Information and Records jobs in the Biotechnology & Pharmaceuticals industry

Records Management Specialist: Position Summary: Ensure records are controlled and managed in a compliant manner throughout their life cycle including storage and archiving, and that the record management system meets the requirements of Genzyme procedures as well as current regulatory requirements and industry practices. Provide customer service and assistance for users needing information or acc...
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Provides medical information with high quality customer service. Researches and responds to inquiries and documents appropriately according to PPD and client guidelines. Identifies and records adverse events (AEs) and product complaints (PCs). If needed, provides clinical trial information, after-hours on call support, as well as processes medical information requests via mail, fax, e-mail. Educat...
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SynteractHCR is a full-service contract research organization (CRO), dedicated to meeting the various clinical development needs of the biotechnology, medical device, and pharmaceutical industries. We have provided clinical trial services on several hundred studies on over 40,000 patients to over 80 commercial clients, including all phases and across a wide range of therapeutic areas, such as onco...
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Johnson & Johnson companies are equal opportunity employers. Senior Counsel, eDiscovery-8348130517 Description The Johnson & Johnson Law Department is recruiting for a Senior Counsel, eDiscovery at Johnson & Johnson World Headquarters located in New Brunswick, NJ. Caring for the world, one person at a time, has inspired and united the people of Johnson & Johnson for 125 years. We embrace research ...
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GENERAL SUMMARY: This is a temporary position, with full-time hours during the summer. This position is characterized by the performance of a variety of administrative and office support duties. Positions require knowledge of company and departmental policies and procedures in order to communicate information involving programs, functions, and services. Duties performed may include preparation of ...
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Job Description: We are seeking a fulltime administrative professional with clerical experience to fill our QA Documents Administrator position. This position will be an integral part of our Quality Assurance staff and will interact with all levels of management and personnel. This position will also assist in over-all office administrative responsibilities. Work includes data entry, scanning and ...
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Growing and well-respected biomedical (clinical, basic and applied) research firm has job opportunities at Wright Patterson Air Force Base. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Research Protocol Coordinator for the Dayton, Ohio...
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IDEXX Laboratories, Inc. is a leader in pet healthcare innovation, serving practicing veterinarians around the world with a broad range of diagnostic and information technology-based products and services. IDEXX products enhance the ability of veterinarians to provide advanced medical care, improve staff efficiency and build more economically successful practices. IDEXX is also a worldwide leader ...
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Ashfield is seeking an experienced Compliance and Quality Assurance professional, with experience in the pharmaceutical sales industry, for an exciting opportunity in Ivyland, PA! Our ideal candidate has experience in CSO and call center operations. Please read the below ad carefully, and if you qualify, we would love to hear from you! Thank you, Ashfield Healthcare, LLC EOE/M/F/D/V General Job Ob...
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Eppendorf, a leader in the bio-tech industry sales, marketing, manufacturing and distribution facilities located in North America, develops, produces and distributes systems for use in life-science research laboratories worldwide. Its product range includes pipettes, dispensers and centrifuges as well as consumables such as micro test tubes and pipette tips. In addition, Eppendorf provides instrum...
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Senior Manager - GMP Quality Assurance North Augusta, South Carolina A Biopharmaceutical manufacturing company is hiring regulatory compliance / GMP Quality Assurance (QA) professionals. This business focuses on 1) industry-scale manufacture of proprietary and generic peptides and specialty chemicals, used as active pharmaceutical ingredients (APIs). 2) Contract research and manufacturing services...
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Primary Responsibilities for role: Responsible for all aspects of the donor center when the Center Manager is not present. Creates appropriate organizational environment and value systems which stimulate the morale and productivity of the work force and its leadership. Collaborates with Training and Quality staff to ensure that training and quality goals are met. Coaches and leads through effectiv...
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● Perform daily donor record file review. ● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual. ● Perform a review of donor center records. ● Perform weekly review of equipment incident logs. ● Verification and release of sample shipment. ● Perform Staging of plasma for shipment. ● Inspection and release of incoming supplies. ● Perform Weekly employee observa...
