Job Description

Perform various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing/preparing standards and samples for analysis and running a variety of equipment or instrumentation independently; troubleshoot and solve instrumental and/or method problems; working efficiently; ensuring that client received quality data by reviewing laboratory data for accuracy, clarity and adherence to GMP and/or GLP regulations; evaluate current systems and suggest process improvements when appropriate; write complete and detailed investigations independently; support multiple projects simultaneously; demonstrate leadership qualities and train newer analysts.

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.
• Perform routine, non-routine and complex analyses; instrumental analyses; including calibration and troubleshooting/repair of instruments independently
• Demonstrate the ability to multitask
• Perform all work independently
• Serve as a trainer for newer analysts
• Review/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
• Demonstrate technical writing skills and initiate/support completing investigations
• Demonstrate desire to learn independently, including new analytical techniques and nonroutine analyses
• Demonstrate leadership qualities including;
  • Effective communication
  • Display confidence
  • Demonstrate motivation and take initiative
  • Follow through on assignments
• Process/review data, generate/review reports, and evaluate data
• Communicate effectively, both orally and in writing
• Independently seek out work
• Perform laboratory maintenance if required
• Support and drive LEAN initiatives
• 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 Chemistry or related science
• 2 year experience in a GMP lab setting
• Authorization to work in the US without immediate or future sponsorship.
• Good dexterity
• Positive attitude
• Solution driven
• Good work habits (organized, efficient, careful, safety-conscious, accurate)
• Attention to detail
• Sound scientific logic; good oral and written communication skills
• Understanding of instrumentation and/or instrumental theory
• Client service focused
• Personal maturity
• Demonstration of organizational skills
• Ability to work with moderate supervision upon training completion on assigned task
• Ability to handle multitasking
• Technical writing skills

Additional Preferences:

- Experience operating or reviewing data from chromatography, HPLC, GC.
- Experience with method development and validation testing
- Experience with Empower
- Experience with wet chemistry

Additional Information

Working schedule will be Full-Time, First Shift, M-F 8am-5pm, weekend availability required. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 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.