Author jobs in medford USA
46 author jobs found in medford: showing 1 - 20
Research Associate, Formulation Development And Manufacturing
Company: Agios |
form characterization techniques including HPLC, dissolution testing, flow and sticking assessments Author and review... and basic chemistry is required Experience working in laboratories and author lab reports Excellent communication...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 02 Mar 2025
Assistant Director For Alumni Relations And Annual Giving
Company: Harvard University |
include writing from author perspectives. Works with vendors, including graphic design (as needed) and print house...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 02 Mar 2025
Senior Medical Writer
Company: Philips |
, and PMCFRs). This person may also contribute to our author other technical documents that support Clinical, Regulatory, Risk...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 01 Mar 2025
Quality Manager
Company: LanceSoft |
Actual Job Title - QUALITY MANAGER Job Responsibilities: Author and review of GxP documents (e.g.- SOPs, Protocols..., e.g. Trackwise Initiate and author investigations related Out of Specification (OOS) or Out of Trend (OOT) results...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 01 Mar 2025
Quality Manger
Company: Katalyst Healthcares & Life Sciences |
Responsibilities: Author and review of GxP documents (e.g.- SOPs, Protocols, Technical Reports, Trend reports... activities as needed. Initiate and investigate deviations, and events in a Quality system, e.g. Trackwise Initiate and author...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 01 Mar 2025
Potency Assay Scientist
Company: Eurofins |
assays. Author and review SOPs and technical reports. Work with cross-functional groups within the client environment...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 01 Mar 2025
Quality Manger
Company: cGxPServe |
Responsibilities: Author and review of GxP documents (e.g.- SOPs, Protocols, Technical Reports, Trend reports... activities as needed. Initiate and investigate deviations, and events in a Quality system, e.g. Trackwise Initiate and author...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 28 Feb 2025
Potency Assay Scientist
Company: Eurofins |
assays. Author and review SOPs and technical reports. Work with cross-functional groups within the client environment...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 28 Feb 2025
Senior Principal Scientist/associate Director - Oncology Pks
Company: Novartis |
, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections/radiation dosimetry of IND/IMPDs and NDA/BLAs as well...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 27 Feb 2025
Associate Engineer, Drug Development Process Improvement (jp13693)
Company: 3 Key Consulting |
and tech transfer. Author, review and/or approve of process documentation needed for process validation and commercialization...Location: Cambridge, MA, USA
| Salary: $30 - 35 per hour | Date posted: 27 Feb 2025
Director, Safety Scientist
Company: Lifelancer |
Inquiries, and Periodic Reporting. Lead analysis of safety data and author relevant safety sections of global regulatory... authorities, IRBs/ECs. Author Health Hazard Evaluations. Contribute to integrated Benefit/Risk assessments. Promote and Advance...Location: Cambridge, MA, USA
| Salary: $179800 - 239800 per year | Date posted: 26 Feb 2025
Scientist
Company: Innova Solutions |
Author and review technical reports and sections of regulatory filings. Support process and method lifecycle management...Location: Cambridge, MA, USA
| Salary: $42 per hour | Date posted: 26 Feb 2025
Scientist
Company: Advanced Bio-Logic Solutions |
investigations and regulatory submissions Author and review technical reports and sections of regulatory filings. Support process...Location: Cambridge, MA, USA
| Salary: $37 - 42 per hour | Date posted: 21 Feb 2025
Scientist
Company: Aditi Consulting |
and regulatory submissions Author and review technical reports and sections of regulatory filings. Support process and method...Location: Cambridge, MA, USA
| Salary: $33.5 - 36.51 per hour | Date posted: 21 Feb 2025
Scientist
Company: Advanced Bio-Logic Solutions |
investigations and regulatory submissions Author and review technical reports and sections of regulatory filings. Support process...Location: Cambridge, MA, USA
| Salary: $37 - 42 per hour | Date posted: 21 Feb 2025
Senior Engineer, Combination Products - Process Engineering
Company: Amgen |
process solutions. Author technical records and ensure they are appropriately maintained in the e.g. Device Master record... (DMR)/Master Manufacturing Record (MMR) Author technical content in Tech Transfer. Represent Process engineering...Location: Cambridge, MA, USA
| Salary: $119195 - 147867 per year | Date posted: 20 Feb 2025
Post-doc - Immunological Evaluation And Formulation Of Lipid Nanoparticles
Company: GlaxoSmithKline |
evaluations, etc. Scientific publications in peer-reviewed journals, with at least 1-2 first author research publications...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 19 Feb 2025
Scientist Ii, T Cell Tolerance
Company: AbbVie |
environment activities. Analyze and interpret experimental data using statistical methods, author protocols and scientific...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 15 Feb 2025
Scientist Ii, T Cell Tolerance
Company: AbbVie |
environment activities. Analyze and interpret experimental data using statistical methods, author protocols and scientific...Location: Cambridge, MA, USA
| Salary: unspecified | Date posted: 15 Feb 2025
Regulatory Affairs Labelling Director
Company: Katalyst Healthcares & Life Sciences |
and review implementation plans to ensure up-to-date, compliant information is provided. Labelling Document Management. Author...