QA AUDITOR III - VACCINES - 2ND SHIFT, THURS - MONDAY Details

QA AUDITOR III - VACCINES - 2ND SHIFT, THURS - MONDAY

PPD - Richmond, VA

Employment Type : Full-Time

JOB DESCRIPTION

Title: QA Auditor III - Vaccines

Department: Quality Assurance

Location: Richmond, VA- flex based (office based with some work at home options)

*This is a 2nd shift position, Thursday through Monday, with a start time of 2-3pm EST.*

PPD clinical research services, Thermo Fisher's clinical research business, is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD clinical research services, we are passionate, deliberate, and driven by our purpose- to improve health!

Envision a workplace where you have a direct impact on improving health, work alongside expert scientists, use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD® Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success.

As a QA Auditor III, you will conduct complex internal and external audits and inspections to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and client contractual obligations.

At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees.

Summarized Purpose:

Conducts complex internal and/or external audits and inspections to ensure compliance with established quality assurance processes, standards, global regulatory guidelines and/or client contractual obligations. Identifies issues impacting the quality and/or integrity of clinical research programs, determines root cause of non-conformance and develops strategies to address issues. May perform technical document review and other GxP practice activities in support of clinical development programs. Provides audit reports to management. Plans and delivers quality services for contracted quality assurance audits, internal site audits, laboratory and file audits for clients and projects.

Essential Functions:

• Provides QA support for second shift, Thursday through Monday work schedule
• Conducts and/or leads a variety of client, internal or GxP audits and regulatory inspections as requested by senior management
• Leads directed site audits, facility, vendor and/or sub-contractor audits
• Provides GxP consultation and support to PPD clinical research services project teams and external clients Leads process audits and may participate as a co-auditor in more complex system audit.
• Performs other types of QA audits or activities (e.g. database audits, clinical study report audits, sample results tables, process improvement)
• Serves as a resource to operational departments on audit or quality assurance subject matter
• Prepares and presents audit findings and/or other related information at departmental, internal operations or client meetings
• Provides mentorship and guidance to junior auditors

#LI-AP1

GD

Job Qualification

Education and Experience:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous QA experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years’) or equivalent combination of education, training, & experience.

Knowledge, Skills and Abilities:

• Meets competencies for QA Auditor I plus: Thorough knowledge of GxP and appropriate regional research regulations and guidelines

• Demonstrated proficiency and led a range of project based or internal GxP audits and vendor audits to high standards required by management

• Excellent oral and written communication skills

• Strong problem solving, risk assessment and impact analysis abilities

• Solid experience in root cause analysis

• Above average negotiation and conflict management skills

• Flexible and able to multi-task and prioritize competing demands/workload

• Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel

  
  

Working Environment:

PPD clinical research services values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Able to work schedule second shift, Thursday through Monday (start time of 2 or 3pm EST)
• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary and/or standing for typical working hours.
• Able to lift and move objects up to 25 pounds
• Able to work in non-traditional work environments.
• Able to use and learn standard office equipment and technology with proficiency.
• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Our 4i Values:

Integrity – Innovation – Intensity – Involvement

If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!

Diversity StatementPPD is proud to be an affirmative action employer that values diversity as a strength and fosters an environment of mutual respect. PPD is committed to providing equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual orientation, disability, veteran status or status within any other protected group.