Project Manager PLM

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Please check this requirement

Position: PLM Project Manager

Remote

Job Description:

Overview:

As a Project Manager specializing in Product Lifecycle Management (PLM) within the pharmaceutical domain and manufacturing sector, you will be responsible for leading and managing projects related to the development, implementation, and enhancement of PLM systems and processes. Your role will involve collaborating with cross-functional teams to ensure the successful execution of projects within specified timelines and budgets while adhering to regulatory requirements and industry standards.

Key Responsibilities:

Project Planning and Execution:

Develop comprehensive project plans, timelines, and budgets for PLM initiatives, considering the specific needs and objectives of pharmaceutical manufacturing processes.

Lead project kick-off meetings, define project scope, objectives, deliverables, and resource requirements.

Coordinate project activities, monitor progress, and identify and mitigate risks to ensure timely and successful project delivery.

Communicate regularly with stakeholders, providing updates on project status, milestones achieved, and any deviations from the plan.

Requirement Analysis and Solution Design:

Work closely with business stakeholders, subject matter experts, and IT teams to gather and analyze requirements for PLM system implementations and enhancements.

Collaborate with vendors and internal development teams to design customized PLM solutions that align with business goals and regulatory compliance requirements.

Ensure that PLM solutions meet the unique needs of pharmaceutical manufacturing processes, including document management, regulatory compliance, change control, and batch record management.

Stakeholder Management:

Build and maintain strong relationships with stakeholders at all levels of the organization, including executives, business users, IT teams, and external vendors.

Engage stakeholders proactively to solicit feedback, address concerns, and manage expectations throughout the project lifecycle.

Act as a liaison between business stakeholders and technical teams, facilitating communication and ensuring alignment between business requirements and technical solutions.

Quality Assurance and Compliance:

Implement best practices and methodologies for quality assurance and compliance within PLM projects, ensuring adherence to regulatory standards such as FDA regulations, GxP guidelines, and industry-specific standards.

Develop and execute test plans, conduct system testing, and coordinate user acceptance testing to validate the functionality, performance, and usability of PLM solutions.

Collaborate with quality and regulatory affairs teams to ensure that PLM systems comply with regulatory requirements for documentation, validation, and audit trails.

Continuous Improvement and Knowledge Sharing:

Identify opportunities for process improvement and optimization within PLM systems and processes, leveraging industry best practices and emerging technologies.

Facilitate knowledge sharing sessions, training workshops, and documentation updates to ensure that stakeholders are equipped with the necessary skills and knowledge to maximize the value of PLM solutions.

Stay abreast of industry trends, advancements in PLM technologies, and regulatory changes affecting the pharmaceutical manufacturing sector, and incorporate relevant insights into project planning and execution.

Qualifications:

Bachelor's degree in Engineering, Computer Science, Pharmaceutical Sciences, or related field. Advanced degree or relevant certifications (e.g., PMP, PLM certification) preferred

Please share resume with contact details

Thank and Regards

Suman Mishra

Rudra Technologies