Sr Quality Specialist
At PPD-Pharmaceutical Product Development, we are looking for a dedicated, highly motivated, and detail-oriented Senior Quality Specialist to join our team. In this role, you will be responsible for developing, implementing, and maintaining quality systems that ensure the safety, efficacy, and quality of all clinical trial materials.You must have a Bachelor's degree in a scientific field such as chemistry, biology, or pharmacy, as well as 5+ years of experience in the Quality Assurance field, preferably in the clinical trial industry. You must also be highly organized, able to work well independently and as part of a team, and have excellent communication and problem-solving skills. If you are ready to take on this exciting role and join our team, we would love to hear from you.
Responsibilities:
Develop, implement, and maintain quality systems for clinical trial materials.
Monitor and review of company documents to ensure compliance with applicable regulations.
Prepare reports and analyze data to support Quality Assurance activities.
Ensure compliance with all applicable quality initiatives, laws, and regulations.
Identify areas for process improvement and recommend changes.
Investigate and resolve customer complaints and quality issues.
Audit internal systems, processes and vendors to ensure compliance with quality standards.
Train and mentor other quality assurance personnel.
Develop and update procedures and standards for quality assurance.
Monitor and report on quality assurance metrics.
PPD-Pharmaceutical Product Development is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply Now
Apply Now
Responsibilities:
Develop, implement, and maintain quality systems for clinical trial materials.
Monitor and review of company documents to ensure compliance with applicable regulations.
Prepare reports and analyze data to support Quality Assurance activities.
Ensure compliance with all applicable quality initiatives, laws, and regulations.
Identify areas for process improvement and recommend changes.
Investigate and resolve customer complaints and quality issues.
Audit internal systems, processes and vendors to ensure compliance with quality standards.
Train and mentor other quality assurance personnel.
Develop and update procedures and standards for quality assurance.
Monitor and report on quality assurance metrics.
PPD-Pharmaceutical Product Development is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply Now
Apply Now