Quality Control Lab Manager

Job Description

Job Description

Are you a Laboratory Manager looking for a new opportunity in Quality Control? Our client is seeking a Quality Control Lab Manager that will be responsible for overseeing daily laboratory operations, ensuring compliance with industry standards, and managing laboratory staff.

If you have a strong technical background in Chemistry, Microbiology, or Material Science, combined with leadership and project management skills - please apply!

Responsibilities

• Supervise day-to-day laboratory activities and ensure smooth operations.
• Clearly communicate priorities and objectives to the team.
• Ensure timely project completion and adherence to established protocols.
• Oversee the receipt, testing, and documentation of samples.
• Ensure all laboratory equipment is properly calibrated, functioning, and maintained.
• Maintain accurate documentation for equipment and procedures.
• Develop, review, approve, and execute laboratory policies and procedures.
• Ensure documentation complies with cGMPs, GOPs, and GLPs.
• Prepare for and participate in internal and external audits by regulatory authorities (e.g., FDA, EU) and customers.
• Address audit findings and ensure corrective actions are implemented.
• Ensure the safety of laboratory personnel and visitors.
• Manage laboratory housekeeping and maintenance of non-calibrated equipment.
• Oversee and manage a team of laboratory professionals or non-professional staff through supervisors.
• Handle hiring, performance reviews, training, and development.
• Assign tasks, manage work schedules, and ensure consistent application of organizational policies.
• Foster positive relationships with internal and external stakeholders.
• Ensure timely and accurate communication regarding laboratory activities and results.
• Contribute to budgetary planning and management.
• Recommend and implement new policies or modifications to existing policies.

Qualifications

• Bachelor's degree in Microbiology, Biology, Engineering, Chemistry, or a related field.
• At least 4 years of experience in a GMP laboratory setting within the pharmaceutical, medical device, or cosmetic industries.
• Proven experience with project management and independent action.
• Familiarity with ISO 17025, CFR requirements, USP / ASTM / ISO / AAMI test methods, and FDA interactions.
• Strong time management skills including prioritization, organization, and detail tracking.
• Technical writing proficiency.
• Ability to diagnose, isolate, and resolve complex issues.
• Effective communication with diverse audiences, including senior management and non-technical stakeholders.
• Ability to control and coordinate concurrent projects with competing priorities and deadlines.
• Willingness to travel up to 10% of the time.

Location

Mundelein, IL

Employment Type

W2 employee, contract and / or contract to hire

Benefits for W2 Employees

• Choice of medical, dental, and vision plans.
• Paid vacation time.
• Competitive hourly rate.
• 401(k)

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm.

With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects.

On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects.

On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings.

We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.

Equal Opportunity Employer Minorities / Women / Veterans / Disabled