying info

Apply Now