DNAjobs.com is proud to feature the following jobs posted February 5 - March 3. 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
Clinical Database Manager
(US-California-San Francisco) Seeking an aggressive, hands-on individual who has the ability and desire to program as well as manage the database process. Will develop data screens, queries, edit checks, and perform QA functions. This is a full time, in-house opportunity to manage an entire database operation and then move into other positions of responsibility as the company experiences high growth.
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SAP Functional Consultant
(US-New Jersey) Seeking candidates with functional SAP skills in all areas. Must be US citizen or in possession of H1B visas,with current residence in US. Job requires consulting background with client exposure. The company is top tier Global Services Organization.
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Forensic Scientist
(US-California-Silicon Valley/San Jose) A grant-supported Scientist position is available in the Genomics Collaboration group to work on novel forensics applications of high-density microarray technology. This position will be responsible for hands-on development of assays based on genotyping and resequencing technologies that will enable use for forensics applications.
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Scientist - Genomics Collaborations
(US-California-Silicon Valley/San Jose) The Genomics Collaborations Scientist will initiate and manage a number of paradigm-shifting collaborations in human genetics with key external scientists. These technologies, which include primarily genotyping and resequencing, will be used to conduct seminal studies across a variety of genetic applications including the study of normal human genetic variation, complex disease association studies, pharmacogenomics, population studies, and forensics.
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Sr. Executive/ Executive - Instrumentation
(India) To maintain and calibrate instruments. Sound knowledge of instruments like HPLC, GC/GC Headspace, FTIR, UV Spectrophotometer. To carry out chemical analysis of semi finished, finished products. To undertake all works relating to software/package. Desired Profile: M.SC / M. Pharma / B. Pharma.
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Lab Attendant
(India-Maharashtra) Knowledge of handling of Lab equipments. Pre & post preparation of Lab experiment activities. Maintaining various equipment Log Books. Preparation of media for experiment etc. Desired Profile: B.Sc with 1-2 years of experience in any Research & Development set up as Lab Attendant.
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Scientist - IPC (Intellectual Property Cell)
(India-Maharashtra) The incumbent should help the IPC cell in patent searches, through research and analysis on cutting edge products that are in the market and those that will enter the market in the future. Its activities involve the protection and management of companies patent portfolios. Desired Profile: The candidate must be M. Pharma / Ph.D. (Pharmaceuticals).
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Microbiologist (Vaccines Production)
(India) The incumbent will be responsible for the job of a Microbiologist. Desired Profile: M. Sc in Microbiology / Biotechnology, M.Tech in Biotechnology.
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Executive - Regulatory Affairs (Biological / Vaccines)
(India-Delhi) Taking care of Registration of products in regulated market. Registration and submission of dossiers/tenders. Updation of regulatory guidelines. Desired Profile Ideal candidate(s) should be M.Sc-Microbiology/Biotechnology or M. Tech, preferably with 1-3 years of experience in QC, QA and production of vaccine facility. Should have knowledge of regulatory affairs and ICH guidelines.
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Officer/ Executive - Process Development Lab
(India) Technology transfer from R&D to Production. Drafting technical directions & BMR. Trouble shooting at production floor. Planning & co-ordination for scale up and Commercial batches. Carrying out Process validations. Preparation of SOPs and DQ,EQ,IQ,OQ & PQ Documentation. Desired Profile: M.Pharma / B.Pharma.
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Officer / Executive - Chemist
(India) Analysis of API and / or pharmaceutical formulation products. To carry out chemical analysis of raw materials, semi finished and finished products. To prepare chemical reagents and standardize. To implement cGLPs, SOPs and STPs Desired Profile: MSC / M. Pharma / B. Pharma. 2 - 4 Yrs experience as chemical analyst experience in pharmaceutical industry.
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Assistant Manager - Utilities (Mechanical / Electrical)
(India-Maharashtra) The person will be responsible for installation, validation and smooth functioning of laboratory machines for GRAND Mumbai. He / She will also be responsible for co-ordination of GRAND project site development with various departments within Panacea Biotec Ltd. and external agencies. The candidate will be responsible for design improvement of new and existing machines to suit the need of research and development.
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Assistant Manager - Accounts
(India) The candidate should have experience in Factory Accounts, Managing A/c., payable, receivables, Reconciliation of A/c., Bill issues, Petty Cash Maintenance, Sales Tax (VAT), Income Tax, Co-ordinating with Auditors, C & F Agents, Branch Office, Head Office. Dealing with banks and financial institutions. Exposure to ERP, preferably SAP will be an advantage. Desired Profile: Chartered Accountant (C.A.)
