Company
pharmaceutical
QAOfficerOperations
Neural analysis suggests this role is
optimal for Mid+ candidates.
“QA Officer Operations. Skills: Quality Assurance, Quality Control, Quality Management Systems, Environmental Monitoring, Release Management, Good Manufacturing Practices (cGMP), Quality Compliance. Manages Quality aspects and projects within area of responsibility. Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems”
What You'll Achieve.
On-time and GMP-compliant release of dosage forms; No complaints about inspections by authorities in your own area of responsibility without these being noticed & communicated beforehand; Successfully support continuous improvement projects
Industry & Context.
Problem Solving Skills
What They're Looking For.
Must Have
Quality Assurance, Quality Control, Quality Management Systems, Technological Expertise, Environmental Monitoring, Release Management, Good Manufacturing Practices (cGMP), Audit & Inspection Management, Quality Compliance, Technological Expertise
Nice to Have
Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge
What You'll Do.
Manages Quality aspects and projects within area of responsibility
Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
Distribution of marketing samples (where applicable)
Executes batch release in compliance with registration
How You'll Work.
Team & Collaboration
Collaborating across boundaries
Communication Scope
Communication skills
Process & Methodology
continuous improvement projects
Full Job Description
**Job Description Summary** -Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. **Job Description** **Major Accountabilities:** * QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones, Functional Breadth, Collaborating across boundaries * Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt * Distribution of marketing samples (where applicable) **Key Performance Indicators:** * On-time and GMP-compliant release of dosage forms * No complaints about inspections by authorities in your own area of responsibility without these being noticed & communicated beforehand * Successfully support continuous improvement projectsExecutes batch release in compliance with registration **Work Experience:** * Quality Assurance * Quality Control * Quality Management Systems * Technological Expertise * Environmental Monitoring * Release Management * Good Manufacturing Practices (cGMP) * Audit & Inspection Management * Quality Compliance * Technological Expertise **Skills:** * Collaboration * Dealing With Ambiguity * Operational Excellence * Regulatory requirements knowledge * Problem Solving Skills * Leadership * Communication skills * Data Integrity * Digital saviness **Languages:** * English. **Skills Desired** Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge
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