Author Jobs in San Diego
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Search Results - Author Jobs in San Diego
Raytheon-San Diego-
/sustainment efforts by working across functional boundaries
• Produce maintenance plans, demilitarization plans, and sustainment plans
• Author and peer review technical support documents for Contract Data Requirements List (CDRL)
• Lead In-service Failure...
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Leidos-San Diego-
Author and maintain tools, techniques, and practices for assuring the testing of the product.
• Guide and mentor less senior members of the test team.
• Plan, scope, and execute testing events.
• Author and execute manual and automated test cases...
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Raytheon-San Diego-
/sustainment efforts by working across functional boundaries
• Produce maintenance plans, demilitarization plans, and sustainment plans
• Author and peer review technical support documents for Contract Data Requirements List (CDRL)
• Lead In-service Failure...
Read more
Techead-San Diego-
active and passive reconnaissance of data, with the ability to assess and author Plans of Milestones and Actions (POA&Ms) containing accurate and verifiable mitigation statements, milestone tracking, and applying to the most relevant security control...
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Raytheon-San Diego-mindmatch.ai-
Support depot/sustainment efforts by working across functional boundaries
• Produce maintenance plans, demilitarization plans, and sustainment plans
• Author and peer review technical support documents for Contract Data Requirements List (CDRL)
• Lead...
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Cellics Therapeutics, Inc.-San Diego-
records, and process controls.
• Partner with Regulatory Affairs and author relevant regulatory submission documents (pre-IND, IND, BLA, etc.) and provide strategic guidance on regulatory interactions relating to process development and validation...
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Monarch Quantum-San Diego-jobvertise.com-
set technical direction and best practices.
• Author technical documentation, invention disclosures, and peer-reviewed publications as appropriate.
• Support transition of designs to production, including design for test and design...
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Cellics Therapeutics, Inc.-San Diego-
and process controls.
• Partner with Regulatory Affairs and author relevant regulatory submission documents (pre-IND, IND, BLA, etc.) and provide strategic guidance on regulatory interactions relating to process development and validation.
• Translate non...
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San Diego-astrion.us-
Develop Custom Test Plans: Author comprehensive test plans and detailed procedures to validate the cyber resiliency of mission-critical platforms.
• Analyze and Report: Meticulously analyze test data and translate complex technical findings into clear...
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Jazz Pharmaceuticals-San Diego-
developing detailed technical work plans and managing performance of vendors.
• Work cooperatively with, or lead, internal and external teams as required.
• Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global...
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San Diego-icims.com-
directly related experience, geographic location, and possible contractual requirements which could fall outside of this range.
Responsibilities:
Test Plan Development
1. Author Test Plans:
• Develop detailed Test and Evaluation Master Plans (TEMP...
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Jazz Pharmaceuticals-San Diego-
initiatives.
Author and/or review drug substance sections of regulatory dossiers and technical reports.
• Support other Technical Operations functions to ensure a smooth transfer of technologies and products to manufacturing sites.
• Clearly and effectively...
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Monarch Quantum-San Diego-workable.com-
development risks as directed.
• Work efficiently as part of a diverse team and engage effectively with customers and suppliers, author reports, and contribute to peer-reviewed publications and invention disclosures.
• Promote, communicate, uphold...
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Blackwatch International-San Diego-
Lifecycle equipment ownership: author specifications, lead vendor selection, oversee factory/site acceptance (FAT/SAT), installation/start-up, qualification (PQ), and handoff to operations.
• Design & analyze DOEs; interpret device/parametric data; apply SPC...
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San Diego-pacira.com-
performed by an individual assigned to this job. Other duties may be assigned.
1. Author, prepare and submit U.S. and global regulatory filings, including Traditional and Special 510(k)s, Letters to File, Pre-Subs, IDEs, technical documentation...
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