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Sr QA Auditor - (1722970) in Bangalore, IN at IQVIA™

Date Posted: 1/25/2018

Job Snapshot

Job Description

IMS Health and Quintiles have come together to be IQVIA. We have created a new way to harness advances in technology, analytics and human ingenuity called Human Data Science, to deliver solutions that help our customers drive healthcare forward and help patients around the globe. Inspired by the industry we help, our employees are committed to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

PURPOSE

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.

RESPONSIBILITIES

 Plan, schedule, conduct, report and close audit activities in any of the countries involved with Quintiles contracts. Audits are conducted to assess compliance with applicable regulations/guidelines, customer requirements, Quintiles 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.

 Prepare and review and approve corrective action plans

 Present educational programs and provide guidance to operational staff on compliance procedures.

 Conduct 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 customer audits,

 Assist in hosting mock regulatory inspections and regulatory facility inspections by acting as scribe and/or reviewing documents and identifying and calling operational staff to answer questions as needed.

 Ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections.

 May perform GLP Archivist duties where needed.

 Assist in training of new Quality Assurance staff.

All responsibilities are essential job functions unless noted as nonessential (N).

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

 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



Job Requirements

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

 Bachelor’s/primary degree

 5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance; GXP experience; or equivalent combination of education, training and experience; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS

 Position requires a significant amount of writing and keyboarding involving repetitive motions with fingers and sitting for prolonged periods of time

 Position requires extensive use of telephone and face-to-face communications, which requires the accurate perception of speech

 Travel required, may include international travel.


Connect to great opportunity™

IQVIA is a strong advocate of diversity and inclusion in the workplace.  We believe that a work environment that embraces diversity will give us a competitive

advantage in the global marketplace and enhance our success.  We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees

builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.


Meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimage healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and help patients around the globe. Whatever your career goals, we're here to confidently get you there!



Job ID: 1722970

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