SENIOR QA SPECIALIST - VALIDATION

Job Description

Job Description

RESPONSIBILITIES:

• Prepares equipment validation procedures and protocols for manufacturing equipment (granulation machines, tablet press and incubator sterilizers)
• Develops and executes matrix type validations where applicable for processes and equipment with adequate supporting rationales.
• Assists in assuring facility, manufacturing, packaging, and Laboratory equipment are qualified to the required cGMP standards.
• Authors/approves and executes qualification protocols and reports.
• Schedules, plans, manages performance qualifications, calibration and maintenance of equipment and utility systems and laboratory Instruments in coordination with operations, Quality Control and maintenance.
• Assists sourcing and procurement of facility equipment and Laboratory Instruments through completion of following tasks

• Qualification of Vendors Selected.
• Input to the development of the URS/FRS/DDS.

• Assists with the routine calibration and maintenance of the Validation Master Plan for the site.
• May present qualification studies to Regulatory and Client Auditors as required.
• Assists with the design, maintenance, and continual improvement of the qualification system in line with cGMP standards.
• Provides technical expertise and guidance on qualification policies and procedures and the implementation of those within the Production and Quality functional areas.
• Occasionally supervises specialized contract personnel and outside vendors in the performance of contract services.
• Summarizes studies and authors qualification reports in compliance with the cGMP standards and in a timely manner.
• Initiates and investigates exception reports and non-conformances, associated with the qualification studies. Troubleshoots and resolves technical issues.
• Other responsibilities and special projects will be assigned based on business and customer needs.

QUALIFICATIONS:

• Bachelor’s degree in sciences or engineering
• 5+years' experience in a highly regulated pharmaceuticals industry or related field
• Knowledge of FDA regulations (21 CFR Parts 210,211 standards) to validate pharmaceutical manufacturing equipment
• Demonstrated experience with qualification commercial processing a packaging equipment.
• Proven track record of managing projects from start to finish on time and on budget.
• Strong working knowledge of cGMP and regulatory standards for validation.
• Experience in writing and reviewing SOPs, GMPs, governmental regulations and/or protocols for accuracy, traceability and compliance.