Proposal Writer – Biologics, Aragen Life Sciences

Job Description

We are seeking a skilled and detail-oriented Proposal Writer – Biologics to join our team. The successful candidate will be responsible for drafting, coordinating, and delivering high-quality technical and commercial proposals related to biopharmaceutical development and manufacturing services, particularly focusing on biologics (e.g., monoclonal antibodies, recombinant proteins, biosimilars). The role requires close interaction with cross-functional teams including Process Development, Manufacturing, Analytical, Regulatory, QA, and Project Management.

Key Responsibilities:
• Develop and write compelling technical and commercial proposals for biologics development and manufacturing projects (drug substance, drug product, analytical services, etc.).
• Coordinate with technical SMEs to capture project scope, timelines, resources, and deliverables accurately.
• Translate client RFPs, RFIs, and scopes of work into structured, customized proposals aligned with business strategy.
• Maintain a library of standard proposal templates, pricing modules, and boilerplate technical content.
• Ensure proposals comply with internal quality standards, brand guidelines, and scientific accuracy.
• Track and manage proposal timelines and deliverables to ensure on-time submissions.
• Assist business development team during client calls and proposal defense meetings, as required.
• Participate in internal meetings to refine service offerings, pricing strategies, and differentiators.
• Continuously update proposal content with latest capabilities, case studies, and regulatory insights.

Required Qualifications:
• Master’s degree in biotechnology, Biochemistry, Pharmacy, or related life sciences discipline. PhD is a plus.
• 6-8 years of relevant experience in Biologics proposal writing, scientific communications, or technical marketing in the biologic’s domain.
• Solid understanding of biologics development workflows (Upstream, Downstream, Analytical, Formulation, Fill-finish.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office Suite; experience with CRM, proposal automation, or document management tools is a plus.
• Strong project coordination and time management skills.
• Detail-oriented with a high degree of accuracy in scientific and technical content.

Preferred Qualifications:
• Prior experience in a CDMO or CRO environment.
• Familiarity with regulatory frameworks (ICH, EMA, FDA) and GMP requirements.
• Understanding of pricing models and commercial proposal structuring.

Work Environment:
• May require flexible working hours to align with global client timelines.
• Remote or hybrid work model available depending on location and team structure.


Interested candidates please share your cv on my email rajashree.hegde.c@aragen.com
Aragen Life Sciences