Entry Level Microbiology Technician- 2nd Shift

EurofinsEurofinsLancaster, Pennsylvania, United States
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Posted

9/9/2026

Employment

Full time

Range

Check website

Work style

On-site

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Core responsibilities

The technician will perform laboratory analyses of bio/pharmaceutical ingredients while ensuring compliance with GMP and GLP regulations. Responsibilities include preparing samples and reagents, documenting results, and maintaining laboratory equipment and workspaces.

Requirements overview

Candidates must have a high school diploma or equivalent and some laboratory experience or college coursework. The role requires the ability to work on-site in Lancaster, PA, without the need for visa sponsorship.

Key skills

MicrobiologyGMPGLPAseptic techniqueLaboratory operationsData analysisReagent preparationSample preparationMicroscopyBiological safety cabinetsTechnical documentationLaboratory maintenanceMicrosoft ExcelMicrosoft WordAttention to detailTeamwork

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Education requirements

high school

About Eurofins

Industry

Medical and Diagnostic Laboratories

Employees

242

Type

Public Company

Size

201-500 employees

It’s so much more than a specimen. It's a life. With over 30 years of specialized expertise in infectious disease, immunology, transplant, and allergy testing for immunocompromised and critical patients, Eurofins Viracor is committed to helping medical professionals, transplant teams, reference labs and biopharmaceutical companies get results faster, when it matters most. Eurofins Viracor is passionate about providing timely, actionable test results, never losing sight of the connection between the testing we perform and the patients our results ultimately serve. Find out more by visiting us at www.eurofins-viracor.com/clinical Eurofins Viracor is an equal opportunity employer.

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Job categories

Science & ResearchManufacturingHealthcare

Description

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description This role is Second Shift 3pm-11pm Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Demonstrates strong client service skills, communicate effectively, both orally and in writing Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Regular attendance and punctuality Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision Perform/Review preparations of reagents, samples, and standards according to procedures. Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors Read and understand analytical procedures (compendial and client supplied) and internal SOP's Use MS Windows applications such as Excel, Word, Outlook email Process data, generate reports, and evaluate data Perform laboratory maintenance and maintain clean workspace Commitment to occasional overtime as workload requires Qualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. Minimum Qualifications: High School diploma or equivalent and some lab experience/college courses Ability to work in the US without immediate or future sponsorship Microscopes and biological safety cabinets Media preparation Organism/culture preparation Aseptic technique Additional Information Working schedule will be Full-Time, Second Shift, M-F 3pm-11pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote. What we Offer: 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.

Requirements

  • Microbiology
  • GMP
  • GLP
  • Aseptic technique
  • Laboratory operations
  • Data analysis
  • Reagent preparation
  • Sample preparation
  • Microscopy
  • Biological safety cabinets
  • Technical documentation
  • Laboratory maintenance
  • Microsoft Excel
  • Microsoft Word
  • Attention to detail
  • Teamwork

Benefits

  • Comprehensive medical coverage
  • Dental options
  • Vision options
  • Life insurance
  • Disability insurance
  • 401(k) with company match
  • Paid vacation
  • Paid holidays

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