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Graduate Trainees - F&D, Q.C, Q.A, R.A
(India-Maharashtra) According to the Knowledge and profile of the candidate. Desired Profile: Freshers with B.Pharma/M.Pharma from a well-reputed institute. Should possess strong analytical and good communication skills, initiative, interpersonal and team skills.
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Microbiologist
(India-Maharashtra) Job Description: All Microbiological Techniques - Microbial Limit Test, Microbiological Assay, Other Microbiological testing, etc. Candidate should be M.Sc. (Microbiology) / B.Pharm. Should be aware of all microbiological techniques. Candidates with FDA approval will be preferred.
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Procurement Specialist
(UK-Home Counties) Our client a major Engineering contractor within the Pharmaceutical industry, are urgently looking for a number of Procurement professionals to work on a new project award based at their offices in Surrey. Candidates must have a minimum of 3-4 years experience working on major Pharmaceutical projects and also have specific experience of small scale production equipment and laboratory instrumentation procurement.
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Associate Director Process Development
(US-Massachusetts) Reporting to the Sr. Director of Process Development and directly supervising 2 Managers you will be directing the development, planning and implementation of product and process development for new products and technologies from the laboratory through pilot plant and into manufacturing scale. You will also provide strategic direction, tactical oversight and technical expertise for all activities within the Product/Process Development area.
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Vice President Regulatory Affairs
(US-Massachusetts) Anticipate consequences and assess impact of new or revised worldwide regulations and guidelines on the company's strategies. Review and approve key segments of regulatory submissions. Represent the company and effectively participate with senior level representatives of regulatory agencies worldwide. Effectively interact with senior company management to influence direction of the Regulatory Affairs group and associated company efforts.
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Regulatory Affairs Manager
(US-Massachusetts) The Manager will be responsible for determining Regulatory strategy for specific projects relating to the development of new formulations, new delivery systems and new indications for commercial products as well as post-marketing commitments and Phase 4 studies. The Manager will also serve as the RA representative on relevant project teams and as the primary regulatory contact with regulatory authorities in the US and Canada.
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Regulatory Affairs Manager
(US-Massachusetts) The Regulatory Affairs Manager develops strategies for worldwide governmental approval to introduce new products to market, provides advice on regulatory requirements, prepares worldwide submissions and negotiates their approval. The incumbent also assists with the training of less senior regulatory affairs personnel and provides work direction on projects of large scale.
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Director of Clinical Research / Operations
(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. The Director will represent Clinical Affairs on Program Teams and provide strategic input on new development-stage products.
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SAS Developer / Programmer
(US-Massachusetts) Design and conduct outcomes studies. Prepare research plans and protocols. Design data collection forms. Conduct analyses of data. Prepare reports and manuscripts for publication. QUALIFICATIONS: Masters with 3-5 years (or Bachelors with 6+ years) of advanced SAS programming experience working with large complex administrative healthcare claims databases.
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Medical Directors
(US-Massachusetts) Act as medical director on selected product development candidate programs. This includes designing clinical trials and an overall clinical development strategy leading to global product registration. Interpret results of Phases 1 - 3 clinical investigations in preparation for new drug applications to relevant regulatory authorities.
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Executives / Officers - Formulation & Development
(India-Maharashtra) The candidate should be M.Pharm with relevant experience in F & D Department in a reputed pharma company, should have knowledge of all dosage forms like tablet, capsule, liquid, cream, ointment, etc., should have knowledge of excepients used in various dosage forms, knowledge of handling of different equipments required for manufacturing, ability to optimize and develop new product, knowledge of preformulation studies, validation, documentation, ability to learn new techniques.
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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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Analytical Chemist - Proteins
(US-Massachusetts) Develop and validate analytical methods to support release, characterization and stability of therapeutic proteins, including HPLC, LC-MS/MS and other analytical techniques for protein and carbohydrate analysis. Independently design analytical strategies to develop complex analytical methods, to develop validation protocols and oversee execution of assay validations.
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General Manager - R&D
(India-Tamilnadu-Chennai) Will be incharge of R&D - Herbal Department. Candidate should be MSc (Chemistry), preference will be given for Ph.D (Phyto chemistry) with Ayurvedic background. Should have 7-10 years experience in research of Herbal products.
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General Manager - Production
(India-Tamilnadu) Will be incharge of fine chemical division activities. Should be BE/B.Tech/M.Tech (Chemical Engineering). 10 Years of experience as plant manager in a reputed Bulk Drug/Fine chemical Organization. Experience in commissioning and erection of new plant. Exposure to CGMP and ISO Standards.
