Author jobs in waltham USA
17 author jobs found in waltham: showing 1 - 17
Manager / Senior Manager Quality Management System & Veeva Quality Systems Administration
Company: Karyopharm Therapeutics Inc. |
-first-time documentation. Author, review, revise, and maintain QMS-related procedures, work instructions, templatesLocation: Newton, MA, USA
| Salary: US$115000 - 145000 per year | Date posted: 03 Jun 2026
Middle School History Teacher
Company: Uncommon Schools |
-to-peer debate, and synthesize arguments. You'll guide students to understand the author's claim and the power of sourcingLocation: Waltham, MA, USA
| Salary: US$71000 - 116000 per year | Date posted: 02 Jun 2026
Middle School Ela Teacher
Company: Uncommon Schools |
. You'll guide students to analyze literary and non-narrative texts, assess an author's purpose, write in a variety of genresLocation: Waltham, MA, USA
| Salary: US$71000 - 116000 per year | Date posted: 02 Jun 2026
Sr. Engineer - Process Development
Company: Yoh |
Author and review MBRs Author and review SOPs Effectively communicate with cross functional teams like ManufacturingLocation: Waltham, MA, USA
| Salary: unspecified | Date posted: 02 Jun 2026
Quality Assurance Associate
Company: Actalent |
and risks in quality and GMP processes. Conduct investigations for deviations, change controls, and CAPAs. Review and authorLocation: Waltham, MA, USA
| Salary: US$43 - 45 per hour | Date posted: 01 Jun 2026
Quality Assurance Associate
Company: Actalent |
and risks in quality and GMP processes. Conduct investigations for deviations, change controls, and CAPAs. Review and authorLocation: Waltham, MA, USA
| Salary: US$43 - 45 per hour | Date posted: 28 May 2026
Senior Associate Scientist / Scientist (analytical R&d)
Company: Cambrex |
product release, stability, and compliance. Author and review analytical protocols, reports, and SOPs in compliance with GMPLocation: Waltham, MA, USA
| Salary: US$74000 - 92000 per year | Date posted: 22 May 2026
Associate Director, Analytical Development - Small Molecule
Company: Ardelyx |
scientific rigor and compliance Participate in the author and review of analytical sections of regulatory submissions (INDsLocation: Waltham, MA, USA
| Salary: unspecified | Date posted: 15 May 2026
Public Affairs & Public Relations Manager - External Communications, Health
Company: Wolters Kluwer |
situations. Ability to read and understand industry specific documents and/or presentations. Ability to author routine reportsLocation: Waltham, MA, USA
| Salary: US$107500 - 188400 per year | Date posted: 15 May 2026
Mrna Process Analytics - Senior Research Associate
Company: Yoh |
processing solutions. Author laboratory standard operation procedures, prepare development reports and deliver presentationsLocation: Waltham, MA, USA
| Salary: unspecified | Date posted: 14 May 2026
Executive/senior Director, Gmp Quality & Quality Management System (qms)
Company: Karyopharm Therapeutics Inc. |
(QRM) processes and ensure integration into QMS decision-making. Author, review, and/or approval documents includingLocation: Newton, MA, USA
| Salary: unspecified | Date posted: 12 May 2026
Scientist I Or Ii, In Vivo Pharmacology, Drug Discovery
Company: ALS TDI |
, molecular biology, or related field Strong publication record with at least two first-author papers Hands on experienceLocation: Watertown, MA, USA
| Salary: US$100000 - 110000 per year | Date posted: 24 Apr 2026
Associate Director, Medical Writing
Company: Alkermes |
plans and ensuring aligned timelines, quality, and resourcing. Independently author and lead the planning, review, commentLocation: Waltham, MA, USA
| Salary: US$175000 - 190000 per year | Date posted: 16 Apr 2026
Drug Safety Program Manager
Company: Alkermes |
. Author, review, and contribute to SOPs, work instructions, and guidance documents, including development and maintenanceLocation: Waltham, MA, USA
| Salary: US$145000 - 158000 per year | Date posted: 10 Apr 2026
Principal Product Manager - Computer Vision
Company: Motorola Solutions |
& Requirements: Author high-quality Market Requirements Documents (MRDs), Product Requirements Documents (PRDs), and user storiesLocation: Waltham, MA, USA
| Salary: unspecified | Date posted: 08 Apr 2026
Senior Scientist, Analytical Development
Company: Alkermes |
analytical strategies and deliver on key objectives Author and review drug substance and drug product analytical sectionsLocation: Waltham, MA, USA
| Salary: US$151286 - 161030 per year | Date posted: 31 Mar 2026
Senior Regulatory Affairs Specialist
Company: Wolters Kluwer |
, MDSAP jurisdictions) Serve as primary author and owner of major submissions, including 510(k), De Novo requests, CE