DNAjobs.com is proud to feature the following positions posted December 3 - 17. For each job, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason Skie
Post Doctoral Fellow
(US-Florida-Miami) Participate in STUDIES OF MECHANISMS OF CELL DEATH IN HUMAN T CELLS AND PANCREATIC ISLETS, with the goal of identifying molecular targets to intervene and prevent cell death leading ultimately to the application in clinical settings. Experience in cell biology and molecular techniques is required. Familiarity with flow cytometry, confocal and electron microscopy is desirable.
Click here for more information.
Sr Scientist - Pharmacokinetics / Pharmacodynamics
(US-Massachusetts) Design and interpretation of PK/TK and PD studies to support non-GLP, GLP programs, Phase I and Phase II clinical trials. Selection and oversight of CRO operations for nonclinical and clinical PK to support regulatory filings. Predictive and population PK/PD modeling of clinical data. Will prepare and review reports and documentation to support IND filings.
Click here for more information.
Regional Sales Manager - Oncology
(India-Tamilnadu-Chennai) For one of our client, which is a top pharma company in India, we are looking for Regional Sales Manager for their oncology division. The candidate should be a Science or Phamacy graduate with 10 to 15 years of pharmaceutical selling preferably oncology / Specialty / Super specialty Products. Apply within one week from the date of this advertisement.
Click here for more information.
Plant Manager / General Manager (Operations / Production)
(India-Gujarat-Vadodara) For one of our clients, which is a top pharmaceutical company based at Baroda, Gujarat, We are looking for a Plant Manager / General Manager (Operation / Production) for a API unit. The candidate should be a graduate in Chemical Engineering with minimum of 10 years experience in USFDA approved Bulk Drug unit.
Click here for more information.
Scientist - Natural Products Chemist
(US-Massachusetts) An experienced Chemist with a Ph.D. and 10 years experience in natural product isolation, characterization, de-replication and bioassay-guided microbial products purification is needed to work on drug discovery programs. The successful candidate is responsible for scale-up purification of secondary metabolites produced by fermentation of actinomycetes.
Click here for more information.
Medical Director - Clinical Development
(US-Massachusetts) Five positions exist! Do you have a minimum of 2 years experience? 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 are some of the areas.
Click here for more information.
Genomics Sales Specialist
(India-Banglore, Hyderabad and Mumbai) High quality representation for Microarray , Proteomics and Molecular diagnostics instrumentations like 2D EPH, Spot cutters and Digestors. Suitable candidate is required to be having a masters with of 0-3 years of experience working in similar field. Preference will be given to those having experience of handling Microarray / Proteomics instrumentation and software support.
Click here for more information.
Manager - Marketing (Medicinal Chemistry)
(India-Andra Pradesh-Hyderabad) MBA Finance. 5-8 Yrs. experience in project management, scheduling, marketing and project coordination. Responsibilities: a) Project coordination and management - for all projects being currently executed at med chem. b) Assist VP Mktg in all matters regarding business development. c) Prepare profitability statements for projects. d) Prepare proposals.
Click here for more information.
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. The group objective is to derive the specific gene expression profile or signature of treatment efficacy (pharmacological effect) and/or toxicity (side effects) leading to the discovery of biomarkers.
Click here for more information.
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.
Click here for more information.
Group Brand Manager
(India-Delhi) As a Group Brand Manager, you shall be at a senior, management level, and will be responsible for overall marketing of brands. Major responsibilities include marketing, planning, strategy development, monitoring & review. You will also be required to provide overall directions to develop new markets and strengthen the existing ones.
Click here for more information.
Medical Sales Representative / Management Trainee - Sales
(India-Punjab, Rajasthan, Gorakhpur, Varanasi, Chennai, Kerala, Hyderabad and Vijaywada ) Responsible for promotion of our brands, management of key accounts in the assigned territories and achieving sales targets through effective implementation of the defined strategies. You should be a Science / Pharmacy Graduate with about 1-2 years of field experience in a reputed pharmaceutical company, having excellent communication skills, good track record and capacity and zeal to achieve results.
Click here for more information.
Postdoc
(Germany-Nordrhein-Westfalen) Looking for a Postdoc in the field of Biology / Biochemistry / Molecular Biology who wants to work independently on his / her own project. Fields to work on include mutated receptor tyrosine kinases in leukemia and epigenetic regulation. Our new colleague should have detailed knowledge of Molecular Biology, vivid interest in research and outstanding capabilities including creativity and high technical skills to perform competitive research.
Click here for more information.
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. There is an additional emphasis on technical report writing and making scientific presentations.
Click here for more information.
Analytical Chemist
(US-Massachusetts) Focused on the discovery and development of biopharmaceutical therapeutics and vaccines for human disease. A qualified candidate should be hands on and familiar with applying various analytical techniques such as HPLC, SEC, AAA, Sequencing, Peptide Mapping, Light Scattering, Carbohydrate Analysis, SDS-PAGE, IEF and MS.
Click here for more information.
Clinical Research
(India-Lalru, Mohali) Candidates applying for the post of AGM should be PhD ) Molecular Pharmacology / Molecular Biology) preferably with 3 - 6 years of experience in drug discovery with a reputed Company. Applicants should have the knowledge of bioinformatics and molecular biology tools and techniques. The applicant should be able to use molecular approaches to study the mechanisms of drug action at the receptor level.
Click here for more information.
