Performing a large variety of analytical tasks for the development and validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution; reading, understanding, and interpreting diverse analytical procedures presented in a variety of written styles
Utilizes technical knowledge in the development of unique analytical methods (including researching projects via literature and internet)
Applies GMP/GLP in all areas of responsibility, as appropriate
Demonstrates and promotes the company vision
Regular attendance and punctuality
Read, understand, and follow the direction of analytical procedures (client and compendial) and internal SOPs
Utilize appropriate resources for information when developing analytical methods
Manage projects and discuss projects with clients when necessary
Perform laboratory operations with good dexterity, good laboratory techniques, and high degree of accuracy and precision
Document testing, observations, deviations, and results clearly and completely
Operate and maintain laboratory equipment, understand principles (theory) of laboratory instrumentation
Understand and perform calculations as required by test methods (some derivation of equations may be required)
Understand and utilize computers for information access, calculations, processing data, and report preparation
Lead projects and perform method development and validation utilizing a variety of analytical techniques, act as technical lead in conference calls with clients
Train others in laboratory procedures
Perform laboratory maintenance, communicate with vendors and repair personnel
Write investigations
Overcheck developmental and investigational work performed by other analysts
Self-teach new analytical procedures and computer programs
Write new SOPs and update existing SOPs
Conducts all activities in a safe and efficient manner
Performs other duties as assigned
The Ideal Candidate would possess:
Experience with MS instrumentation, such as, TOF or QTOF for the purpose of RNA/DNA and/or oligonucleotide identification/quantification
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
BS with 5+ years or MS with 3+ years or PhD with 3+ years in Chemistry or related field
Authorization to work in the United States indefinitely without restriction or sponsorship
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
As a part of Eurofins BioPharma Product Testing - the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide - Eurofins Lancaster Laboratories provides comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies. Our service offering includes comprehensive chemistry, biochemistry, microbiology, molecular and cell biology and biosafety testing of drug substances, final products, intermediates, and starting materials for both small and large molecule drug products.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com .
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
