EMINENT Services Corporation is a growing investigational drug management and information technology management services provider to pharmaceutical/biotechnology industry and the Government.
We are seeking motivated candidates for the following immediate full-time positions. Email your resumes to HR@emiserv.com (No Phone Calls).
| ID | TITLE | DESCRIPTION |
| J01 | Staff Pharmacist | Pharmacist License in the State of Maryland with at least 2 years experience. Responsibilities include clinical protocol review and monitor receiving, shipping, and patient specific packaging/labeling of Investigational Drugs. Knowledge of cGMP regulations is a must. Must be willing to serve on call. |
| J22 | Research Associate | Research Associate in Frederick City area. Implement Quality Assurance/Quality Control procedures and current good manufacturing and practice regulations. Develop familiarity with current Good Manufacturing Practice regulations and applicable Federal, State and Local regulations related to the operation of Biological Specimen Repository, Biological Research Laboratory and Packaging & Labelling operations. Coordinate semiannual physical inventories and assist in the preparation of protocols for clinical study products. Assist in the preparation of commercial batch records and execute the commercial labelling batch records as per GMP guidelines and deadlines for release of finished products to market. Organize and assist in the archival and retrieval of biological specimen while gaining a strong understanding of the ISBER best practices for biological repositories. Participate in Investigational Drug development programs and gain a deeper understanding of the field. Requirements: Bachelor’s in Pharmacy or related field and 2 years of experience. Alt Occupations: Technician. Mail resume to Anbu S. Devasahayam, EMINENT Services Corporation, 7495 New Technology Way, Frederick, MD 21703 USA, email: hr@emiserv.com. EOE. (Salary - $61,900). |
| J23 | Research Associate, Pharmaceutical Research Laboratory | Assist in investigational drug development programs, QA/QC, analysis, analytical methods & documents development. Preparation of specifications and test SOPs, calibrate analytical equipment's, prepare test protocols, and develop formulations. Experience in High Performance Liquid Chromatography (HPLC), Ultra-performance liquid chromatography (UPLC), Ultra Visible Spectro Photometer (UV), Fourier Transform Infrared Spectroscopy (FTIR), Autotitrator, Particle size analyzer, and SDS-Page analysis is required. Bachelors or equivalent in Chemistry or Pharmaceutical Science or related field, and 2 years' lab experience preferred. |
| J24 | Manager, Pharmaceutical Research Laboratory | Manage Pharmaceutical Research Laboratory, review analytical test, stability evaluation, method development, and instrument qualification protocols. Control the Laboratory Information Management System (LIMS) data entry; Check the LIMS data prior to QA/QC review. Check laboratory data for accuracy and approve test results. Manage laboratory technicians and research associates, plan and execute the analytical testing, stability evaluations, and method validations for the pharmaceutical products and bulk drug substances as per the approved protocols adhering to the cGMP (Current Good Manufacturing Practices). Review the results and approve the reports for method development and validation. Maintain and generate Standard Operating Procedures (SOP) for various Operations. Operate Ultra Performance Liquid Chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Ultra Visible Spectro Photometer (UV), Fourier Transform Infrared Spectroscopy (FTIR), Particle size analyzer, Dissolution test apparatus, Autotitrator and SDS Page Analysis. Masters or equivalent in Chemistry or Pharmaceutical Science or related field degree with minimum 3 years laboratory experience, or Bachelors with minimum 5 years of laboratory experience preferred. |