



Job Information
Actalent Chemist in Shawnee, Kansas
Chemist
Job Description
Performs routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications. Designs and executes method transfer protocols, method validations, and assists in writing method transfer/validation reports. Designs and executes cleaning validation protocols and assists in writing reports. Supports activities to develop analytical methods to assess the purity, potency, and stability of drug substances and finished products. Proficient at HPLC/GC analysis and preparation of reagents and sample solutions for testing. Operates laboratory analytical instrumentation and assists in troubleshooting and calibration of laboratory equipment. Maintains accurate, detailed records of work performed. Assists in ensuring testing adheres to schedules through a team-oriented process. Serves as backup for the laboratory supervisor. Reads and interprets USP, EP, JP compendial monographs, and analytical methodology. Writes SOPs, laboratory protocols and reports, memos, and other interdepartmental correspondence. Provides training and guidance to other personnel and becomes a subject matter expert in general and advanced laboratory practices. Utilizes root cause analysis tools and technical writing to complete laboratory investigations. Independently conducts and documents laboratory investigations and acts as a backup for the laboratory supervisor.
Responsibilities
Perform routine analysis of finished pharmaceutical dosages and/or raw materials.
Design and execute method transfer protocols and validations.
Assist in writing method transfer/validation reports and cleaning validation protocols.
Develop analytical methods to assess purity, potency, and stability of drug substances and finished products.
Conduct HPLC/GC analysis and prepare reagents and sample solutions for testing.
Operate and troubleshoot laboratory analytical instrumentation.
Maintain accurate, detailed records of work performed.
Ensure testing adheres to schedules through a team-oriented process.
Serve as backup for the laboratory supervisor.
Read and interpret USP, EP, JP compendial monographs, and analytical methodology.
Write SOPs, laboratory protocols, reports, memos, and other interdepartmental correspondence.
Train and provide guidance to other personnel and become a subject matter expert in laboratory practices.
Utilize root cause analysis tools and complete laboratory investigations.
Essential Skills
Bachelor’s degree in chemistry or related science field.
Work experience in cGMP and/or GLP chemistry lab environment (0-2 years + PhD, 5 years+ with a Master’s degree, 7 years with a Bachelor’s degree).
Proficient in HPLC and GC.
Experience in a pharmaceutical lab.
Protocol writing, method development, and method validation.
Experience with small molecules and wet chemistry.
Skills & Qualifications
Ability to read and interpret USP, EP, JP compendial monographs.
Experience in writing SOPs, laboratory protocols, and reports.
Training and guidance capabilities for other personnel.
Proficiency in root cause analysis tools and technical writing.
Work Environment
The standard work schedule is Monday to Friday, 8 am to 5 pm.
Pay and Benefits
The pay range for this position is $35.00 - $43.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision• Critical Illness, Accident, and Hospital• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available• Life Insurance (Voluntary Life & AD&D for the employee and dependents)• Short and long-term disability• Health Spending Account (HSA)• Transportation benefits• Employee Assistance Program• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Shawnee,KS.
Application Deadline
This position is anticipated to close on Apr 2, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.