Senior Scientific Group Lead - QA & Mentorship

Eurofins USA BioPharma Services

Lancaster (Lancaster County)

On-site

USD 95,000 - 130,000

Full time

8 days ago
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Benefits offered by this job

Life and disability insurance
401(k) with company match
Paid holidays and vacation
Dental and vision options

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking a Scientific Group Leader II to oversee a quality-focused team and ensure cGMP compliance. You will lead, mentor and coach staff, manage workflow, and drive continuous improvement in a fast-paced environment.

The role requires a Bachelor’s degree in chemistry/biology/biochemistry or related field and at least 2 years of supervisory experience in a cGMP setting.

Qualifications

  • Bachelor’s degree in chemistry, biology, biochemistry or related degree concentration.
  • Minimum of 2 years of experience in supervisory experience in a cGMP environment.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

  • Ensure that the quality policy program is understood, implemented, and maintained; identify, prevent, or correct any departures from the quality system
  • Enforces safety policies across all areas of responsibility
  • Perform laboratory tasks as required to deliver on department objectives
  • Monitor and control cost
  • Perform all functions in support of and in compliance with all state and federal employment regulations
  • Communicates effectively with client staff members
  • Conducts all activities in a safe and efficient manner
  • Performs other duties as assigned
  • Foster a positive and professional work environment
  • Communicate a clear vision and motivate staff to excel
  • Monitor and approve employees’ time worked through time-entry system
  • Follow communication plan policy for regular meetings as directed by your business unit
  • Coach, train, and develop others within the group with respect to their personal development to maximize performance
  • Manage workflow and perform daily monitoring to meet customer service needs and KPI
  • Conduct semi-annual performance reviews and interview applicants
  • Ensure data integrity record keeping to maintain compliance
  • Confront and address problems, concerns and performance issues in real time
  • Expand self-awareness and develop leadership skills as defined; attend applicable leadership training based on identified needs
  • Effectively delegate and exercise accountability of self and others
  • Mentor direct reports toward successful higher-level development/promotion
  • Perform succession planning in preparation for growth of team and self
  • Customer Service: Independently act as technical lead in calls/audits for non-escalated issues
  • Numeracy: Review and approve quotes as role requires. Identify and take action when pricing is inaccurate
  • Comprehensive understanding of instrumental and/or analytical theory for all technical disciplines they oversee and provides support beyond own team
  • Independent accurate impact assessment of data, with recognition of which issues require escalation to upper management for awareness
  • Lead investigations independently through technical writing, root cause analysis, robust CAPA, and complete impact assessment for on time closure
  • Continually evaluate systems and processes, making adjustments to help improve overall productivity, efficiency and quality in the department
  • Propose and lead new LEAN initiatives in the department and support LEAN initiatives in the division

Skills

Supervisory experience in cGMP

Education

Bachelor’s degree in chemistry/biology/biochemistry or related field

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking a Scientific Group Leader II to oversee a quality-focused team and ensure cGMP compliance. You will lead, mentor and coach staff, manage workflow, and drive continuous improvement in a fast-paced environment.

The role requires a Bachelor’s degree in chemistry/biology/biochemistry or related field and at least 2 years of supervisory experience in a cGMP setting.

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