Formulation R&D Technician
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Job Location:
Ballwin, MO - USA
Monthly Salary:
Not Disclosed
Posted on:
24-10-2025
Vacancies:
1 Vacancy
Job Summary
Formulation R&D Technician Oral Product Development
Humanwell Pharmaceuticals US St Louis MO
Summary
Humanwell Pharmaceutical US Inc. based in St Louis MO is committed to advancing pharmaceutical research and development with a particular emphasis on novel therapeutics that address unmet medical needs. The organization strives to enhance the quality of life for patients and shape a healthier future. Humanwell seeks individuals motivated by a desire to make a meaningful impact and is currently recruiting a dedicated Formulation R&D Technician. The individual will collaborate closely with senior scientists and management to execute hands-on pharmaceutical development activities.
Primary Duties and Responsibilities
- Maintain compliance cleanliness and organization within the operational areas of the pilot plant.
- Set up operate maintain and sanitize a broad array of formulation equipment and testing instruments including but not limited to scales high shear and fluid bed granulators blenders tablet press film coater homogenizer density tester and hardness tester.
- Document laboratory activities in accordance with Good Documentation Practices.
- Summarize study outcomes and assist in the preparation of technical reports and presentations.
- Independently plan and accomplish assigned responsibilities within established timelines as directed by supervisory personnel.
- Conduct physical inventory for both controlled and non-controlled substances.
- Contribute to the development revision and delivery of training on manufacturing Standard Operating Procedures (SOPs).
- Comply with current Good Manufacturing Practices (cGMP) and all applicable regulatory guidelines.
- Work extended hours occasionally as necessitated by project requirements.
- Be available to travel up to 10% of the time.
- Perform additional duties and assignments as required.
Required Qualifications and Skills:
- Bachelors or Masters degree in Pharmaceutical Science Chemical Engineering Chemistry or a closely related discipline.
- Preferably possesses relevant experience within the pharmaceutical industry.
- Preferably possesses hands-on experience in pharmaceutical research and development as well as GMP manufacturing environments.
- Demonstrates willingness and capability to comply with FDA OSHA and DEA regulations.
- Exhibits a proven ability to collaborate effectively as part of a cross-functional team.
- Displays excellent oral and written communication skills.
Job Type: Full-time
Job Location: Ballwin MO
Required Experience:
IC
Key Skills
- Laboratory Experience
- Vendor Management
- Design Controls
- C/C++
- FDA Regulations
- Intellectual Property Law
- ISO 13485
- Research Experience
- SolidWorks
- Research & Development
- Internet Of Things
- Product Development
