Bostwick Laboratories® a full-service laboratory specializing in uropathology, dedicated to the diagnosis, treatment and subsequent management of prostate cancer, kidney disease, cancer of the bladder and other urologic conditions is currently seeking an experienced Microbiology Supervisor . The qualified team leader, Manages and coordinates the procurement of laboratory supplies and equipment; Monitors standing orders, negotiating supply contracts, continued evaluation pricing/discounts, and termination of agreements with vendors. Supervise and control inventory distribution; Plans the testing and calibration procedures according to validation protocols for instruments and equipment; Maintains continued service of laboratory equipment. Notification of vendors in the event of equipment malfunctioning; and, Prepares Quality Control documents, temperature control log sheets, equipment maintenance log sheets, discrepancy logs, calibration logs, and general work performance logs.
Successful applicants should possess a BS Degree or higher in Clinical Laboratory Sciences including comprehensive knowledge of Microbiology and have eight (8) to ten (10) years experience gained through increased responsibility in a management position, with a minimum of three years experience in Microbiology. Experience with CAP and NYSDOH proficiencies and regulations, ASCP Certified as a MT and NY State License is required.
Job Title: Post Doctoral Fellows
Company: Roche NimbleGen, Inc
Location: Madison, WI
Description:
Make your mark. Improve lives.
Follow your passion: Roche NimbleGen, Inc., a Madison, Wisconsin based growing leader in the life science industry is adding Post Doctoral Fellows in a variety of disciplines. These are one year appointments, and involve working under the direction of Senior Scientists and Directors in our Research and Development department. Our success is built on innovation, curiosity and diversity, and on seeing each other’s differences as an advantage. Roche has ambitious plans to keep learning and growing – and is seeking people who have the same goals for themselves.
The Position:
The Fellows will join Roche NimbleGen’s research and development group. The individuals in these roles may participate in interdisciplinary projects with Roche’s Pharmaceutical Division, as well as projects focusing on the development of high profile applications of our microarray platforms. Successful completion of the key projects will advance RNG’s R&D efforts, identify and develop new microarray applications, and foster adoption of RNG technology within Roche, its affiliates and the larger research community.
These roles will provide opportunities to work in an industry setting in areas including:
Sequence Capture
Expression
Methylation
ChIP-chip
Comparative Genomic Hybridization (CGH)
Copy Number Variation (CNV)
Who you are:
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point. Your experience includes:
Ph.D. in life sciences
Advanced understanding of the research literature, concepts and methods related to microarrays (cellular biology, molecular biology, biochemistry, and bioinformatics).
Advanced knowledge of the quantitative and qualitative methods related to microarray research.
Capabilities related to authoring and/or co-authoring of research-based reports/articles.
Demonstrated ability to communicate effectively within an R&D environment and throughout the organization.
Basic knowledge related to methods and tools related to microarray analysis desired, advanced skills are preferred.
For more information visit our careers page.
Roche NimbleGen, Inc. develops DNA microarray and chemistry technologies, providing the highest density arrays available in the industry in a fraction of the time of conventional microarrays. The company's patented Maskless Array Synthesizer (MAS) technology provides highly customized oligonucleotide array design, manufacture, hybridization, and analysis services to researchers in biotechnology, pharmaceuticals, government and universities. NimbleGen's products and services aid researchers in high-throughput, low-cost screening for genotyping, gene expression analysis and toxicity screenings.
Job Title: Sales Rep-New Business Devel.
Company: ISIS
Location: San Carlos, CA
Description:
ISIS Services, a Bay Area life science company, provides contract research and development services to the medical device, pharmaceutical and biotechnology communities. We are seeking an experience sales professional to help support our continued growth. Candidates should have a demonstrated track record of success in sales. Responsibilities include sourcing and developing new client leads, qualifying them for further development and then working in conjunction with internal staff to complete a sale.
SPECIFIC DUTIES AND RESPONSIBILITIES:
Engage potential new clients in the medical device, biotechnology, pharmaceutical and life sciences communities through cold calls, facility visits, on site and web presentations, conference calls, trade shows, etc. in order to grow sales.
Facilitate introduction of potential new clients to our content experts by setting up opportunities to meet or consult on protocol development.
Attend local industry networking events and dinners as necessary.
