Formulation R&D Technician

Humanwell Pharmaceutical US•Ballwin, MO

16d

About The Position

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.

Requirements

Bachelor's or Master’s degree in Pharmaceutical Science, Chemical Engineering, Chemistry, or a closely related discipline.
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.

Nice To Haves

Preferably possesses relevant experience within the pharmaceutical industry.
Preferably possesses hands-on experience in pharmaceutical research and development as well as GMP manufacturing environments.

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.