GMP documentation practices jobs Skill: GMP documentation practices Analytical Chemist - III
Net2Source · Pearl River, USContract · Senior
Materials Management Compliance & Process Improvement Specialist
Tailored Management · Houston, US+1 more · On-site · Contract
Senior Specialist, Manufacturing NPI & Clinical Readiness
VetJobs · Bothell, US· On-site · Full-time · Senior
+10K new in the last hour
Net2Source · Posted Nov 6, 2026
Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products.
Perform laboratory testing of raw materials, drug substances, drug products, in-process samples, stability samples Conduct routine wet chemistry and analytical testing using laboratory instrumentation Accurately document and review analytical results using electronic laboratory systems (LIMS) Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines Participate in peer review of data and laboratory documentation Bachelor's or master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Related scientific discipline Nice to have: 5-7 years of pharmaceutical QC laboratory experience Nice to have: Experience using Empower chromatography software Nice to have: Previous involvement in audit-ready environments Nice to have: Experience reviewing laboratory documentation and SOPs Tailored Management · Posted Nov 3, 2026
Own quality records, controlled documentation, and operational improvement initiatives supporting onsite Supply Chain and Materials Management operations.
Houston, Texas, United States 14905 Kirby Drive, Texas, United States Pay Rate: $26.67/hr on W2
Own and drive Materials Management deviations, CAPAs, and change controls through completion in TrackWise Gather evidence, facilitate investigations and root-cause analysis, and develop clear documentation Coordinate impact assessments, corrective and preventive actions, implementation evidence, and effectiveness checks Maintain visibility of record status, due dates, dependencies, and outstanding actions Prepare records for review and closure in accordance with site procedures Bachelor’s degree in a relevant field or an equivalent combination of education and relevant experience VetJobs · Posted Nov 5, 2026
The Senior Specialist, Manufacturing NPI and Clinical Readiness plays a key role in enabling clinical readiness for cell therapy products through ownership of manufacturing documentation, MES readiness, change control assessment, risk assessments, and operator training.
Bothell - WA - US: $96,832 - $117,338
Author and own the development, revision, and lifecycle management of batch records, procedures, and SOPs supporting clinical manufacturing. Ensure documentation readiness aligns with manufacturing timelines, change control requirements. Act as point person for technical issues and liaison with internal groups (QA, QC). Improve processing efficiency and ensure optimized technical support for scale-up. Collaborate with IT/MES teams to support design and review of electronic batch records. Bachelor’s degree in Engineering, Life Sciences or related technical field High School Diploma Nice to have: cell therapy manufacturing Nice to have: biologics manufacturing Nice to have: FMEA
Nice to have: pharmaceutical or biotechnology warehousing
Nice to have: Supply Chain
Nice to have: Materials Management
Nice to have: TrackWise Medical Coverage – HDHP, PPO, and Surest plan options Minimum Essential Coverage (MEC) Dental Insurance Vision Insurance Short-Term Disability (STD)
discretionary incentive cash stock opportunities
Senior Specialist, Manufacturing NPI & Clinical ReadinessVetJobs · Bothell, US