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    Principal Investigator/Senior Scientist - Moscow, United States - Alturas Analytics, Inc

    Alturas Analytics, Inc
    Alturas Analytics, Inc Moscow, United States

    3 weeks ago

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    Description

    Job Description

    Job DescriptionDescription:

    We are seeking a highly skilled and experienced Principal Investigator to join our dynamic team. As a Principal Investigator, you will play a crucial role in leading and overseeing our bioanalytical projects and studies, with a strong focus on mass spectrometry and LC-MS/MS techniques.

    The ideal candidate will have extensive experience in bioanalytical contract research organization (CRO) settings, demonstrating a deep understanding of the field and a proven track record of successful project management. At Alturas Analytics, Inc., we offer a supportive and collaborative environment that encourages innovation and provides leadership opportunities.

    Relocation assistance may be available. Located in a vibrant college town, Moscow, Idaho is a friendly community with beautiful natural surroundings and a lively cultural scene. You'll enjoy walkable streets, live music, and access to some of the best outdoor recreation opportunities in the country.

    Benefits

    We have a relaxed yet professional environment. We strive to be a part of our community as well as a part of each other's lives through volunteering at local schools and community events as well as parties and monthly catered lunches. We're growing and doubling our lab capacity this year, so promoting from within and offering professional development opportunities are top priorities. We pay 100% of your premiums for health insurance, dental, vision, life and short- and long-term disability. We also have paid vacation and holidays, a Safe Harbor 401K with an automatic 3% employer contribution, and a bonus program based on company-wide goals.

    About the Role

    The Principal Investigator/Senior Scientist is responsible for method development, method validation, analysis of samples, and generation of plans, data, reports and other applicable documentation to support drug development studies according to, and within compliance of, all applicable procedures and regulations.

    Essential Duties and Tasks:

    • Ensures that project details (e.g., time lines, data, reports) are reported fully to laboratory management and clients
    • Acts as a project manager to ensure projects are kept on-track
    • Provides scientific expertise in the development of methods and method validations
    • Acts as a resource for lab personnel regarding operations of the laboratory
    • Develops and validates methods in accordance with procedures, regulations, and guidelines
    • Analyzes samples and generates data and reports in accordance with procedures, regulations and guidelines
    • Maintains laboratory equipment, including troubleshooting and repair of LC-MS/MS and GC-MS/MS instruments
    • Works closely with QA personnel to ensure compliance
    • Evaluates equipment, procedures and techniques to improve laboratory procedures
    • Prepares laboratory technical procedures
    • Prepares and/or reviews correspondence, notifications, reports and other documents
    • Prepares documents and materials for scientific publications, presentations, short-courses and workshops
    • Travels occasionally for professional development or to represent the company at client sites, professional organization and trade show venues
    • May fulfill a supervising role for other laboratory or facility personnel

    Additional Duties and Tasks Roles:

    • May perform QC review of data if needed
    • May participate in research projects for publications and poster presentations
    • May represent the company by leading webinars or seminars or by presenting information at professional meetings.
    • May provide technical training to other employees on laboratory skills, procedures, systems
    • Provides assistance to laboratory management
    • Performs other duties as needed or assigned
    Requirements:

    Education and Experience Requirements:

    • Graduate degree (M.S. or Ph.D.) in chemistry, or related field, plus 2 years work experience in a bioanalytical CRO or a Bachelor's degree in chemistry, or related field plus 4 years work experience in a bioanalytical CRO
    • At least 2 years work experience in a regulated bioanalytical mass spectrometry laboratory, including method validation, analytical instrument maintenance, data acquisition and management, and sample analysis
    • 1-3 years minimum of supervisory or managerial experience in a laboratory setting preferred
    • Knowledge of Good Laboratory Practices (GLPs) and other regulatory guidance preferred
    • Working knowledge of complete MS Office suite and Adobe Acrobat
    • An equivalent combination of education and experience may qualify the appropriate personnel for this position

    Skills and Abilities Requirements:

    • Skills in laboratory techniques and procedures
    • Skills in verbal and written communication
    • Skills in problem solving and supervising staff towards meeting client deadlines
    • Skill in supervising personnel, to include delegating responsibility, training and evaluating performance
    • Ability to function effectively in stressful situations
    • Ability to interpret and apply agency regulations and guidelines
    • Ability to communicate with other employees in order to develop sound procedures and policies
    • Ability to travel occasionally for professional development

    Physical Requirements:

    • Sitting up to 2/3 of the time
    • Working in front of a computer monitor up to 2/3 of the time
    • Walking up to 1/3 of the time between departments/offices
    • Standing up to 2/3 of the time
    • Using hands to handle or feel up to 2/3 of the time
    • Reaching with hands and arms up to 2/3 of the time
    • Talking or hearing over 2/3 of the time
    • Lifting up to 10 lbs. up to 2/3 of the time
    • Lifting up to 50 lbs. less than 2/3 of the time
    • Close vision (clear vision at 20 inches or less) needed to read small labels
    • Depth perception

    About Us

    Alturas Analytics, Inc. is a bioanalytical laboratory dedicated to supporting pharmaceutical drug candidates from discovery through late phase clinical trials. Our vision: supporting transformative medicines for a healthier future. More specifically, we provide expert GLP and Non-GLP LC-MS/MS and GC-MS/MS quantitation and PK/TK analytical services in both small and large molecules. We are a growing, privately-owned CRO specializing in method development, validation, and sample analysis in all biological matrices in support of therapeutic development programs.

    Community Involvement

    Our goal is to build an enduring company of integrity in an environment that provides rewarding career paths, and empowers individuals to engage in the well-being of the communities in which they reside.

    We seek to inspire the next generation of scientists through involvement of educational programs at every level. From making science fun for elementary-aged students, active participation in science fairs and guest lecturing at the undergraduate university level, we are stepping towards fostering a generation where science is exciting and an integral component of everyday life.

    In addition to company support for community programs, Alturas offers employees paid time-off for individual volunteer activities and matching monetary donations to numerous 501(c)(3) organizations.

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.



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