DNAjobs.com is proud to feature the following jobs posted April 17 - 24 (listed in chronological order). For each position, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason
PH.D. or M.D. in Cardiovascular Sciences
(US-Texas-Houston) A four-year funded postdoctoral position is available for a Ph.D. or M.D. at the section of Cardiovascular Sciences, Department of Medicine. The position will utilize molecular genetic approaches to study the mechanisms involved in heart failure. Highly motivated application is encouraged to send resume with three names of references (Salary: $24,000 to $26,000). Must have a green card or H1. Background check and verification of education will be required.
Click here for more information.
Research Technician Cardiovascular Sciences
(US-Texas-Houston) A research technician position is available at the section of Cardiovascular Sciences, Department of Medicine. A successful candidate with B.S and experience in basic molecular and cellular biology including mouse genotyping is desirable. Send resume with two names of references (Salary: $22,000 to $24,000). Background check and education verified. Must have H-1 Visa or Green Card.
Click here for more information.
Manager/Assoc Dir, Oncology Sales Training
(US-New Jersey) The Training Manager for Oncology Sales is responsible for directing, developing, and implementing product and skill training for new and existing Sales Specialists. Specific Responsibilities are to: Proactively identify training needs of the Oncology Sales team through needs assessments, soliciting input from Sales/Marketing/Medical Affairs/Operations, developing and implementing training initiatives, completing ongoing assessments, and continuously improving upon training materials and processes. Direct, develop, and implement product training for new and existing Oncology products. Lead and participate in the development of on-going training for tenured Sales Specialists regarding ways to effectively communicate our selling messages, employ new sales campaigns, deal with competitive activity and new market entrants, effectively use clinical studies, and developing of core messages to support the Oncology Sales and Marketing Model. Be an integral member of the Oncology product teams by leading in creating training strategies and tactics to support brand strategies. Collaborate with marketing to ensure promotional materials align and support the Oncology Marketing and Sales model.
Click here for more information.
Regulatory Affairs Manager, Therapeutic Area
(US-New Jersey) Assist the Director in assuring compliance with Federal and State regulations. Compile and submit documents for all types of applications to regulatory agencies. Act as liaison to FDA for assigned projects. Maintain up-to-date knowledge of laws, regulations and policies enforced by the Federal and State governments as they relate to pharmaceuticals and devices. Assist the Director with the review of advertising/promotional materials and labeling for marketed products. Compile and submit applications (IND, NDA, Biologics, Devices) to government agencies in support of research and marketed products. Maintain up-to-date knowledge of the data, information, and formats required for inclusion in these applications. Act as liaison to the FDA in matters pertaining to applications and regulatory compliance. Track applications through FDA reviewing divisions. Compile and submit responses to FDA communications. Attend FDA meetings and participate in negotiations with FDA as necessary. Requirements: Bachelor's degree required. 4-6 years broad Regulatory experience required. Experience with filing NDAs and INDs required.
Click here for more information.
Sr Quality Assurance Manager
(US-New Jersey-Central) Assist the designated director in conducting and maintaining quality assurance programs, procedures and controls to ensure that quality and distribution of products conform to established corporate standards. Under supervision, assures compliance of company I Quality and company Regulatory Affairs procedures with the company Quality System. Reports to the Associate Director of Quality in the Regulatory Affairs and Quality Assurance department. Works with Marketing and Logistics representatives regarding HT product quality operations Conduct internal and external ISO/GMP audits. - Perform vendor audits, as required, for compliance to cGMP's and Company quality requirements. Requirements: A Bachelors degree is required. Advanced degree preferred. Minimum of four years experience as a quality professional is required. Broad pharmaceutical experience base in related areas such as development, regulatory etc. is desired. Works independently with minimum supervision. Excellent communication and organizational skills are required. Some travel required.
Click here for more information.
Senior Scientist, Cell Biology
(US-California-Silicon Valley/San Jose) Vitra Bioscience, Inc., a dynamic biotechnology company in Silicon Valley, California, is offering a Senior Scientist position in its Cell Biology research group. The selected candidate will be working in the development of cell-based assays for drug discovery using Vitra’s innovative technology. A Ph.D. in cell biology or related area is necessary. Experience working with different types of primary cell lines, and cell-based assays is a must. Knowledge of microscopy and image analysis is a big plus. Familiarity with drug screening processes and methods also a big plus. The ideal candidate should have a minimum of 5 years experience working in an industrial setting and be well organized, innovative, independent, and have excellent communications skills. Vitra Bioscience is an Equal Opportunity Employer that offers excellent salaries, a competitive benefits package, and employee stock options.
Click here for more information.
Senior Scientist, Product Development
(US-California-Silicon Valley/San Jose) Vitra Bioscience, Inc., a dynamic biotechnology company in Silicon Valley, California, is offering a Senior Scientist position to lead its Product Development group. Areas of specific responsibility and attention will include the following: Working with the scientific founders and others in senior management, participate in the development of the overall strategic direction for the company. Provide support to the reagent manufacturing, assay development, software and hardware. Oversee the transfer of new processes and protocols from applied research through development and into manufacturing. Lead the smooth progress from research through product development into commercialization.Qualifications: Ph.D. or equivalent. Proven record of accomplishment in a relevant technology based or life science products oriented company. A minimum of 5 years experience in leading the cycle of product commercialization from research through development to commercial product launch in the life sciences.