EDUCATION/EXPERIENCE/SKILLS REQUIRED:
Professional appearance essential, as well as ability to present and communicate verbally and in writing in an effective and persuasive manner.
Minimum of Bachelor’s Degree.
Sales professional with demonstrated experience in sales and/or business development required.
Experience in the life sciences, pharma or medical device industries a plus.
Must be proficient in electronic communication modalities such as Microsoft Office, email, PDA, etc.
Excellent customer service skills.
Excellent interpersonal and organizational skills.
Mostly Bay Area travel
Job Title: PhD Level Microbiologist
Company: CDC
Location: Atlanta, GA
Description:
Microbiologist will serve to provide international laboratory training and support for surveillance of the key bacterial respiratory and meningitis pathogens-- Streptococcus pneumoniae, Haemophilus influenzae, and Neisseria meningitidis. Flexibility for international travel is essential, as are good interpersonal skills and an ability to work in developing country settings with a variety of partners. Principal roles of the position are to provide laboratory bacterial surveillance training and to evaluate the challenges and needs of laboratories involved in surveillance in developing countries. In addition the individual will perform large-scale strain characterization for international surveillance projects. Necessary training to carry out these roles will be provided for the individual in the CDC Division of Bacterial Diseases Streptococcus and Meningitis Laboratories. The individual must be flexible and able to adapt to routine testing for long duration, interspersed with more specialized scientific studies.
The position requires familiarity with high-throughput strain characterization at the molecular and phenotypic levels and knowledge of molecular diagnostics and molecular protocol development strategies that will be applied for these three bacterial pathogens. The fellow will assist in developing multiplexed real time and conventional PCR assays for identifying and characterizing these species. The individual will also carry out technologically advanced, large scale, molecular studies from clinical specimens when viable strains are not obtainable in order to identify the etiologic agents as well as serotype and genotype them. High throughput classical bacteriology procedures will also be performed, including strain isolation, culture, long term storage, serotyping, and antibiotic susceptibility testing. This individual will be required to interpret complex strain characterization data and requires skills required to routinely summarize data in scientific presentations.
Qualifications.
Ph.D. in Microbiology or related field, with at least one year post-doctoral laboratory experience.
Authorship/coauthorship of at least 5 peer-reviewed papers pertaining to Microbiology.
Experience working with or in developing country laboratories.
Clinical lab experience is highly desirable.
Proficiency in a language useful in some developing country settings is highly desirable.
Job Title: Biostatistics Manager
Company: SciencesCrossing
Location: Thousand Oaks, CA
Description:
Biostatistics ManagerResponsibilities:
Contributes to study design and planning, including choice of endpoints, choice of statistical methods, sample size and power calculations, study design, and randomization specification.
Contributes to the design of case report forms and data checks, prepares Statistical Analysis Plans, supports and works with statistical programmers, writes TLG specifications to support the work of statistical programmers, drafts summaries of clinical trial results, supports completion of study reports, integrated summaries, abstracts, papers, presentations and annual updates.
Responds to team and regulatory requests for ad hoc data analyses, helps team members interpret both planned and ad hoc analyses, monitors statistical soundness of data presentations and explains assumptions required for validity.Requirements:
A Graduate degree in statistics, biostatistics is required.
0-1 years of pharmaceutical experience with a PhDis required.
2+ years of experience with a Master's degree is required.
Experience in oncology is preferred.
Knowledge and ability to apply statistical method routinely used in clinical trials.
Knowledge of relevant regulatory guidance regarding statistical analysis and methodology.
Proficient use of statistical analysis software.
Project management skills.For further information, please visit us online at http://www.sciencescrossing.com Please send your resume to SciencesCrossing at Register to View Apply Now
There will be charge of $29.95 per month (or a lower monthly rate based on agreement length) after your 7 day FREE Trial to use our service.
Job Title: Laboratory - Supervisor, Microbiology - 0800005841
Company: St. Joseph Medical Center Towson
Location: Essex, MD
Description:
THIS POSITION IS LOCATED IN TOWSON, MARYLAND
Job Summary: This job is responsible for the coordination and oversight of administrative and clinical activities relating to the daily operations of a laboratory function in accordance with established business objectives and applicable accreditation/regulatory requirements. An incumbent serves as the point-person for issues impacting the assigned lab facility. Work includes: 1) timely, responsive and cost-effective staffing/scheduling of lab professional and support staff for the assigned facility; 2) serving as liaison with various internal departments in coordinating and troubleshooting various business-related issues; and 3) directly supervising staff engaged in lab-related work activities. An incumbent is a first-line "working supervisor", and may spend a moderate amount of time (10%-20%) performing laboratory work that requires professional certification MT (ASCP preferred).
