Our Senior Formulation Scientist, Development is responsible for managing and supporting formulating new products and any new formulations for existing products for continuous process improvement. This role will collaborate with the development team to support the Pharmacy Services and Technical Services department in developing new and improving existing formulations that will be transferred into commercial products. The Senior Formulation Scientist, Development will also support the Technical Services team as a subject matter expert with addressing important manufacturing issues. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
What The Senior Formulation Scientist, Development Does Each Day
- Innovate and develop new products/patents
- Design and develop protocols for new product development and improvement of existing products
- Supports administrative activities and meetings for formulation process strategies
- Collaborates with Pharmacy Services in developing new product formulations
- Collaborates with Technical Services in transferring new products to commercial products
- Ensures product deadlines are met and projects are handled in a professional manner
- Present ideas for modifying existing procedures and suggest alternative methods to improve results
- Perform scientific literature searches and evaluations as required
- Collaborating with development in producing for writing new drug formulations
- Recommending scientifically sound drug formulations for new products and existing products
- Review drug/diluent compatibilities
- Ensures pharmaceutical formulations are correct for specific procedures and processes
- Supports the Technical Support team with process validations and qualifications
- Ensures all proper policies and procedures/work instructions are followed correctly within R&D development
- Ensures that Master Formularies are up to date and makes any changes pursuant to process improvements and investigations
- Ensures all duties and processes are in adherence with ISO standards, USP, and current good compounding practices
- Perform change control processes and assist with managing timelines
- Writing, maintaining, and improving standard operating procedures related to developed products
- Practice and monitors good documentation practices
Our Most Successful Senior Formulation Scientist, Development
- Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)
- Has good coordinating abilities, attention to detail with positive communication skills
- Has excellent organizational skills with ability to manage multiple projects
- Is proficient in Microsoft Office
Minimum Requirements For This Role
- Ph.D. in analytical chemistry or equivalent or Master’s degree with extensive experience
- 7+ years’ experience with formulation development in a pharmaceutical environment
- 10 years advanced R&D at scientist/engineer level in pharmaceutical fields
- Experience working with controlled substances & sterile injectables
- Understanding of cGMP, FDA, ICH principles, guidance and regulation
- Experience writing SOPs and critical regulated documents for internal and external business
- 18+ years of age
- Able to successfully complete a drug and background check
- Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas
Benefits Of Working At Quva
- Set, full-time, consistent work schedule
- Comprehensive health and wellness benefits including medical, dental and vision
- 401k retirement program with company match
- 17 paid days off plus 8 paid holidays per year
- Occasional weekend and overtime opportunities with advance notice
- National, industry-leading high growth company with future career advancement opportunities
About Quva
Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.
Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”
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