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Computer System Validation Csv Pharmaceutical Jobs in Oregon

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Support computer system validation activities for lab instruments. * Create and manage validation ... Experience in biotechnology, pharmaceutical, or related industries. * Ability to travel between ...

Showing results 21-40

Computer System Validation Csv Pharmaceutical information

What is the difference between Computer System Validation Csv Pharmaceutical vs Quality Assurance Specialist?

AspectComputer System Validation Csv PharmaceuticalQuality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, Validation certificationsGxP, ISO, QA certifications
Work EnvironmentPharmaceutical manufacturing, regulated labsQuality departments across industries, including pharma
Employer & IndustryPharmaceutical companies, biotech firmsPharma, biotech, healthcare organizations
Primary FocusEnsuring computer systems meet validation and compliance standardsMaintaining quality standards and process improvements

Computer System Validation Csv Pharmaceutical specialists focus on validating computer systems to ensure compliance with industry regulations, while Quality Assurance Specialists oversee overall quality processes. Both roles require GxP knowledge and are vital in pharmaceutical environments, but their core responsibilities differ in scope and focus.

What are common challenges faced by computer system validation (CSV) professionals in the pharmaceutical industry?

CSV professionals in the pharmaceutical industry often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for audits, and ensuring thorough validation of complex systems within tight project timelines. Collaboration with cross-functional teams, such as IT, quality assurance, and manufacturing, is essential to address technical and compliance issues. Additionally, balancing the need for robust validation with operational efficiency requires strong communication and project management skills.

What are the key skills and qualifications needed to thrive as a computer system validation (CSV) professional in the pharmaceutical industry?

To thrive as a Computer System Validation (CSV) professional in pharmaceuticals, you need a strong background in life sciences or engineering, knowledge of regulatory standards (such as FDA 21 CFR Part 11), and experience with validation protocols. Familiarity with validation lifecycle management tools, quality management systems (QMS), and industry guidelines like GAMP 5 is typically required, along with certifications such as ISPE or PMP being advantageous. Outstanding attention to detail, analytical thinking, and strong communication skills help ensure compliance and effective coordination with cross-functional teams. These competencies are vital for maintaining regulatory compliance, data integrity, and patient safety in pharmaceutical operations.

What is computer system validation (CSV) in the pharmaceutical industry?

Computer System Validation (CSV) in the pharmaceutical industry is a process used to ensure that computerized systems used in drug manufacturing and related processes work as intended and comply with regulatory standards, such as FDA 21 CFR Part 11. CSV involves planning, testing, documenting, and maintaining systems to guarantee the accuracy, reliability, and integrity of data. This is critical for patient safety and product quality, as well as for meeting legal and regulatory requirements. The process typically includes risk assessment, validation planning, protocol execution, and ongoing monitoring of system performance.
What are popular job titles related to Computer System Validation Csv Pharmaceutical jobs in Oregon? For Computer System Validation Csv Pharmaceutical jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Csv Pharmaceutical jobs in Oregon look for? The top searched job categories for Computer System Validation Csv Pharmaceutical jobs in Oregon are:
What cities in Oregon are hiring for Computer System Validation Csv Pharmaceutical jobs? Cities in Oregon with the most Computer System Validation Csv Pharmaceutical job openings:

Instrumentation Specialist

Lonza

Bend, OR • On-site

Full-time

Medical, Dental, Vision

Re-posted 23 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

The actual location of this job is in Bend, Oregon. Relocation assistance is available for eligible candidates and their families, if needed.

In this role, you will play a key part in ensuring the reliability and compliance of laboratory instrumentation that supports critical quality control processes. This is an exciting opportunity to contribute to life-saving therapies while developing your technical expertise.

This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Lonza Pharma & Biotech has an opening for an Instrumentation Specialist at our Bend, OR site. In this role, you will support Quality Control operations by maintaining, calibrating, and troubleshooting analytical laboratory instruments.

What you will get
  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Competitive compensation and performance-based rewards
  • Medical, dental, and vision insurance
  • Opportunities for professional growth and development
  • A collaborative and supportive team environment
What you will do
  • Maintain, calibrate, and troubleshoot analytical laboratory instruments.
  • Develop and maintain validation procedures for laboratory systems.
  • Support computer system validation activities for lab instruments.
  • Create and manage validation documents, including protocols and reports.
  • Coordinate on-site repairs and manage vendor relationships.
  • Order and maintain spare parts and inventory levels.
  • Support audits and provide technical expertise to ensure compliance.
What we are looking for
  • Bachelor's degree or equivalent experience in a related field.
  • Experience working with laboratory instrumentation and systems.
  • Experience maintaining and repairing analytical instruments.
  • Knowledge of regulated environments such as GMP or similar standards.
  • Familiarity with validation or qualification of laboratory equipment.
  • Experience in biotechnology, pharmaceutical, or related industries.
  • Ability to travel between local Bend sites as needed.
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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