Senior Technical Lead – Peptide Development & GMP (Hybrid)

Perspective Therapeutics; New Jersey; Hybrid; USD 100,000 - 140,000; Full time

Job summary

Perspective Therapeutics is hiring a CMC Technical Manager for Peptide Development in Somerset, NJ. This hybrid role involves overseeing peptide programs and ensuring compliance with GMP standards. The candidate will manage all technical aspects from development to commercialization.

Qualifications include a B.S. in a relevant field and over 7 years in the pharmaceutical industry. Technical writing skills and experience in regulatory settings are essential. Strong project management and communication skills are required.

Qualifications

• Minimum 7+ years’ experience in the Pharmaceutical Industry.
• Experience with peptide synthesis, purification, and regulatory settings.
• Familiarity with regulatory and quality assurance aspects.

Responsibilities

• Oversee peptide programs at CDMO and in-house.
• Review and approve master batch records and test methods.
• Manage clinical projects from raw materials to release.

Skills

Project management skills

Communication skills

Attention to detail

Technical writing

Knowledge of GMP standards

Ability to multitask

Education

B.S. degree in Chemistry, Biochemistry or related field

Tools

Microsoft Office

Job description

Perspective Therapeutics is hiring a CMC Technical Manager for Peptide Development in Somerset, NJ. This hybrid role involves overseeing peptide programs and ensuring compliance with GMP standards. The candidate will manage all technical aspects from development to commercialization.

Qualifications include a B.S. in a relevant field and over 7 years in the pharmaceutical industry. Technical writing skills and experience in regulatory settings are essential. Strong project management and communication skills are required.