DNAjobs.com is proud to feature the following jobs posted June 3 - 19. 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 Skie
Curriculum Creators
(Anywhere-Telecommute) To further develop innovative bioscience, biomedicine, and biotechnology integrated curriculum and laboratory instructional lessons for standards-based teaching and learning. Collaborators of curriculum designers and writers will expand on existing works, to further develop field-test drafts of instructional lessons and units across K-12 grade levels and content areas.
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Application Specialist - Mass Spectrometry
(India-Karnataka-Bangalore) Candidates shall be M.Sc Chemistry, preferably Ph.D . Relevant Experiance of 6-10 yrs in handling and operating Mass Spectrometers of various makes in Labs with Pharmaceutical Companies. Job requires extensive travel. Salary 4 - 6 lakhs INR p.a. Higher salary may be considered for extremely suitable candidates.
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Business Development Manager
(India, South Africa, Bangkok, Kuala Lumpur) Relevant work experience in business development with a Pharmaceutical company in bulk drugs, formulations and other Nutraceuticals (herbal products, Dietary supplements, herbal extracts, cosmeceuticals etc). Job involves extensive traveling.
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Pharmaceutical Sales Representative
(US) We currently have an exciting new opportunity partnering with a top pharmaceutical company, and we are seeking individuals who have the desire and drive to become part of high impact, successful sales team promoting Diabetes products to physicians and pharmacies. Qualifications include: Minimum of a 4-year bachelor degree. Previous business-to-business sales experience preferred. Proven track record in pharmaceutical sales or equivalent; medical device sales experience is preferred.
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Medical Director - Clinical Development
(US-Massachusetts) Currently we have several companies searching for just the right person to lead their clinical development team. Areas of interest are numerous but could include Oncology, Neurology (drugs or devices), Cardiovascular (drugs or interventional) ), Gastroenterology, Urology, Inflammation and Infectious Disease.
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Cell Culture Scientist
(India) To work with team involved in recombinant mammalian cell lines and Hybridomas for production of Biotherapeutics, Chimeric antibodies or Monoclonal antibodies. The ideal candidate should have working experience with cell culture techniques, preferably with recombinant mammalian cell lines and hybridomas for production of Biotherapeutics, Chimeric antibodies or Monoclonal antibodies at lab as well as pilot scale.
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Marketing Franchisee
(India-Karnataka-Bangalore) As our Marketing Franchisee, you will operate independently promoting our products in the biotech, research and medical industry. We will support you in terms of marketing material, leads, technical backup. You will be entitled to a percent on the sales created in your territory. This will give you an oppurtunity to get an insight into this new field of biotechnology, allow you to develope your contacts with ease of working independently.
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Research Scientist II
(US-New York-Albany/Poughkeepsie) Principal responsibilities are to provide specific technical expertise to execute internal and external projects in the areas of ADMET, metabolite synthesis and synthetic biocatalysis and to apply a wide range of purification and analytical techniques to isolate, purify, analyze and characterize products of various biotransformations, including metabolites.
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Clinical Project Manager
(US-Massachusetts) Provide operational perspective to planning of clinical studies. Generate timelines for initiation to completion and reporting of clinical studies. Coordinate generation and assembly of all documentation associated with clinical studies. Participate in site selection and qualification. Negotiate investigator and CRO budgets in collaboration with Finance Department.
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Chemist, Scientist, Laboratory Technician
(India) Physical and Chemical testing of all building materials including cement as per Indian Standards in Stationary Laboratory. Controlling the system, from the collection of sample to the testing as per Indian Standard and submission of the finalized report to concern authority for implementation of Quality Control on site.
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Microbiologist
(India) Job includes handling the microbiology department of a pharma company into manufacturing of formulations and injectables. The candidate should be an M.Sc. (Microbiology) with through knowledge of working with a pharma company.
