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4.0

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331 Sandoz Jobs

Project Manager DDIT Dev. Regulatory Affairs (RA)

5-9 years

Hyderabad / Secunderabad

1 vacancy

Project Manager DDIT Dev. Regulatory Affairs (RA)

Sandoz

posted 10d ago

Job Description

The Project Manager for Regulatory Affairs (RA) team is responsible for capturing and addressing both global and local demands and projects from the RA business. This role involves close collaboration with other DDIT functions to ensure the delivery of high-quality services and innovative solutions to stakeholders.
As a key contributor to the organizations strategy, the Project Manager will implement objectives related to technology strategy development, solution discovery, service management, risk management, and relationship management.
In this role, the PM must drive the development and implementation of cutting-edge solutions that leverage best-in-class technologies to enhance our products and services. PM is required to manage stakeholders and act as a strategic business partner.

Job Description
Roles and Responsibilities:
  • Identify project goals, objectives, and direction. Lead the project team by clearly setting expectations related to quality and performance
  • Deliver projects as per Novartis Standards, Follow the established IT Controls and Keeping the costs within the approved budget.
  • Support business stakeholders on Identifying opportunities to streamline or improve processes through the implementation of innovative solutions to gain efficiencies.
  • Stay up to date with the latest advancements in IT Domain and Identify and evaluate opportunities to integrate the technologies into our existing products and services.
  • Work closely with the Business and DDIT stakeholders to understand their priorities and collaborate on the implementation of the defined roadmap for innovative solutions.
  • Work closely with stakeholders to understand their needs and translate them into actionable projects.
  • Be curious and engaged with our business stakeholders to establish a trustful and solid partnership.
  • Manage relationships with internal and external stakeholders, including executives, business units, and partners.
  • Act as a strategic business partner, providing guidance and insights on how the adoption of technologies can drive business growth and competitive advantage.
  • Collaborate with external partners and stay engaged with the wider innovation community to leverage industry best practices. Monitor and evaluate the performance of implemented solutions, making iterative improvements as necessary.
Essential Requirements:
  • At least 10+ years of experience in Project Management, preferably managing Digital & Automation projects within Pharma domain.
  • Excellent problem-solving and planning skills. A passion for innovation and a curiosity to explore technologies.
  • Strong communication and presentation abilities, with the ability to effectively convey complex ideas to both technical and non-technical stakeholders.
  • Experience in stakeholder management and strategic business partnering.; working with cross-functional teams.
  • Demonstrated ability to work in a fast-paced, dynamic environment and adapt to changing priorities.
  • Excellent communication skills.
  • Must have proven strong knowledge of SDLC, Validation & Compliance, Agile methodology
  • Proficiency with tools such as Jira, Confluence, HPQC, MS Project, Smartsheets and other project management tools
  • Experience in Data migration and System integration related projects.
  • Experience in managing GxP Projects and related fields
  • Multi-national global experience in interacting with senior management, collaborating across boundaries and relationship management, and influencing without authority.
  • Budget Management, Commercial Acumen, Influencing Skills, Performance Management (PM), Risk Management, Service Delivery Management, Strategic Planning, Waterfall Project Management
Desirable:
  • Implementation experience of Veeva Submission and Registration module is a plus.
  • Experience in Regulatory Affairs business processes is a plus (e.g. Registration Management, Submission Management, Submission Content management, Submission Publishing & Clinical Publishing, Product Labelling)
Education & Qualifications:
  • Bachelor s degree in engineering, pharmaceutical, computer science, management, or a related field. A master s degree in a relevant discipline (MBA, MS etc.) and related accreditations in project management, agile, quality and compliance is a plus.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired
Agile (Programming Methodology), Budget Management, Change Management, Cost Budgeting, Decision Making Skills, Project Finance, Project Management, Project Risk Management, Project Team Management, Regulatory Affairs, Stakeholder Engagement, Waterfall Model

Employment Type: Full Time, Permanent

Read full job description

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People are getting interviews at Sandoz through

(based on 15 Sandoz interviews)
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Company Website
34%
20%
13%
13%
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What people at Sandoz are saying

Regulatory Affairs salary at Sandoz

reported by 1 employee with 7 years exp.
₹5.4 L/yr - ₹6.9 L/yr
6% more than the average Regulatory Affairs Salary in India
View more details

What Sandoz employees are saying about work life

based on 381 employees
67%
49%
55%
91%
Flexible timing
Monday to Friday
No travel
Day Shift
View more insights

Sandoz Benefits

Submitted by Company
Competitive compensation
Pay equity
Pay for sustainable performance
Differentiated benefits and wellbeing programs
Values & integrity
Balanced rewards
Submitted by Employees
Free Transport
Health Insurance
Cafeteria
Job Training
Free Food
Soft Skill Training +6 more
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