Quality Assurance Manager

at  Cerba Research Nederland

9000 Ghent, Oost-Vlaanderen, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Dec, 2024Not Specified25 Sep, 2024N/AGood communication skillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

As the Quality Assurance (QA) Manager you are responsible to drive and ensure patient safety, data integrity and compliance with the relevant regulations and internal Cerba Research processes covering the clinical laboratory and diagnostic solutions part of clinical trial protocols, in close collaboration with the Scientific and Project Management Teams.
We are Cerba Research, a global partner for integrated clinical laboratory and diagnostic solutions. We help accelerate therapies through the development of highly specialized custom assays, deep biomarker expertise, and a passion for scientific innovation across complex therapeutic areas.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities:

The QA Manager is an ambassador for quality, both within and outside of the department. This position enjoys building relationships and working together collaboratively with others to meet shared objectives. This role is part of a team of QA professionals who strive to embed a quality culture across the organization, energized and motivated by teamwork in a positive and supportive working environment.

  • Master’s Degree in science preferred or equal by experience
  • Extensive knowledge and practical hands-on experience in GCP and CGLP and applicable legislation in Central Lab
  • Comprehensive understanding of pharmaceutical regulatory requirements and impacton the various functions within the business
  • Strong experience in ICH GCP clinical trial or central lab role including quality assurance and quality management related responsibilities
  • Experience in international Clinical trial or Central Lab projects
  • Experience in using or managing QA clinical trial Data Management and CTMS databases
  • Excellent communication skills and teamwork
  • Flexible in dealing with problems and solution oriented
  • Punctual and having eye for details
  • Fluent in English (written and spoken language


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Software Testing, Clinical Pharmacy

Graduate

Proficient

1

9000 Ghent, Belgium