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                        Biotechnology & Pharmaceuticals industry jobs

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                        Brief Description Onyx Pharmaceuticals has an immediate opening for an AP Manager! Position will manage all aspects of the accounting processes for accounts payable. Primary responsibilities will involve managing the accounts payable process, including payment of vendor invoices and processing of T&E payments. This individual will play a key role in overseeing the department and implementing effic...
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                        Work Location: Not Applicable Shifts: 2nd Positions Available: 1 Position Summary Under general supervision of the Warehouse Supervisor or other supervisory/management-level position within the facility, responsible for performing a variety of warehouse-related duties such as receiving and storage of goods, preparing orders for shipment by picking items from shelves and placing them in totes, and ...
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                        As a member of the Vertex GIS team, the Project Manager/Business Analyst is responsible for managing IT driven projects and process improvements, including documentation of business requirements, functional specifications, project charter, business case and project tracking. PM/BA will work with all areas of marketing including Digital Marketing, HCP Marketing, Patient Marketing, Patient Services ...
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                        Join the CLIA laboratory that is dedicated to improving healthcare through revolutionary genetic analysis solutions. The rapidly growing Sequenom Center for Molecular Medicine is on the forefront of ground-breaking clinical diagnostic tests. Sequenom Center for Molecular Medicine, a wholly-owned subsidiary of Sequenom, is a CAP accredited and CLIA-certified specialty reference laboratory dedicated...
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                        NATURE AND SCOPE: Responsible for advanced network administration, applies advanced network knowledge, principals, theories, concepts and industry practices. Follows industry standards to analyze requirements, coordinate the installation, testing and problem resolution of the company’s voice and data communications. In depth knowledge of local area networks (LAN’s), wide area networks (WAN’s), dem...
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                        Hollister Inc - Boston, MA (1 hour ago)
                        ACCOUNTING MANAGER - Prestigious Global Firm Job Number: 72357 ACCOUNTING MANAGER - Prestigious Global Firm Job Description: We are searching for a sharp and detail oriented Accounting Manager to who will (along with Corporate Controller) lead the core accounting, financial reporting and consolidation services, and the preparation of financial statements for the numerous company entities and partn...
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                        Assistant Buyer Primary Responsibility: Strong organizational skills and the ability to prioritize and multitask are essential. Primary responsibilities will be assisting the Procurement Agent with administrative tasks including: placing routine orders, sourcing information, processing returns, data entry, generating reports, creating spreadsheets, order follow up/tracking, and communicating with ...
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                        An opportunity exists for an exceptional individual in the area of biopharmaceutical product performance. Wolfe Laboratories conducts rational formulation development that leverages a molecular understanding of the pharmaceutical and biopharmaceutical attributes for the delivery of drugs, including poorly soluble drugs, via conventional and non-conventional oral formulations as well as complex par...
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                        An international biopharmaceutical company is seeking a Medical Writer to join their Clinical Development Team. The successful candidate will research, write, and edit complex documents for submission to regulatory agencies and for publication and presentations to meet the objectives of Clinical Research and Development. This is a full-time position and outstanding opportunity to join a dynamic te...
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                        Position Summary: The Sr. Specialist, GMP Quality Assurance will perform a wide array of Quality Assurance activities focusing on quality compliance as defined by Cubist Quality procedures in support of early/late phase/ commercial active pharmaceutical ingredient (API) and drug product (DP) manufacturing (including secondary packaging and labeling activities). Candidate should have experience wor...
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                        Lead Financial Analyst - Planning R&D Business Unit: Sandoz - United States Division: Sandoz Company/Legal Entity: USA Sandoz Inc Princeton NJ Job Reference Code: 98444BR Financial Responsibilities • Maintain financial responsibility for the D&R organization and serve as a key finance resource through: Forecasts - Provide timely, accurate and well planned financial forecasts that enable management...
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                        Position Summary: The Engineer III will primarily collaborate with other Cubist departments for the scale-up and engineering of processes and the management of technology transfer to Contract Manufacturing/Research Organizations (CMO/CRO) for both pipeline and commercial products. The candidate will effectively collaborate with other Cubist departments within and outside Tech Ops (e.g. Regulatory,...
