Job Description

We are seeking an experienced and detail-oriented Senior Analytical Chemist to join our client’s team and support critical pharmaceutical development projects. This onsite, contract-to-hire position, based near North Vernon, IN , focuses on performing advanced laboratory testing and method development for raw materials, packaging components, in-process samples, and finished products. The role plays a key part in ensuring compliance with cGMP standards while driving innovation in analytical testing and method validation.

Compensation:

• $35-$47/hour based on experience

Work Schedule:

• Monday through Friday, 8:30 am – 5:30 pm

Key Responsibilities of the Senior Analytical Chemist:

• Perform routine and complex chemical and physical tests on raw materials, active pharmaceutical ingredients (APIs), packaging, in-process, and finished products
• Utilize advanced techniques including HPLC, GC, dissolution, Karl Fischer titration, wet chemistry, and particle size analysis
• Develop and validate analytical test methods in alignment with ICH, FDA, and USP requirements with minimal supervision
• Conduct analytical research to evaluate new raw materials, packaging materials, and reference standards
• Draft and revise SOPs for laboratory processes and ensure compliance with regulatory guidelines
• Prepare technical documents to support regulatory submissions (IND, NDA, ANDA)
• Troubleshoot laboratory methods and instrumentation, recommending and implementing improvements
• Provide peer review of analytical data and ensure accuracy of laboratory records
• Train and mentor junior chemists on instrumentation, methodology, and best practices
• Support method transfers and contribute technical insight for the purchase of new laboratory equipment
• Collaborate with cross-functional teams to ensure testing and reporting timelines are met

Qualifications and Skills for the Senior Analytical Chemist:

• Bachelor’s degree in Chemistry or related field required; advanced degree preferred
• 8–12 years of experience in pharmaceutical product analysis within a cGMP-regulated laboratory
• Strong expertise in method development, method validation, and analytical instrumentation (HPLC, GC, dissolution, wet chemistry, ICP-MS, particle size analysis)
• In-depth knowledge of cGMP, FDA, ICH, and USP/NF guidelines
• Proven ability to write and edit technical documentation and regulatory reports
• Skilled in troubleshooting laboratory instrumentation and analytical methods
• Proficiency in Microsoft Word and Excel, LIMS, and Chromatography Data Systems
• Excellent communication skills with the ability to lead projects and mentor junior analysts
• Strong organizational, problem-solving, and time management abilities

Why Join Us?

This opportunity provides the chance to work on complex, cutting-edge projects within a collaborative pharmaceutical laboratory environment. You’ll play a critical role in developing analytical methods that directly impact drug product quality, while being part of a team that values technical expertise, mentorship, and professional growth.

About Us:

Contemporary Staffing Solutions (CSS) is a trusted leader in providing contract, temporary, temp-to-hire, and direct hire staffing solutions. With decades of experience, we’ve grown from a staffing agency to a nationwide provider of workforce management solutions. Our niche recruitment expertise spans Accounting & Finance, Call Center & Office Support, Human Resources, Sales & Marketing, and Information Technology.

Explore more about CSS and how we connect great talent with exceptional opportunities by visiting

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