Biotech Jobs in Fort Washington, Pennsylvania

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140 Fort Washington, PA Biotech jobs found on Monster.

Jobs 1 to 20 of 140
Johnson & Johnson companies are equal opportunity employers. ASSOC DIR CLIN PHARMA/PHARMACOKINETICS-9892140505 Description Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies, Inc., is recruiting for an Associate Director, Clinical Pharmacology/Pharmacokinetics located in Fort Washington, PA. McNeil Consumer Healthcare markets a broad range of well-know...
Corporate Summary: Established in 1972, Nutrisystem Inc. (NASDAQ: NTRI), was founded on the principle of helping people change their lives and is now the leading provider of home-delivered weight loss meal plans. Nutrisystem offers balanced nutrition in the form of low glycemic index meal plans designed for men and women, including seniors, vegetarians and the Nutrisystem® D® program for people wi...
Johnson & Johnson companies are equal opportunity employers. Scientific Director, Discovery Immunology (IBD)-1719140529 Description Janssen Research & Development, L.L.C., a Johnson & Johnson Company is hiring Scientific Director to be located in Springhouse, PA to provide oversight of a group within the Immunology therapeutic area with a focus on driving innovative new approaches in drug disco...
Johnson & Johnson companies are equal opportunity employers. Associate Scientific Director, PK/PD Modeling-9659140429 Description Janssen Research & Development, L.L.C., a Johnson & Johnson company, is recruiting an Associate Scientific Director to be located in Spring House, PA. Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwi...
Johnson & Johnson companies are equal opportunity employers. Head of Clinical Development, Cell Therapy-0392140514 Description Janssen Research & Development is currently recruiting for a Head of Clinical Development for the Cell Therapy group to be located in Spring House, PA. Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide...
ePharmaSolutions is a leading eClinical trial software provider to the life science industry. Our continued growth is leading to the expansion of our Product and Portfolio Management Team. As an eClinical Product Manager, you will work closely with clients and internal teams to lead the development of ePharmaSolutions’ next generation Electronic Trial Master File (eTMF) and Investigator Site File ...
Requirements: - BS Life Sciences or Healthcare (or equivalent experience) - 1-2 Years of experience in Regulatory Affairs for a pharmaceutical company (may consider candidates coming from quality background too) - Experience with eCTD preferred - Experience working for a CMC group within Regulatory Affairs , preferably in the generic pharmaceutical industry, working with parenteral drug applic...
SAS Administrator – Full time Perm Opportunity in Horsham, PA For additional information please email your resume to ***** Install, maintain, and support SAS enterprise applications and ensure high level of SAS application availability. In addition, responsibilities include providing technical support to SAS developers and may include implementing additional functionality to sup...
The Director, USOR has the primary responsibility for planning and managing outcomes research (OR) activities for in-line and developmental drugs that are prioritized by the US Market Leadership Team. This includes all phases of outcomes research including design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic mode...
If you have extensive experience interpreting clinical trial protocols for the purpose of establishing and designing documentation requirements for a Trial Master File system, learn more about how you can be a part of ICON’s Document Management group that’s responsible for verifying clinical trial documentation is consistent with the TMF specifications, applicable SOPs, ICH/GCP guidelines and othe...
Feasibility Manager ICON is looking for a strategic expert to manage the process of clinical project feasibility as a part of our global team based in US. Key Responsibilities: • To perform as technical expert in feasibility process for internal and external clients and to provide strategic input to Business Development Operations to Sponsors through Bid defence and supervision of other feasibi...
Company Overview: At Quaker Chemical, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. Since 1918, we have been an integral part in the growth of the world’s largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worl...
Pharma client seeks Scientific Associate II - Microbial Molecular Biology for a 6 month contract. Responsible for implementing and optimizing experimental protocols in the areas of virology, molecular biology, serology, and cell biology. Previous experience with influenza, tissue culture, virus propagation and titration, antibody cloning, and conducting serological and cellular-based assays (eg. ...
Under the guidance of an Executive Director, Global Health Outcomes (GHO), the Director, Outcomes Research has the primary responsibility for planning and managing Outcomes Research activities for in-line and developmental Respiratory products and devices. Responsibilities include and are not limited to the following: All phases of outcomes research including design and implementation of retrosp...
Under the guidance of an Executive Director, Global Health Outcomes (GHO), the Director, Outcomes Research has the primary responsibility for planning and managing Outcomes Research activities for Osteoporosis. Responsibilities include and are not limited to the following: All phases of outcomes research including design and implementation of retrospective database studies, assessment of patient...
The Quality Control Technician is responsible for the analysis of manufacturing samples to a standard test method and escalation of issues to management. Records and maintains product analysis data. Contributes effectively to the team, meeting both team and personal objectives as set. Immediately communicates out of specification test results. And assists in resolving internal non-conformances. E...
Lyophilization Technology, Inc. (LTI), established in 1992, is a unique Contract Development and Manufacturing Organization enjoying a leadership position in the health care and related industries. The company conducts applied research, provides scientific services and technical support, and manufactures clinical supplies for freeze dried pharmaceuticals, biologics, diagnostics, biopharmaceuticals...
ESIS HSE will be the preferred provider of HSE consulting and compliance services in the unbundled market while maintaining our underwriting and loss control capabilities to support ACE. Our relentless focus on the customer experience will build our brand preference. Our customers will describe us as customer-focused, experienced, flexible, creative, and efficient. KEY OBJECTIVE: Provide superio...
Position Overview: The Clinical Program Leader is responsible for all aspects of clinical delivery for a portfolio of the client accounts and projects. S/he is responsible for clinical quality, clinical timelines, clinical task oversight, and clinical team performance across his/her assigned portfolio for the full project life cycle. The Clinical Program Leader will proactively build and maintain...
Saint-Gobain is the world's largest manufacturer and distributor of building materials, and a leader in the production of high-performance materials and glass containers with more than 1,000 subsidiaries in 64 countries. Saint-Gobain was founded in 1665 and is headquartered in Paris, France. Saint-Gobain had sales of $55.5 billion in 2012 and employs nearly 193,000 people worldwide. ABOUT CERTAIN...

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