Technical Manager – Peptide Development

Perspective Therapeutics

CMC Technical Manager overseeing peptide programs at Perspective Therapeutics, ensuring compliance with GMP standards and supporting regulatory submissions. Responsible for managing clinical projects from raw materials to release/stability.

Posted 7/29/2026full-timeRemote • 🇺🇸 United StatesSeniorLead💰 $125,000 - $160,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing peptide programs, ensuring compliance with regulatory standards, and overseeing the technical and quality aspects of clinical projects. Proficient in technical writing for regulatory submissions and familiar with quality assurance processes in the pharmaceutical industry.

Highest-signal resume keywords

Peptide SynthesisRegulatory SubmissionsTechnical WritingQuality AssuranceCMC Peptide Programs

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Peptide PurificationLyophilizationMethod ValidationBatch Record ReviewTechnical Auditing

Tools & Technologies

Microsoft Office

Industry Keywords

Pharmaceutical IndustryRadiopharmaceuticalsSOP ComplianceCAPAIND/IMPD CMC

About the role

Key responsibilities & impact

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
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 clinical projects from raw materials to manufacturing to packaging, distribution and release/stability
Perform ongoing review of batch records as part of product release, working closely with quality on deviations and CAPAs, and ensuring appropriate communication of issues, development and plans
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

Requirements

What you’ll need

Minimum B.S degree in Chemistry, Biochemistry or related field
7+ years’ experience in Pharmaceutical Industry in a similar function
Prior experience with peptide synthesis, purification and lyophilization
Prior experience working with CMC peptide programs in regulatory settings with external collaborators/vendors
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)

Benefits

Comp & perks

Health insurance
Retirement plans