Oral Solid Drug Development Scientist (2nd Shift)

Catalent; Kansas City (MO); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Career development

Diverse culture

PTO & holidays

401K match

Benefits from day one

Tuition reimbursement

Job summary

Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. The Pharmaceutical Development Senior Associate Scientist I role supports formulation design and development of oral solid drug products.

The position requires a Bachelor’s or Master’s degree in life/physical sciences with related experience, strong documentation, and GMP/SOP compliance; it is a 2nd

Qualifications

• Bachelor’s degree in a related life science or physical science field with at least 2 years of related experience, or an MS.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Physical requirements: ability to stand, walk, sit, use hands for manipulation, and reach with hands and arms for up to 8 hours per day; ability to wear a respirator; and occasional lifting up to 50 pounds.

Responsibilities

• Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs.
• Draft technical documents such as laboratory notebook writeups, protocols and batch records.
• Trains others on procedures and laboratory techniques.
• Executes efficiency improvement project with guidance.
• Has applied knowledge of the principles and concepts of a discipline.
• Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team.
• Performs parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
• Develop and executes procedures, methods, manufacturing processes with minimal complexity, with high quality.
• Demonstrated ability to lead small team projects.
• All other duties as assigned.

Skills

Train others

Documentation

GMP knowledge

Regulatory compliance

Education

Bachelor’s degree in life/physical science

Master’s degree in life/physical science (MS preferred)

Job description

Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. The Pharmaceutical Development Senior Associate Scientist I role supports formulation design and development of oral solid drug products.

The position requires a Bachelor’s or Master’s degree in life/physical sciences with related experience, strong documentation, and GMP/SOP compliance; it is a 2nd