Group Leader - Bioanalytical LCMS Assay Services - M - F Second Shift

Work Schedule

Monday to Friday, 2:30 p.m. – 11:00 p.m. EST (Second Shift – Afternoons).

Environmental Conditions

• Able to lift 40 lb without assistance.
• Cold room/freezers: –22 °F (–6 °C).
• Office environment.
• Use of personal protective equipment (safety glasses, gowning, gloves, lab coat, ear plugs, etc.).
• Work with hazardous/toxic materials.

Location & Eligibility

This is a fully onsite role in the bioanalytical laboratory at 8700 Quioccasin Road, Richmond, VA. Applicants from any U.S. location may apply; relocation assistance is not provided. Candidates must be legally authorized to work in the United States without sponsorship and must pass a comprehensive background check, including a drug screening.

Key Responsibilities

• Provide management and direction to laboratory staff and resources for project activities.
• Oversee daily operations to monitor quality and project timelines.
• Assist in preparation and implementation of company policies, quality systems, and training programs.
• Ensure responsiveness to customers and overall client satisfaction.
• Plan and monitor progress and quality of projects using financial and quality management tools.
• Prepare, review, and approve study protocols, status reports, final study reports, and other technical documents.
• Design experimental studies and participate in technical troubleshooting.
• Review data for technical quality and compliance with protocols, methods, and SOPs.
• Review and approve laboratory investigations, deviations, and QA facility and data audits.
• Lead client and FDA audits.
• Allocate, schedule, and manage laboratory resources for project activities and update project status.
• Review timesheet reports for billing accuracy.
• Respond to client questions, lead technical meetings, and assist in proposal preparation.
• Identify new opportunities within the client base and collaborate with business development.
• Coordinate and prioritize project activities with internal functional groups and support functions.
• Assist management in their responsibilities and implement PPD SOPs and operational policies.
• Recommend and ensure adherence to quality system improvements.

Education & Experience Requirements

• BS degree + 8 years of experience (including ≥1 year of people‑management responsibility), OR
• MS degree + 6 years of experience (including ≥1 year of people‑management responsibility), OR
• PhD + 3‑5 years of experience (including ≥1 year of people‑management responsibility).
• Equivalency may be considered based on a combination of education, training, and directly related experience.

Knowledge, Skills, and Abilities

• Proven leadership and ability to cultivate a collaborative work environment.
• Effective negotiating skills.
• Knowledge of QA metrics and ability to write/recommend changes to SOPs.
• Troubleshooting of multiple systems/methodologies.
• Independent optimization of analytical methods.
• Understanding of basic financial terms as they apply to the business.
• Understanding of proposal and project scope related to pricing and resource management.
• Project and time‑management skills.
• Strong written, oral, and presentation communication skills.
• Ability to train and mentor junior staff.

Work Environment

• Thermo Fisher Scientific supports employee health and wellbeing.