Manager/Senior Manager, Quality Assurance, Bioanalytical

Celerion

Tempe, Arizona

JOB DETAILS
SKILLS
Artificial Intelligence (AI), Biotech and Pharmaceutical, Clinical Research, Code of Federal Regulations, Communication Skills, Conflict Resolution, Detail Oriented, Drug Development, FDA (Food and Drug Administration), GCP (Good Clinical Practices), GLP (Good Laboratory Practices), GxP, Leadership, Maintain Compliance, Medicine, Multicultural, Multitasking, Presentation/Verbal Skills, Process Improvement, Quality Assurance, Quality Management, Regulations, Team Lead/Manager, Team Player, Translational Research, Vendor/Supplier Evaluation, Willing to Travel, Writing Skills
LOCATION
Tempe, Arizona
POSTED
30+ days ago
Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

Are you a Bioanalytical Quality Professional with experience in quality assurance and team management looking to make an impact in a dynamic clinical research environment?
 
At Celerion, we're transforming clinical research through translational medicine.  We're seeking a talented Manager/Senior Manager, Quality Assurance, Bioanalytical for our Global QA department to drive quality and compliance of our studies, processes and systems which is key to our mission of accelerating medicine for patients.
 
Ideally this role would be locally based at our Lincoln, Nebraska US location or alternatively at our Tempe, Arizona US location. Hybrid working and willingness to travel from other locations in the United States would also be considered. 

What You’ll Do:

  • QA Bioanalytical Team Direction and Management
  • Driving QMS and Process Improvement Initiatives
  • Oversight of Study Audits, System/Process Audits and Vendor Audits
  • Hosting Sponsor Audits and Regulatory Inspections
  • Actively contributing to Global QA Strategy

What You’ll Bring:

  • Ability to communicate and interact at all levels within multicultural environment
  • Ability to organize and manage multiple priorities
  • Strong problem solving, comprehension and analytical skills
  • Collaborative team player, open minded, ethical and culturally sensitive
  • Ability to manage and resolve conflict
  • Good, well-developed leadership skills
  • Excellent written and oral communication skills
  • Attention to detail, tactful and diplomatic
  • Advanced Computer skills and literacy

What is Required:

  • Bachelor’s degree in Business, Science, or related field or equivalent experience
  • Minimum of 8 to 10 years experience in Quality Assurance
  • Minimum of 4 to 5 years team management experience
  • Proficient knowledge of GXP (specifically GLP and/or GCP) and FDA 21 CFR Part 11 regulations
  • Robust knowledge of Bioanalytical techniques, regulations and industry guidelines
  • Well-developed Pharmaceutical Industry network
If this role is what you are looking for as the next step in your career, then please apply!

Celerion Values:       Integrity   Trust   Teamwork   Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

About the Company

C

Celerion

We Are Celerion

Our 40+ years of experience, innovative strategies, global capabilities, and expertise in early phase research make us faster than our competitors. That means you get key data sooner, enabling you to make earlier go/no-go decisions about your drug's development. It’s all in the name: Celerion is derived from the Latin celeritas (meaning swiftness and speed), which reflects our founding principle—that fast, reliable research is vital to a product's success.

Celerion’s focus is on the implementation of innovative strategies to generate key data very early to enable go/no-go decisions in drug development. With a large clinical capacity of more than 600 beds, efficient bioanalytical laboratories and experienced scientific staff, Celerion offers one of the most experienced clinical pharmacology research networks in the industry.

Why Join Celerion?

Celerion is one of the most experienced and successful CROs in the world. One of our key assets and greatest resources is the experience and expertise of our employees. Our vision to be the premier provider of early stage drug development solutions will only be achieved by ensuring that we have the brightest minds in the industry working with us.

We are looking for individuals who enjoy working in a fast-paced environment and who demonstrate leadership, teamwork, and are passionate about what they do.

If you want to build a meaningful career in a successfully growing company, and make a positive contribution to the health and well-being of people around the world, join our team.

COMPANY SIZE
1,000 to 1,499 employees
INDUSTRY
Biotechnology/Pharmaceuticals
EMPLOYEE BENEFITS
401K
WEBSITE
https://celerion.com/