bengaluru karnataka pharmaceutical quality assurance Jobs – 47 Open Jobs Today

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- Full-time
- Research
- Bachelor's degree
- Communication skills
15h
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QA Mgr

IQVIA -
Bengaluru, Karnataka

Apply Now

Job details

Full-time
15 hours ago

Qualifications

Research
Quality assurance
Bachelor's degree
Risk analysis
Research & development
Communication skills
Negotiation

Full job description

Bengaluru, India | Full time | Hybrid | R1515072

Job Overview
Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.

Essential Functions

Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions
Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers
Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures
Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans
Manage Quality Issues
Present educational programs and provide guidance to operational staff on compliance procedures
Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closures for quality events arising from Quality Issues, Audits, Inspections or during simillar QA activities
Provide quality assurance consultancy activities and projects for clients within budget and established timelines
Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements
Host audits/inspections,Ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections
May perform GLP Archivist duties where needed
Manage/oversee quality events updates in eQMS and/or Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle
Lead/collaborate/support in QA initiatives/projects for quality, process improvements
Assist in training of new Quality Assurance staff

Qualifications

Bachelor's Degree Pref
5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance. GXP experience. Equivalent combination of education, training and experience.
Knowledge of word-processing, spreadsheet, and database applications..
Extensive knowledge of pharmaceutical research and development processes and regulatory environments..
Knowledge of quality assurance processes and procedures..
Strong interpersonal skills..
Excellent problem solving, risk analysis and negotiation skills..
Strong training capabilities..
Effective organization, communication, and team orientation skills..
Ability to initiate assigned tasks and to work independently..
Ability to manage multiple projects..
Ability to establish and maintain effective working relationships with coworkers, managers and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

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pharmaceutical quality assurance jobs in bengaluru karnataka

QA Mgr

Principal AX Developer (Microsoft Dynamics AX 2012/D365 F&O)

APC & PO Specialist/Consultant/Expert

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