> Markdown version of [/jobs/ext/2866682-technical-manager-peptide-development](https://www.wearedevelopers.com/jobs/ext/2866682-technical-manager-peptide-development). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Technical Manager - Peptide Development - **Company:** Perspective Therapeutics, Inc. - **Location:** United States - **Experience:** Expert - **Salary:** $125,000.0 - $160,000.0 - **Contract:** Permanent contract - **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Office, Microsoft PowerPoint, Model Validation - **Published:** September 12, 2026 - **Apply:** https://startup.jobs/technical-manager-peptide-development-perspective-therapeutics-10017372 ## About the Role To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This is a hybrid position that will require travel to manufacturing sites., * Minimum B.S degree in Chemistry, Biochemistry or related field is required. * 7+ years' experience in Pharmaceutical Industry in a similar function. * Prior experience with peptide synthesis, purification and lyophilization. * Demonstrated experience leading peptide CMC programs through late-stage clinical development and/or commercialization, including scale-up, technology transfer, process validation, and regulatory interactions with external manufacturing partners. * Experience supporting quality systems and quality-related activities, including deviations, CAPAs, change controls, investigations, and regulatory inspections. * Technical writing experience to support CMC module 3. * Familiarity with Regulatory and Quality Assurance aspects in manufacturing processes of peptide products. * Technical auditing and Radiopharmaceutical experience are a plus. * Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). Knowledge / Skill / Ability * Broad knowledge of risk-based quality systems approaches consistent with ICH Q10 for pharmaceuticals. * Full understanding of GMP and peptide manufacturing, methods validations, specifications, and release/stability. * Deep understanding of peptide process development, scale-up, manufacturing controls, and commercialization requirements for late-stage clinical and commercial products. * Strong project management skills, including contracting, budgeting, and timeline oversight. * Must have excellent communication skills (verbal and written). * Highly organized with a strong attention to detail, clarity, accuracy and conciseness. * Ability to multitask and manage parallel workstreams in a fast-paced drug development environment. * Ability to travel up to 15%. ## Description Reporting to the Senior Director, CMC Operations, the CMC Technical Manager, Peptide Development is responsible for the technical oversight of peptide programs at CDMO manufacturing sites and in-house R&D activities. This role supports phase-appropriate development, disposition, and distribution of Perspective Therapeutics' peptide-based radiopharmaceuticals across Phase I-III clinical and pre-commercial programs. The individual will serve as a key technical lead for late-stage peptide development and commercialization activities, including process scale-up, technology transfer, process validation, regulatory submissions, and commercial readiness efforts. This role will ensure compliance with GMP standards, provide oversight of quality-related activities, and serve as a subject matter expert throughout clinical development and commercialization., * Responsible for overseeing all the peptide programs at CDMO and ensuring the activities are completed in a timely manner to support peptide based radiopharmaceutical drug candidates. * Lead peptide CMC activities supporting process scale-up, technology transfer, process validation, and commercial readiness at internal and external manufacturing sites. * Responsible for review and approval of master batch records, method validation protocols and reports, test methods, specifications, etc. for early phase clinical, late phase clinical and commercial peptide products. * Manage the technical and quality aspects of peptide development programs from raw materials through manufacturing, packaging, distribution release and stability, ensuring phase-appropriate GMP compliance and inspection readiness. * Provide technical leadership for batch record as review, deviation investigations, CAPAs, change controls, product impact assessments, and disposition activities in partnership with Quality Assurance (QA). * Work closely with QA and early Discovery organizations throughout the development and manufacturing processes. * Ensure all relevant SOPs are followed to support activities carried out at CDMOs. * Acting as SME when needed and in providing or reviewing responses to regulatory agency findings from inspections. * Draft and technical review of IND/IMPD CMC sections, briefing packages, and any other regulatory submissions. ## Related Videos - [Geometric deep learning for drug discovery](https://www.wearedevelopers.com/videos/264-geometric-deep-learning-for-drug-discovery) - [In-depth .NET Azure Functions: Isolated mode, performance and durable AI agents](https://www.wearedevelopers.com/videos/100207-in-depth-net-azure-functions-isolated-mode-performance-and-durable-ai-agents) - [Developing the Rich Text Editor for DeepL.com](https://www.wearedevelopers.com/videos/1172-developing-the-rich-text-editor-for-deepl-com) - [Engineering/Manager Pendulum: Generating compound interest on your career](https://www.wearedevelopers.com/videos/100348-engineering-manager-pendulum-generating-compound-interest-on-your-career) - [From Syntax to Singularity: AI’s Impact on Developer Roles](https://www.wearedevelopers.com/videos/900-from-syntax-to-singularity-ai-s-impact-on-developer-roles) - [Your Manager Doesn’t Come with a User Manual (But You Can Totally Write One)](https://www.wearedevelopers.com/videos/1495-your-manager-doesn-t-come-with-a-user-manual-but-you-can-totally-write-one) ## Related Articles - [How We Built a Worry-Free System That Runs for 10+ Years – And What We’d Do Again](https://www.wearedevelopers.com/magazine/751-how-we-built-a-worry-free-system-that-runs-for-10-years-and-what-we-d-do-again) - [Should Tech Managers Be Developers First? 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