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Product Manager - Devices
(India-Maharashtra) The product owner will be responsible for business development activities either through business units or external third parties. Activities will include, but not limited to, anything that will help maximise sales and profitability of the products. The product owner will develop strategic plans for product development, brand identity, market positioning, pricing and distribution channels in conjunction with the business units/and or third parties.
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Center Manager
(India-Maharashtra) To ensure the smooth functioning of the day-to-day technical and management functions of the clinic. To develop, plan, and schedule clinic workflow, based on the approved policies and procedures as framed by Goldshield Group and to achieve the business targets set by the group. To review, monitor, and revise the policies and procedures in close coordination with Goldshield Operations Manager.
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Director of Clinical Development
(US-Massachusetts) Reporting to the Global Head of Oncology, the Director of Clinical Development will plan, direct, implement and manage the strategy and clinical development of oncological biopharmaceutical products. The position will contribute to the planning of clinical trial programs for investigational new drugs based on an oversight of pre clinical, regulatory, manufacturing and quality assurance issues.
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Officer - Regulatory Affairs
(India-Maharashtra) Preparation of Registration Dossiers for Regulated and Non Regulated markets. Cordination with R&D and Production Departement for samples for Registration. Arranging Reports like pharmacology, toxicology, and clinical data. Maintenance and updating of existing authorisations.
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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. Along with the Medical Monitor, you will be responsible for study site selection; patient accrual, documentation of protocol violations; tracking study progress via standard reports; and management of adverse event reporting.
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Clinical Scientist / Experimental Medicine
(US-Massachusetts) Is your expertise in early clinical development? MD and / or PhD? If so - read on. A unique opportunity exists to lead the clinical sciences effort for an oncology drug discovery company! Here is what is needed: Phase 1, 2A experience. Implementing biomarkers. Proof of concept. Oncology. Clinical trial management. CRO / staff selection and management.
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Officer Q.C.
(India-Maharashtra) Raw material analysis, semi finished / finished product analysis, Packaging material analysis, Stability sample analysis. Desired Profile: Knowledge of handling of analytical instruments like HPLC, FTIR, disolution, Good analytical skills and ability. Ready to work in shift duties.
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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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Gene Expression / Data Mining
(US-Massachusetts) 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. To propose mechanisms and pathways affected by drug therapy which will be confirmed and validated by additional experiments. To extract implicit and novel information from complex and large databases to characterize genes involved in the physiological and/or the pathological state following drug therapy.
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Manager - Purchase
(India-Maharashtra) To formulate long term and short term strategic purchase planning. Will be responsible for Proposal Evaluation, Cost effective purchase with timely delivery, credit terms. To assess performance of vendors. To ensure optimum inventory levels. To implement the purchasing process. To maintain standards and quality through effective purchasing. Identify areas of opportunity that would result in cost savings and/or quality improvement.
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Clinical Program Manager
(US-Massachusetts) The Clinical Program Manager works within the Department of Clinical Operations to manage clinical studies that are designed to establish the safety and effectiveness of Company products. This person initially will focus on early clinical development, but will have the ability to bring one or more of these products to Phase III development, as necessary.
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Senior Scientist - Pharmaceutical Development
(US-California) Develop and transfer to contract sites drug product manufacturing processes. Develop formulations for typical oral and parenteral dosage forms including aseptic solutions and freeze-dried parenterals, capsules, tablets, oral solutions and suspensions. Develop dosage forms and processes consistent with all requirements of corporate partner(s) and US or EU regulations.
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Marketing Manager
(India-Maharashtra) To understand marketing guidelines. To implement marketing strategies, building and maintaining customer base. To effectively manage all interfaces of the Clinic with individuals and corporate. To make sales call to various target groups like doctors, corporate, and other laboratories and facilities. To prepare and achieve monthly / quarterly / yearly targets.
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Formulation Scientist
(US-Massachusetts) Scientific Ph.D. or equivalent combination of education and working experience with 4+ years of working in the protein formulation development or related fields. Must have strong analytical skill with relevant physical and chemical analytical instrumentation for protein characterization. Experiences with liquid and solid protein drug formulation, process and maintaining product stability program are essential.
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Molecular Biologist
(US-Massachusetts) 1) The selected individual will be responsible for mode of action (MOA) studies to further the developmental pipeline; 2) Target identification and validation; 3) Determination of mode of action of small molecule compounds; 4) RNAi. The candidate will be an active contributor to both exploratory and drug discovery project teams.
