<p>Job Title: QC Chemist</p> <p>Job Description</p> <p>We are seeking a skilled QC Chemist who practices the principles of quality on a daily basis. The ideal candidate is hard-working and extremely ambitious, with the ability to learn and manage responsibilities in a dynamic business environment. The analytical group is responsible for analyzing raw materials, in-process materials, stability, and finished products in accordance with cGMP regulations. The group also handles scheduling, calibration, maintenance of equipment, and performs method development and validation for various analytical methods. As a team member, you will be expected to follow and help plan daily operations within the lab, communicating with all areas in the company to meet client and company deadlines.</p> <p>Responsibilities</p> <ul> <li>Demonstrate expertise with analytical instrumentation, including HPLC, UHPLC, Dissolution, Spectrophotometer, GC, KF (potentiometric and coulometric), and ICP-MS. </li><li>Understand and apply USP, ICH, and CFR regulatory requirements. </li><li>Perform analytical techniques such as Method Development/Validation, chromatography, pipetting, and solution preparation. </li><li>Utilize electronic systems like LIMS, electronic laboratory notebooks, TrackWise, OpenLAB, Excel, and Word. </li><li>Conduct various analytical tests, including Assay, dissolution, degradants, moisture, hardness, viscosity, and pH. </li><li>Execute against monographs, protocols, and SOPs in a cGMP laboratory environment. </li><li>Prevent deviations and investigations. </li><li>Conduct stability scheduling and studies. </li></ul> <p>Essential Skills</p> <ul> <li>Bachelor's Degree in Chemistry from an accredited US college or university. </li><li>At least 1 year of hands-on QC Chemistry experience in a small molecule GMP lab. </li><li>Previous related lab experience is required. </li><li>Experience with HPLC (Agilent 1100 or 1290). </li><li>Experience with Dissolution and FTIR/IR. </li><li>Proficiency with LIMS and GMP. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience with electronic systems such as TrackWise and OpenLAB. </li><li>Capability in Method Development and Method Improvement. </li><li>Understanding of wet chemistry and pharmaceutical processes. </li></ul> <p>Work Environment</p> <p>This position requires you to spend the majority of your time in the lab. Please note that salaried employees are compensated for a 50-hour work week.</p> <p>Job Type & Location</p> <p>This is a Permanent position based out of Horsham, PA.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $80000.00 - $80000.00/yr.</p> <p>Health, dental, vision and 401k available</p> <p>2 weeks of vacation</p> <p>Holiday and sick time available</p> <p>Workplace Type</p> <p>This is a fully onsite position in Horsham,PA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Dec 15, 2025.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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.</p>