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19-Oct-2018Nashville, NC+17 milesTechnology Jobs
Job details Technical Writing role writes, or supports the development of, various technical documents such as: requirements, specifications, test plans, and user manuals within this research-based pharmaceutical company. ONLY WANT LOCAL RESUMES, MUST BE WITHIN AN 1-2 HOURS WITHIN ROCKY MOUNT, NC HQ Responsibilities Understands validation concepts in order to produce documentation for validated...
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Position title : Sr. Quality Specialist Location : Rocky Mount, NC Duration : eighteen months Contract The Sr. Quality Specialist shall independently conduct and write complex formal investigation reports with input from area SMEs. The applicant will function as an independent reviewer of drafted investigations providing constructive feedback and in some instances act as a coach to the investig...
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Interprets federal and state and/or international regulations as they apply to laboratory processes supporting GMP operations. Identifies and/or leads key projects for continual improvement of compliance in laboratories and may extend to other site operations as appropriate. Major Accountabilities Assists with investigations and resolving compliance problems, questions, or complaints received f...
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Summary of Work Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures within this pharmaceutical industry innovator. Assists in writing and performing method validations and method transfers. Assists in pro...
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ROLE SUMMARY The R2 Manufacturing Quality Engineer provides oversight and guidance in R2 SVP manufacturing operations, ensuring continuous facility and GMP compliance. The R2 Manufacturing Quality Engineer will coach manufacturing personnel on proper GMP and SOP compliance and empower them to identify and escalate quality issues, to ensure quality product. ROLE RESPONSIBILITIES Conduct evaluati...
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Our client has been a leader in the pharmaceutical industry for over 60yrs. They are committed to finding, developing, and introducing innovative medicines that meet the evolving needs of healthcare professionals, patients, and caregivers. Summary of Work Support the 2016 Network projects which drive simplification and increases efficiency of our data network. Contribute to all aspects of enter...
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Our client has been a leader in the pharmaceutical industry for over 60yrs. They are committed to finding, developing, and introducing innovative medicines that meet the evolving needs of healthcare professionals, patients, and caregivers. Position description Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, ...
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The Quality Manager is responsible for establishing and reviewing process controls, emphasizing customer satisfaction, continuous improvement, and waste reduction. Measurement systems and inspection techniques are to be developed and maintained to advance department goals and objectives in support of plant goals and objectives as monitored and reported through Key Performance Indicators (KPI). ...
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Position description Our Client, a leader in the pharmaceutical industry, is seeking a Technical Writer familiar with SAP and has strong computer skills. This position can sit in Durham and/or Wilson. There will be occasional travel to/from each location. Will support 2 projects- one with SAP manufacturing system (SAP QM module) the other project is POMS the MES validation system rewriting vali...
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