Regulatory Affairs Biosimilars Consultant
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com.
This is a remote position.
Responsibilities
• Provide expert regulatory affairs guidance and support for biosimilars development projects.
• Review and analyze regulatory requirements and guidelines related to biosimilars in various regions.
• Assist in the preparation, submission, and maintenance of regulatory submissions for biosimilars, including INDs, BLAs, and variations.
• Collaborate with cross‑functional teams to ensure alignment on regulatory strategy and objectives.
• Stay updated on regulatory developments and trends impacting biosimilars globally.
• Participate in meetings with regulatory authorities as needed.
• Provide regulatory support and expertise during regulatory agency inspections and audits.
Qualifications
• Bachelor's degree in a scientific or related field; advanced degree preferred.
• Minimum of 8 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with specific expertise in biosimilars preferred.
• Strong understanding of regulatory requirements and guidelines governing biosimilars development and approval processes.
• Experience with regulatory submissions for biosimilars, including INDs, BLAs, and variations.
• Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders.
• Proven ability to work independently and manage multiple projects simultaneously.
• Regulatory affairs certification (RAC) preferred but not required.
This is a unique opportunity for biosimilars consultant professionals to leverage their regulatory expertise on biologic medical products and make a meaningful impact in the pharmaceutical and medical device industries. Competitive compensation packages are available.
Be part of our network of Subject Matter Experts.
Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact [email protected].
Follow us on LinkedIn for more company updates and opportunities.
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This is a remote position.
Responsibilities
• Provide expert regulatory affairs guidance and support for biosimilars development projects.
• Review and analyze regulatory requirements and guidelines related to biosimilars in various regions.
• Assist in the preparation, submission, and maintenance of regulatory submissions for biosimilars, including INDs, BLAs, and variations.
• Collaborate with cross‑functional teams to ensure alignment on regulatory strategy and objectives.
• Stay updated on regulatory developments and trends impacting biosimilars globally.
• Participate in meetings with regulatory authorities as needed.
• Provide regulatory support and expertise during regulatory agency inspections and audits.
Qualifications
• Bachelor's degree in a scientific or related field; advanced degree preferred.
• Minimum of 8 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with specific expertise in biosimilars preferred.
• Strong understanding of regulatory requirements and guidelines governing biosimilars development and approval processes.
• Experience with regulatory submissions for biosimilars, including INDs, BLAs, and variations.
• Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders.
• Proven ability to work independently and manage multiple projects simultaneously.
• Regulatory affairs certification (RAC) preferred but not required.
This is a unique opportunity for biosimilars consultant professionals to leverage their regulatory expertise on biologic medical products and make a meaningful impact in the pharmaceutical and medical device industries. Competitive compensation packages are available.
Be part of our network of Subject Matter Experts.
Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact [email protected].
Follow us on LinkedIn for more company updates and opportunities.
Apply tot his job
Apply To this Job