Drug development principles jobs

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Jobgether · Posted Nov 11, 2026

Open

Romania
Contract · Senior
8+ years

Apply with Referso

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Jobgether · Posted Nov 11, 2026

Open

Romania
Contract · Senior
8+ years

Apply with Referso

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Jobgether · Posted Nov 11, 2026

Open

France
Senior
8+ years

Apply with RefersoAI Apply on careers page

Experienced Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products, ensuring compliance throughout the product lifecycle.

Responsibilities

Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.

Requirements

Bachelor's degree
Master's degree
PhD degree
Nice to have: Small-molecule CMC regulatory activities

Skills

Regulatory CMC Small Molecule Veeva RIM North American regulatory framework

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Jobgether · Posted Nov 11, 2026

Open

Spain
Senior
8+ years

Apply with RefersoAI Apply on careers page

Seeking an experienced Regulatory CMC Consultant to support regulatory affairs activities for small-molecule pharmaceutical products in a senior consulting role.

Responsibilities

Support regulatory affairs activities for small-molecule pharmaceutical products, with a focus on Chemistry, Manufacturing, and Controls (CMC) requirements.
Apply knowledge of the North American regulatory framework to support product compliance and lifecycle activities.
Contribute to processes for maintaining products on the market, including regulatory reporting and ongoing surveillance.
Interpret and assess relevant regulatory guidelines and requirements, translating them into practical recommendations.
Apply an understanding of drug development principles and related regulatory concepts to assigned projects.

Requirements

Bachelor's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
Master's degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
PhD degree in Biology, Chemistry, Pharmacy, Regulatory Affairs, or another life sciences discipline
Nice to have: Small-molecule CMC regulatory activities

Skills

Regulatory CMC Small Molecule

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Responsibilities

Requirements

Skills

Benefits

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Responsibilities

Requirements

Skills

Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Responsibilities

Requirements

Skills

Benefits

Benefits