Essential Duties:
Supervises daily operations of the assigned laboratory to provide adequate coverage for all shifts and balance workflow to maximize utilization of resources; observes and monitors staff adherence to established policies, standards and procedures, and facilitates ongoing compliance of these and other applicable laboratory regulatory agencies (e.g. JCAHO, CAP, etc).
Assigns, supervises and evaluates the work of subordinate staff engaged in technical and professional lab activities; interviews job candidates and makes hiring recommendations, ensuring that employees are qualified and properly trained to perform job duties; communicates performance objectives and evaluates individual performance.
Receives notification from employees who are not able to report to work for assigned schedule (e.g. sick, FMLA, etc) or who are requesting planned time off (e.g. vacation, holidays, in-service training, etc).
Participates directly in staff development activities, to include LEAN and Rapid Process Improvement initiatives; coordinates the general orientation and training of assigned staff, and records/reports progress of individual employees.
Tracks and enters Quality Incident Monitor forms (QIMs) into tracking database; identifies and alerts manager of significant issues; suggests improvements to reduce incidents via LIS change forms and feedback to manager and staff.
Participates inadministrative departmental budget planning and oversees the ordering of lab supplies and ensures adequate inventory is available and logged in according to established guidelines; alerts manager and Inventory Specialist of reagent lot # or back-order situations.
Reviews QC on an as-needed basis, or at least monthly by each analyte;
Takes action to address and resolve operational or service issues (as received from physicians, nurses, clients and staff) in accordance with established standards; initiates and reviews IRIS incident reports according to established timelines; follows up on any unresolved issue(s) with manager in a timely manner, including coordinating with internal departments and/or external agencies as necessary; monitors and evaluates general customer service work practices and procedures, providing recommendations to improve operational efficiency and regulatory compliance.
Attends hospital operational meetings (e.g. Safety, Disaster Planning, etc) as representative of the assigned Lab, and communicates general information and upcoming changes to Lab Staff and Lab Operations Mgr.
Keeps abreast of organizational initiatives and trends, technologies and regulatory requirements with potential for impacting matters within designated scope of responsibility; researches nature/scope of impact on existing activities and recommends effective solution/response.
May perform the professional duties of a Medical Technologist (refer to Medical Technologist job description, job code 2099) as necessary.
Job Requirements
Education:
Bachelor of Science Degree in Medical Technology or related field of Laboratory Science.
Experience:
Four years of related clinical laboratory experience as an MLT or MT, obtained in a hospital setting within the last 8 years.
Experience in a “lead,” MT Coordinator or supervisory role is strongly preferred.
License/Certification:
MT (ASCP)
Additional Responsibilities:
Demonstrates a commitment to service, organization values and professionalism through appropriate conduct and demeanor at all times
Adheres to and exhibits our core values: Reverence: Having a profound spirit of awe and respect for all creation, shaping relationships to self, to one another and to God and acknowledging that we hold in trust all that has been given to us.Integrity: Moral wholeness, soundness, uprightness, honesty and sincerity as a basis of trustworthiness. Compassion: Feeling with others, being one with others in their sorrows and joys, rooted in the sense of solidarity as members of the human community. Excellence: Outstanding achievement, merit, virtue; continually surpassing standards to achieve/maintain quality.
