Analytical Lab Director

Quicksilver Scientific•Louisville, CO

About The Position

We're seeking an experienced, strategic, and hands-on Analytical Lab Director to lead our laboratory operations. If you thrive in a fast-paced environment, this is your opportunity to make a meaningful impact at a mission-driven company.

Requirements

At least 10+ years of relevant analytical chemistry management and leadership experience.
Ph.D. in chemical, physical, biological, or clinical lab science .
Be board-certified by an approved certifying body (e.g., ABB, ABCC, ABMM, ABMGG).
Considerable knowledge of the use of laboratory apparatus and equipment, with the ability to aid in troubleshooting technical problems.
Instrumentation Proficiencies: HPLC-DAD, HPLC-RID, GC-MS, LC-MS-MS, ICP-MS, MTT
Considerable knowledge of the methods, materials, and techniques used in laboratory work.
Exceptional communication skills, including cross-functional team leadership skills and the ability to work in close collaboration with others.
Ability to work independently, adapt to change, and manage multiple tasks.
Ability to problem-solve and make decisions on complex issues, often in a cross-functional team setting.
Knowledge of federal, state, and local standards, regulations, guidelines, and requirements affecting the operations of a clinical reference laboratory.
Must meet CLIA requirements for a laboratory Director in a high-complexity laboratory.
Proficiency with MS Office and laboratory data systems.

Nice To Haves

Experience within the nutritional or pharmaceutical industrie s is preferred.

Responsibilities

Direct the day-to-day operation of the laboratory to ensure smooth flow of samples and testing.
Provide leadership, mentoring, and professional development opportunities for the analytical lab staff.
Handle team management, including PTO request approval, progressive disciplinary actions, staff coaching, and performance reviews.
Work with HR on recruitment efforts, interviewing potential hires, and training new hires.
Develop, implement, and refine policies and procedures to enhance laboratory efficiency and compliance.
Oversee the analytical lab to ensure that scheduling of laboratory staff is sufficient to meet production schedules.
Coordinate testing responsibilities and change laboratory schedules as workflow permits, based on business needs.
Support team members in resolving analytical challenges and troubleshooting technical issues.
Responsible for in-house method development.
Developing and maintain all SOPs.
Method development and analysis of biological samples for plasma and whole blood uptake of new QS products.
Management Reviews and Summaries, Risk assessments, Deficiency reports, Non-Conformance reports.
Ensure adherence to regulatory standards and safety requirements.
Understand and stay updated on regulatory requirements for the industries we service (i.e., CLIA, FDA, etc.).
Responsible for receiving and maintaining accreditation from accrediting bodies (CLIA, A2LA).
Perform in-house analysis on QS products for potency - coordinating with manufacturing to satisfy testing needs and consulting with 3rd party testing laboratories.
Expand in-house analytical testing for supplements and in-house clinical testing.
Responsible for training staff on in-house potency testing methods and finalizing all potency reports.
Run tests as needed to support R&D and manufacturing problem-solving.
Curating and purchasing of new analytical instruments.
Maintain all instrumentation, perform repairs and/or coordinate with 3rd party for repairs as needed.
Proficiency in all basic laboratory and wet-chemistry skills.
Coordinate with and inform the laboratory director and founder of all laboratory progress, issues, and needs.