Grants Proposal Writer

The work we do at BioTechnique has never been more important and we are looking for talented candidates to join us. We re growing our locations our capabilities and our teams and looking for passionate missiondriven people like you who want to make a real difference in people s lives. Join BioTechnique and help create the next vaccine cure or gene therapy in partnership with some of the most innovative biopharma companies across the globe. Here you ll work alongside and learn from some of the most dedicated scientists engineers and manufacturers in the industry. We re proud to cultivate a culture that will fuel your passion energy and drive. Join us and discover a community that thrives on diversity and never scares away from a complex challenge. At BioTechnique you determine what s possible.

BioTechnique is a highly potent sterile injectable and clinical oncolytics manufacturing company dedicated to providing cytotoxic and high potency sterile injectable fillfinish services. BioTechnique s project management and client services staff work closely with our clients to meet all manufacturing needs. From IND applications through commercial scale production we provide formulation and compounding fillfinish and optional lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team s expertise to work with our clients to create a process design for their product that suits their needs.

The Experience

With operations spanning the globe and featuring a multicultural team BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team you will be offered the ability to feel inspired in your career explore your professional passions and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such you will not only be offered a compensation and benefits structure that rewards you but also be provided with the tools that will help you grow and learn.

At BioTechnique it s about more than just a job it s about your career and your future.

Your Role

As a Grants Proposal Writer at BioTechnique you will be responsible for developing and writing grant proposals to government entities such as BARDA ASPR the BioMap Consortium the Medical Technology Enterprise Consortium the Rapid Response Partnership Vehicle (RRPV) DARPA and others. You will collaborate with our project teams to create compelling narratives that align with the missions of these agencies and demonstrate BioTechnique s capabilities and expertise as a leading CDMO. This role supports 8PM 5AM PH timezone.

• Research and identify grant opportunities relevant to BioTechnique s strategic goals in the pharmaceutical manufacturing sector.
  
• Lead the development and writing of all grant proposals ensuring they meet the stringent requirements and guidelines of government agencies.
  
• Collaborate with scientific technical and project management teams to gather necessary information and align proposal content with project objectives and agency priorities.
  
• Write revise and edit drafts including executive summaries conclusions and organization credentials.
  
• Ensure proposals are submitted in a timely manner and comply with all agency protocols.
  
• Monitor and manage the proposal submission process including preparation of supporting documents budget narratives and appendices.
  
• Stay current with all regulatory industry and grantrelated updates by attending relevant workshops and reviewing publications.
  

Requirements

• Bachelor s degree in a relevant field such as Life Sciences English Journalism or Communications. Advanced degrees or certifications in grant writing or project management are highly preferred.
  
• 5 years of experience in a grant writing role supporting government projects within the pharma/biotech industries.
• Proven track record of successful grant writing specifically with proposals to government agencies mentioned above or other agencies.
  
• Strong understanding of the pharmaceutical industry and the specific needs of a CDMO.
  
• Excellent writing editing and proofreading skills with the ability to produce clear concise and persuasive copies.
  
• Strong research skills and the ability to understand complex scientific and technical information.
  
• Exceptional organizational and project management skills with the ability to manage multiple projects under tight deadlines.
  
• Experience in collaborating with diverse teams including scientists engineers and project managers.
  
• Proficient in Microsoft Office and familiar with grant submission portals and requirements.
  
• Must be able to support working hours of 8PM5AM PH timezone.
  

Equal Opportunity Employment Statement:

PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees interns and applicants for employment. Consistent with this commitment our policy is to comply with all applicable federal state and local laws concerning employment discrimination. Accordingly the Company prohibits discrimination against qualified employees interns and applicants in all aspects of employment including but not limited to: recruitment interviewing hiring (or failure or refusal to hire) evaluation compensation promotion job assignment transfer demotion training leaves of absence layoff benefits use of facilities working conditions termination and employersponsored activities and programs including wellness social and recreational programs. Employment decisions will be made without regard to an applicant s employee s or intern s actual or perceived: race color religion sex (including pregnancy gender identity and sexual orientation) national origin age (40 or older) disability genetic information or any other status protected by law.

#LIFF1

Bachelor s degree in a relevant field such as Life Sciences, English, Journalism, or Communications. Advanced degrees or certifications in grant writing or project management are highly preferred. 5+ years of experience in a grant writing role supporting government projects, within the pharma/biotech industries. Proven track record of successful grant writing, specifically with proposals to government agencies mentioned above or other agencies. Strong understanding of the pharmaceutical industry and the specific needs of a CDMO. Excellent writing, editing, and proofreading skills with the ability to produce clear, concise, and persuasive copies. Strong research skills and the ability to understand complex scientific and technical information. Exceptional organizational and project management skills, with the ability to manage multiple projects under tight deadlines. Experience in collaborating with diverse teams including scientists, engineers, and project managers. Proficient in Microsoft Office and familiar with grant submission portals and requirements. Must be able to support working hours of 8PM-5AM PH timezone. Equal Opportunity Employment Statement: PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant s, employee s, or intern s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-FF1