role could open the possibility of becoming the QA team lead...This requires experience in a comparable QA position, as well as an interest in DevOps-related areas...This role is an excellent opportunity, as in the future we expect the QA team to grow and therefore this
role could open the possibility of becoming the QA team lead...This requires the candidate to have experience in a similar QA position and also have an interest in..This role is an excellent opportunity, as in the future we expect the QA team to grow and therefore this
You will be responsible for the assigned processes and activities within QA Operations and will mainly..well as the support of health authorities’ inspections and corporate audits.The Senior Specialist, QA..This position will be working closely with the QA Operations management to identify and handle process..The Senior Specialist, QA Operation is capable of working autonomously carry escalation and follow all..release of product on the Boudry manufacturing site.This position is responsible for quality assurance (QA
JOB TITLE: QA Engineering/Validation Expert START DATE: ASAP DURATION: 8 months Services: The objective
and QA Does identify required project documentation with the team, using the QRM-methodology and the..previous projects Defines qualification documents in collaboration with quality engineers, Validation, QA-Val
the governance for GCP/GEP and GVP compliance, as well as to develop and to lead strategic Clinical QA..team to raise the necessary GxP metrics to the functional level review.• Be responsible to promote QA..Sound experience in GCP QA environment and GVP is required.• Experience in a GLP environment is an asset..Consistently build GxP QA capability, by providing continuous coaching, mentoring and advice to all direct
and QA Does identify required project documentation with the team, using the QRM-methodology and the..previous projects Defines qualification documents in collaboration with quality engineers, Validation, QA-Val
Support as QA validation the periodic review and requalification of equipment/processes to ensure that..with writing and reviewing documents (procedure, work practice) prepared by SMEAs required, provides QA..Support the QA team to perform evaluation of deviations, CAPA, and change control in his area of responsibility
and QA - Does identify required project documentation with the team, using the QRM-methodology and the..previous projects - Defines qualification documents in collaboration with quality engineers, Validation, QA-Val
and QA Does identify required projectdocumentation with the team, using the QRM-methodology and the..ofprevious projects Defines qualificationdocuments in collaboration with quality engineers, Validation,QA-Val
and QA Does identify required project documentation with the team, using the QRM-methodology and the..previous projects Defines qualification documents in collaboration with quality engineers, Validation, QA-Val
learnt of previous projectsqualification documents in collaboration with quality engineers, Validation, QA-Val
previous projects.Defines qualification documents in collaboration with quality engineers, Validation, QA-Val
previous projectsDefines qualification documents in collaboration with quality engineers, Validation, QA-Val
technical agreements, and applicable regulatory requirements.Responsible for:internal batch record review, QA
process gap assessments and risk assessments on Bio manufacturing processes.Directly interface with CMO QA
Ensure that any compliance issues are raised to Quality Assurance (QA), supervisor and the relevant leadership
Directly interface with CMO QA and project management regarding any potential compliance gaps, deviation
