Biotech Jobs in Malvern, Pennsylvania

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86 Malvern, PA Biotech jobs found on Monster.

Jobs 1 to 20 of 86
Alliance Pharma, Inc. is a contract research organization (CRO) specializes in bioanalysis, drug metabolism and DMPK support. We are currently seeking a QC specialist with a minimum of 4 years GLP bioanalytical experiences in CRO industry with Bachelor's Degree or higher. Advanced knowledge in specific compliance discipline (GLP, GCP),knowledge of the drug development process, regulation awarenes...
We are currently seeking a full-time Immunoassay group associate director whose responsibilities will include: * Managing a staff of bioanalytical scientists in the development/validation of PK and immunogenicity assays on standard and novel immunoassay platforms in a regulated environment. Analyzing non-clinical and clinical study samples and ensuring the scientific quality of data in order to m...
Responsibilities: The candidate will take a team role to develop and scale-up cell therapy process processes In this role, the candidate will develop processes, scale-up procedures, troubleshoot process scale-up issues and recommend procedures to improve the existing process The candidate may conduct development studies to identify and determine ranges of critical process parameters: media prep...
Alliance Pharma, Inc. is a contract research organization (CRO) specializes in advanced bioanalytical and drug metabolism services. We are currently seeking a QA specialist with a minimum of 4 years QA (Quality Assurance) and GLP bioanalytical experiences in CRO industry with Bachelor's Degree or higher. Advanced knowledge in specific compliance discipline (GLP, GCP),knowledge of the drug develop...
Eldredge, Inc. Plant Operations Center Job Title LLaboratory Chemist Qualification BS in Chemistry or Environmental Science, preferred Lab experience Role Summary Ensure compliance of all Responsible Care® Management System, codes and initiatives. Responsible for the analysis of all incoming waste to determine the treatability methodology to be used for processing the material in a safe and...
Job Title: Regulatory Labeling Consultant Position Responsibilities Lead relevant Company Core Data Sheets labeling teams; providing regulatory affairs labeling expertise and guidance to ensure successful development and update of CCDS. Lead regional labeling teams for EU SmPC and US PI. Provide labeling expertise to other regional labeling teams to facilitate the development and update of reg...
Job Title: Regulatory Affairs Manager Position Responsibilities Prepare, compile, review/quality control and process regulatory submissions including INDs, BLA, NDA, amendments/supplements, annual reports, study protocols, study reports, investigator brochures, safety reports, etc. Attend and participate in assigned project/regulatory product development and submission teams, providing clear an...
Senior Safety Scientist Essential Duties and Responsibilities Receives safety related information via telephone calls, faxes, e-mails, etc., from Sponsors, CROs, healthcare professionals, study coordinators, allied health personnel, patients, caregivers and other parties reporting potential adverse events Enters data into safety database Prepares draft MedWatch and CIOMS I forms Follows up on...
Abacus Service Corporation is a nation-wide staffing firm based out of Farmington Hills, Michigan that services Fortune 500 companies in varying industries across the US. Our client is looking for a Regulatory Affairs Manager in Wayne, PA. Job Title : Regulatory Affairs Manager Duration : 6 months contract (Possibility of an extension) Location : Wayne PA-19087 Job Description: Primary Duties...
Job Title: Regulatory Associate Position Responsibilities In collaboration with Global Regulatory Affairs Labeling staff, review potential differences between country labeling and Company Core Datasheets. Assess the clinical relevance of these differences, research company databases for documentation to support regulatory labeling submissions, and work with product teams to progress any require...
Job ID: JD-13 Date: 10/24/2014 Job Title: Quality Manager Department: Quality Reports To: Director of Quality and Regulatory Affairs Location: KOP, USA Summary of Position Quality Manager is responsible for ensuring that a product meets specific requirements for the company and its customers. Quality Manager handles legal compliances, customer expectations and coordinate activities in order ...
Job Title: GMP Monitor Position Description Assist the supervisor in coordinating monitoring activities to meet the needs of Quality Control and Compliance. Assume delegated responsibilities for group personnel training, authoring and review of Certificates of Analysis and Records of Analysis. Ensures proper documentation and compliance with cGMPs. Follow and work in accordance with company p...
Job Title: Associate Scientist Position Description Bench Scientist performing molecular biology techniques, such as RNA isolation, RT-PCR, immunoblot analysis and cell culture. Analyze and summarize experimental data using a variety of laboratory instrumentation and computer software. Skilled in the simultaneous maintenance of multiple mammalian cell lines. Responsible for following standard...
Saint-Gobain, the world leader in the habitat and construction markets, designs, manufactures and distributes building materials, providing innovative solutions to meet growing demand in emerging economies, for energy efficiency and for environmental protection. Saint-Gobain is a welcoming, solid, open-minded company that offers long-term career opportunities. About CertainTeed A subsidiary of S...
Saint-Gobain, the world leader in the habitat and construction markets, designs, manufactures and distributes building materials, providing innovative solutions to meet growing demand in emerging economies, for energy efficiency and for environmental protection. Saint-Gobain is a welcoming, solid, open-minded company that offers long-term career opportunities. About CertainTeed A subsidiary of S...
Summary of Position The primary purpose of this position is to develop and maintain the regional Labware Laboratory Information Management System or LIMS. The position creates and maintains procedures, configures and customizes the system and provides support and training to staff members. It is accountable for testing and documenting system changes as required by ISO standards. Geographically di...
Start: immediately, upon background check process completion Duration: five months/role could extend and/or become permanent Location: Wayne, PA 19087 DESCRIPTION This role is responsible for working individually or within a team of analysts and/or projects to improve and maintain business processes within various teams. Basic Qualifications A four-year degree, or the equivalent in work expe...
Seeking candidate with expertise developing clinical trial strategies for innovative therapies focused in immunology. Our pharmaceutical company focuses on advanced research developing new products for a myriad of health conditions. Your responsibilities include leading a team of clinical affairs personnel and providing medical expertise to prescribers, providers, and regulatory authorities. Othe...
TechData Service is a top staffing company with openings for contract positions with many pharmaceutical companies in the NJ, CT, MA and PA areas. We work with many companies to place clinical, IT, and professional positions with many large pharmaceutical clients. Often times we can help you with the specific company where you would like to work. We are available for career discussions to determin...
Johnson & Johnson companies are equal opportunity employers. Senior Product Development Engineer, Trauma-8185141028 Description DePuy Synthes, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Product Development Engineer, Trauma to be located in West Chester, PA. DePuy Synthes is a Johnson & Johnson company that is one of the leaders in the medical device industr...

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