Click here for more information.
Regulatory Affairs CMC Associate, Manager and/or Associate Director
(US-Massachusetts) Provide Regulatory guidance, strategic advice and contribute to a Regulatory project team planning on CMC issues. Handles all aspects of CMC-related activities for assigned biological development project. RESPONSIBILITIES: Review and assessment of all CMC documents for consistency. Accuracy and conformance with all regulatory requirements; Identification of content, responsibility and timing of CMC documents for regulatory submissions; Coordinating and monitoring the progress of all CMC regulatory submissions; Providing regulatory guidance for CMC issues, processes and templates by working closely with Manufacturing and Quality through all phases of drug development; defining current regulatory requirements for technical submission (INDs, CTXs, BLAs, and DMFs); Directly interacting with regulatory authorities(internal) and Manufacturing and Quality (external) on CMC issues requiring agency feedback; and participating in pre-approval inspection activities.
Click here for more information.
Process Development Engineer
(US-Massachusetts) Responsible for the development of new products, processes and technologies based on core technologies to meet market needs and corporate objectives. Generates new concepts/technology in the area of tissue protection, regeneration and healing. SPECIFIC RESPONSIBILITIES: 1. Work with research and business development to identify market needs and evaluate technologies to design and develop cost effective products. Develop appropriate design inputs defining product performance requirements. 2. Use experiments, literature searches, internal and external interactions to develop formulations, characteristics and delivery systems that address product performance requirements. 3.Lead the product design efforts for new product concepts. Direct internal resources and coordinate external collaborations to design and test product concepts. 4. Design processes to cost effectively produce product meeting critical product attributes. Perform experiments to screen critical process control factors. Use experimental design techniques to develop robust processes at the laboratory scale.
Click here for more information.
Quality Engineer
(US-Massachusetts) Introduce robust quality programs and practices to evaluate processes and identify areas that lead to efficiency or quality issues, evaluate cause of problems and analyze quality data, implement root cause corrective actions, and evaluate results. Designs, evaluates and implements quality assurance programs and systems for manufacturing and development to ensure compliance with regulatory requirements. Develops methods, protocols and assays to ensure that appropriate quality tests and analyses are being conducted. Works with quality and manufacturing to create and /or modify methods and procedures to ensure those appropriate tests are conducted and that products, materials and manufacturing equipment meet required standards. SPECIFIC RESPONSIBILITIES: 1. Investigate and perform root cause analyses of process deviations and out of specification results. Prepare detailed reports summarizing investigation results and outlining recommended corrective actions. 2. Coordinate the implementation of corrective actions and routine change controls. Work closely with manufacturing, QA, QC, engineering and facilities implement changes. Regularly report status to Director of Quality and provide summaries of open items.
Click here for more information.
APPLICATION SCIENTIST - GENOMICS
(India - Mumbai) RESPONSIBILITY: To provide scientific support in the form of protocol and technique development to scientists in various DBT, DST, ICAR, CSIR institutions for DNA Microarray technology, high-throughput capillary sequencing and other aspects of drug-discovery programs. In addition, to conduct seminars, workshops and training programs for customers and sales team. BACKGROUND: Ph.D. in Molecular Biology or Biotechnology with 2-3 years' experience in Gene Expression Studies and the above mentioned areas. SALARY: Rs. 35,000 - 40,000 per month Please apply with complete Curriculum Vitae to: HRD Manager Amersham Biosciences Ltd., India Branch Office FF-3, First Floor, Palani Centre, 32 Venkatnarayana Road T.Nagar, Chennai 600 017, INDIA
Click here for more information.
APPLICATION SCIENTIST - PROTEOMICS (Mass Spectrometry)
(India - Chennai) RESPONSIBILITY: The person appointed will assist in providing a high quality interface between customers and the Central Proteomics Product management. He/ she will be responsible for conducting seminars, demo-ing the Mass Spec and 2D product line. In addition he/she will handle technical queries and provide technical support to customers. The job holder will also provide technical support/training to field colleagues in support of sales opportunities. BACKGROUND: Applicants should ideally be a Ph.D. level candidate in an appropriate Life Sciences subject with four to five years experience in Mass Spectrophotometry (using Maldi-TOF or LCMS). Knowledge of related proteins analytical techniques like protein purification, 2D-electrophoresis etc. will be an added advantage. SALARY: Rs. 30,000 - 40,000 per month Please apply with complete Curriculum Vitae to: HRD Manager Amersham Biosciences Ltd., India Branch Office FF-3, First Floor, Palani Centre, 32 Venkatnarayana Road T.Nagar, Chennai 600 017, INDIA
Click here for more information.
