Global GCP/PV Auditor job opportunity at Novartis.



DateMore Than 30 Days Ago bot
Novartis Global GCP/PV Auditor
Experience: 5-years
Pattern: full-time
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeOND
loacation Barcelona Provincial, Spain
loacation Barcelona Prov..........Spain

Job Description Summary In this role you will lead, support and report independent GCP/PV audits and approve follow-up corrective and preventive activities according to the Novartis Quality Systems and Standards, Good Clinical Practice(GCP)/Good Pharmacovigilance Practice(GPvP) and the current GCP/PV regulations. You will provide GCP/PV related quality guidance and assist in the identification and implementation of quality assurance training needs for Global GxP Audit and other business partners. The audits performed on behalf of Global GxP Audit include all audit types across GCP and PV disciplines including internal and external targets.   Job Description We pursue amazing talent across Spain! This position offers the possibility of being fully remote, with flexibility in location. We’re excited to welcome you to our team whether you're based in Madrid or Barcelona . Please note that the role requires travel of up to 60% of the time. Major accountabilities: P la n , lead, c ondu ct, do c u me n t, report and follow-up of GCP/PV a ud i ts according to the requirements specified in the respective Novartis procedures as well as applicable regulations, standards, quality agreements, and guidance documented. For this entry-level global auditor role, audits will typically be limited to low risk GCP/PV activities such as Investigator site audits, single service vendors, systems/process, Patient Oriented Programs, etc).  Assist in supporting complex audits (Country Organizations, multiservice vendors, high risk vendors, etc). Pr o vi de t e c hn i c a l g u i d a n ce a n d t rai n i n g o n a ud it a ct ivi t ie s. E n s u r e appropriate esc ala t i o n to responsible management in case o f c ri t i c a l a u dit f i n d i n gs and support immediate follow-up measures according to the Novartis requirements on Management Escalations and other relevant procedures.  Ensure adequate efinition and recording of mitigation plans when applicable. A ssess t h e a de q u a cy o f r e s p o n ses (C A P A pl an s) t o a u dit fi n d i n gs i n c oo pe ra t i o n with CAPA Approver a n d CAPA Coordinator . Maintain current knowledge of regulations, standards, and guidance documents. Minimum Requirements: Education: Degre e i n n a t u ral/ b i o l o gi c a l sc ie n c e s o r e qu ivale n t (o r a n e qu ivale n t mi x o f e du c a t i o n a n d ex p erie n c e). 5 years GCP/GPvP/clinical /industry/health authority experience or equivalent; 1-2 years of GCP auditing experience preferred. Ability to manage and objectively evaluate compliance issues and address a variety of tasks within the same timeframe while maintaining oversight. maintain a moderate degree of independence with respect to decision making and problem solving. T ho r ou g h k no w le d g e o f a p p li c a b l e G C P , G PvP a n d Gx P reg u la t i on s, g u i d eli n e s, po li c ie s a n d p r o c e du re s. E x p erie n ce w i th H eal th Au t ho ri ty i n s p e ct i on s a n d i n t era ct i o n a p l u s. G oo d qu ali ty a n d c o m p lia n ce lea d er s h i p a n d f a c ili t a t i o n s kill s. Fluent English, written and spoken. Other languages are a plus. Why Novartis:   Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?   https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network:   Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up:   https://talentnetwork.novartis.com/network Benefits and Rewards:   Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:   https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion :  Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.   Skills Desired Auditing, Audit Management, Communication Skills, Compliance Audits, Compliance Risk, Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gmp Procedures, Inspection Readiness, Organizational Skills, People Management and Leadership, Qa (Quality Assurance), Regulatory Compliance, Risk Management, Self-Awareness, Technological Expertise

Other Ai Matches

Regional Value and Access Manager Centro Applicants are expected to have a solid experience in handling Job related tasks
Assoc Dir, Clinical Data Acquisition and Mgmt Applicants are expected to have a solid experience in handling Clinical Data Acquisition and Mgmt related tasks
People Partner Applicants are expected to have a solid experience in handling Job related tasks
Produktionsmitarbeiter (m/f/d), Kundl, Tirol, Austria Applicants are expected to have a solid experience in handling Kundl, Tirol, Austria related tasks
Assoc. Dir. DDIT ISC Threat Hunting Applicants are expected to have a solid experience in handling Job related tasks
Assoc. Dir. - HPC Infrastructure Sr. Engineer (Location: Czech Republic OR Mexico OR India) Applicants are expected to have a solid experience in handling Job related tasks
Vodja kakovosti (m/ž/d) / Site Quality Head (m/f/d) Applicants are expected to have a solid experience in handling Job related tasks
【契約社員】Associate, General Affairs Applicants are expected to have a solid experience in handling General Affairs related tasks
Sr. Specialist- Solution Delivery for Infrastructure Services- AWS/ Azure Applicants are expected to have a solid experience in handling Job related tasks
Therapeutic Data Strategy Director Applicants are expected to have a solid experience in handling Job related tasks
Product Manager- Oncology Applicants are expected to have a solid experience in handling Job related tasks
Vzorčevalec (m/ž/d) / Sampling operator (m/f/d) Applicants are expected to have a solid experience in handling Job related tasks
Data Steward Expert (with language proficiency in Mandarin/Thai/ Vietnamese/Japanese/Arabic/Korean) Applicants are expected to have a solid experience in handling Job related tasks
Senior Global Program Safety Team Lead Applicants are expected to have a solid experience in handling Job related tasks
Senior QA Operations Specialist Applicants are expected to have a solid experience in handling Job related tasks
Engineering & Maintenance Technician I/II Applicants are expected to have a solid experience in handling Job related tasks
Director Data Platform Applicants are expected to have a solid experience in handling Job related tasks
G2G Young Professional Applicants are expected to have a solid experience in handling Job related tasks
Material Coordinator Applicants are expected to have a solid experience in handling Job related tasks
Principal Scientist, Mid/Large Scale Oligonucleotide Synthesis, xRNA Therapeutics Applicants are expected to have a solid experience in handling Mid/Large Scale Oligonucleotide Synthesis, xRNA Therapeutics related tasks
Associate Director IT Solution Architect (HPC) Applicants are expected to have a solid experience in handling Job related tasks
Supply Chain Planning & Logistics Senior Specialist Applicants are expected to have a solid experience in handling Job related tasks
ED, Head of Analytics Engineering Applicants are expected to have a solid experience in handling Head of Analytics Engineering related tasks