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Author jobs in waltham USA

21 author jobs found in waltham: showing 1 - 21

Supervisor, Analytical Development
Company: Alkermes |

Location: Waltham, MA, USA

| Salary: US$131000 - 142000 per year | Date posted: 14 Aug 2026
analytical data, reports, and documentation Author, revise or review SOP's, analytical protocols, analysis reports
Mrna Analytical Development Scientist - Analytical Sciences
Company: Sanofi |

Location: Waltham, MA, USA

| Salary: US$85500 - 123500 per year | Date posted: 12 Aug 2026
design and execute complex experiments under general supervision. Author method development and investigation reports
Technical Operations Engineer
Company: Anduril Industries |

Location: Waltham, MA, USA

| Salary: US$146000 - 194000 per year | Date posted: 12 Aug 2026
. Troubleshoot issues in real-time, applying analytical thinking and hands-on problem-solving skills. Author training documentation
Technical Field Operations Engineer
Company: Anduril Industries |

Location: Waltham, MA, USA

| Salary: US$146000 - 194000 per year | Date posted: 12 Aug 2026
. Troubleshoot issues in real-time, applying analytical thinking and hands-on problem-solving skills. Author training documentation
Director/senior Director, Cmc Drug Substance Development
Company: Enanta Pharmaceuticals |

Location: Watertown, MA, USA

| Salary: unspecified | Date posted: 11 Aug 2026
, author, and review drug substance sections of regulatory documents. You will: Lead Drug Substance Strategy: Serve as the..., formulation development, analytical development, Quality Assurance, and CMC Regulatory Affairs. Author and Review CMC
Senior Application Engineer
Company: Synopsys |

Location: Waltham, MA, USA

| Salary: US$167627 per year | Date posted: 03 Aug 2026
on industrial problems, develop application best practices. Support Ansys field and digital marketing, author conference
Oncology Translational Medicine Lead Director
Company: AstraZeneca |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 01 Aug 2026
Interpretation and Communication: Drive data reviews; author and review clinical study reports; present to governance; contribute
Principal Engineer, Process Development - Osd
Company: Alkermes |

Location: Waltham, MA, USA

| Salary: US$173000 - 193000 per year | Date posted: 31 Jul 2026
at external partners. Develop, review, and approve process development source documents, and author and review drug product
Sr. Process Development Engineer - Osd
Company: Alkermes |

Location: Waltham, MA, USA

| Salary: US$140000 - 154000 per year | Date posted: 31 Jul 2026
improvement. Author CMC sections for IND, NDA, and other regulatory filings. Develop process trains and flows, ensuring
Advanced Practice Clinician - Watertown
Company: LHC Group |

Location: Watertown, MA, USA

| Salary: US$109500 - 164000 per year | Date posted: 30 Jul 2026
monitoring and management of patients with acute and chronic illnesses. Serves as the care plan author and supervisor. Adjusts
Senior Test Engineer
Company: ICS |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 25 Jul 2026
Planning: Author comprehensive Software Test Plans and Procedures across the entire Software Development Life Cycle (SDLC.... Documentation: Author the final reporting process, including Test Summary Reports (TSR) and detailed defect justifications
Senior Principal Scientist, Analytical Sciences
Company: Eli Lilly |

Location: Watertown, MA, USA

| Salary: US$71250 - 187000 per year | Date posted: 20 Jul 2026
, providing technical oversight, troubleshooting, and ensuring assay robustness and compliance. Author and review methods
Senior Quality Scientist I
Company: Addgene |

Location: Watertown, MA, USA

| Salary: US$84000 - 92000 per year | Date posted: 14 Jul 2026
on a variety of samples through different means. Author, update, and maintain new SOPs for developmental processes. Cross-train
Medical Director, Clinical Development (neurology)
Company: Deciphera |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 09 Jul 2026
Attend and contribute to study team meetings Present clinical trial findings to management Author clinical documents... (protocol, investigator brochure) Author clinical portions of regulatory documents (IND, CTA, NDA, MAA or equivalent
Sr. Engineer - Process Development
Company: Yoh |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 07 Jul 2026
Author and review MBRs Author and review SOPs Effectively communicate with cross functional teams like Manufacturing
Senior Advisor, Manufacturing Science And Technology
Company: Eli Lilly |

Location: Watertown, MA, USA

| Salary: unspecified | Date posted: 17 Jun 2026
in mitigation plans. Author regulatory and technical documents for regulatory submissions in support of custom raw materials
Senior Systems Test Engineer - Electrophysiology
Company: Boston Scientific |

Location: Waltham, MA, USA

| Salary: US$89200 per year | Date posted: 17 Jun 2026
decisions and verify system functionality. Author and maintain test procedures, test reports and design verification plans
Senior Systems Test Engineer - Electrophysiology
Company: Boston Scientific |

Location: Waltham, MA, USA

| Salary: US$89200 per year | Date posted: 17 Jun 2026
decisions and verify system functionality. Author and maintain test procedures, test reports and design verification plans
Director, Medical Writing
Company: Alkermes |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 16 Jun 2026
author and lead the planning, review, comment resolution, and delivery of routine and complex clinical and regulatory
Principal Research Scientist Ii - Analytical Development
Company: AbbVie |

Location: Waltham, MA, USA

| Salary: unspecified | Date posted: 10 Jun 2026
testing results. Participate in the preparation and review of technical documents for late-stage programs. Author and review
Senior Associate Scientist, Ard
Company: Cambrex |

Location: Waltham, MA, USA

| Salary: US$74000 - 92000 per year | Date posted: 21 May 2026
product release, stability, and compliance. Author and review analytical protocols, reports, and SOPs in compliance with GMP