4 technical documentation engineer jobs at 2 companies in Rich Square, NC

2mo
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Staff Validation Engineer, Media Fills
Greenville, North Carolina, United States
OnsiteFull Time
Thermo Fisher Scientific
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
8+ YOE8+ years in pharmaceutical/biotech validation; aseptic processing and media fill experience; sterile manufacturing background; strong technical writing; ability to lead validation projects.
GMP, cGMP, validation protocols, procedures, optimization, risk assessment, documentation
1w
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Interior Communications SOVT Technical Writer
Suffolk, Virginia, United States
$70k-$78k/yr OnsiteFull Time
Akima
Akima: Delivers mission-critical services and technology to federal agencies.
0+ YOEAbility to develop SOVTs and SPEG-compliant test documentation; able to obtain Secret clearance; BA typically required; 0–2 years experience; proficiency with MDTST, Microsoft Word, and Visio; proofreading/editing and cybersecurity/CUI familiarity.
Modern Digital Tactical Software for Testing (MDTST), Microsoft Word, Microsoft Visio
1mo
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Staff QA Engineer
Greenville, North Carolina, United States
OnsiteFull Time
Thermo Fisher Scientific
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
6+ YOEIn-depth GMP and ISO 9001/13485 knowledge, audit and inspection experience, expertise in CAPA/change control/document control, FMEA and root cause analysis, validation (IQ/OQ/PQ), TrackWise/SAP experience, advanced degree +6 yrs or BS +8 yrs in technical field; travel up to 25%.
TrackWise, SAP, FMEA
2mo
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Validation Manager
Greenville, North Carolina, United States
OnsiteFull Time
Thermo Fisher Scientific
Thermo Fisher ScientificNYSE: TMO: Sells equipment and chemicals for scientific research and healthcare.
6+ YOE3+ MgmtBachelor's degree in engineering, science, chemistry, biology or related technical discipline; 6-8 years pharma/biotech manufacturing; 2+ years validation experience; 3+ years people management; strong cGMP knowledge; regulatory inspection experience.
cgmp, validation management, change control, statistical analysis, documentation tools