Eurofins Lancaster Laboratories

Technical Manager

Eurofins Lancaster Laboratories • $80K — $90K *
Groton, CT 06340In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
1 month ago
Job Overview by Ladders

Qualifications

  • M.S. or Ph.D. in Pharmaceutical Sciences, Chemistry or related field.
  • 3+ years of GMP/GLP laboratory experience (3 years with M.S. or 2 years with PhD).
  • 3+ years in formulation of solid dosage forms or pharmaceutical drug product development preferred.
  • 2+ years of demonstrated independent leadership experience.
  • Strong scientific, organizational, and reasoning skills with attention to detail.
  • Proficient communication skills, both oral and written.
  • Self-motivated and adaptable, able to prioritize under shifting demands.

Responsibilities

  • Lead teams to foster collaboration and high morale.
  • Deliver technical contributions through hands-on lab research.
  • Train employees on safety and quality for efficient lab operations.
  • Utilize operational tools to manage and optimize laboratory resources.
  • Ensure compliance with quality standards and GMP/GLP regulations.
  • Track and report key performance indicators (KPIs) for productivity.
  • Maintain positive relations with clients and ensure superlative service.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
Full Job Description
Job Description

In this position, you will perform hands-on laboratory experiments, balancing technical bench work with team leadership and operational management responsibilities.
  • Leads teams (Group Leaders and Direct Reports) serving clients in a laboratory setting and requires a strong laboratory presence. Provides role model leadership that fosters high morale and collaboration.
  • Delivers technical contributions through hands on research to advance projects and initiatives. Serves as a technical expert in the lab generating data.
  • Ensures proper training of all employees to ensure safety, quality, productivity, teamwork, and client service. Organizes inter-team cross-training to ensure service continuity.
  • Uses Operational Excellence and Lab Management tools (ie training and capabilities matrices, standard Day and capacity/resource planning tools, etc.) to ensure efficient laboratory operations. Uses tools to organizes technical resources and staff to accomplish client goals within given deadlines. Monitors and adjusts resource allocation across teams.
  • Ensure adherence to highest quality and efficiency standards in laboratory operations. Applies GMP/GLP in areas of responsibility; as appropriate.
  • Tracks key KPIs including quality, safety, training and service metrics to ensure teams are meeting productivity and quality standards.
  • Fosters positive client relations by interfacing effectively with clients and staff to create a superlative service culture.
  • Continuously seeks to improve processes and efficiencies. Manages process improvement and cost savings initiatives.
  • Oversees performance management and development of staff. Manages employee development and cross-training plans for staff.
  • Manages communications between clients, group leaders, and other cross-functional groups. Facilitates meetings and disseminates administrative communications.
  • Leads and manages recruiting for areas of responsibility.
  • Demonstrates and promotes the company vision. Ensures compliance with company policies and contributes to the overall success of the organization.
  • Communicates regularly with Regional Manager/Director for update on operations.
  • Manages to ensure compliance with all laws and prevention of co-employment.
  • Performs other duties as assigned.


Qualifications
  • M.S. or Ph.D. in Pharmaceutical Sciences, Chemistry or other related degree concentration.
  • M.S. 3+ years of relevant GMP/GLP laboratory experience or PhD, 2+ years of relevant experience within the pharmaceutical industry.
  • 3+ years formulation of solid dosage forms experience or 3+ years pharmaceutical drug product development experience preferred.
  • 2+ years of successful independent leadership experience, including team succession planning, developing and managing schedules, establishing, monitoring and reporting KPIs and metrics.
  • Strong scientific, computer, organizational skills, and reasoning skills, including logical thinking and deductive reasoning.
  • Excellent communication (oral and written) and attention to detail.
  • Ability to work independently and as part of a team, self-motivated, and adaptable. High energy and positive approach to situations and interactions.
  • Able to prioritize and able to quickly adapt to shifting priorities.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.


Additional Information

The position is full-time, Monday-Friday, 8:00am-5:00pm, with overtime as needed.
  • Target Compensation: $80-90k
  • 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.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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