Proposal Writer / Bid Writer - Pharmaceutical Contract Manufacturing (CDMO) Remote / home-based (UK) | 6-12 month fixed-term contract | Competitive salary
The opportunity
Our client is a global contract development and manufacturing organisation (CDMO) specialising in biopharmaceuticals. They are looking for an experienced Proposal Writer to join their Global Proposals team on a 6-12 month fixed-term contract and take ownership of RFP and bid responses for new pharma customers.
What you'll be doing
- Writing and managing proposals and RFP responses end to end, from receipt through to submission, driving the writing, review and approval cycle to tight deadlines
- Interpreting RFPs and client needs, and meeting technical SMEs to define project scope, budget and timelines
- Pulling together pricing and forecast data to support proposal generation
- Using templates and writing standards to ensure every bid is consistent, readable and high quality
- Partnering with Business Development to support pre-sales conversations, and acting as the link between the site and prospective customers, including supporting client visits
- Spotting trends in the pipeline and helping identify strategic opportunities
- Maintaining the proposal database, legal files and Business Development Master Index
About you
- Previous CDMO experience (essential)
- Full-cycle proposal writing experience (essential), from RFP review and scoping through to pricing, drafting, review and submission
- Degree in Chemistry or a related science (an advanced degree in Business is desirable)
- Ideally 5+ years in pharma; ADC experience is a plus
- Excellent written and verbal communication, with a strong eye for detail and flow
- Confident with Microsoft Office, including MS Project, Excel, Word and PowerPoint
- Organised and self-directed, able to prioritise and deliver to deadlines while working remotely
- A natural relationship builder, comfortable with colleagues and customers alike
Please note
This is a home-based role. Occasional site visits may be required, which may involve time in a pharmaceutical manufacturing or laboratory environment, with PPE provided where required.
Why apply?
Flexible home-based working, a specialist and growing biologics business, and real influence over how new business is won, with the chance to make an immediate impact.
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Proposal Writer employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