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Medicinal Chemists - Research Associates
(US-Massachusetts) Independently proposes, designs and conducts synthetic organic chemistry reactions to meet project goals. Synthetic work will encompass the preparation of single compounds as well as libraries. Purifies and characterizes materials by analytical methods such as NMR, HPLC, LC-MS. Maintains accurate and up-to-date experimental data.
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Senior Clinical Research Associate
(US-Massachusetts) The key responsibilities of this position will be to contribute to the development of clinical programs including protocols, study procedure handbooks, and case report forms; to insure compliance of study activities with FDA regulations, Guidelines and principles of Good Clinical Practice.
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Product Manager - ST & NE
(India-Maharashtra) Candidate should be exp in pharma company. Handling all activities pertaining to Marketing & promotion of entire range of Surgical technologies & neuro Endoscopy; Support to the sales team, handling training & induction, product demos. Candidate should be graduate in Bsc / B, Pharma+MBA-Mkt, Engineer, 5-8 yrs exp in sales Marketing; Sound Conceptual knowledge.
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Manager - Biomedical
(India-Delhi) Person will be responsible for looking after project of a large superspeciality hospital. Responsibility will be to manage the installation of bio medical equipments and hand over the running machine. Candidate should be B.E.Electronics/ Instrumentation or a biomedical engineer with 6 to 10 years of relevent experience in looking after bio medical project i.e, installation , commissioning of bio medical equipments particularly in a hospital environment.
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Biochemist
(US-Massachusetts) The candidate should have skills in general protein biochemistry and a quantitative background with experience in LCMS, biosensor analysis, flow cytometry, fluorescence spectroscopy or other biophysical methodology. The candidate will participate in the development, execution and analysis of biochemical assays for drug screening and characterization.
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Pharmacist
(India-Karnataka-Bangalore) Diploma in Pharmacy / Bpharma.
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Bioinformatics Consultant
(Mexico-Mexico City) The successful candidate will be involved in: 1. Development of JAVA software for the interchange of molecular data between bioinformatics tools. 2. Training of CIMMYT staff in JAVA software development. We are seeking candidates with the following qualifications, skills, characteristics and interests: 1. Degree in Biological or Computational Sciences. 2. At least two years experience in JAVA software development for Bioinformatics.
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Senior Biostatistician
(US-Massachusetts) A large portion of effort will be directed to oversight of biostatistical services provided by clinical CROs. An understanding of industry standards for data management procedures used to collect, compile, and present clinical data is required. Responsibilities will include activities that support the planning, analysis, review, and interpretation of clinical data sets from research projects and protocols conducted by the clinical research group.
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Scientist - Analytical Development
(US-Massachusetts) Developing, validating and transferring appropriate analytical methods for chemical raw materials, chemical intermediates, in-process controls, and final drug substances, as well as assessing purity, potency and stability of drug substances and drug products. Assisting in the setting of specifications of drug substances, raw materials, synthetic intermediates and drug products.
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Cell Culture Scientist
(India) Engaged in R&D and production of recombinant proteins for biopharmaceutical, therapeutic & diagnostic antibodies. Must have knowledge in molecular cloning, protein expression, cDNA, viral isolation culture and assay for antiviral activities, recombinant antigen antibodies production,able to develop new approach, methods. Able to cordinate the R&D lab.
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Senior Research Scientist
(India-Andra Pradesh-Hyderabad) Responsible for using a variety of techniques in the design, synthesis, analysis and process optimization of compounds destined for toxicological and clinical evaluation. Requirements include a M.Sc. or Ph.D. in organic chemistry or related discipline. Individuals with relevant postdoctoral and/or industrial experience are highly desired.
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Regulatory Affairs Manager
(US-Massachusetts) The Manager, Regulatory Labeling and Promotion, is responsible for the management of regulatory activities in the support of external commercial communications, labeling development, and labeling maintenance. This person represents regulatory in cross-functional teams that review and/or approve promotional materials, sales training materials, press materials, and other external communications.
