Biotech Jobs in Rockville, Maryland

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144 Rockville, MD Biotech jobs found on Monster.

Jobs 1 to 20 of 144
Overview Teva Pharmaceuticals USA is recruiting a highly talented individual to be responsible for assay development, validation, and execution to support the development of biologics and synthetic peptides within the Global Bioassay and Technology group in West Chester, PA. Broad experience with a variety of biological in-vitro systems is required. Prior experience in assay validation, and techno...
Overview Teva Biopharmaceuticals, USA (TBU) is responsible for developing innovative and biosimilar biologics for Teva Pharmaceuticals—the largest generics company in the world. Located in Rockville, MD the staff of 75, specializes in biologics CMC and bioassay development. We have a range of products in various stages of clinical development from IND through BLA filing including, innovative mAbs,...
Overview The successful candidate will plan and execute the pharmaceutical development activities in area of Formulation Development and Container Closure System (Extractables and leachables and container closure integrity) for early and late phase candidates in Teva biologic pipeline. PLEASE NOTE: Our Rockville site will be relocating to West Chester, PA in the third quarter of 2015. The candidat...
Responsibilities Lead and/or support mammalian and microbial cell culture process development leading to commercialization of recombinant therapeutic proteins Design and execute cell culture studies in laboratory and in pilot plant, either individually or in team Perform process optimization and process characterization Author technical reports for documentation of development activitie Maintain a...
Health, Education, and Social Programs Public Health and Survey Research Rockville, Maryland About ICF International If you want to work on the leading issues of the day, if you want your work to reflect your passion in life, if you truly want to make the world a better place, then you want to work at ICF International. Whether ensuring efficient use of energy resources, protecting the environment...
Director, Promoting the Quality of Medicine Programs Job Description The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug...
Health, Education, and Social Programs Public Health and Survey Research Rockville, Maryland About ICF International If you want to work on the leading issues of the day, if you want your work to reflect your passion in life, if you truly want to make the world a better place, then you want to work at ICF International. Whether ensuring efficient use of energy resources, protecting the environment...
Health, Education, and Social Programs Survey Research Washington, DC Metro area, Boston Metro or NYC Metro About ICF International If you want to work on the leading issues of the day, if you want your work to reflect your passion in life, if you truly want to make the world a better place, then you want to work at ICF International. Whether ensuring efficient use of energy resources, protecting...
MSN's client is seeking a Clinical Research Associate II/III with CRO experience! The ideal candidate should have experience working in the Oncology or Pediatrics. Position Summary: Incumbent contributes to the preparation of study protocols, informed consents, case report forms, and study support documents (manuals, training tools, diary cards, source document worksheets). Collects and reviews es...
MSN's client is seeking a Laboratory Operations Assistant for their Rockville, MD location. Major duties and responsibilities: General Inventory & Vendor Oversight Monitor inventory quantities to determine if inventory levels are sufficient and monitor expiring materials to minimize company losses Receive, open, unpack, and re-stock shelves as appropriate Adjust inventory levels to reflect product...
QC Scientist III – Microbiology Lead ABL is seeking to hire a QC Scientist III – Lead Microbiologist for Hands-on performance and oversight of a GMP environmental monitoring (EM) program which includes HVAC (ISO classes 5, 7 and 8), purified water and compressed gases systems in a Quality Control Laboratory in a GMP facility that produces biopharmaceuticals (vaccines, biologics, viral vaccines, mo...
REMOTE, PERMANENT CLINICAL PROJECT MANAGER WITH CNS AND CRO EXPERIENCE Position Summary: Seeking a project manager who has CRO experience with experience managing project budgets/timelines etc. Project Manager acts as liaison between site, vendor, sponsor, clinical staff, and other departments (e.g. BCDM, Regulatory, QA, Pharmacovigilance) for the management and coordination of all aspects of assi...
MSN's client is seeking a Administrative Assistant to provide support to Development (includes Manufacturing, Cell Culture Sciences, Purification Sciences, Analytical Sciences, and Drug Product Sciences) Quality (includes Quality Assurance and Quality Control) and Regulatory Affairs Applicants must meet the following requirements: BA/BS degree preferred Minimum of five years of experience providin...
Sr. Staff Scientist, Upstream Process Development ABL is seeking to hire a Sr. Staff Scientist, Upstream Process Development to provide scientific ideas and technical expertise in protein purification for the GMP manufacture of protein products. Context of the Job and Major Challenges: As leader of the Upstream Process Development effort, the Senior Staff Scientist – Upstream will be accountable f...
MSN's client is seeking a Product Safety Specialist for their Rockville, MD site. The selected candidate will be responsible for (including supervising others): Management of CRO or contractor safety staff, as appropriate, to ensure that safety-related project milestones are met within required timelines. Ensuring complete case compilation by acquisition of all relevant event information, data ent...
The Director, PQM Programs is a leadership position within the Global Health Impact Programs department. It is responsible for strategizing, planning, organizing, directing and overseeing the implementation of programmatic and operational activities as part of the Promoting the Quality of Medicines program (PQM) cooperative agreement (HRM-A-00-00-00017-00) in accordance with the U.S. Agency for In...
Director, Promoting the Quality of Medicines Program The Director, PQM Programs is a leadership position within the Global Health Impact Programs department. It is responsible for strategizing, planning, organizing, directing and overseeing the implementation of programmatic and operational activities as part of the Promoting the Quality of Medicines program (PQM) cooperative agreement (HRM-A-00-0...
Regulatory Submissions Publishing Associate At Workforce Integration - Wi? - we know people are the key to successful organizations. So we have concentrated on getting people down to a Science. Ask us Wi? Our client is seeking a Regulatory Submissions Publishing Associate to work out of their Rockville, MD location. This role is critical to the company's continued success. Major duties and respons...
Regulatory Submissions Publishing Associate At Workforce Integration - Wi? - we know people are the key to successful organizations. So we have concentrated on getting people down to a Science. Ask us Wi? Our client is seeking a Regulatory Submissions Publishing Associate to work out of their Rockville, MD location. This role is critical to the company's continued success. Major duties and respons...
MSN's client is seeking a Regulatory Operations Associate to perform Word and PDF publishing and formatting of regulatory submission documents to ensure that they meet style and publishing guidelines. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Provide support and technical assistance for formatting of regulatory submission documents • Format Word documents by applying appropriate styles/templates •...
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