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Project Manager, Manager* (On-Site

Job in Santa Clarita, Los Angeles County, California, 91382, USA
Listing for: Lief Labs
Full Time position
Listed on 2026-02-28
Job specializations:
  • Management
    Operations Manager, Program / Project Manager, Healthcare Management
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Project Manager, Manager* (On-Site)

Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements. Our in‑house product development and R&D team creates the best‑tasting and cutting‑edge supplement formulations. Lief also houses a state‑of‑the‑art, full‑service Current Good Manufacturing Practice (cGMP) manufacturing facility, which offers custom solutions for many supplement categories. Lief collaborates with entrepreneurial firms to help them build premier brands.

Our turnkey solutions allow us to engage in seamless partnerships that help brands with scalability and sustainable growth.

Lief Labs is in the Santa Clarita Valley (Valencia, CA.).

Summary

The Manager of Project Management you will be responsible for overseeing and coordinating projects across various departments within the organization. You will lead a team of project managers, providing guidance, support, and direction to ensure the successful execution of projects from initiation to completion. This role will require strong leadership skills, excellent communication, and a proactive approach to problem‑solving.

Responsibilities
  • Leadership and Team Management:
    • Lead and manage a team of project managers, providing coaching, mentoring, and support to ensure project success.
    • Foster a collaborative and high‑performing team culture focused on delivering results and driving continuous improvement.
  • Project Planning and Execution:
    • Develop project plans, timelines, and budgets in collaboration with cross‑functional teams to ensure alignment with organizational goals and objectives.
    • Oversee the execution of projects, monitoring progress, identifying potential risks and issues, and implementing mitigation strategies as needed.
    • Ensure projects are delivered on time, within budget, and meet quality standards.
  • Stakeholder Engagement:
    • Build strong relationships with key stakeholders across departments, including R&D, manufacturing, quality assurance, and regulatory affairs.
    • Communicate project status, updates, and milestones to stakeholders, ensuring transparency and alignment throughout the project lifecycle.
  • Continuous Improvement:
    • Identify opportunities to streamline processes, improve efficiency, and enhance project management methodologies.
    • Implement best practices and lessons learned to drive continuous improvement in project delivery and execution.
  • Compliance and Quality:
    • Ensure compliance with relevant regulatory requirements, quality standards, and company policies throughout the project lifecycle.
    • Work closely with quality assurance and regulatory affairs teams to address any compliance‑related issues or concerns.
  • Additional duties as assigned.
Supervising Responsibilities

In accordance with applicable policies/procedures and Federal/State laws, may perform the following supervisory responsibilities:
Interviewing, hiring, orienting, coaching and developing employees; planning, assigning, and directing work; appraising, managing and rewarding performance; addressing complaints and resolving problems.

Minimum Qualifications Education

Bachelor's degree in business, project management, engineering, or a related field. Advanced degree or certification (e.g., PMP, PRINCE2) is preferred. PMP certification.

Experience
  • 5+ years of experience in project management, preferably in the pharmaceutical, nutraceutical, or consumer health industry.
  • Proven track record of successfully leading and delivering complex projects on time and within budget.
  • Strong leadership skills with the ability to motivate and inspire cross‑functional teams.
  • Excellent communication and interpersonal skills, with the ability to effectively engage and influence stakeholders at all levels of the organization.
  • Solid understanding of project management methodologies, tools, and techniques.
  • Experience working in a regulated environment (e.g., FDA, cGMP) is highly desirable.
  • Ability to thrive in a fast‑paced, dynamic environment and adapt to changing priorities and deadlines. Proven experience as a Project Manager in pharmaceutical or nutraceutical product development.
  • Strong understanding of regulatory requirements and quality standards in the nutraceutical industry.
  • Proficiency in project…
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