RxLogix Looking for Manager – IT QA at Noida, Uttar Pradesh Full Time

Job Status: Full Time

Essential Duties & Responsibilities:
Note: This opportunity is not a fit for the software testing professionals. The candidate must possess experience in the Pharmaceutical IT Compliance areas and CSV and a good understanding of regulations for LifeScience industries such as GAMP 5, CFR , EU Annex 11, ICH etc.

1. CSV:
Provide application validation expertise on GxP products for drug safety space.

Be accountable for reviewing and supporting key CSV deliverables – Requirement Specifications, Validation

Plan, Test Plan, Traceability Matrix, Test Summary Report, Qualification Scripts and Validation Summary Report

Understanding of implementing projects on SaaS Models

Understanding needs of Infrastructure , Operation and Performance qualification in alignment with Software Engineering Practices.

Requirements Analysis and Risk Assessment, Profiling and Mitigation in collaboration with the SME

Sound Defect management skills

Provide adequate understanding and expertise on Change Control Procedure, Deviation Handling, Document Management and CAPA management

Understanding of risk-based system validation approach and V-Model

2. Quality Assurance Operations:
Knowledge of GxP, QA best practices

In depth understanding of the regulatory guidelines for IT systems– primarily FDA, EMA, MHRA and PMDA

In depth understanding of 21 CFR Part 11, EU Annex 11 compliance

Minimum 10 years’ experience of client, internal and regulatory audits

Anchor updates to QMS

Engage in Continual Improvement programs

Coordinates the revision, review, and approval of IT SOPs and other GxP documents

3. Team and Stakeholder Management Skills:
Client engagement and ability to convince based on RxLogix Best Practices

Ability to manage Stakeholder needs and do multi tasking

Oversee work of direct reports and cross-train staff on different quality areas

Interview, hire, train, develop and manage employees

Capacity planning and forecasting resource requirements

Performance evaluation and appraisals

Motivating agent for the team and fosters the spirit of teamwork

Coach, mentor and develop staff, including overseeing new employee onboarding and providing career development planning and opportunities

Closely work with clients, project team and product owners to support product releases and implementations

4. Other Must-have skills:
Well-organized and detailed oriented professional, with strong verbal and written communication skills

Self- motivated with ability to manage, organize and prioritize multiple tasks

Should be able to achieve the optimum balance for Quality vs. Productivity

Minimum Requirements:
1. Exposure to pharmacovigilance domain and drug safety applications – Argus or ArisG/J –strong preference

2. Experience with electronic QMS/DMS is a plus.

3. Experience in Manual execution and ALM Tool based executions

4. Experience with training coordination and management

5. Worked in Agile / Scrum team structure

6. Experience in SQL and PLSQL writing

Preferred Qualifications:
1. BE/ B.Tech./ MCA/ B.Pharma/ M.Pharma from recognized institute with good academic scores

2. IT Quality Assurance professional with 09-12 years of experience with computerized system validation in Life Sciences industry. Hands on experience is performing Validation activities both Manual and ALM tools based.

Travel Expectations:
0-5%