Manager/ Senior Manager Quality Engineer
4 weeks ago
This position is responsible for supporting the site Technical Operations processes related to
cGMP such as Commissioning, Qualification and Validation (CQV), Computer System
Configuration Management and Computer System Validation (CSV).
Responsibilities and Duties:
- Implement / execute computer system validation and general CQV.
- Work with site facility and operations teams to ensure compliance with Validation Master Plan activities.
- Provide support for change control technical assessment/evaluation process.
- Align on change control requirements to manage the requested change.
- Implement qualification procedures.
- Responsible for system compliance aspects across the sites project portfolio.
- Support the sites quality system management with measurement and control strategies.
- Support regulatory inspections and audits.
- Manage the risk assessment process for qualification and validation.
- Support vendor qualification and compliance audits.
- Review technical/investigation reports as appropriate.
- Write, review, and approve proposed changes to systems and procedures, as appropriate.
- Write, review, and approve protocols and summary reports.
- Track, review, and report metric information for use in continuous improvement of areas of responsibility.
- Support QE Director on continuous improvement initiatives and projects within the sites quality organization.
- Perform other duties and tasks as assigned.
Qualifications and Requirements:
- Bachelors degree in technical discipline (Computer Science/ Industrial Engineering or similar).
- Minimum of 3 years of Quality Engineering with related experience such as Computer System Validation in a GMP environment (Drug Substance or Drug Product).
- Knowledge of quality systems and pharmaceutical regulatory requirements (21 CRF Part 11/210/211, ICH 8, ICH 9, and ICH 10).
- Quality Engineering Certification, ASQ, Black Belt/Green Belt certifications, preferred.
- Proficiency in Computer System Validation in a GMP environment (Drug Substance or Drug Product).
- Automation, equipment, and utility IQ/OQ/PQ/PV.
- Quality Assurance, GMPs, Health Authority Regulations and Validation practices/principles.
- Strong knowledge of GMP, GAMP, SOPs, and quality systems.
- Experience with internal and external audit principles.
- Strong knowledge of change control practices/strategies.
- Proficient in MS Word, Excel, PowerPoint, and other applications.
- Ability to communicate and work independently with scientific/technical personnel.
- Strong communication and coordination skills, good language skills and the ability to analyze and solve problems with a positive work attitude.
by Jobble
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