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Quality Assurance Group Leader

Eurofins Scientific

Lancaster, PAFull-timeNo compensation foundPosted 4w agoVerified open 6 days ago

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At a glance

Compensation
No compensation found
Location
Lancaster, PA
Schedule
Full-time
Work Authorization
US work authorization required

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Eurofins Scientific is hiring a Quality Assurance Group Leader. The Quality Assurance Group Leader will delegate responsibilities, provide support and feedback to direct reports, and prioritize employee development through cross-training and goal communication. This role involves coaching direct reports, interacting with other departments to ensure quality data, and supporting management initiatives to improve quality and productivity. The leader will also perform higher-level QA tasks including investigation writing, root cause analysis, and data trending.

Key focus areas include Delegate responsibilities and project ownership to direct reports, Provide follow-up, support, and constructive feedback for delegated tasks, and Make employee development a top priority.

Successful candidates bring Bachelor’s Degree In Biology/Chemistry Or Equivalent Experience, 2-3 Years Laboratory Experience, and 4-5 Years High-level Laboratory Experience. Preferred (not required): Delegate Responsibilities, Project Ownership, Provide Follow-up, and Provide Support.

Skills & qualifications

RequiredNice to have

Skills

Delegate ResponsibilitiesProject OwnershipProvide Follow-UpProvide SupportConstructive FeedbackEmployee DevelopmentProject Cross TrainingDepartment Cross TrainingTechnical Skills DevelopmentJob PlansCommunicate ExpectationsCommunicate GoalsCoach Direct ReportsReal-Time FeedbackInteract With Other DepartmentsEducate Other DepartmentsProfessional BehaviorSupport Upper ManagementImprove Quality MetricsCAPA ImplementationInvestigation WritingInvestigation ReviewRoot Cause AnalysisDocumentationTechnical ReviewTracking Action ItemsDriving to CompletionIdentify Trends in Recurring EventsEffective CommunicationDisplay of ConfidenceMotivationFollow Through on AssignmentsData TrendingData AnalysisSupplier AuditsInternal AuditsValidation WritingValidation ReviewChange Control WritingChange Control ReviewBatch Record ReviewEM Report ReviewAssist With Agency InspectionsReview QAU ProceduresWrite QAU ProcedurescGMP Quality Systems21 CFR Part 21021 CFR Part 211EU GMP AnnexComputer Skills

Qualifications

Bachelor’s Degree in Biology/Chemistry or Equivalent Experience2-3 Years Laboratory Experience4-5 Years High-Level Laboratory ExperienceExperience in Regulated IndustriesAuthorization to Work in the United States

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Employee Responsibilities:

  • Delegate responsibilities and project ownership to direct reports.  

  • Provide follow-up, support, and constructive feedback for delegated tasks.

  • Make employee development a top priority – project/department cross training, technical skills development, involvement/ownership, job plans in place, expectations/goals clearly communicated. 

  • Be available and coach direct reports though challenges, without doing the work for them.  

  • Provide direct reports with constructive, positive feedback for continuous improvement and development.  

  • Provide real-time feedback. Interact with and/or educate other departments (technical and support) to ensure that Eurofins, as an organization, is providing quality data in a timely manner that meets the clients needs.

  • Demonstrate professional behavior and support upper management in initiatives to improve quality/productivity.  

  • Work with the laboratory and support groups to improve quality metrics, and enable CAPA implementation.  

  • Also support the technical and supports groups with investigation writing and review, including thorough root cause analysis

  • Technical writing and review; tracking action items and driving to completion; ability to identify trends in recurring events.

  • Demonstrate leadership qualities such as: effective communication, display of confidence, motivation, and follow through on assignments.

  • Perform higher level QA tasks including but not limited to: major investigation writing/review, in-depth root cause analysis, data trending/analysis, supplier audits, internal audits, validation/change control writing/review, batch record/EM report review, assist with agency inspections, review/write QAU procedures. The ideal candidate would possess   :

  • Familiarity with cGMP Quality Systems (21 CFR Part 210, 211, EU GMP Annex)

  • Strong computer, scientific, and organizational skills

  • Ability to Multi-task and to make decisions when required.

  • Excellent communication (oral and written) and attention to detail

  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude

  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

  • Strong leadership, initiative, and team building skills Basic Minimum Qualifications   :

  • Bachelor’s degree in Biology/Chemistry with a minimum of 2-3 years experience in the laboratory or a minimum of 4-5 years of experience in the laboratory at a high level of performance (if possessing no degreee)

  • Experience in regulated industries (Pharmaceuticals, Medical Device) Biologics)

  • Authorization to work in the United States indefinitely without restriction or sponsorship Position is Full-time, Monday-Friday, 8:00 a.m.-5:00 p.m. , with overtime as needed.  Candidates currently living within a commutable distance of Lancaster, PA  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.

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