Site Director

Job Title: Site Director

In this role, you will provide strategic and operational leadership, directing the development, planning, implementation, and maintenance of manufacturing methods, processes, and operations for new or existing products and technologies. You will ensure the effective use of material, equipment, and personnel to produce quality products, developing and overseeing budgets, and monitoring labor and capital expenditures. The role requires you to formulate and recommend manufacturing policies, procedures, and programs while overseeing all operations at the site, including Manufacturing, Supply Chain, Engineering, and Maintenance.

Responsibilities

• Optimize manufacturing processes including batching, filling, inspection, and packaging to meet demand forecasts and customer needs.
• Drive cross-functional alignment through matrix reporting structure involving Quality Assurance, Quality Compliance, Finance, and Human Resources.
• Ensure compliance with specifications, Standard Operating Procedures, FDA regulations (GMP’s), and New Drug Applications for product quality, safety, and efficacy.
• Support preventative maintenance, calibration programs, process improvements, technology upgrades, and related engineering projects.
• Lead Supply Chain planning, procurement, production scheduling, material management, and inventory control.
• Ensure effective Operations and Quality controls for sterile manufacturing requirements.
• Oversee capital project planning, site budgets, manufacturing schedules, and performance requirements.
• Enhance product quality based on customer feedback.
• Resolve complex problems with in-depth evaluation of situations or data.
• Regularly interact with management or executive levels concerning multiple functional areas and customer divisions.

Essential Skills

• BS in Engineering, Life Sciences, or related field; MS preferred.
• 5+ years of sterile/injectable manufacturing experience.
• 5+ years of experience leading and managing a team.
• Experience with FDA/cGMP compliance and sterile manufacturing practices.
• Strong knowledge of IV bag production processes and equipment.
• 8+ years of manufacturing experience.
• Strong leadership experience.

Additional Skills & Qualifications

• Experience in pharmaceutical and sterile environments.
• Understanding of GMP regulations.
• Knowledge of FDA standards.
• Proficiency in strategic planning and operational leadership.

Work Environment

The role is based in a very large GMP-regulated manufacturing facility undergoing expansion, with multiple buildings on campus. The facility is in the process of adding new manufacturing lines and filling/compounding suites. The environment promises growth and development opportunities.

Job Type & Location

This is a Permanent position based out of Cleveland, OH.

Pay And Benefits

The pay range for this position is $89.00 - $96.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Cleveland,OH. Application Deadline This position is anticipated to close on Mar 2, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] for other accommodation options.