Responsibilities include, but are not limited to, the following:
· Perform non-routine analytical activities by independently developing and characterizing stability-indicating methods for early-phase pharmaceutical small to medium molecules with pre-set timelines using instrumentation such as, but not limited to, UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration
· Participate in technical discussions with project leads to recommend alternatives, research new methods/techniques and discuss potential solutions to problems.
· Plan critical laboratory experiments to investigate aberrant results, determine root cause and recommend action plan
· Write Standard Operating Procedures (SOPs), assist in generating technical reports, prepare data for presentations/technical discussions and transfer methods internally and externally
· Prepare method protocols, & technical reports for characterization of analytical methods based on separation techniques (HPLC, UPLC, GC), Spectro-analytical technique (Ultraviolet-Visible Spectrophotometry), and dissolution testing
· Assist and mentor junior-level scientists on analytical techniques and troubleshooting issues.
· Ensure project deliverables are scientifically accurate and meet timeline expectations
· Comply with all laboratory safety guidelines including Personal Protective Equipment (PPEs)
· Maintain general cleanliness of the lab, including personal bench space and common use areas
The ideal candidate would possess:
· Deep understanding of analytical sciences, drug development process, GMP/GLP requirements, and pharmaceutical industry trends
· Previous experience in pharmaceutical oral solid dosage & parenteral drug product analytical testing
· Good knowledge of three main pharmacopoeias (Japanese; JP, US; USP and European; Ph. Eur.) and ICH guidelines related to method development and validation
· Experience in developing pharmaceutical small molecules analytical chemistry methods for dissolution multi-media screening and analyzing data using compendial methods
· Understanding of experimentation and data analysis using Empower software
· Excellent project management skills; Ability to communicate complex scientific findings/recommendations and project resource requirements (material, manpower, time, etc.), and elevate relevant issues to project lead and line-management
· Excellent communication (oral and written), attention to detail, effective problem-solving and decision-making skills
· Ability to work independently and as part of a team with internal and external clients, 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
· Experience in exploration and application of innovative technologies/approaches to analytical development activities
· Experience with transfer of analytical technologies
· Ability to drive performance by tracking and managing key performance indicators using internal and external metrics
· Ability to prioritize complex workloads and manage changing priorities
· Proficiency in IT related skills such as Microsoft excel, word, PowerPoint etc
Basic Minimum Qualifications:
· Bachelor's degree in analytical chemistry, biochemistry, 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 a related major)
· At least ten years of related experience with separation science to support pharmaceutical oral solid dosage & parenteral drug product/substance analytical testing
Position is Monday- Friday 8:00 am- 5:00 pm. Overtime as needed. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
