Biotech Jobs in Fort Washington, Pennsylvania

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146 Fort Washington, PA Biotech jobs found on Monster.

Jobs 1 to 20 of 146
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...
Ensure quality and compliance in all my actions by:  Ensuring that the complaint records in the PQMS system contains all required information for an investigation to be conducted by the site.  Performing initial review of lot-specific alert limits.  Ensuring that alerts are entered into the PQMS system within the stipulated procedural timeline.  Ensuring that change logs are processed with...
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, Immunology-0636140321 Description Janssen Research & Development, L.L.C., a Johnson & Johnson Company is hiring an Associate Director, Immunology to be located in Springhouse, PA. Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worldwide. Resea...
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...
PerkinElmer is a global technology leader driving growth and innovation in the Environmental and Human Health Science markets. The company is a leading force in the development, production, marketing, servicing, and support of laboratory instrumentation and ancillary services throughout the world. PerkinElmer is searching for a Lead Lab Computing IT Service Engineer to join our OneSource team and...
SUMMARY OF POSITION: The Sr. Financial Analyst, Business Planning & Analytics (BP&A) is responsible to support all goals and objectives of the BP&A function. Reporting to the Sr. Manager or Director, BP&A, this resource will support key analytical and data quality functions, as well as supporting the development and growth of the BP&A reporting environment. The Sr. Assoc. BP&A will support the de...
SUMMARY OF POSITION: The Senior Proposal Analyst position is responsible to develop pricing and proposals for related client RFPs and any associated revisions. The Senior Analyst will lead and coordinate the associated RFP response activities with sales, Senior Management, functional departments and contract management. ESSENTIAL FUNCTIONS: The successful candidate will be responsible for leadi...
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 ...
Overview Do YOU have great ideas? Want to work in an environment that will nurture your professional development? Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is, today, a worldwide leading generic pharmaceutical company and one of the top 10 pharmaceutical companies in the world. As a forward-looking global pharmaceutical company, Teva...
Overview Do YOU have great ideas? Want to work in an environment that will nurture your professional development? Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is, today, a worldwide leading generic pharmaceutical company and one of the top 10 pharmaceutical companies in the world. As a forward-looking global pharmaceutical company, Teva...
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...
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...
Overview Do YOU have great ideas? Want to work in an environment that will nurture your professional development? Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is, today, a worldwide leading generic pharmaceutical company and one of the top 10 pharmaceutical companies in the world. As a forward-looking global pharmaceutical company, Teva...
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...
Must have: - Master's degree in epidemiology (or closely related discipline, such as public health or biological sciences) - Three years job related experience (e.g. clinical/epidemiology research), or equivalent experience a plus - Must have strong communication, organizational and project management skills - Pharmaceutical experience preferred Responsibilities: Under general supervision of...
Basic Qualifications: High School Diploma minimum 2 years manufacturing experience in the pharmaceutical or biotechnology industry Ability to work a production shift schedule of a 12 hours, work nights, and every other weekend. 12 hour shift: 5AM - 5PM or 5PM – 5AM Preferred Qualifications Associates or Bachelors Degree with less than one year prior manufacturing experience in the pharmaceut...
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...

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