Advanced Manufacturing Tech Solutions (AMTSOL) -
A Leader in Life science Manufacturing Technology solutions we are looking for top talent to be part of the dynamic team and drive the growth of the business.
Job Title: Computer System Validation (CSV) Engineer / Specialist
Role Overview
We are looking for a Mid-Level CSV Engineer to support validation activities for GMP-regulated computerized systems across manufacturing packaging and laboratory environments. The role focuses on hands-on execution of CSV lifecycle deliverables working closely with Quality Engineering IT and project teams to ensure compliance and timely delivery.
Key Responsibilities
- Execute CSV lifecycle activities for GMP computerized systems including MES DCS SCADA and automated equipment
- Prepare review and support approval of CSV documentation (Validation Plans URS Risk Assessments IQ/OQ/PQ Reports)
- Support risk-based validation approaches for new and existing systems
- Ensure CSV activities comply with cGMP GAMP 5 Annex 11 and 21 CFR Part 11
- Support project teams to align validation activities with project timelines
- Participate in validation risk assessments to define appropriate testing scope
- Review system specifications design documents installation records and qualification documentation
- Support CSV activities across manufacturing packaging and laboratory systems
- Generate track and support closure of validation deviations and discrepancies
- Support investigations and assess data integrity risks during validation and routine operations
- Perform periodic reviews of computerized systems and assist in identifying compliance gaps
- Support the development and maintenance of CSV / Qualification SOPs
- Assist in regulatory inspections and internal audits
- Collaborate with local and global CSV teams to ensure consistent execution
- Escalate potential quality or compliance issues to senior CSV or Quality leads
- Follow EHS and site safety procedures during commissioning and validation activities
Qualifications & Experience
- Bachelors degree in Engineering Life Sciences Computer Science or related discipline
- 47 years of experience in Computer System Validation within a regulated pharma / biopharma environment
- Solid understanding of CSV regulations and quality expectations
- Hands-on experience validating GAMP Category 3 4 and 5 systems
- Experience executing validation protocols and managing validation documentation
- Working knowledge of Annex 11 21 CFR Part 11 and GAMP guidelines
- Experience supporting investigations root cause analysis and CAPAs
- Strong documentation and cross-functional collaboration skills
Advanced Manufacturing Tech Solutions (AMTSOL) - A Leader in Life science Manufacturing Technology solutions we are looking for top talent to be part of the dynamic team and drive the growth of the business. Job Title: Computer System Validation (CSV) Engineer / Specialist Role Overview We are l...
Advanced Manufacturing Tech Solutions (AMTSOL) -
A Leader in Life science Manufacturing Technology solutions we are looking for top talent to be part of the dynamic team and drive the growth of the business.
Job Title: Computer System Validation (CSV) Engineer / Specialist
Role Overview
We are looking for a Mid-Level CSV Engineer to support validation activities for GMP-regulated computerized systems across manufacturing packaging and laboratory environments. The role focuses on hands-on execution of CSV lifecycle deliverables working closely with Quality Engineering IT and project teams to ensure compliance and timely delivery.
Key Responsibilities
- Execute CSV lifecycle activities for GMP computerized systems including MES DCS SCADA and automated equipment
- Prepare review and support approval of CSV documentation (Validation Plans URS Risk Assessments IQ/OQ/PQ Reports)
- Support risk-based validation approaches for new and existing systems
- Ensure CSV activities comply with cGMP GAMP 5 Annex 11 and 21 CFR Part 11
- Support project teams to align validation activities with project timelines
- Participate in validation risk assessments to define appropriate testing scope
- Review system specifications design documents installation records and qualification documentation
- Support CSV activities across manufacturing packaging and laboratory systems
- Generate track and support closure of validation deviations and discrepancies
- Support investigations and assess data integrity risks during validation and routine operations
- Perform periodic reviews of computerized systems and assist in identifying compliance gaps
- Support the development and maintenance of CSV / Qualification SOPs
- Assist in regulatory inspections and internal audits
- Collaborate with local and global CSV teams to ensure consistent execution
- Escalate potential quality or compliance issues to senior CSV or Quality leads
- Follow EHS and site safety procedures during commissioning and validation activities
Qualifications & Experience
- Bachelors degree in Engineering Life Sciences Computer Science or related discipline
- 47 years of experience in Computer System Validation within a regulated pharma / biopharma environment
- Solid understanding of CSV regulations and quality expectations
- Hands-on experience validating GAMP Category 3 4 and 5 systems
- Experience executing validation protocols and managing validation documentation
- Working knowledge of Annex 11 21 CFR Part 11 and GAMP guidelines
- Experience supporting investigations root cause analysis and CAPAs
- Strong documentation and cross-functional collaboration skills
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