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Listed five days ago
Work with Engineers to develop Computer Validation Strategy, plans, protocols, reports, risk assessment, requirement traceability matrix etc for...
Work with Engineers to develop Computer Validation Strategy, plans, protocols, reports, risk assessment, requirement traceability matrix etc for...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
5d ago
5d ago
Listed twelve days ago
Responsible for qualification and validation activities for laboratory systems and equipment, ensuring compliance with GMP and regulatory...
Responsible for qualification and validation activities for laboratory systems and equipment, ensuring compliance with GMP and regulatory...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
12d ago
12d ago
Listed fifteen days ago

Be an early applicant

This is a Full time job

We are looking for Validation Engineers to lead the commissioning, qualification, and validation of critical facility systems (HVAC, cleanrooms,...
We are looking for Validation Engineers to lead the commissioning, qualification, and validation of critical facility systems (HVAC, cleanrooms,...
subClassification: Electrical/Electronic EngineeringElectrical/Electronic Engineering
classification: Engineering(Engineering)
15d ago
15d ago
Listed twenty one days ago

This is a Full time job

$4,000 – $6,000 per month
Join a dynamic & highly regulated GMP environment where you’ll lead impactful validation projects across equipment, facilities, utilities, & processes
Join a dynamic & highly regulated GMP environment where you’ll lead impactful validation projects across equipment, facilities, utilities, & processes
subClassification: Laboratory & Technical ServicesLaboratory & Technical Services
classification: Science & Technology(Science & Technology)
21d ago
21d ago
Listed twenty one hours ago
The Quality Assurance is responsible for maintaining quality systems and supporting continuous improvement initiatives.
The Quality Assurance is responsible for maintaining quality systems and supporting continuous improvement initiatives.
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
21h ago
21h ago
Listed eight days ago
Work closely with cross-functional teams and external partners, ensure the smooth execution of product, technology transfer and validation activities
Work closely with cross-functional teams and external partners, ensure the smooth execution of product, technology transfer and validation activities
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
8d ago
8d ago
Listed more than thirty days ago
Develop commissioning and validation plans for high technology facilities in the bio-pharmaceutical and/or semiconductor industry. Formulate...
Develop commissioning and validation plans for high technology facilities in the bio-pharmaceutical and/or semiconductor industry. Formulate...
subClassification: ManagementManagement
classification: Engineering(Engineering)
30d+ ago
30d+ ago
Listed nine days ago
Join a dynamic & highly regulated GMP environment where you’ll lead impactful validation projects across equipment, facilities, utilities, & processes
Join a dynamic & highly regulated GMP environment where you’ll lead impactful validation projects across equipment, facilities, utilities, & processes
subClassification: Laboratory & Technical ServicesLaboratory & Technical Services
classification: Science & Technology(Science & Technology)
9d ago
9d ago
Listed eight days ago

Be an early applicant

This is a Full time job

Responsible for ensuring risk based cleaning validation policies and standards have robust quality oversight and are in compliance to GMP standards...
Responsible for ensuring risk based cleaning validation policies and standards have robust quality oversight and are in compliance to GMP standards...
subClassification: Pharmaceuticals & Medical DevicesPharmaceuticals & Medical Devices
classification: Healthcare & Medical(Healthcare & Medical)
8d ago
8d ago
Listed six days ago
We are seeking a QA Validation Manager to provide site-level quality oversight of validation and qualification activities across manufacturing...
We are seeking a QA Validation Manager to provide site-level quality oversight of validation and qualification activities across manufacturing...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
6d ago
6d ago
Listed twelve days ago
As the Quality Engineer (Validation), you’ll have the chance to ensure that change control and validation activities are executed in a timely...
As the Quality Engineer (Validation), you’ll have the chance to ensure that change control and validation activities are executed in a timely...
subClassification: Mechanical EngineeringMechanical Engineering
classification: Engineering(Engineering)
12d ago
12d ago
Listed more than thirty days ago
Own, execute and improve the validation lifecycle from Plan to Retire, for manufacturing processes and equipment. This includes, but is not limited...
Own, execute and improve the validation lifecycle from Plan to Retire, for manufacturing processes and equipment. This includes, but is not limited...
subClassification: Pharmaceuticals & Medical DevicesPharmaceuticals & Medical Devices
classification: Healthcare & Medical(Healthcare & Medical)
30d+ ago
30d+ ago
Listed twenty one days ago
  • Bachelor's degree in Life Sciences, Engineering, or a related field
  • 2–4 yrs experience in CSV within the Pharmaceutical or Medical Device industry
  • Familiarity with CSV lifecycle management and automation systems validation
  • Bachelor's degree in Life Sciences, Engineering, or a related field
  • 2–4 yrs experience in CSV within the Pharmaceutical or Medical Device industry
  • Familiarity with CSV lifecycle management and automation systems validation
Our client is seeking a Computer System Validation (CSV) Consultant – Pharmaceutical / Medical Device to join their team!
Our client is seeking a Computer System Validation (CSV) Consultant – Pharmaceutical / Medical Device to join their team!
subClassification: OtherOther
classification: Consulting & Strategy(Consulting & Strategy)
21d ago
21d ago
Listed more than thirty days ago

