Bachelor's degree in chemistry, biology, biochemistry, or related field with 3+ years of lab experience.
Experience in laboratory investigations and audit support.
Authorization to work in the U.S. indefinitely without restriction or sponsorship.
Responsibilities
Manage pharmaceutical microbiology testing, both routine and non-routine.
Coordinate sample collection and data entry for environmental monitoring in cleanrooms and labs.
Apply GMP/GLP principles to maintain quality standards.
Supervise team members to meet client requirements and turnaround times.
Conduct performance reviews and maintain training records for staff.
Develop and implement operational improvements to enhance productivity.
Communicate effectively with clients and support technical documentation.
Benefits
Comprehensive medical, dental, and vision coverage.
Life and disability insurance.
401(k) plan with company match.
Paid vacation and holidays.
Full 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
About Eurofins Lancaster Laboratories
Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
