|Reference # :||18-01164||Title :||Assistant/Associate Scientist|
|Location :||East Syracuse, NY|
|Experience Level :||Start Date / End Date :||02/20/2018 / 08/19/2018|
The Syracuse Biologics Manufacturing operation produces clinical, commercial and launch biologics drug substance at its 5000L scale manufacturing facility (mammalian cell process) in Syracuse, NY
The role of the research scientist is to conduct experiments for the purposes of commercial support for downstream biopharmaceutical manufacturing and cold chain transportation. The candidate will support network bulk fill, freezing, storage and cold chain shipping operations for biologics drug substance. Responsibilities include the operation, cleaning and maintenance of laboratory equipment, preparation of buffers and reagents, documentation of experimental data and results, data verification and the preparation of study protocols and final reports. Appropriate GLP/GMP procedures must be followed. This position also involves troubleshooting and problem solving of process related problems observed at manufacturing scale through the effective design of scale-down studies and the evaluation of data from manufacturing lots. The successful candidate will work effectively in cross-functional project teams and also work independently to accomplish project goals. The position offers the opportunity to interface with Process Development, Manufacturing, Manufacturing Support, Quality Assurance, Analytical, Supply Chain and Global Regulatory Sciences groups. Strong communication and technical writing skills are required.
• B.S. degree in Pharmaceutical Sciences, Biological or Chemical Sciences/Engineering or related disciplines
• Knowledge of common protein analytical tools and demonstrated experimental skills for lab work are required.
• Knowledge of protein freezing/thawing, formulation and stability is desired.
• Knowledge of cold chain shipping qualification is desired.
• Process development, characterization, and/or validation experience are desired.
• Candidates must possess good organizational skills and strong attention to details, excellent experimental/troubleshooting aptitude, and be self motivated.
• Experience with cGMP regulations, regulatory requirements, and CMC authoring for biologics processes are a plus.
The candidate should also possess good verbal and written communication skills, as well as excellent interpersonal skills with the ability to work in a team environment
If interested, please contact:
212 258 2279
ECLARO is a company that delivers talent. We provide fully customizable, comprehensive talent acquisition and management of seasoned professionals through a number of business models, including: Consulting, Professional Hire, Global Integrated Delivery™ and Managed Services.
ECLARO recruits and manages a staff of highly skilled individuals in an array of specialized disciplines. This approach enables our clients to leverage new opportunities, respond to increased and changing demands and increase their profitability. Please visit www.eclaroIT.com to see why the Right People are The Answer™.
Specialties: Customized solutions for Human Capital and Talent Acquisition, Permanent placement and retained search, Recruiting, Staff Augmentation, Contract Labor, Managed Services, RPO, MSP, VMS, IT solutions, management and support, offshore business process outsourcing.
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
Industry: Staffing and Recruiting
Type: Privately Held
Company Size: 501-1000 employees