Analytical Chemist
(India-Andra Pradesh-Hyderabad) M.Pharm / Ph.D in Analytical Chemistry with 3-5 years experience in clinical research.
Click here for more information.
Clinical Chemist
(US-Massachusetts) Supervise mass spectrometry and biochemical testing in support of clinical trials and post marketing activities. You will be responsible for clinical data management and laboratory quality control. Requires a MS or Ph.D. degree in Biochemistry or Clinical Laboratory Science with previous clinical laboratory supervisory experience.
Click here for more information.
Director of Formulation
(US-Massachusetts) The Director of Formulation will be responsible for developing solid and injectible dosage formulations for drug products. Oversee the development of final dosage formulations for drug products; Initiate and coordinate all outside interactions with CROs working on formulation development.
Click here for more information.
Molecular Biologist
(India-Karnataka-Bangalore) MSC OR PHDin chemistry / biochemistry / biotechnology WITH 2 to 5 YEARS OF EXPERIENCE IN DNA SYNTHESIS or oligonucelotides. Should be able to work in Night shifts.
Click here for more information.
Research Manager
(US-Massachusetts) This unique opportunity exists to manage the Protein Engineering section of the Research Group. You will be responsible for leading a team of several Scientists who are responsible for the development of second generation therapeutic proteins using a variety of methods including protein and carbohydrate modification, and conjugation techniques.
Click here for more information.
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.
Click here for more information.
Clinical Operations - Electronic Case Report Form Development Specialist
(US-Massachusetts) Provide and maintain trial specific eCRF pages and plausibility and consistency checks for eCRF applications for clinical trials. Develop complimentary validation and monitoring reports using SAS and/or other reporting tools. Provides input into specifications of data structures and database applications for clinical trials.
Click here for more information.
Director / Sr Director Toxicology
(US-Massachusetts) Responsible for managing the overall preclinical safety and ADME assessment of compounds in all stages of preclinical research and development. Working with experienced drug development scientists and research scientists on various project teams, you will oversee the design and conduct of studies intended to support the progression of compounds through the key phases of preclinical and clinical development.
Click here for more information.
Scientist Drug Metabolism
(US-Massachusetts) A staff scientist is sought to bring expertise in drug metabolism to the drug discovery and development teams advancing new chemical entities for emerging small molecule programs. Responsibilities: The identification and evaluation of new tests and procedures to assess metabolic liabilities.
Click here for more information.
Staff Investigator / Investigator - Formulations Development
(US-Massachusetts) As a member of our Formulation Development / Pharmaceutical Operations department, you will identify and develop dosage forms of new chemical entities. Working closely with Medchem, PK and Pharmacology to identify candidates and compound selection for clinical development via preformulation studies (solubility, pKa, crystallinity, effects of pH, temperature, moisture and excipients on chemical stability).
Click here for more information.
Trainee Scientists - Chemoinfomatics / Bioinfomatics
(India-Karnataka-Bangalore) Fresh M.Sc. in Organic / Medical / General Chemistry or M.Sc. with specialization in Molecular Biology / Biochemistry.
Click here for more information.
Life Sciences Business Development Manager
(US-New Jersey) Drive the sales of all solutions into a vertical Line of Business. Solutions include, but are not limited to E-commerce, E-procurement, Customer Relationship Management (Broadvision, Epiphany, SAP, Oracle CRM), Supply Chain Management, Enterprise Wide Infrastructure (Cisco), Application Hosting, Knowledge Management, Data Warehousing, ERP Service existing clients, including Fortune 500 firms.
Click here for more information.
VP - Business Development
(US-Connecticut-Danbury/Bridgeport) Responsibilities include contributing to the formulation of the Company strategic plan, research and analysis of potential opportunities such as in-licensing, out-licensing or partnerships, in-depth evaluation of new opportunities and negotiating deals. It will manage 2 professional people. The position reports to the President of the BioPharmaceutical division.
Click here for more information.
Senior Regulatory Submissions Specialist
(US-California-Silicon Valley/San Jose) The Sr. Regulatory Submissions Specialist will prepare and submit pre-market applications to the FDA. This position will approve proposed product changes and modifications as well as labeling, packaging, and promotional materials. This position will support preparation of international product pre-marketing, registration applications and approves international labeling and packaging.
Click here for more information.
Sr. Director Development and Medical Affairs
(US-New Jersey) Clinical Development Plans and key clinical documents. Develop clinical trial protocol designs, data review / synthesis and publications. Interact with regulatory authorities, scientific societies & institutions and scientists. Interface with marketing concerning new products and act as senior advisor for business development and licensing opportunities.
Click here for more information.
Director of Manufacturing / Solid Dosage Forms
(US-California-Silicon Valley) Director, Manufacturing will direct the manufacturing of all my clients products at the facilities of their partners and outside contractors, and will manage my clients product supply chain, including purchasing and planning. The Director, Manufacturing will coordinate the contract manufacturing of bulk and finished products and activities at third party distribution centers.
Click here for more information.
Clinical Monitor
(Netherlands) Monitoring of the largest European Clinical Studies within Post Market. Establish good working relationships with Clinical Investigators. Work closely with the Project Manager and the CRA in charge of the Clinical Study. Ensure that clinical trials are conducted in compliance with the protocol, Sops and regulatory requirements. Monitoring e-Case Report Forms against protocols and source documents at Clinical Investigations sites.
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.
