Entry Level Chemist- Package Testing

Eurofins; Lancaster, Northern (Lancaster County, KY); Hybrid; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Medical Devices in Lancaster, PA, is seeking a full-time laboratory analyst to support GMP/GLP compliant testing of bio/pharmaceutical ingredients and products.

The role involves preparing standards, reviewing data for accuracy, operating instruments, and generating reports while delivering high-quality data under supervision or guidance. Training, teamwork, and commitment to safety are essential on this 2nd/3rd shift position.

Qualifications

• Bachelor's degree in microbiology, biology, biochemistry, or related field with no industry laboratory experience
• Authorized to work in the US indefinitely without restriction or sponsorship
• Med device experience is a plus

Responsibilities

• Applies GMP/GLP and maintains quality in all responsibilities.
• Reviews and prepares standards and samples; operates equipment independently when trained.
• Documents data and deviations clearly in compliance with regulatory requirements.
• Performs calculations and uses computer tools for reporting.
• Reads procedures and SOPs; uses Excel/Word/Outlook for communication.
• Maintains safety, housekeeping, and equipment; supports overtime as needed.
• Demonstrates strong teamwork and client service

Skills

GMP/GLP compliance

Analytical lab techniques

Data analysis

Attention to detail

Communication skills

Education

Bachelor's degree in microbiology, biology, biochemistry, or related field

Tools

MS Windows

Excel

Word

Outlook

Job 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

**Please note this position is a 4/10 schedule on 2nd or 3rd shift**

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 and promotes the company vision
• Demonstrates strong client service skills, teamwork, and collaboration
• Proactively plans and multitasks to maximize productivity
• 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
• Understand and perform calculations as required by test methods
• Understand and utilize computers for information access, calculations, and report preparation
• 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
• Communicate effectively, both orally and in writing
• Independently seek out work
• Perform laboratory maintenance
• Commitment to occasional overtime as workload requires
• Conducts all activities in a safe and efficient manner
• Ensures good housekeeping with a neat, clean and orderly workspace
• Performs other duties as assigned
• Communicates effectively with client staff members

Qualifications

Minimum Qualifications:

• Bachelor's degree in microbiology, biology, biochemistry, or related degree concentration and noindustrylaboratory experience
• Authorized to work in the US INDEFINITELY without restriction or sponsorship
• Med device experience is a plus

Additional Qualifications:

• good work habits (organized, efficient, careful, safety-concious, accurate)
• sound scientific logic
• good oral and written communication skills
• understanding of instrumentation
• client service focused
• demonstration of organizational skills
• ability to work with moderate supervision upon training completion on assigned task
• ability to handle multitasking

Additional Information

Working schedule will beFull-Time, Second or Third Shift, Sun-Wed or Wed-Sat, 2pm-12am or 12am-10am.Candidatescurrently living within a commutable distance of Lancaster, PAare encouraged to apply. No relocation assistance will be given.25% travel may be required. This position isNOTremote.

• 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 Medical Devices is a Disabled and Veteran Equal Employment Opportunity employer.