SEARCH CAREER OPPORTUNITIES

GENERAL SUMMARY OF POSITION: 

The Research Associate I is responsible for carrying out downstream process development activities, supporting the development and optimization of downstream processes as well as performing scale up and scale down studies.  The incumbent will contribute to scale down comparability and virus clearance studies for the production of monoclonal antibodies to support product discovery, process development and assay development activities.  The Research Associate I will also be involved in the technical transfer of processes to the manufacturing group.

MAJOR RESPONSIBILITIES:

• Operates and maintains standard laboratory and department-specific equipment.
• Prepares buffers, packs chromatography columns, carries out purification experiments, and makes detailed observations.
• Performs analytical biochemistry assays and other laboratory testing as required.
• Keeps timely and accurate documentation per cGMP, GLP, and MBL SOPs in notebooks and in electronic documents.
• Coordinates with other group members to maintain and organize assay request and data entry on common projects.
• Analyzes experimental data and provides accurate, concise and pertinent summaries and reports.
• Provides support for protocol writing, project summaries and technical reports.
• Prepares written and oral reports for presentation to the supervisor(s) and development group.
• Maintains reagent and equipment inventories, orders supplies and cleans laboratory areas, hoods and common equipment.
• Exercises technical discretion in the design, execution and interpretation of experiments that contribute to project strategies within defined parameters. 
• Perform additional job related duties as required.

REQUIRED QUALIFICATIONS:

• Requires a bachelor’s degree in Chemistry, Biology, or related field with a minimum 0-2 years of relevant experience
• Ability to follow instructions precisely, recognize deviations, and recommend corrective action within scope of training
• Ability to troubleshoot within scope of training
• Computer literate and proficient in MS Word, Excel and other relevant electronic systems
• Strong critical thinking, time management and organizational skills.  Demonstrated ability to manage and prioritize multiple projects and consistently meet deadlines
• Possesses strong attention to detail, ability to maintain accurate records and excellent proofreading skills
• Excellent written and verbal communication skills. Ability to communicate effectively with others
• Ability to work effectively both independently and as a member of a team
• Occasionally projects require flexibility in work schedule to meet business needs

• Working knowledge on protein purification and hands-on experience on chromatography workstations preferred