About this role
Employee Responsibilities:
Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques
Determine if data is compliant and defendable based on industry regulations and methodology
Verify data is of sound quality following all method, industry, and client requirements where applicable
Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area; perform complex calculations
Produce written reports (e.g., SOP, OMC, client reports)
The Ideal Candidate would possess:
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Familiarity with Microsoft Word, Excel, and Outlook
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Minimum Qualifications:
Bachelor's degree in biology or other related degree concentration, or equivalent directly-related experience
Authorization to work in the United States indefinitely without restriction or sponsorship Positions are full-time, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to Lancaster, PA are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance401(k) with company matchPaid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.