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Scientist - Head of Gene Expression Sciences
(US-Massachusetts) Leading a group of scientists responsible for the interpretation of gene expression patterns from genomics and proteomics studies. Derive the specific gene expression profile or signature of treatment efficacy (pharmacological effect) and/or toxicity (side effects) leading to the discovery of biomarkers.
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Microbiologist
(India-Andra Pradesh-Hyderabad) Should have exposure in Molecular Biology along with General Administration of Clinical Reference Laboratory. The Candidate should have good communication, interpersonal and leadership skills. Should also have experience in people management as well as the management of performance from fellow colleagues. Requires MD in Microbiology.
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BioStatistician
(India-Maharashtra-Mumbai City) Contribute to the development of long-term goals and operating policies for the organization, through his/her leadership role on the management team; Manage multiple projects locally but may also additionally manage some globally; Manage timelines, quality and preparation of statistical reporting deliverables and ensure that they comply with global regulatory guidelines.
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Regulatory Affairs CMC Associate, Manager and/or Associate Director
(US-Massachusetts) 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.
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Scientist - Immunologist / Assay Development
(US-Massachusetts) Your principle responsibility is to oversee the design, development, and validation of assays that are used to support clinical immunogenicity testing. These assays include but are not limited to ELISA, RIA, western blot, neutralization and radioimmunoprecipitation techniques.
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QC Chemist - Noida
(India) QC CHEMIST IN PHARMACEUTICAL COMPANY. BSC/MSC/B.PHARM/M.PHARM/PHD.
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Vice President - Regulatory Affairs
(US-Massachusetts) Anticipate consequences and assess impact of new or revised worldwide regulations and guidelines on company strategies. Review and approve key segments of regulatory submissions. Represent the company and effectively participate with senior level representatives of regulatory agencies worldwide.
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Director of Drug Safety
(US-Massachusetts) The Director is responsible for all activities related to the monitoring and reporting of the safety profile of marketed products on an ongoing basis. This includes the management of potential risks associated with these products, ensuring compliance with FDA regulations on expedited and periodic reporting of Adverse Events, developing and adhering to Corporate Standard Operating Procedures (SOP).
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Head of Clinical Sciences
(US-Massachusetts) You will actively manage/participate in the development of oncology clinical projects within phase I/II. Specific responsibilities include: Design clinical oncology studies draft and refine protocols and case report forms implement biomarkers; mechanistic studies clinical trial management CRO / staff selection and management.
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Manager Drug Safety
(US-Massachusetts) Manage the processes and reporting of adverse events (AE) of marketed products and products under development while assuring compliance with regulatory requirements and internal SOPs. Responsibilities also include the management and oversight of Drug Safety Associates and their roles for adverse event report processing, Periodic Reports, registry functions, case report documentation triage of individual case reports.
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Director of Clinical Affairs
(US-Massachusetts) The Director of Clinical Affairs will be responsible for all aspects of clinical trial management. These responsibilities include the management of contract research organizations (CROs), design and writing of protocols and clinical trial reports, preparation and monitoring of budgets and trial timelines, and recommendation on resource requirements.
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Clinical Program Manager
(US-Massachusetts) Develop clinical development plans and study timelines. Participate in the development of clinical protocols, Investigator Brochures, consent forms, training material, and other clinical documents, as required by the project. Provide a liaison function between clinical investigators and scientific personnel in the development of programs and clinical studies.
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Director Sales / Business Development
(US-New York-New York City) The number 2 home care organization in New York seeks a sales professional from the healthcare industry (home care, pharmaceuticals, medical sales, hospitals, nursing homes). Reports to COO. Indentify new opportunities for expansion. Develop marketing/sales plans. Ensure department budget.
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Pharmaceutical Research
(India-Maharashtra-Mumbai ) A pharmaceutical major is looking for a talented & enthusiastic M.Pharm for their R&D operations. Requires M.Pharm. (Pharmaceutics) with pharmaceutical background. Exposure on Oral forms / Liquid dosage injections / NDDS.
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