Quality Associate

Overview

• Support quality assurance activities, ensuring compliance with industry standards and regulations in a dynamic pharmaceutical environment.
• Collaborate with cross-functional teams to maintain and improve quality systems and processes.
• Assist in the review and documentation of quality-related procedures and protocols.
• Contribute to the preparation and execution of internal audits and inspections.
• Provide support in the investigation and resolution of quality-related issues.
• Ensure proper documentation and record-keeping for compliance purposes.
• Work closely with the team to meet project deadlines and quality objectives.
• Participate in training sessions to stay updated on industry best practices and regulations.

Key Responsibilities & Duties

• Conduct quality checks and assessments to ensure compliance with established standards.
• Assist in the development and implementation of quality management systems.
• Support the creation and revision of standard operating procedures (SOPs).
• Participate in root cause analysis and corrective action planning for quality issues.
• Maintain accurate and organized records of quality assurance activities.
• Coordinate with suppliers and vendors to ensure quality standards are met.
• Provide support during regulatory inspections and audits.
• Monitor and report on quality metrics to identify areas for improvement.

Job Requirements

• Bachelor of Science (BS) degree in a relevant field is required.
• Minimum of 1 year of experience in quality assurance or a related field.
• Preferred 2 years of experience in pharmaceutical or healthcare industries.
• Strong understanding of quality assurance principles and regulatory requirements.
• Proficiency in documentation and record-keeping practices.
• Excellent analytical and problem-solving skills.
• Ability to work effectively in a team-oriented environment.
• Willingness to work on-site and adhere to organizational policies.