Life Sciences Management Consultant - (GRC)

Responsibilities :

We are looking for smart, self-driven, high-energy people with top-notch communication skills, intellectual curiosity and passion for excellence. Our analysts have a blend of in-depth domain expertise, strong analytical and conceptual thinking skills and excellent soft skills. We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation, Risk Management and Audits At IC-LS, you will:

Be responsible for the delivery of business results to global health and life sciences clients.

Serve as a team member, track lead or engagement lead on business consulting engagements for clients.

Execute consulting engagements in a global delivery model, working with consultants across regions.

Analyze problems, and structure complex business analyses.

Work with cross functional client teams to perform gap analysis and identify improvement options.

Effectively collaborate with the internal and external stakeholders.

Participate in a variety of firm building events

Additional Responsibilities:

Knowledge of validation tools and templates used in the pharmaceutical industry.

Proven ability in supporting multiple projects, responding quickly to changing situations in complex environments.

Preferable IT background to understand complexities on the program.

Experience in Agile and waterfall methodology

Knowledge and hands on experience in conducting periodic or control maturity assessment and Audits

Knowledge in Saas/Cloud Qualifications

Technical and Professional Requirements:

4 †14 years of professional experience in the Life Sciences industry working for a consulting services organization and/or industry.

Good understanding of key pharmaceutical compliance regulations like 21 CFR Part 11, GxP and GAMP 5.

Experience creating, reviewing and approving / acknowledging validation deliverables.

Knowledge of risk management process and quality management requirements which assures that IT Projects meet Quality and Regulatory requirements

Experience in validation of Enterprise applications such as SAP / S4 HANA projects, Trackwise, QMS, DMS and etc.

Functional knowledge in any of the domain applications such as Clinical applications like EDC, CTMS etc., Regulatory applications like CDR, or any other applications/system used in Pharma industry.

Thorough Knowledge in compliance and validation concepts. (Change, Deviation, Supplier management)