Malvern
Biotech Jobs in Malvern, Pennsylvania
142 Malvern, PA Biotech jobs found on Monster.
Johnson & Johnson companies are equal opportunity employers. Senior Contracts & Grants Analyst-7846130508 Description Janssen Pharmaceutical Research & Development, L.L.C., a member of the Johnson & Johnson Family of Companies, is recruiting for a Senior Contracts & Grants Analyst located in either Malvern PA, Spring House PA, Raritan NJ or Titusville NJ. Janssen Rese...
Consider joining Eurofins Lancaster Laboratories, Inc. where people are the most important element in our chemistry. Celebrating 50 years of service, Eurofins Lancaster Laboratories, Inc. is a leading contract lab providing testing and research services in the pharmaceutical and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, Inc., a nationally recognized laborato...
Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating over 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized labor...
Environmental Chemist / Executive Management Track Position Environmental Standards, Inc., a leader in developing innovative solutions to client environmental liabilities, has an Environmental Chemist (non-laboratory) position available at our Valley Forge, PA office. Since our inception in 1987, we have enjoyed long-term relationships with Fortune 500 companies and continue to provide high-qualit...
Leading pharma client seeks a Clinical Data Manager/Sr Manager for a long term contract opportunity. The primary responsibility of the Data Management (DM) Outsourcing Project Leader is to lead and manage DM tasks outsourced to external vendors and ensure that milestones, deliverables, quality and timelines are met within budget and in accordance with regulatory requirements to support innovative...
Position Summary: Auxilium is seeking an Senior Biostatistician to join the Clinical Development team in our Chesterbrook office. The Senior Biostatistician will provide all aspects of design and statistical analyses and reporting on clinical development projects and ensure timely completion of statistical analyses and reports. PLEASE APPLY FOR THIS POSITION VIA OUR WEBSITE: https://home.eease.com...
The Senior Manager/ Associate Director, Data Management is responsible to ensure data management activities for clinical trials within assigned research program(s) are completed in a timely and accurate manner and lead the evaluation and implementation of data management technologies, processes, sourcing, strategies and business relationships. Leads and manages DM tasks outsourced to external vend...
This is a contract position with possibility of going full-time SUMMARY OF POSITION: Responsible for all phases of pilot scale catalyst preparation and execution of laboratory experiments. Skilled in the preparation of a broad range of catalyst types. Also responsible for efficient organization of his/her own time, careful documentation of all experiments and preparations, and compliance with all...
SUMMARY OF POSITION: Johnson Matthey’s research and development activities are focused on improved catalyst performance and operational efficiency. This position will support the definition of experimental approaches, conduct and coordinate experimental work, analyze results, complete documentation, and ensure that process & washcoat rheology control of catalyst formulations is optimized, understo...
This position will report to the Associate Director - Environmental, Health, and Safety and will based at the Wayne, PA laboratory. The position has responsibility for overseeing all aspects of environmental, health and safety programs related to central laboratories globally and for facilitating a collaborative approach to implementing such programs with site management. Prior lab experience is h...
Senior Clinical Statistical Programmer Description: Minimum of a Bachelors degree, Masters Preferred Minimum 8 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries The Clinical SAS Programmer creates SAS programs in support of sponsors clinical trials according to SOPs and guidelines. This programmer will create, document, validate...
Basic Qualifications: 1. Minimum 5 years in pharma working on clinical trials 2. Minimum of a Ph.D. in statistics 3. Minimum 5 years experience using SAS The Sr. Statistician will be responsible for the following: " Participate in the design and review of clinical protocols and case report forms including preparation of statistical sections, sample size calculations, randomization, and study desig...
Basic Qualifications: 1. Minimum 1 years in pharma working on clinical trials 2. Minimum of a Masters in statistics 3. Minimum 1 years experience using SAS The Statistician will be responsible for the following: " Participate in the design and review of clinical protocols and case report forms including preparation of statistical sections, sample size calculations, randomization, and study design...
Develop and enhance applications based on specifications. Codes and tests according to design specifications. Skilled in coding, testing, and implementing configuration changes to software applications to meet both functional and technical requirements. Unit test applications and develops system and user documentation.Some responsibility over other developers with less experience. Minimum of a Bac...
FUNCTION: Serve as primary expert in inorganic analysis of customer samples. Provide technical leadership, evaluate and institute new technologies relevant to qualitative and quantitative analysis , manage projects, provide technical assistance within and external to the department. ACCOUNTABILITIES: 1. Perform IC, ICP-OES and ICP-MS analysis of raw materials, polymers, polymer related samples, an...
Quality Control Reviewer Provides timely and accurate review of test records generated in cGMP testing on both hard copy test records and/or the electronic data for release, stability, validation and qualification purposes. •Provide periodic review of instrumentation log and reference standards logs. •Compile and prepare documentation records for QA final review and archiving. •Additional responsi...
JOB TITLE: Absorption Systems is an industry-leading biopharmaceutical contract research organization currently seeking an Associate Scientist/Scientist to work with our Molecular and Cellular Biology teams in our Exton, PA facility. Description: Absorption Systems is seeking a motivated individual with a strong science background in Molecular and Cellular Biology and Life Sciences to join a team...
Company Information Fibrocell Science Inc. is an autologous cellular therapeutic company focused on the development of innovative products for aesthetic, medical and scientific applications. Fibroblasts are responsible for the production of collagen and contribute to the formation of connective tissue fibers. We believe that these cells have a broad application. Our vision is to develop and bring...
Get referred to this job Schedule: Full-time Organization: Business Process Outsourcing (BPO) Service Delivery Operations Location: Wayne, PA Individuals within the BPO Service Delivery Operations (SDO) provide clients with proven solutions, proprietary software assets and industry best practices to deliver an outsourcing solution at a fraction of the cost required to run the process in house. The...
Absorption Systems is an industry-leading biopharmaceutical contract research organization currently seeking a Associate Scientist for it’s Exton, PA facility and reports to the Associate Director, Pharmacokinetics and Bioanalysis Absorption Systems is seeking a motivated individual with a strong science background (biology or chemistry) to join a team involved in the bioanalysis of preclinical in...
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