<p>Job Title: QC Chemist</p> <p>Job Description</p> <p>Job Summary: We are seeking a dedicated and detail-oriented QC Chemist to join our team. The QC Chemist will be responsible for conducting routine and non-routine analyses of raw materials, in-process, and finished products to ensure they meet quality standards and safety regulations. The ideal candidate will have a strong analytical mindset, meticulous attention to detail, and extensive knowledge of laboratory procedures and equipment.</p> <p>Responsibilities</p> <ul> <li>Conduct various chemical and instrumental analyses on raw materials, in-process samples, finished products, packaging, and composites. </li><li>Prepare and analyze samples using various procedures, including internal SOPs, specifications, analytical methods, compendial monographs, client procedures, research procedures, and protocols. </li><li>Utilize Wet Chemistry techniques (pH, Viscosity, and Titration) and Analytical Testing methods (GC, UV/Vis, and IR). </li><li>Maintain sophisticated analytical instruments, schedule preventative maintenance, and ensure trouble-free operation. </li><li>Ensure products meet quality standards and specifications, making critical pass/fail decisions. </li><li>Troubleshoot quality issues and identify root causes, preventive, and corrective actions. </li><li>Prepare and report results from timely preparation of monthly reports. </li><li>Maintain compliance with relevant regulations, standards, and guidelines. </li><li>Maintain accurate and complete records of all analytical activities. </li><li>Provide technical assistance to internal and external customers. </li><li>Make risk analysis and usage decisions of non-conformances. </li></ul> <p>Essential Skills</p> <ul> <li>Quality control </li><li>GMP </li><li>QC testing </li><li>Chemistry </li><li>Laboratory </li><li>Gas chromatography (GC) </li><li>Wet Chemistry techniques (pH, Viscosity, Titration) </li><li>UV/Vis </li><li>IR </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field. </li><li>1+ years of experience in a QC role within a cGMP facility. </li><li>Proficiency with Wet Chemistry techniques such as pH, Viscosity, and Titrations. </li><li>Familiarity with analytical techniques such as GC, UV/Vis, and IR. </li><li>Strong understanding of cGMP environment and regulatory standards. </li><li>Excellent attention to detail and problem-solving skills. </li><li>Ability to work independently and as part of a team. </li><li>Strong communication and documentation skills. </li></ul> <p>Work Environment</p> <p>The QC Chemist will work in a cGMP-compliant laboratory setting, utilizing a range of sophisticated analytical instruments and equipment. The role requires adherence to safety protocols and regulatory guidelines. The work environment is collaborative, and you will have the opportunity to provide technical support to both internal and external customers. Flexibility and the ability to work independently and within a team are essential.</p> <p>Additional Information:</p> <p>This plant is a 24/7 operation and the QC department works a rotating shift (no set shifts, each employee must do the rotating shift). Ex: 4 12hr night shift followed by 7 days off then 5 8hr day shift followed by 3 days off then back to night.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $30.00 - $30.00/hr.</p> <p>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:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully onsite position in Newark,DE.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Apr 2, 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>Diversity, Equity & Inclusion</p> <p>At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:</p> <ul> <li>Hiring diverse talent </li><li>Maintaining an inclusive environment through persistent self-reflection </li><li>Building a culture of care, engagement, and recognition with clear outcomes </li><li>Ensuring growth opportunities for our people </li></ul> <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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>