Eurofins

Global lab testing and analytics network

Group Leader 2 Microbiology

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeIndianapolis, IN, USANo salary listed

About the Job

Requirements

A bachelor's degree in chemistry, biology, biochemistry, or a related degree concentration and at least 3 years of laboratory experience.
Experience conducting laboratory investigations and supporting audit responses.
Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

Manage routine and non-routine pharmaceutical microbiology testing.
Coordinate sample collection, data entry, and team operations for environmental and utility monitoring programs in cleanrooms, laboratories, or industrial settings.
Apply Good Manufacturing Practice and Good Laboratory Practice principles and maintain quality standards in all areas of responsibility.
Ensure the quality policy program is understood, implemented, and maintained; identify and correct departures from the quality system.
Supervise assigned employees in performing work and meeting client requirements; coordinate workflow and monitor daily operations to meet turnaround times.
Conduct semi-annual performance reviews, interview applicants, maintain training records, and develop succession plans for assigned employees.
Coach, train, and develop team members to maximize performance and support effective implementation of operational improvements.
Develop and implement operational improvements; continually evaluate systems and processes to enhance productivity and quality.
Apply technical knowledge of instrumental and analytical theory; troubleshoot and resolve technical and method issues.
Communicate with client staff members and support the writing of investigations to strengthen technical documentation.
Monitor and approve employee time entries; address performance issues and foster team motivation and morale.
Expand leadership skills through applicable training; perform functions in compliance with state and federal employment regulations and safety requirements.
Perform additional duties as assigned to ensure smooth department operations.

Job Description

Management of pharmaceutical microbiology testing (routine and non-routine):
Coordinates sample collection, data entry, and team operations for environmental and utility monitoring programs in cleanrooms, laboratories, and or industrial settings.
Apply GMP/GLP principles and maintain the highest quality standards in all areas of responsibility
Ensure the quality policy program is understood, implemented, and maintained; identify and correct any departures from the quality system
Supervise assigned employees in performing work and meeting client requirements; coordinate workflow and monitor daily operations to meet turnaround times
Conduct semi-annual performance reviews, interview applicants, maintain training records, and develop succession plans for assigned employees
Coach, train, and develop team members to maximize performance and support effective implementation of operational improvements
Develop and implement operational improvements; continually evaluate systems and processes to enhance productivity and quality
Demonstrate strong technical knowledge of instrumental and analytical theory; troubleshoot and resolve technical and method issues
Communicate effectively with client staff members and support the writing of investigations to strengthen technical documentation
Monitor and approve employee time entries; address performance issues and foster team motivation and morale
Expand leadership skills through applicable training; perform all functions in compliance with state and federal employment regulations and safety requirements
Perform additional duties as assigned to ensure smooth department operations

Qualifications

Bachelor's degree in chemistry, biology, biochemistry, or related degree concentration and at least 3 years of laboratory experience
Experience in conducting laboratory investigations and supporting audit responses
Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

This is a full-time position, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to Indianapolis, IN are encouraged to apply.

Excellent full time benefits including:

Comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

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