Job Description
The Site Lead is responsible for overseeing all aspects of biotechnology product manufacturing and delivery at a designated site. This includes managing production processes, quality assurance, supply chain operations, regulatory compliance, and the integration of technology with manufacturing. The role ensures timely, budget-conscious execution of operations while maintaining high standards of safety, quality, and compliance. The Site Lead also collaborates across functions and with external stakeholders to meet contractual obligations and drive continuous improvement.
ResponsibilitiesLead and manage a cross-functional team including Operations, Quality, and Technology.Foster collaboration across departments to ensure alignment with production goals and customer expectations.Supervise biotechnology product manufacturing, ensuring adherence to schedules and quality standards.Monitor equipment performance and coordinate maintenance.Implement lean manufacturing techniques to improve efficiency and product quality.Collaborate with Technology teams to ensure processes meet delivery expectations.Troubleshoot production issues and resolve bottlenecks in coordination with Product and Sales teams.Oversee end-to-end supply chain operations from raw material procurement to product distribution.Manage inventory to meet production schedules while minimizing excess stock and optimizing working capital.Conduct audits and inspections to ensure compliance with GMP and other regulatory standards.Monitor KPIs related to efficiency, quality, timelines, and compliance.Ensure adherence to safety protocols and environmental regulations.Provide regular updates to senior leadership on operational performance and challenges.Identify and escalate risks related to efficiency, compliance, or product quality.Lead crisis management efforts during operational disruptions or safety concerns.Essential SkillsBachelor’s degree in science, engineering, or a related field required.10+ years of relevant experience, including leadership roles.Knowledge of microbiology and BSL-2-level pathogen handling.Experience with cell culture, cryopreservation, and biotech product testing.Proficiency in MS Office and relevant software tools.Familiarity with ISO quality systems and GMP practices.Strong organizational and communication skills.Additional Skills & QualificationsAdvanced degree preferred.Preferred certifications: PMP, Six Sigma Black Belt, Lean Manufacturing.Work Environment
The Baltimore site is primarily a biotechnology manufacturing facility, with work conducted in BSL-2 laboratory conditions, meaning there may be exposure to biohazardous agents but within controlled safety protocols. Benefits include a 10k sign-on bonus, up to 20% yearly bonus, and opportunities for global career growth and development. The company invests in technical, professional, and leadership development, rewarding performance with bonuses, long-service awards, and career advancement opportunities.
Pay and Benefits
The pay range for this position is $120000.00 - $145000.00/yr.
up to 20% bonus
Career Growth & Development
-Global Opportunities: With over 19 sites worldwide, employees have access to internal mobility and international assignments.
-Learning & Development: The company invests in technical, professional, and leadership development, helping employees reach their full potential 3.
-Recognition & Progression: Performance is rewarded through bonuses, long-service awards, and career advancement opportunities.
Workplace Type
This is a fully onsite position in Baltimore,MD.
Application Deadline
This position is anticipated to close on Aug 15, 2025.
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 actalentaccommodation@actalentservices.com for other accommodation options.