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General Manager - HR
(India-Tamilnadu-Chennai) Over all incharge of HR & Admin activities. Candidate should be a post graduate preferably MBA from reputed institute with HR & IR as core subjects. Experience of 10-15 preferably from either FMCG or pharmaceuticals industry. Holding at least senior Management level. Should be well versed with IR, HR and Training function. Should be a good team leader. Candidates working in BPO industry will also be considered.
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General Manager - Sales
(India-Tamilnadu-Chennai) Will be incharge of sales and distribution activities of all over India. Candidate should be a Post Graduate with MBA from reputed Institution. Should have 10 - 15 years of experience in FMCG Industry. Exposure to National Level is must.
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Biotechnology Curriculum Writers
(Anywhere-Telecommute) Rebirth is seeking experienced school curriculum writers to create and develop biotechnology curriculum for Kindergarten through High school textbooks. Must be experienced in designing and writing standards-based elementary curriculum, instruction, and assessment. In addition to the above, you may have experience in chemistry, biology, molecular biology, or physics.
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Service Engineers
(India) Installation of Biomed Equipment. Maintainance of Biomed Equipment. After Sales Service. Proactive calls to Customer. Job involves fieldwork. Data update in the system. Desired Profile Must be B.E/B.Tech or Diploma (Electronics/Bio Med, Medical Instrumentation). Relevant Experience in the similar field. Good Communication skills. High degree of customer centricity.
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Application Specialist
(India) Has to solve the queries regarding the products, Demonstration. Training to Technicians. Desired Profile Candidate should be Diploma/Degree in Bio Instrumentation, B.Pharma etc. Product Demonstration and Problem Solving.
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Business Executives / Management Trainee - Diagnostics Products
(India) Responsible for assigned territory. Has to promote monopolistic product to various blood banks, laboratories and institutions. Has to achieve the desired targets within a stipulated time period. Desired Profile: Candidate has to be graduate in science / Microbiology / Biotechnology / B.Pharma.
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Business Executives / Management Trainee - HomeHealth
(India) Responsible for assigned territory. Has to promote point of care products like blood pressure monitor, blood sugar monitors and weighing scales, heating pads, massager etc. to retailers, sports shop, chemist and customers directly. Has to achieve the desired targets within a stipulated time frame. Desired Profile: Candidate has to be graduate in science/commerce, preferably with diploma in engineering.
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Department Manager - Bioinformatics
(India) Manage, direct and provide leadership to the team professionals trained in biology, statistics and other related disciplines, organized in several departments. Overall product responsibility for all bioinformatic products from design to customer service. Accountabilities: Monitor new technologies and innovate new products. Communicate with customers and experts to understand unmet needs and translate them into features or products.
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Associate Product Manager
(US-Pennsylvania-Pittsburgh) Urgent need for an Associate Product Manager in the Pittsburgh area. This position would be the general manager of their business responsibility as well as accountable for all aspects of running his/her business. This person will also serve as the lead marketing role in commercialization of new products. The Product Manager is expected to possess all skill sets necessary to run the business, effective marketing mix development and implementation.
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Product Manager
(US-Pennsylvania-Pittsburgh) This position will support inbound and outbound marketing activities such as: 1.Product management responsibility for selected products in product-line. 2.Product line performance reporting, including detailed price and margin trend analysis, to identify opportunities and drive improvements. 3.Develop and implement targeted promotional and training activities. 4.Develop annual five-year product portfolio plans. 5.Develop business case analysis and financial modeling of new product opportunities.
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Associate Scientist - Molecular Diagnostics
(US-California-Silicon Valley/San Jose) Helping in the design and execution of moderately complex experiments in chemistry, molecular biology, and biochemistry, with minimal supervision. Maintaining and organizing laboratory in a compliant manner (ordering supplies and equipment; calibrating laboratory instrumentation regularly and keeping calibration records; maintaining lab records, material safety data sheets, equipment manuals, and standard operating procedures; etc.)
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Director Business Development
(US-Massachusetts-Boston) Director of Genomics Business Development will represent company in the industry and actively increase revenue from current and potential customers within the Genomics Programs and Services sector of the business. Will define and execute the strategies necessary to penetrate and expand customer base and achieve revenue growth.
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Product Manager and Genomics Specialist
(India) Require Highly motivated and charged species who have their genes expressing to have desired levels of traits which can help in marketing and establishing our offered solutions for genotyping and gene expression. For Product managers the ideal candidate should atleast have a Masters/Phd Degree in life science with prior expereince of hands on wet lab Microarray or any other Genotyping/Expression toools.