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                        Sandoz, a global leader in the rapidly growing generics industry, is a company in which doctors, pharmacists and patients worldwide have placed their trust for more than 100 years. With our 23,000-plus employees in more than 130 countries, we save and improve lives by developing, producing and distributing high-quality, affordable pharmaceuticals. Choosing Sandoz is always "a healthy decision". Th...
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                        Position Summary: Responsible for the development of manufacturing processes for pharmaceutical drug product, technology transfer and phase 3 clinical productions at contract manufacturing organizations. This includes planning and managing the implementation of drug product processes for registration, validation and commercial launch. Provide technical support for drug products at either the comme...
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                        Responsibilities include: Medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of regional contract CRAs, and organizes the files and budgets associated with several clinical studies. Provides medical support which may include: Adverse Event Reporting - the investigation and reporti...
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                        Our client, a global leader in the pharmaceutical industry is seeking a Administrative Assistant I to join the Cambridge, MA location Under limited direction and on own initiative, provides a variety of advanced secretarial and administrative functions for the office of the Division Head. High working knowledge of Outlook Works closely with Division Head Executive Assistant. Makes travel arrangeme...
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                        JOB SUMMARY: We require a highly motivated Research Scientist to work on protein stability & aggregation as it relates to therapeutic protein development. The current project is designed to understand the fundamental mechanism/s of protein instability, sub-visible particulate formation and aggregation using variety of chromatographic, biophysical and biochemical tools. DUTIES AND RESPONSIBILITIES:...
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                        Smith Hanley Consulting Group - Telecommute(2 hours ago)
                        Position Overview Perform and coordinate all aspects of the clinical monitoring process in accordance with GCP and global SOP to assess the safety and efficacy of investigational products and/or medical devices. Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation. Represents company in the global medical research community and develops collabor...
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                        Contract hire will be responsible for testing and interpreting results for raw materials, active pharmaceutical ingredients, finished pharmaceutical products, and stability samples. With an expertise in laboratory techniques commonly used in the analysis of pharmaceutical products, this position will help to ensure that suitable methods are in place to evaluate samples using equipment to analyze, ...
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                        Validation Engineer Specific experience in Cleaning Validation, including CIP and SIP is highly preferred! Duties: Field execution of commissioning, qualification, and validation related activities at the direction of field supervision (project leader and/or project manager) and client. Duties include but are not limited to preparation, execution, and review of protocols, standard operating proced...
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                        The successful candidate will facilitate compliance with DEA regulations for the company’s controlled pharmaceuticals and regulated list 1 chemicals. Other responsibilities include but are not limited to: o Quarterly reports and other documentation as needed per DEA requirements. o Training appropriate personnel regarding DEA regulations. o Conducting periodic audits of manufacturing and respectiv...
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                        Position Summary: The Director, International Markets and Clinical Supply Chain Management will serve as the primary point person in Technical Operations for the supply chain organization for all CMC projects. This supply chain leader will collaborate across Tech Ops and partner organizations in identifying, developing and implementing supply chain strategies for pipeline products. In addition, th...
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                        Our client is looking for a Safety Surveillance Scientist for a 7+ month position in Thousand Oaks, CA. Position Description: To provide medical and safety input into the clinical scope, review criteria, analysis and interpretation of safety data. To develop and execute the safety surveillance strategy for product candidates/products in clinical development programs/approved products. To support t...
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                        DESCRIPTION: · Performs a variety of qualitative and quantitative analytical assays to support raw material, in-process, intermediate and final product testing according to standard operating procedures and regulatory requirements. · Performs laboratory operations necessary to support testing, such as reagent preparation/qualification, equipment and assay troubleshooting. Analyzes results and noti...
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                        Position Summary: Under the direction of the Sr. Director, Supply Chain, the Manager, PPIC will be responsible scheduling of all CMO's within Cubist's manufacturing network and management of inventory levels in support of corporate goals. Minimum Basic Qualifications: B.S. Degree in Business Administration, Supply Chain, or Life Sciences A minimum of 7 years experience in pharmaceutical or biotech...
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