What are the responsibilities and job description for the CSV Engineer II position at Germer International - Pharmaceutical Recruiting?
The Computer System Validation Engineer will be responsible for executing validation activities for computer systems and software applications, ensuring compliance with regulatory requirements, industry standards, and company policies. This role involves preparing validation documentation, conducting validation testing, and supporting cross-functional teams in achieving validation objectives.
Primary Responsibilities:
• Execute CSV activities in accordance with regulatory requirements (e.g., FDA, EMA, GxP) and industry standards (e.g., GAMP 5).
• Prepare and review validation documentation, including validation plans, protocols, and reports.
• Conduct and document risk assessments to identify potential validation issues and develop mitigation strategies.
• Perform validation testing, including installation qualification (IQ), operational qualification (OQ),and performance qualification (PQ).
• Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure successful validation of computer systems and software applications.
• Identify and troubleshoot validation issues, providing technical support and recommendations for resolution.
• Maintain accurate and complete validation records and documentation.
• Support the CSV Manager in planning and coordinating validation projects to ensure timely completion and adherence to project timelines.
• Stay current with industry trends, regulatory changes, and best practices related to computer system validation.
• Assist in the preparation for regulatory inspections and audits, including presenting validation documentation and addressing inquiries.
• Participate in continuous improvement initiatives to enhance the CSV process.
Education, Experience, & Qualification:
• Bachelor's degree in Computer Science, Information Technology, Engineering, Life Sciences, or a related field.
• Minimum of 3 years of experience in computer system validation within the pharmaceutical,biotechnology, medical device, or related industry.
• Experience with the validation of various computer systems, including ERP systems, LIMS, MES,and other software applications.
• Certification in computer system validation or quality management (e.g., ASQ, ISPE) is a plus.
Key Competencies:
• Excellent analytical and problem-solving skills, with a keen attention to detail.
• Effective communication and interpersonal skills, with the ability to collaborate and build
relationships with cross-functional teams.
Salary : $70,000 - $80,000