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Technical Manager

Eurofins
Posted 4 days ago, valid for 7 days
Location

New London, CT 06320, US

Salary

$80,000 - $90,000 per year

Contract type

Full Time

Life Insurance
Disability Insurance

By applying, a Eurofins account will be created for you. Eurofins's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

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  • Eurofins Lancaster Laboratories is seeking an experienced team member for their Professional Scientific Services team, focusing on laboratory experiments and team leadership.
  • Candidates should have an M.S. with 3+ years or a Ph.D. with 2+ years of relevant GMP/GLP laboratory experience in the pharmaceutical industry.
  • The role involves leading teams, ensuring safety and quality, and managing operational efficiency while fostering positive client relations.
  • The target compensation for this full-time position is between $80,000 and $90,000 annually, with excellent benefits included.
  • The position requires strong scientific and organizational skills, effective communication, and the ability to work independently as well as part of a team.

Company Description

Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry.  Celebrating over 55 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.

Eurofins Lancaster Laboratories, a nationally recognized laboratory, is seeking a highly motivated, experienced, team member to work in our Professional Scientific Services team.

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

 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

  • Compensation: USD 80000 - USD 90000 - yearly



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    By applying, a Eurofins account will be created for you. Eurofins's Privacy Policy and Terms & Conditions will apply.

    SonicJobs' Terms & Conditions and Privacy Policy also apply.