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Senior QA Officer
(UK) Our client has requested the expertise of a candidate with the following criteria: Product release; Batch Review; Product Review; GMP; QA systems in production; Preparation of QA procedures and reports. 5 years QA experience within the pharmaceutical sector. Knowledge of GxP. Aseptic Processing. Isolator technology (viall filling).
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Engineer, Teperature Control
(US-California-Oakland/East Bay) This person will be an expert for temperature control skids used by major manufacturers in the pharmaceutical industry. As an engineer, this person will be working with current products and new product development including computer- controlled refrigeration systems. The job includes a wide range of disciplines including familiarity with electrical, mechanical, biochemical, and software engineering.
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Managing Consultant, Revenue Cycle
(US-California-San Francisco) We are seeking an experienced revenue cycle professional with Patient Access and/or Patient Financial Services expertise. The individual must have prior, hands-on responsibility for assessing, planning implementing and directing the transformation of key revenue cycle business processes.
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Lab Manager
(US-Florida-Gainesville/Jacksonville) The successful candidate will have at a minimum 5 years of experience as a polarized light microscopist for asbestos bulk sample analysis and have attended at least one week of formal training in PLM for asbestos identification. The successful candidate will have at least 3 years experience as a NVLAP laboratory manager or assistant manager.
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Electrophysiologist
(Canada) The successful candidate will join an interdisciplinary, highly motivated team dedicated to the identification of new drug candidates using both conventional and automated patch-clamp technologies. Responsibilities will include whole cell patch clamp analysis and optimizing automated patch-clamp instrumentation towards screening for high affinity and selective drug candidates against a number of ion channel targets.
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Manufacturing Technician
(Spain-Madrid) Our client, Pharmaceutical company is looking for 18 manufacturing technicians Part of the sterile Manufacturing Department, you will be in charge of: Manufacturing sterile products to GMP standard Generate, record and check data on Manufacturing records. Other tasks: general maintenance and cleaning production areas.
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QC Manufacturing Supervisor
(Spain-Madrid) Part of the sterile Manufacturing Department, you will be in charge of the following: Managing a team of manufacturing technicians: assignment, attendance checking, training QC supervision Responsibility on specific Manufacturing sterile products activities to GMP standard. To check and validate the data on Manufacturing records.
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Senior Scientist I
(US-California-San Francisco) Will be responsible for analytical related activities including method development/validation for small molecule, in-process support of the API manufacturing , drug product development, analytical method generation, and analytical technology transfer. Will also be responsible for release and stability testing, set up specifications, investigate out of specification or out of trend results, and troubleshooting of methods/ developing separation technology and preparing analytical and stability reports and documents for regulatory submissions.
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Informatics Scientist
(Canada) Our Drug Discovery Division is expanding and we are looking for an Informatics Scientist to facilitate drug discovery via best use of the relevant scientific data, information and software tools such as Accelrys Accord, DIVA, MDL, ISIS Base, and Pipeline Pilot. The Informatics Scientist will administer computer-based applications supporting biology and chemistry data acquisition and handling, ensuring that the information is both catalogued and available across the research groups.
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R&D Scientist
(India-Delhi-New Delhi Suburbs) A new company started and funded by international venture capitalists together with scientific professionals, will be in the areas of a) technical consulting, b) contract research and c) applied research is looking to hire dynamic professionals in the following areas: Molecular Biology; Cell Biologists; Protein Biochemists; Bioinformatics; Genomics and Microarray Specialists.
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Director of Oncology
(US-New York-Westchester) Oncology Director needed. Requirments: Registered Nurse/Masters in nursing, business or health care adminstration- 5-10 yrs of progressive mgmt experience. 3-5 years of related clinical experience. Current national certiciation/ny license.
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Clinical Nurse Educator
(US-New York-Westchester) Clincial nurse educator needed. Graduate degree in nursing. Current nys state licensure. Minimum 5 years experience in pediatric setting. Pediatric icu experience. Help hospital prepare for jcaho results. Develop and implement clinical skills training programs for nurse in long term car, rehab and acute care facilities.
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Patient Care Director for Surgical/Ortho Floor
(US-New Jersey) NJ hosptial seeking a patient care director w/ current nj nursing licensure.
BSN required, masters in nursing - prior proven experience and expertise in clinical area relevant to unit patient. Proven experience and expertise in leadership - certification in area of specialization. Surgical or pacu experience.
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Grant Writer
(US-New York-Westchester) Grant writer needed to work w/ various departments to develop fundable projects, research grant opportunities, coordinate grant proposals - to report to executive director familiarity with section 3 hrsa grants preferred.
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