Validation Engineer - Davie

We currently have an exciting opportunity available for a Engineer, Validation in Boca Raton, · The Engineer, Validation provides validation support to Immunotherapy Production, · This role also provides activity updates to Validation Manager on a regular basis to ensure complian ...

Support aseptic process validation activities for sterile injectable products with a strong focus on vial filling and fill-finish operations in a cGMP manufacturing environment. · Support aseptic process validation for sterile injectable and vial filling operations. · ...

We are seeking a Validation Engineer to support aseptic process validation activities for sterile injectable products with a focus on vial filling and fill-finish operations in a cGMP manufacturing environment.Prepare review and execute IQ/OQ/PQ protocols and validation reportsSu ...

Job summaryADMA Biologics is a biopharmaceutical company that creates products for immunodeficient patients. We have an exciting opportunity available for an Engineer in Boca Raton FL · The Engineer provides validation support to Immunotherapy Production Quality Control and Plant ...

We currently have an exciting opportunity available for a Engineer, · Validation in Boca Raton, FL. · The Engineer, · Validation provides validation support to Immunotherapy Production, Quality Control and Plant Engineering. ...

The Validation Engineer is responsible for ensuring the reliability, · consistency, and regulatory compliance of manufacturing processes, · equipment, and computerized systems.Lead the preparation, · execution, and review of validation documentation. · Independently lead · and co ...

We currently have an exciting opportunity available for a Engineer, · Validation in Boca Raton, FL.This role provides validation support to Immunotherapy Production, · Quality Control and Plant Engineering. · ...

We currently have an exciting opportunity available for a Engineer, · Validation in Boca Raton, · FL · The Engineer, · Validation provides validation support · To Immunotherapy Production, · ...

The Validation Engineer is responsible for ensuring the reliability, consistency and regulatory compliance of manufacturing processes equipment and computerized systems. · This role leads the development and execution of validation documentation and activities including process e ...

Walk through production lines and understand equipment and production processes to identify quality issues and their root causes. · ...

The company is seeking a Quality Engineer with strong expertise in Computer System Validation and digital manufacturing systems to support regulated operations. · This role focuses on ensuring compliant validation strategies for manufacturing, utilities, and digital platforms whi ...

++The company is seeking a Quality Engineer with strong expertise in Computer System Validation and digital manufacturing systems to support regulated operations. · + ...

A Validation/Project Engineer is needed for 2-4 years of related experience in the field. · Bachelor's degree in engineering or a related field. · At least 2 years experience as a validation engineer in a similar industry. · ...

The Validation Engineer will support aseptic process validation activities for sterile injectable products within a cGMP-regulated manufacturing environment.This role has a strong emphasis on vial filling and fill-finish operations, ensuring validated processes meet FDA and regul ...

Seeking a Validation Engineer with hands-on experience in aseptic processing and sterile injectable manufacturing. · This role will support process validation activities with a strong focus on vial filling and fill-finish operations in a cGMP-regulated environment. · ...

The GxP / Computer System Validation (CSV) Engineer is responsible for ensuring that computerized systems used in regulated environments comply with applicable GxP regulations and industry standards.This role leads and supports validation activities throughout the system lifecycl ...

We are seeking a highly capable and detail-oriented Commissioning & Qualification Calibration Consultant to join our client's operations for a 6-month assignment. · ...

The Validation Engineer will support aseptic process validation activities for sterile injectable products within a cGMP manufacturing environment. · Support aseptic process validation for sterile injectable manufacturing. · ...

+Job summary · No C2C*. Must be a US Citizen or Permanent Resident · The GxP / Computer System Validation (CSV) Engineer is responsible for ensuring that computerized systems used in regulated environments comply with applicable GxP regulations and industry standards.Plan, execut ...

The Validation Engineer II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. · Perform critical review of Validation Engineer I project plans and related documents to ensure impleme ...