BioProcess Analytical Chemist
Job Description
The Purification Process Development (PPD) group is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development.
We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the group in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing.. Knowledge and expertise in analytical biochemical techniques including real-time qPCR, ELISA, fragment analysis, HPLC, and capillary gel electrophoresis (CGE)are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects.
** Job Responsibilities and Requirements:**
Experience with protein chemistry, protein analytics, and bioprocess technology is required
Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process
Hands on experience and working knowledge on techniques including but not limited to RT-qPCR, spectrophotometry, liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), ELISA, CGE and SDS-PAGE are preferred
A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred
Work closely with colleagues by providing quality data to support product development through all clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data
Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices
Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices
Qualifications
4-6 years of relevant experience
Experience with RT-qPCR, ELISA, and fragment analysis
Ability to follow established procedures independently and be accountable for prioritizing own workflow to meet defined metrics and timelines
Strong oral and written communication skills
Additional Information
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Andover, MA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.