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 Brownstown, 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:
- $38-$47/hour based on experience
Work Schedule:
- Monday through Friday, 8:30am – 5:30pm
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 www.ContemporaryStaffing.com.