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Formulation Development Scientist - St Asaph, Denbighshire, United Kingdom - CONTRACT PHARMA
3 weeks ago
Description
Each day we Bring Science to Society as we work towards improving the quality of life for patients who benefit from the therapies that we manufacture.
Each day we Bring Science to Society as we work towards improving the quality of life for patients who benefit from the therapies that we manufacture.
Whether you are working hands-on in developing, manufacturing, or, testing the products or if you are utilizing your expertise in any other way, through your work here you will have an opportunity to positively affect countless lives.
We encourage our employees to continue their personal and professional development in various ways.Formulation Development Scientist II
We are looking for a Product Development II .
In this role, you will support research directed toward the development of new formulations and/or formulation platforms for a significant PD project or a number of small projects with complex features.
Lead development activities for client-based projects with supervision, ranging from preclinical studies to NDA submission.Execute prototype, scale,e-up, and process transfer activities including manufacture, data evaluation, troubleshooting product/process issues and risk assessments.
pharmaceutical development reports, investigation plans, and outcomes for development problems.
Maintain knowledge of equipment, instrumentation, and procedures related to product development.
Maintain and expand knowledge of current and new formulation development technologies and
Perform literature and patent searches ta o provide a background basis for development plans.
Attend cGMP training sessions and comply with site-wide and departmental procedures including but not limited to change control, documentation, deviation reporting, cGMP compliance, safety, and electronic data security.
Work closely with Analytical Development, Quality Assurance, and Validation groups.May serve as lead for product development activities within cross-departmental project teams.
Bachelor's degree in Pharmaceutics, Physical Organic Chemistry, Pharmaceutical Chemistry, Chemical Engineering or similar with 5 years of relevant work experience, or Master's degree in one of the areas above with 3 years of relevant work experience.
Familiarity with common pharmaceutical raw materials, their applications, and the principles of formulation development.
Working knowledge of MS Office (Word, Excel, PowerPoint, Access, and Outlook), Minitab, JMP, or equivalent.
We offer a competitive total rewards package that includes health benefits, annual performance bonuses, stock options, generous paid time off, holiday shutdowns, parental leave, matching 401k contributions, and much more
Societal is a bi-coastal contract development and manufacturing organization (CDMO) with expertise to deliver on our client's needs, regardless of complexity level.
These projects span pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms.
We provide industry-leading support for small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging, and logistics services to the global pharmaceutical market.
We do all of this in our best-in-class facilities in San Diego, California, and Gainesville, GA.If you would like to apply for this position, please visit our website at and click on the "Careers" section.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law.
If you require an accommodation to complete the application or interview process, please contact .Societal is a bi-coastal contract development and manufacturing organization (CDMO) with expertise to deliver on our client's needs, regardless of complexity level.
These projects span pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms.
We provide industry leading support for small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging and logistics services to the global pharmaceutical market.
We do all of this in our best-in-class facilities in San Diego, California and Gainesville, Georgia.NextRoll and our advertising partners process personal data to:
