Department: Small Molecule

Location: Middleton, Wisconsin

Details: Full time, fully onsite

This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.Must be legally authorized to work in the United States withoutsponsorship.Must be able to pass a comprehensive background check, whichincludes a drug screening.

As a Group Leader you will provide management and direction to laboratory staff and resources for project activities and needs, oversee daily operations to monitor quality and project timelines, and assist in preparation and implementation of company policies, quality systems and training programs. You will ensure responsiveness to the customer and overall, client satisfaction. Additionally, plans and monitor the progress and quality of projects by utilizing the financial and quality management tools available.

Essential Functions:

• Prepares, reviews and approves study protocols, project status reports, final study reports and other project-related technical documents.

• Designs experimental study and participates in technical troubleshooting.

• Reviews data for technical quality and compliance to protocols, methods and SOPs. Reviews and approves laboratory investigations, deviations, and QA facility and data audits. Leads client and FDA audits.

• Allocates, schedules and manages laboratory resources for group's project activities and updates project status. Reviews timesheet reports for billing accuracy.

• Responds to client's questions and needs; leads client technical meetings.

• Assists in preparation of proposals by provided project definition.

• Identifies new opportunities within client base and ability to work with business development to pursue opportunities.

• Coordinates and prioritizes project activities with internal functional groups (physical testing, analytical development, microbiology, etc.) and support functions (QA, sample management, etc.).

• Assists management in their responsibilities.

• Prepares and implements PPD SOPs and company operational policies. Ensures adherence and makes recommendations to quality system improvements.

• Bachelor's degree in lab sciences such as biology, biochemistry, immunology, chemistry, molecular biology or similar

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years9) or equivalent combination of education, training, & experience.

• 1+ years of management responsibility

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

• Proven leadership skills

• Demonstrated experience with performance management and process improvement

• Ability to cultivate a collaborative work environment with a team

• Effective negotiating skills

• Demonstrated knowledge of QA metrics of program base; ability to write and recommend changes to PPD SOPs

• Ability to troubleshoot multiple systems/methodologies

• Ability to independently optimize analytical methods

• Understanding of basic financial terms and definitions as it applies to the business

• Understanding of proposal and project scope as it relates to pricing, resource management and the impact on business

• Project and time management skills

• Effective written and oral communication skills as well as presentation skills

• Ability to train and mentor junior staff

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

• Able to work upright and stationary and/or standing for typical working hours.

• Able to lift and move objects up to 25 pounds.

• Able to work in non-traditional work environments.

• Able to use and learn standard office equipment and technology with proficiency.

• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.