Senior Principal Quality Auditor (Remote)

Senior Principal Quality Auditor (Remote)
Empresa:

Precision Medicine Group


Detalles de la oferta

Senior Principal Quality Auditor (Remote)Senior Principal Quality Auditor | Precision For Medicine | SpainPrecision for Medicine is hiring a Senior/Principal Quality Auditor to join our team.
Candidates can be based in either the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.Position SummaryThe Senior/Principal Quality Auditor supports the audit program and clinical projects to ensure compliance with regulations and Precision procedures.Essential FunctionsSupport the Quality Management System including SOPs, training, and CAPA.Process and maintain documentation for controlled documents, as required.Develop and administer training for employees and/or consultants.Host client/sponsor audits and support regulatory inspections.Coordinate and conduct assessments of potential and contracted vendors, including vendor audits as warranted.Coordinate and conduct internal audits of quality systems.Coordinate and conduct investigator site audits.Coordinate and conduct trial master file audits.Participate on computer systems validation projects and systems change control process.Provide QA consultation and support to assigned project teams internally and externally.Support and manage reported quality issues and any associated corrective and preventive actions.Monitor quality systems to provide feedback on compliance risks to QA management and identify opportunities for improvement.Maintain Q&C trackers, databases, metrics, and files.Follow applicable regulations and standards, including but not limited to local regulations (US FDA and EU), ICH, ISO, and company policies and procedures.QualificationsMinimum Required:Requires two to five years of applicable experience or equivalent combination of education and experience.Clinical research experience in a non-QA role considered (e.G., clinical research associate experience).Working knowledge of GCP/ICH guidelines and FDA regulations and standards.Hands-on experience leading clinical site audits.Other Required:Bachelor's degree in a science, healthcare, or related field of study.Availability to travel up to 50% domestically and/or internationally.Preferred:CRO, Pharmaceutical, and/or Medical device experience.QA certification preferred (e.G., CQA, SQA, etc.
).Experience with electronic clinical trial systems (e.G., EDC, CTMS, IxRS, ePRO, etc.
).SkillsExcellent interpersonal and problem-solving skills, effective verbal and written communication, and computer skills.CompetenciesStrong knowledge of GCP/ICH guidelines and FDA regulations and industry standards.Intermediate proficiency in Microsoft Word, Excel, and PowerPoint, and some knowledge of Access or similar database.Must possess a customer service demeanor; demonstrate collaboration and flexibility, teamwork, and a keen attention to detail.Ability to work independently and in a team environment.Ability to work with cross-functional groups and management under challenging situations.Ability to prioritize work and handle multiple and/or competing assignments.Excellent verbal and written communications skills.Must be fluent in the English language.At Precision for Medicine, we believe that the era of one-size-fits-all medication is giving way to a next generation of treatments, medicines that will be more effective because they are prescribed according to the unique biology of an individual patient.
Our mission is to help innovative biotech and pharmaceutical companies accelerate the development of these life-changing treatments.
Precision does this by developing assays that utilize biomarkers to help identify the right patient for the right drug.
We handle every aspect of clinical trials from initial strategy and design to selecting sites and executing quality clinical trials.
This is where you come in!Any data provided as a part of this application will be stored in accordance with our Privacy Policy.
For CA applicants, please also refer to our CA Privacy Notice.Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at ******.#J-18808-Ljbffr

Requisitos

Senior Principal Quality Auditor (Remote)
Empresa:

Precision Medicine Group


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