Chemistry Data Review- Sci II

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 SOPs 
• 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:

• Bachelors 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.

Remote Work :

No

Employment Type :

Full-time