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Required Technical Skills : Knowledgeable of IPS elements as they pertain to pharmaceuticals, vaccines, and blood products; Understanding of the Army and DoD field medical force structure; Proficiency with MS Office Suite; Must possess excellent writing and verbal skills and be able to author supporting documentation for the DoD acquisition process and be able to brief medical logistics requirements to PdMs and PjMs.
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Author and utilize standard procurement tools such as Statement of Work (SOW), Project Order, Letter of Intent, Non-Disclosure Agreements (NDA), and/or Confidentially Disclosure Agreements (CDA.
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As required by specific animal research protocols, documentation shall be performed to standards required by the Good Laboratory Practices (GLP) regulations. Minimum of five (5) years' experience in laboratory animal clinical medicine and surgery, with non-human primate expertise, rodents, and rabbits.
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Submit required employment documentation, including all official post-secondary transcripts, in a timely manner. Adjunct Job Description Adjunct faculty in Human Services will have a Master’s Degree in a related field (e.g., Counseling, Social Work, Human Services), and is licensed as an LCPC , LPC , LCSW -C, LCSW , LMSW , or LCADC , with a focus on counseling, addictions, social work, or the human services fields.
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Must meet Biological Personnel Reliability Program (BPRP) and Controlled Substance-Personnel Reliability Program (CS-PRP) requirements. The Alaka`ina Foundation Family of Companies (FOCs) is looking for a Laboratory Research Veterinarian to support our government customer located in Fort Detrick, Maryland.
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Your team, consisting of a secretary, paralegal, support specialist, will assist you in preparing necessary legal documentation, conducting depositions, investigating/researching, and evaluating cases for settlement, arbitration, and trial.
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Oversee logistics for apartment setups for newly arrived refugee families, including: monitoring and matching Good Neighbor Partner (GNP) groups with families; communicating necessary client information and setup guidance; liaising with GNP and case management staff, ensuring the furnishings and supplies are provided through home setups in accordance with program guidelines, and appropriate documentation is completed.
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Maintain robust CAPA, nonconformance, QMS electronic documentation and complaint management systems. Ensure participation in project team meetings as a Quality representative and contribute toward development of relevant design control and risk management documentation for commercial diagnostic products.
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Maintain and update RMS and Procore for applicable project documentation. We are seeking an experienced Construction Quality Control Manager (QCM) and Site Safety & Health Officer (SSHO) to join our dynamic HGC team, a subsidiary of Bristol Bay Construction Holdings LLC (BBCH.
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As a Drafter / Designer for NVR , parent company of Ryan Homes and NVHomes , you will be part of the team responsible for developing the construction documentation and programming used throughout the sales, permitting, and homebuilding processes.
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Establish process and documentation for EM monitoring program to support cGMP manufacturing (MFG) operations. Knowledge of cGMP requirements and good documentation practices. Serve as liaison between MFG and contract cleaning services to monitor cleaning service effectiveness, adapt to MFG schedule, etc.
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Follows food quality standards, accurate documentation of heating and cooling HACCP compliance, and maintains temperature logs. Committed to the Revolution Foods mission that all children will have access to nutritious, tasty food to support the development of healthy minds and bodies.
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Support and follow the Site Safety manager with site safety observations and safety documentation organization. Support and follow the Site Construction Manager with vendor and manpower observations, schedule tracking, and project documentation.
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This is an exciting opportunity to join Thermo Fisher Scientific where you will support the manufacturing documentation review department by facilitating timely release of batch records to ensure that customer needs are met while adhering to cGMP quality and compliance standards.
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Duties may include venipuncture, medication and vaccine administration, measurement, and documentation of vital signs, and assisting providers with patient exams, and telephone and clerical support.
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author documentation jobs in Frederick, MD
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