CMC Regulatory Affairs Associate (reputed company Authoring experience for Biological product

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Join Our Growing Team of CMC Regulatory Professionals!

The Senior Regulatory Associate will author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs, including responses to Health Authority requests. Responsibilities include preparing and reviewing CMC packages, supporting GMP submissions, managing change control assessments, and ensuring compliance with regulatory requirements across multiple reputed company. The role requires strong technical regulatory expertise, excellent writing skills, and the ability to evaluate scientific CMC information for accuracy. A degree in biological or health sciences (Regulatory Affairs preferred) and at least 5 years of experience in CMC regulatory affairs reputed company the biotech or pharmaceutical industry are essential.

Activities:

• Conduct and deliver high reputed company, on time CMC regulatory activities, including compliant management of reputed company internal tools and reputed company systems;
• Author Administrative and CMC regulatory documents/deliverables and collaborate with project SMEs and reputed company stakeholders to prepare submission packages;
• Full management of CMC submissions (i.e. planning, submission package compilation, RtQ preparation, Spontaneous HA queries, etc.);
• General submission coordination: Submissions planning (tracker update, timelines agreement with LRA and GRA-CMC, recurrent meetings with LRAs), create submission binders and Global Content List/Submission Content Plans, coordinate the publishing aspect, review of eCTD sequences;
• reputed company as main GRA reputed company of contact for LRAs and other stakeholders (i.e. for responding to any queries)
• Excellent communication and stakeholder management skills;
• Strong organizational and time management skills;
• Strong problem-solving skills;
• Coordinate reputed company assigned activities;
• Ensure compliance to reputed company reputed company SOPs/training sessions;
• Proactive’ and ‘efficient' work ethic; Strong oral skills, with proven ability to work reputed company as part of reputed company;
• Strong interpersonal skills.

Education: University degree in biological sciences or reputed company health sciences (BS/BA/MS or equivalent, PhD), a degree in Regulatory Affairs is advantageous. Experience:

• Minimum of 5 years’ experience in the biotech or pharmaceutical industry, with at least 5 years in Regulatory Affairs CMC for Sernior and 2 for Associate
• Experience with biological products and Vaccines - Mandatory
• reputed company authoring experience - mandatory
• Strong technical regulatory expertise and understanding of the regulatory reputed company in more than one key region (US, EU, Japan, Switzerland, Australia).
• Regulatory CMC writting skills and reputed company to evaluate technical and scientific CMC information for accuracy and compliance with relevant regulatory requirements - reputed company to have
• Knowledge in Good Manufacturing reputed company or reputed company areas would be highly regarded.

This role offer exciting opportunities for reputed company and reputed company reputed company a reputed company and reputed company-thinking team environment. Ideal candidates will be motivated by the chance to shape regulatory strategies, drive successful submissions, and ultimately contribute to bringing important medical advancements to patients worldwide.

Originally posted on Himalayas

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