About this role
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 analysisTechnical 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 skillsAbility to Multi-task and to make decisions when required.Excellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivation, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesStrong leadership, initiative, and team building skillsBasic 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.