Biotech Jobs in King of Prussia, Pennsylvania

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187 King of Prussia, PA Biotech jobs found on Monster.

Jobs 1 to 20 of 187
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...
Primary Duties:  Work with the Global Medical Team leader , neuroscience to develop and execute multi-year global medical strategy for the specified Product/Disease Area, appropriately aligned with overall strategy and incorporating R&D functional strategies (clinical, regulatory, HEOR, PV, compliance)  Work with the Global Medical Team leader, neuroscience on the development and in-year imple...
Primary Role Work with the Global Medical Team leader , neuroscience to develop and execute multi-year global medical strategy for the specified Product/Disease Area, appropriately aligned with overall strategy and incorporating R&D functional strategies (clinical, regulatory, HEOR, PV, compliance) Work with the Global Medical Team leader, neuroscience on the development and in-year implementati...
Position Title : Manager Regulatory Affairs CMC Location: Chesterbrook, PA Duration: 6+ months Position: 2 Under the guidance of the Director of Regulatory Affairs, manage Regulatory Affairs activities for execution of global CMC strategies for investigational and marketed products in all regions, especially EU and International regions. Lead the preparation and filing of CMC sections for regu...
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. ...
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...
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 ...
Please note this a 8 months contract position Skills: Clinical manufacturing environment, Biopharmaceutical/ or Pharma Industry Performs out of specification (OOS), out of trend (OOT), laboratory events and deviations, environmental monitoring events, atypical event and non-conformance investigations for the Malvern site. These investigations include, but are not limited to Remicade drug substan...
Johnson & Johnson companies are equal opportunity employers. Associate Director, Bioassay Methods Development-2408140602 Description Janssen Research & Development, LLC., a Johnson and Johnson Company is hiring an Associate Director, Bioassay Methods Development to be located in Malvern, PA. Janssen Research and Development , LLC develops treatments that improve the health and lifestyle of peo...
Company: Yoh Safety Physician needed for a contract opportunity with Yoh's client located in Collegeville, PA area. What You'll Be Doing: - Provides high level medical expertise in the safety evaluation and risk management of key assets or other highly complex products in clinical development and/or the post-marketing setting - Ensures that adverse event and other safety information is efficie...
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...
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 s...
Overview The Manager/Sr. Manager, Promotional Review & Labeling will be primarily responsible for the regulatory review of advertising and promotional materials for assigned products within the Teva pharmaceuticals portfolio. The portfolio includes products in the respiratory, CNS, oncology, pain, and women’s health therapeutic areas. Overview Do YOU have great ideas? Want to work in an environ...
Responsibilities: Excellent employment opportunity for a Scientist in the Malvern, PA area. The scientist will be part of a team effort to provide cell banking services to PDMS, other R&D customers, company Chain and other clinical and commercial manufacturing sites. The scientist will perform cell culture according to Standard Operating Procedures using Good Manufacturing Practices. Primary r...
Validation Engineer (Malvern, PA) pi is seeking an experienced candidate with strong eye for detail who can perform activities related to the qualification and life-cycle management of computerized lab instruments and mechanical equipment in an analytical laboratory in a pharmaceutical GMP facility. The role will require excellent interpersonal skills, and the ideal candidate must be able to deve...
Requirements: - Bachelor's Degree in Scientific discipline or equivalent work experience - Prefer RAC certification - 3+ years experience in FDA regulated industry - Working knowledge of Medical Device Regulations (FDA required, international a plus) - Demonstrated direct interaction with FDA reviewers/inspectors - Demonstrated interpersonal, written, oral, communication, organizational and ...
Eurofins is the world leader in the food, bio/pharmaceutical product testing. It is also number one in the field of environmental laboratory services and one of the global market leaders in agroscience, genomics, discovery pharmacology, and central laboratory services. With over $1 billion in annual revenues and 13,000 employees across 170 sites in 35 countries, Eurofins is a leading international...
Contractor Environmental Monitoring Specialist (CEMS) Must have: Education: • Bachelor's degree in Microbiology or Biology is preferred. Candidates with BS in Chemistry, Engineering, Pharmacy, or equivalent will be considered with relevant experience in environmental monitoring, laboratory operations, or sterile/vaccine production setting. Required Experience and Skills: • At least one year o...

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