Maintains confidentiality and protects sensitive data at all times
Adheres to organizational and department specific safety standards and guidelines
Works collaboratively and supports efforts of team members
Demonstrates exceptional customer service and interacts effectively with physicians, patients, residents, visitors, staff and the broader health care community
Job Title: SCIENTISTS IN BIOTECHNOLOGY INDUSTRY
Company: Privately Placed in The Day
Location: New London, CT
Description:
BECAUSE Our CAUSE is Greg and his cancer. Greg, Patient Opportunities in Development Sciences at Genentech For more than 30 years, Genentech has been at the forefront of the biotechnology industry, using human genetic information to develop novel medicines for serious and life-threatening diseases. Today, Genentech is among the world s leading biotech companies, with multiple therapies on the market for cancer and other serious medical conditions. The core mission of Development Sciences is to enable the identification, selection, development and commercialization of safe and effective small molecule and antibody-based therapeutics by providing key scientific and strategic input from the sciences of pharmacokinetics, pharmacodynamics, molecular diagnostics, biomarkers, toxicology, pathology and bioanalytics. These various functions work together in a highly cross-functional manner along with colleagues in Research and Clinical Development to select molecules for development, develop molecules into potential therapies and ensure that future Genentech therapies are safe and effective for patients through clinical trials. Our group drives the development of breakthrough therapies through innovation, decisive leadership, teamwork and effective partnerships with regulators and collaborators. Our expanding pipeline in the areas of small molecule, macromolecule and antibody drug conjugate has created opportunities for talented scientists at all levels, including Directors, in the following departments in our South San Francisco, CA, headquarters: * Clinical Pharmacokinetics and Pharmacodynamics * Modeling and Simulation * Early Stage Pharmacokinetics and Pharmacodynamics * Pharmacodynamic Biomarkers * Toxicology * Investigative Safety Assessment We aim to provide employees with a stimulating and collaborative environment where they can make important contributions to medicine and thrive as professionals. Our unique culture is characterized by a commitment to science, a dedication to patients and a respect for individuals and their contributions. To learn more about our current opportunities and apply for a position, please visit careers.gene.com. Use Ad The Day when a source is requested. For immediate consideration, please email your resume to Register to View Genentech is an equal opportunity employer. In October 2008, Genentech was named top employer in the biopharmaceutical industry by Science magazine.TDDClick to view ad from The Day
Job Title: MicroBiologist I
Company: Bio-Rad Laboratories - Clinical Diagnostics Group
Location: Hercules, CA
Description:
Join us at the forefront of scientific discovery! At Bio-Rad Laboratories, you will participate in exciting new developments at the cutting-edge of science and technology. Our teams of dedicated professionals work together in an entrepreneurial atmosphere, providing a broad range of innovative tools and services to the clinical diagnostics and life science research markets. Bio-Rad was founded more than 40 years ago, and we are recognized as a world leader in science and research. Visit us at www.bio-rad.com
Position Responsibilities: Preparation/qualification of media/reagents. Lab monitoring, maintenance and cleanup. Quality documentation, including data entry, equipment logs and inventory lists. Routine/investigational analyses of DI water system and environmental samples, including bio-burden, Total Organic Carbon, airborne particulates (TAP, VAP), and surface viable (SV). Knowledge, ability and skills to apply GLP and GMP on a daily basis.
Job Requirements
Education: B.S. degree in Microbiology; or equivalent degree in Biological Sciences with lab and coursework in Microbiology.
Experience: Minimum 6 months to 1 year of laboratory work experience, preferably in a microbiology laboratory or pharmaceutical/GMP environment.
Skills: Aseptic technique, environmental monitoring, bench-top testing, documentation/record keeping. Following written procedures and/or verbal instructions precisely with a commitment to testing accuracy. Problem solving and trouble shooting. A responsible and reliable team player. Good and open verbal/written communication; proficient data entry and computer skills.
Description:
Global biotech company seeks salesperson for a territory based in the general Baltimore / DC area. Seeking Biology or related degree, post graduate experience in the lab a +. Scientific sales experience preferred.
Please attach a current resume in Word in reply. All inquiries will be treated with the utmost confidentiality and discretion.
Location: Baltimore / DC & vicinity
Compensation: up to 95k base DOE car allowance, commission
Principals only. Recruiters, please don't contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
Job Title: Technologist Trainee to Senior Technologist-Microbiology
Company: Laboratory Corporation of America
Location: Burlington, NC
Description:
Performs tests and analyses in an entry level capacityaccording to established testing procedures indesignated technical department. Gains knowledge ofdepartment procedures and operations.1st ShiftTuesday-Saturday8:00am-4:30pmRequired Skills:B.S./B.A. Degree in Biology, Chemistry or related
science (or 24 credits in Chemistry/Biology constituting
a biological science major) as required by CLIA.
Req. Code : 096107a
Division/Department : LabCorp