Project Manager - Technical Services Pharmaceuticals

Hikma Pharmaceuticals - Columbus, OH

Full-time - Mid Level

Columbus, OH

5,001-10,000 employees

Wholesale Trade Agents and Brokers

About the position

The Project Manager, Technical Services at Hikma Pharmaceuticals is responsible for leading and managing cross-functional project teams to ensure the successful commercialization of generic products. This role involves overseeing project planning, execution, and completion while adhering to key performance indicators such as timing, cost, and process robustness. The Project Manager will work closely with various stakeholders to manage risks, facilitate communication, and ensure compliance with applicable regulations in the pharmaceutical industry.

Responsibilities

• Manage and deliver organizational and project leadership for Generic commercialization, Site Transfers, Buy-ins, Third Party, Alternate API, and process changes.
• Proactively identify and manage risks that could adversely affect successful project completion.
• Lead and facilitate multiple cross-functional teams, managing project team resources and experts to address relevant issues and manage progress.
• Ensure integration of technical and commercial information necessary for project success, utilizing project management skills and tools.
• Assess critical data to facilitate 'Go / No Go' project decisions and provide proactive communication to stakeholders regarding issues and risks.
• Facilitate change management requirements and manage tactical and strategic change meetings.
• Develop and manage implementation plans, ensuring document review prior to final implementation.
• Assess completed projects for lessons learned to drive improvement in project performance.

Requirements

• B.S. degree in a scientific and/or related operations discipline with 1-3 years of experience in pharmaceuticals or project management.
• M.S. degree in a scientific and/or related operations discipline with 3-5 years of experience preferred.
• Proficient knowledge of applicable regulations (cGMP, DEA, FDA, EMEA) and pharmaceutical supply chain operations.
• Demonstrated knowledge of project management methodology with an active PMP certification.
• Ability to communicate effectively at various levels and manage complex projects.

Nice-to-haves

• Active Six Sigma certification preferred.
• Experience in change management, analytical, and/or drug regulatory affairs.

Benefits

• 401(k) with company matching
• Dental insurance
• Disability insurance
• Employee discount program
• Health insurance
• Life insurance
• Paid holidays
• Annual performance bonus
• Generous paid time off (PTO) starting with 20 days
• Tuition reimbursement
• Paid maternity and parental leave