JOB TITLE: Food Scientist DEPARTMENT: Product Development Status Level: Exempt ACCOUNTABILITY: Vice-President of Technical Services JOB SUMMARY: Provide technical service and support to ou...

JOB SUMMARY: Provide technical service and support to our customers and internally to Manufacturing, Sales, Marketing, Purchasing and Quality Control as required to generate and maintain sales to Industrial and Food Service accounts; and train and provid...

JOB TITLE: Senior Food Scientist – Meat Specialist DEPARTMENT: Product Development Status Level: Salary ACCOUNTABILITY: Vice President of Technical Services JOB SUMMARY: Provide technical service an...

McCormick & Co., Inc., a global leader in the spice, flavor & seasonings industry, is seeking a full time Senior Research Chef in its World Class Technical Innovation Center (TIC), located at 202-204 Wight Avenue in Hunt Valley (Baltimore), MD. This posi...

Reg. Full-time Description: Essential Duties and Responsibilities: Ability to follow assay protocols including assay calculations and dissection of tissue; perform all basic lab functions including but not limited to dilutions, general solutio...

Major Duties and Responsibilities (including supervising others): Perform formulation development, optimization, product characterization and stability studies of protein therapeutics. Design and execute experiments to support preformulation, form...

Major Duties and Responsibilities (including supervising others): Design and perform protein formulation stability and characterization studies to support the development of therapeutic protein products. Assist in development of methodologies for ...

This is a paid 6-month internship position, beginning immediately. Those seeking summer internship only need not apply. Major Duties and Responsibilities (including supervising others): • Assist in the formulation development, optimiza...

Position Summary: This position will provide technical, operational, and strategic leadership for the Biological Analysis group within the Analytical Biochemistry department. Technical areas include: bioassay, immunoassay, PCR, and biosensor method develo...

Major Duties and Responsibilities (including supervising others): MedImmune has a new Scientist II / Senior Scientist position in the Protein Characterization Group within the Analytical Biochemistry Department. The successful candidate will provid...

MedImmune, Inc. has a new opportunity for a Scientist I/II in the Mass Spectrometry Group within the Analytical Biochemistry Department. The successful candidate will provide bio-analytical support for Research and Development. The responsibilities includ...

MedImmune has a new opportunity for an R&D Associate I/II in the Bioassay Group within the Analytical Biochemistry Department in Gaithersburg. The successful candidate will play an important role in the development, qualification and validation of cel...

The successful candidate will be responsible for the characterization of protein biopharmaceuticals in preclinical/clinical development. The candidate will perform routine characterization assays, and assist in the development, optimization, and validatio...

MedImmune has a new opportunity for an Associate Scientist II/Scientist I in In-process Testing Group within the Analytical Biochemistry Department. The successful candidate will utilize chromatographic and spectroscopic methods to support biopharmaceutic...

MedImmune is committed to advancing science to develop better medicines that help people live healthier, longer and more satisfying lives. The company has meaningfully impacted the health of millions of children and adults by developing products that meet...

The Training Specialist III (TS III) position will support the Medical Organization Training and Standards Department (MOTSD) team in delivery of quality training services to the Medical Organization (MO). This position will provide for all MO Functional ...

Major Duties and Responsibilities: o Review and track documents for the Trial Master File o Proficient in current Clinical Trial Management System o Schedule project and group meetings o Create meeting agendas and assist in...

The Regulatory Writing Operations Associate is responsible for providing quality control (QC) review of clinical regulatory documents developed within the Medical Writing group, and for providing other operational support as needed. Major Duties an...

Primary responsibilities will include participating in special projects to effectively assist the Medical Organization with key decision support in managing the business operations, oversight of the Medical Organization invoice process, tracking, reportin...

The Manager, CRPS is responsible for planning for and managing all aspects of Clinical Trial Material preparation, distribution & reconciliation as well as budgeting for CTM-related clinical trial costs. This person is responsible for multiple trials ...

The Director /Senior Director of Training provides technical and organizational leadership, oversight, and direction for the design, development and implementation of training functions and activities to achieve the Medical Organization’s goal to be...

Position Summary: The Clinical Supply Specialist II (CSS II) coordinates the packaging & labeling activities required to provide Investigational Product (IP) for clinical trials in time for scheduled First-Patient-In (FPI) date. This person is also re...

Major Duties and Responsibilities: o Lead operational activities for multiple trials o Lead multiple cross functional project teams o Manage all CRO activity for assigned trials o Plan and lead Investigator Meetings ...

Major Duties and Responsibilities: o Lead operational activities for multiple trials o Lead multiple cross functional project teams o Manage all CRO activity for assigned trials o Plan and lead Investigator Meetings ...

The Central Services Associate I supports the Clinical Study Teams with a special emphasis on study start up activities and CTMS support. Major Duties and Responsibilities: • Contributes to the clinical study team through all stu...

Major Duties and Responsibilities (including supervising others): The MedImmune Clinical Research and Development Intern will gain a hands-on experience of working in a clinical research and development biotechnology company. The 10-12 week intern...

The Director/Senior Director, Clinical Development, Oncology will be based in Gaithersburg, Maryland, and reports to the Vice President and Therapeutic Area Head of Oncology. The Director/Senior Director will have full responsibility for the planning, imp...

The Clinical Scientist will work under the supervision of the Medical/Clinical Research personnel (Clinical Leader, Medical Director, or Senior Clinical Scientist) to assist in the preparation of Investigational New Drug Applications (INDs), Clinical Deve...