Senior Quality Assurance Auditor

Posted 12 Days Ago
Hiring Remotely in Pennsylvania
Remote
5-7 Years Experience
Pharmaceutical
The Role
The Senior Quality Assurance Auditor at Parexel is responsible for leading, planning, scheduling, performing, and reporting a range of GxP audits across all phases of Clinical Research. They must have a minimum of 2 years' experience in quality assurance, auditing, and at least 5 years' experience in relevant areas of life science. The role requires international travel for audits and a deep understanding of Good Practices (GxPs) and regulations related to clinical trials.
Summary Generated by Built In

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do.

At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life- changing medicines to patients. We are seeking a Senior Quality Assurance Auditor to join our team. Our Senior Quality Assurance Auditor works toward building a deeper connection and understanding with those who count on us most. Through questioning the status quo and collaborating cross-functionally, the Senior Quality Assurance Auditor is responsible for leading, planning, scheduling, performing, and reporting a range of GxP audits across all phases of Clinical Research.

Title: Senior Quality Assurance Auditor (GCP Auditor)

Who we’re looking for:

  • Minimum of 2 years’ experience in quality assurance, auditing, including sound experience of applicable GxP auditing.
  • At least 5 years’ experience in regulatory affairs, clinical research, monitoring, data management, safety/pharmacovigilance, pharmacy, laboratory, or other relevant area in life science such as technology, third party supplier management.
  • Ability to travel internationally for audits as required. Travel time could be up to approx. 60%.
  • Excellent knowledge, understanding and experience of Good Practices (GxPs) and international, national, and local regulations and laws related to clinical trials and other clinical research.
  • Ability to rapidly learn, understand and apply applicable Parexel and client procedures.
  • Client focused approach to work.
  • Excellent interpersonal, verbal, and written communication skills, including the ability to present at conferences, meetings, and training sessions.
  • Ability to mentor / train auditors and other personnel.
  • A flexible attitude to work assignments and new learning and the ability to adjust to changing priorities and unforeseen events.
  • Ability to diplomatically address sensitive issues confidentially and professionally.
  • Auditors must be detail oriented, good at decision making, able to maintain a ‘big picture’ / overview on the project / business.
  • Ability to follow up on multiple tasks and projects, and to handle confidential information diplomatically.

What you’ll do:

  • Lead, Perform and Report audits for area of specialization, work with internal customers and develop and execute strategic audit plans for the area.
  • Manage GxP audits.
  • Lead and coordinate internal regional and global process/system audits across regions and develop all necessary tools such as report templates, checklists, and standard emails.
  • Report outcome and trends of audit program to the process owner, QA Senior Management.
  • Review audit reports, responses, and other program deliverable to ensure consistent high quality.
  • Act as QA Lead on audits program(s).
  • Arrange meetings with client and other key stakeholders as required to plan a program of contracted audits.
  • Support Serious Breaches (SB) investigations and help oversee the project teams to reach final conclusion regarding the reportability of a critical Quality Event.
  • Support auditor training and mentoring of new / less experienced auditors by performing co-audits, assist in developing training materials/tools, delivering training, and sharing knowledge and experience.
  • Maintain QA records / systems.
  • Process improvements: Optimize new and existing processes to maintain and improve quality standards including supporting quality initiatives as assigned.
  • Provide local, regional, and global consultancy and interpretation on regulatory compliance to internal/external clients, Parexel management, and staff with regards to the implementation of GxP and safety/PV requirements, and implementation of appropriate regulatory requirements.
  • Support Sponsor Audits and Regulatory Inspections, as assigned.
  • Liaise with external industry and regulatory inspectorate contacts and networks to determine best practice regarding implementation of relevant GxP requirements across the Parexel Corporation.
  • Maintain sound knowledge of Parexel policies, procedures, and guidelines and promote compliance within Parexel.
  • Maintain compliance with training curriculum.
  • Build, develop, and maintain good working relationships with internal and external customer groups.
  • Work well in a team environment.
  • Perform other quality related tasks or initiatives as assigned.

Additional Details:

Ability to travel internationally for audits as required. Travel time could be up to approx. 60%.

Why join us:

Be part of groundbreaking projects that are pushing the boundaries of the industry.

Experience a collaborative and inclusive work environment that highly appreciates your expertise. Unlock your full potential with professional growth and development opportunities.

Enjoy work life balance and flexible working hours.

Parexel US Benefits:

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings Accounts

Work/Life Balance

401(k) with Company match

Pet Insurance

Full list of benefits available here: https://www.parexel.com/us-benefits

If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!

At Parexel we embrace flexibility and understand that in today’s fast-paced world, employees need to balance their careers with their personal lives. Come join us where learning is constant, and you’re exposed to a world of experiences and open doors.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

The Company
HQ: Durham, North Carolina
20,524 Employees
On-site Workplace

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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