This is a Full time job

• Collaborates with Customers and provides technical input and recommendations to ensure all aspects of Customer validation requirements are fully...
• Collaborates with Customers and provides technical input and recommendations to ensure all aspects of Customer validation requirements are fully...
subClassification: Electrical/Electronic EngineeringElectrical/Electronic Engineering
classification: Engineering(Engineering)
30d+ ago
30d+ ago
Listed more than thirty days ago
Ensure that change control and validation activities are executed in a timely manner. MAIN RESPONSIBILITIES Comply to all policies and...
Ensure that change control and validation activities are executed in a timely manner. MAIN RESPONSIBILITIES Comply to all policies and...
subClassification: Pharmaceuticals & Medical DevicesPharmaceuticals & Medical Devices
classification: Healthcare & Medical(Healthcare & Medical)
30d+ ago
30d+ ago
Listed twelve days ago
Responsible for qualification, requalification, relocation, decommissioning, and retirement of GMP laboratory equipment while ensuring compliance...
Responsible for qualification, requalification, relocation, decommissioning, and retirement of GMP laboratory equipment while ensuring compliance...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
12d ago
12d ago
Listed twenty nine days ago

Expiring soon

This is a Full time job

$6,000 – $9,000 per year
Consultancy Firm
Consultancy Firm
subClassification: Pharmaceuticals & Medical DevicesPharmaceuticals & Medical Devices
classification: Healthcare & Medical(Healthcare & Medical)
29d ago
29d ago
Listed twenty two days ago
* Support validation and decommissioning activities for GMP laboratory systems and equipment * Execute and review CSV deliverables including: *...
* Support validation and decommissioning activities for GMP laboratory systems and equipment * Execute and review CSV deliverables including: *...
subClassification: Laboratory & Technical ServicesLaboratory & Technical Services
classification: Science & Technology(Science & Technology)
22d ago
22d ago
Listed seventeen days ago
We are helping a pharmaceutical MNC company to recruit for pharmaceutical quality assurance in document control and audits
We are helping a pharmaceutical MNC company to recruit for pharmaceutical quality assurance in document control and audits
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
17d ago
17d ago
Listed fifteen hours ago

Be an early applicant

This is a Full time job

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to...
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
15h ago
15h ago
Listed twenty two days ago
We are seeking an MES Validation Engineer to support validation activities for Electronic Batch Record (EBR) systems within a GMP-regulated...
We are seeking an MES Validation Engineer to support validation activities for Electronic Batch Record (EBR) systems within a GMP-regulated...
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
22d ago
22d ago
Listed twenty two days ago
Validate MES systems and maintain compliance within a GMP manufacturing environment
Validate MES systems and maintain compliance within a GMP manufacturing environment
subClassification: Quality Assurance & ControlQuality Assurance & Control
classification: Manufacturing, Transport & Logistics(Manufacturing, Transport & Logistics)
22d ago
22d ago
Listed twenty days ago
This role’s focus is on the provision of technical guidance, planning, coordinating and resourcing validation projects on-site. He/She ensures the...
This role’s focus is on the provision of technical guidance, planning, coordinating and resourcing validation projects on-site. He/She ensures the...
subClassification: Biological & Biomedical SciencesBiological & Biomedical Sciences
classification: Science & Technology(Science & Technology)
20d ago
20d ago
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