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Johnson & Johnson companies are equal opportunity employers. Clinical Research Scientist III (Raynham, MA)-3275130307 Description DePuy Synthes, a member of the Johnson & Johnson Family of Companies is recruiting for a Clinical Research Scientist III. This position is located in Raynham, MA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic ...
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JOB SUMMARY: The Document Systems Analyst supports Meridian’s Quality System by developing and maintaining electronic form records and approval processes. The Document Systems Analyst works with cross functional teams to identify areas that can be streamlined or improved by implementing electronic forms processes that meet regulatory requirements and standards for electronic documentation. KEY DUT...
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This position performs activities to support the strategic corporate goals in the area of human resources, by providing guidance, and support to management and supervisors in best HR practices. Providing employees support regarding policies, procedures and handling employee issues and concerns. Responsible for both office, Woburn and Des Plaines in recruitment, orientation, benefits administration...
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JOB TITLE: Technician I, Chemical/Pharmaceutical Operations (Manufacturing Lab Technician)-Third Shift At Cardinal Health, we're developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities. Business Segment: Pharmaceutical Segment Business Unit: Nuclear Ph...
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Johnson & Johnson companies are equal opportunity employers. Equity Analyst (New Brunswick, NJ)-7975130509 Description Johnson & Johnson Corporate Headquarters is recruiting for an Equity Analyst to be located in New Brunswick, NJ. Caring for the world, one person at a time, has inspired and united the people of Johnson & Johnson for 125 years. We embrace research and science - bringing innovative...
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*This position is open at two levels - Microbiologist I and Microbiologist II POSTION SUMMARY Responsible for performing assays that support the release of intermediates and finished products. These include routine and non-routine microbiological tests on in-process and final container products, as well as environmental monitoring samples. ESSENTIAL DUTIES AND RESPONSIBILITIES include the followin...
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The Process Operator I is responsible for the processing and encapsulation of the Methylphenidate, Dexmethylphenidate, Verapamil, or Morphine operation processes. This includes receiving order instructions (Batch Records), weighing and staging of materials, solution preparation, solution application (coating beads), drying, and screening, machine set-up, sampling, and packaging and storing of the ...
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The Process Operator I is responsible for the processing and encapsulation of the Methylphenidate, Dexmethylphenidate, Verapamil, or Morphine operation processes. This includes receiving order instructions (Batch Records), weighing and staging of materials, solution preparation, solution application (coating beads), drying, and screening, machine set-up, sampling, and packaging and storing of the ...
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Johnson & Johnson companies are equal opportunity employers. STAFF TPM ENGINEER/ME2 CHAMPION-7452130502 Description The Ethicon Surgical Care business offers a broad range of products, platforms and technologies-including sutures, surgical staplers, clip appliers, trocars and synthetic mesh devices-that are used in a wide variety of minimally invasive and open surgical procedures. Specialties incl...
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Primary Responsibilities for role: Responsible for all aspects of the donor center when the Center Manager is not present. Creates appropriate organizational environment and value systems which stimulate the morale and productivity of the work force and its leadership. Collaborates with Training and Quality staff to ensure that training and quality goals are met. Coaches and leads through effectiv...
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Description Medline Industries has an immediate opening for Associate QA Specialist-Supplier Quality position, located in Mundelein, IL headquarters. The Associate QA Specialist will be responsible for quality assurance activities related to the Supplier Quality group within the QA/RA Division. The position will be responsible for maintaining design control files and device master records for FDA ...
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The Company DPT Laboratories, Ltd. is a Contract Development & Manufacturing Organization (CDMO) headquartered in San Antonio, TX. DPT has extensive experience in providing fully integrated semi-solid, liquid and sterile dosage form development, as well as, manufacturing services to many of the world’s leading pharmaceutical, biotechnology and healthcare companies. With its primary facility in San...
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