What are the responsibilities and job description for the Analytical Scientist position at Actalent?
The Analytical Scientist III plays a key role in developing, validating, and optimizing analytical methods independently. This position leads method development initiatives, ensures timely completion of projects, and provides technical oversight through report reviews and regular updates. The ideal candidate demonstrates urgency, initiative, and consistency in managing tasks and major projects.
Core Responsibilities
Analytical Testing
Support Quality Release testing, special requests, and stability studies for raw materials and finished products using SOPs, in-house methods, compendial standards, or methods under development.
Evaluate testing methodologies across various sample matrices and review results from contract labs to confirm compliance with agreed methods and parameters.
Instrumentation & Software
Troubleshoot analytical instruments including HPLC, GC, ICP-MS/OES, and LC-MS/MS.
Apply strong knowledge of experimental design, chemical principles, and instrumentation theory.
Proficient in laboratory software such as Empower, Tiamo, MassHunter, and MassLynx for chromatographic and spectroscopic analysis.
Mentorship & Collaboration
Actively mentor and train junior chemists in laboratory techniques and data interpretation.
Provide technical leadership in optimizing analytical methods for both marketed and developmental products.
Assist in onboarding and training new personnel following SOPs and established programs.
Safety Compliance
Maintain a safety-first approach, adhering to all safety protocols and regulatory requirements.
Manage hazardous waste in compliance with RCRA and SCDHEC regulations.
Ensure proper calibration and maintenance of laboratory instruments.
General Duties
Plan and coordinate analytical activities to ensure successful project execution.
Serve as a liaison for resolving product quality and technical issues.
Collaborate with cross-functional teams (Operations, Innovations, Marketing, etc.) to address quality and compliance concerns.
Develop and validate robust analytical methods for raw materials, finished products, and stability studies.
Execute method transfer protocols and maintain ISO 17025 competency.
Stay current with scientific advancements and act as a subject matter expert for the Quality department.
Skills
- FDA
- HPLC
- Analytical chemistry
- Wet chemistry
- Method validation
- Pharmaceutical method development
- UV/VIS
- FTIR
- Chromatography
- ICP
- GCMS
Additional Skills & Qualifications
Qualifications
Minimum Requirements
Ability to develop chromatographic, spectroscopic, titrimetric, and wet chemistry methods.
Skilled in troubleshooting laboratory instruments and interpreting complex data.
Advanced knowledge of instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS/MS, GC-MS, ICP-MS/OES, and HPTLC.
Familiarity with botanical compound characterization and analytical column selection.
Strong understanding of sample preparation techniques and statistical analysis (DOE, trend analysis).
Thorough knowledge of FDA, ICH guidelines, and GMP/GLP compliance.
Education & Experience
Bachelor’s degree in Chemistry with 7 years of experience in method development and validation within a GMP environment; or Master’s/Ph.D. with 5 years of relevant experience.
Hands-on bench experience is required.
Experience Level
Expert Level
Job Type & Location
This is a Permanent position based out of Lancaster, SC.
Pay and Benefits
The pay range for this position is $80000.00 - $110000.00/yr.
Comprehensive Health Coverage: Competitive medical, dental, and vision plans for employees and their families.
Educational Assistance: Opportunities for training and professional development to support career growth.
Supportive Work Culture: A family-oriented environment that values faith, servant leadership, and collaboration.
Community Engagement: Volunteer opportunities and mission trips organized by the company to give back locally and internationally.
Employee Recognition & Perks: Birthday cards with gift cards, family days at the zoo, Thanksgiving dinners, and other thoughtful gestures.
Work-Life Balance: A culture that prioritizes employee well-being and fosters a positive, supportive atmosphere.
Workplace Type
This is a fully onsite position in Lancaster,SC.
Application Deadline
This position is anticipated to close on Dec 12, 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.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Salary : $80,000 - $110,000