Pharmatech Associates Jobs in United States

Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the world. · Principal/Executive Consultant, Qua ...

Fostering a professional, inclusive and diverse environment is our commitment. · Key Responsibilities: · Developing global CMC regulatory strategy · Determining best ways to present information in assigned regulatory submissions · ...

A pharmaceutical consultancy is seeking a Regulatory Consultant/CMC for small molecule drug development. · Key Responsibilities: · Developing global regulatory strategies · Ensuring compliance with regulations · ...

Senior Quality Consultant – Bilingual · We are seeking an experienced Senior Quality Consultant to deliver quality and compliance-related services. · Conduct gap assessments · Evaluate inspection readiness programs · Participate in complex investigations · ...

Job Description for Remote ANDA Regulatory Strategist · The goal of this position is to support pharmaceutical companies in guiding their regulatory strategy and submissions. · FDA regulations understanding · ANDA submissions expertise · ...

Regulatory Strategists · We are seeking a highly experienced Regulatory Consultant to guide strategy and manage 505(b)(2) NDA submissions. · 10+ years of experience in regulatory affairs with FDA regulations · Proven track record in regulatory strategy development · This is a ful ...

Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the world. · We are seeking a highly experience ...

Regulatory Consultant/CMC, Small Molecule · This role plays a key global leadership position in Regulatory Affairs for CMC and clinical aspects of regulatory documents and submissions. · The candidate will act as a CMC SME for SMALL MOLECULE drug development and regulatory elemen ...

Senior Quality Consultant · We are seeking a Senior-level Quality Consultant to assist with delivering quality and compliance-related services. · Conduct gap assessments · Evaluate inspection readiness programs · ...

Pharmatech Associates is seeking a Regulatory Affairs Consultant to work on ongoing projects with 10-20 hours per week. This role involves leading the development and execution of regulatory strategies, engaging with relevant authorities, and providing guidance throughout product ...

About the Job · We are seeking a senior-level Quality Consultant to assist with delivering quality and compliance-related services. The nature of our projects varies from client to client and can often be supported remotely. · Conducting gap assessments of a company's QMS against ...

regulatory affairs consultant job involves developing strategies for product registration, managing regulatory submissions, and providing guidance to clients across all stages of product development. · key responsibilities · lead the development of regulatory strategies with exec ...

A prominent pharmaceutical consultancy is looking for a highly experienced Regulatory Consultant to guide and support their regulatory strategy and submissions. This remote role requires a proven track record in ANDA submissions and a strong understanding of FDA regulations. The ...

Regulatory Consultant · We are seeking a highly experienced Regulatory Consultant with deep expertise in 505(b)(2) NDA submissions. · Lead and manage 505(b)(2) NDA submissions in compliance with FDA regulations. · ...

Pharmatech Associates is seeking a Global Regulatory CMC Lead to oversee global CMC strategies. · About the Role · Leverage expertise to manage complex projects. · Ensure compliance with global regulations. · ...

Key Responsibilities: · a leading pharmaceutical consulting firm is seeking a skilled regulatory consultant to develop regulatory strategies and lead 505(b)(2) nda submissions from a remote location. · the ideal candidate possesses over 10 years of experience in regulatory affair ...