PRODUCT MANAGER - Separation Techniques
(India - Hyderabad) RESPONSIBILITY: Marketing and Sales of Separation range of products like Laboratory / Industrial scale chromatography systems, filtration and media. Previous experience is selling FPLC, HPLC, Bioprocess and Filtration systems would be an added advantage. BACKGROUND: M.Sc. in Life Sciences with 4-5 years' of work experience in similar areas. SALARY: Rs. 25, 000 - 35,000 per month Please apply with complete Curriculum Vitae to: HRD Manager Amersham Biosciences Ltd., India Branch Office FF-3, First Floor, Palani Centre, 32 Venkatnarayana Road T.Nagar, Chennai 600 017, INDIA
Click here for more information.
Post Doc
(US-Florida-Tampa) POSTDOCTORAL POSITION available immediately for studies of the molecular and cell biology of horizontal transfer of functional genes between multicellular organisms. Strong background in molecular techniques, cell biology or electron microscopy required. Send curriculum vitae and three letters of reference to: Dr. S. K. Pierce, Department of Biology, SCA 110, Univ. of South Florida, Tampa, FL 33620. email: pierce@cas.usf.edu. The University of South Florida is an Affirmative Action/EqualOpportunity Employer.
Click here for more information.
Scientists, Animal Housing Specialists, and Technicians
(France - Paris) BioProtein Technologies is a dynamic and rapidly expanding biotechnology company based in central Paris. The company is permanently seeking self-motivated scientists, animal housing specialists, and technicians. BioProtein currently proposes internships for students specializing in animal housing. Experience with rabbit housing is an asset. If you want to join us and participate in our success, please send your CV : by E-mail: contact@bioprotein.com by post: Human Resources BioProtein Technologies 63-65, Boulevard Massena 75013 PARIS, FRANCE
Click here for more information.
Project Manager
(US-Texas-El Paso) If you are a bilingual(English and Spanish), mechanical engineer, we have an exceptional opportunity for you! Our client is a leading medical device manufacturer that concentrates on proprietary OEM products and private label fluid disposables. They are in need of an exceptional project manager who is experienced at production line transfer. You will be responsible for the administration of new products, transfer of projects, and documentation functions. You will be required to identify and ensure adequate and appropiate resources are assigned to projects to ensure the design is controlled, the company’s goals for the sucessful completion of the projects are achieved and the customer needs met. For consideration you must posses an engineering degree and have knowledge of FDA/GMP regulations.
Click here for more information.
Product Manager
(Germany) As a young company in the field of Fluorescence Diagnosis and Photodynamic Therapy we are currently looking for a: Product-Manager (f/m) - Your task includes the acquisition of new customers and support service of our cooperation partners as well as the representation of our products at trade fairs. Prerequisites are knowlegdes in the field of diagnostic and therapeutic techniques in medicine and biotechnology. Desirable is a scientific education of comparable knowledge. If you can picture yourself in one of these positions, please send your application with CV to: Biocam GmbH Friedenstraße 30 D-93053 Regensburg GERMANY Tel: +49 941 785398 0 Fax: +49 941 785398 10 eMail: info@biocam.de
Click here for more information.
Bioinformatician: 0401
(France) We have an open position in bioinformatics. The bioinformatic team is dedicated to the handling, storage and tracking of all data downstream from our endonuclease screening platform. Candidates should have training in both informatics and biology as well as experience working in industry. The ability to understand the challenges of both wet and dry labs is essential. Application including C.V and references should be send to: CELLECTIS SA Service de recrutement 102 route de Noisy F-93235 Romainville Cedex
Click here for more information.
Field Applications Specialist
(US-Illinois-Chicago) Beckman Coulter, Inc. is a leading provider of instrument systems and complementary products that simplify and automate laboratory processes. Our products span the biomedical continuum, from life sciences to clinical diagnostics and cellular analysis –and are backed by service that is second-to-none. Systems Biology Field Application Specialist: Your mission, as an Application Specialist, will be to combine your consultative skills, technical expertise, and training savvy to seamlessly integrate Beckman Coulter genetic analysis and protein separation products into our clients’ operations. Your responsibilities will include: Product training, technical, and application support for our automated genetic analysis system, the CEQ2000XL, and CEQ8000. Product training, technical, and applications support for PA-800 and PF2D protein systems. Technical assistance to our sales force. Application support for our genetic and protein analysis applications that are integrated with our robotics solutions. Preferred Candidate Profile: Degree in Chemistry, Biochemistry, Molecular Biology or related discipline Prior laboratory or field service experience in HPLC/CE and protein analysis.
Click here for more information.
Director of Sales and Marketing
(US-Florida-Ft. Lauderdale) MEDICAL DIAGNOSTIC COMPANY - MANUFACTURER OF IN VITRO DIAGNOSTICS FOR USE IN DOCS OFFICES AND OTC - NEEDS DIRECTOR OF SALES & MARKETING. EXPERIENCE REQUIRED. EMAIL RESUME + SALARY REQUIREMENTS.
Click here for more information.
Post / Search Jobs & Resumes for free at DNAjobs.com
Our employment services are free for Job Seekers, Employers, and Recruiters.
Click here to post a job or resume.
