QC Chemist

QC Chemist I And II We are currently hiring multiple QC Chemist I and II roles in Columbus. These are 2nd and 3rd shift positions and will be supporting a pharmaceutical manufacturing company. The QC Scientist I performs hands-on bench testing to support the development and release of multisource pharmaceutical products. This role focuses on chemical and physical analyses, including sample preparation and wet chemistry, and provides analytical support for registration materials and regulatory submissions. Over time, the QC Scientist I receives training on advanced instrumentation such as HPLC and GC and works across Oral Dose Solids and Nasals departments while adhering to cGXP standards, standard operating procedures, and company practices. Responsibilities Perform routine bench testing, including sample preparation, wet chemistry, standard weighing, and dilutions, in support of product development and quality control activities. Conduct chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products. Provide analytical support for the release of registration materials required for regulatory submissions. Assist with analytical method validation and method transfer activities to ensure robust and reliable analytical procedures. Execute assigned analytical tasks to support product development, registration lot release, and pre- and post-regulatory submission activities within established timelines. Work in compliance with cGXP guidelines, internal SOPs, and company practices and procedures at all times. Follow written work instructions and analytical procedures accurately and consistently. Document analytical activities, observations, and results clearly and completely, ensuring data integrity and right-first-time documentation. Identify execution challenges with analytical methods and support troubleshooting activities to resolve technical issues. Collaborate with colleagues in both the quality group and manufacturing areas to accomplish assigned tasks using a team-based approach. Manage multiple analytical tasks in a fast-paced environment while maintaining high quality and attention to detail. Apply scientific judgment and professional competency when working under supervision to interpret data and make appropriate recommendations. Essential Skills Bachelors degree in a science field is required. Preferred bachelors degree in Chemistry or Biochemistry; candidates with degrees in Biology, Microbiology, Physics, Environmental Science, or Pharmaceutical Science are considered if they have strong chemistry lab experience. Strong chemistry laboratory experience, gained either through academic coursework or outside of academia. Prior laboratory experience is required; experience in non-academic lab settings is strongly preferred. Hands-on experience with sample preparation, wet chemistry techniques, standard weighing, and preparing dilutions. Ability to work effectively in a team environment to accomplish shared objectives. Ability to handle multiple tasks simultaneously in a fast-paced environment. Good written and verbal communication skills for documenting results and collaborating with cross-functional teams. Ability to work under supervision while using sound scientific judgment and professional competency. Commitment to following cGXP guidelines, SOPs, and established company practices. Additional Skills & Qualifications Experience in quality control or chemical testing environments. Exposure to biochemistry techniques and principles. Familiarity with HPLC and GC instrumentation, or strong interest and aptitude to be trained on these technologies. Experience working in pharmaceutical, environmental, or related scientific laboratories. Demonstrated ability to identify issues in analytical method execution and contribute to troubleshooting. Strong attention to detail and commitment to maintaining data integrity and accurate documentation. Comfort working in a structured environment with defined procedures and regulatory expectations. Ability to adapt to changing priorities and support both development and manufacturing-related activities. Work Environment This role is based in a fast-paced pharmaceutical manufacturing and quality control environment. The QC Scientist I spends significant time in the quality group performing bench testing and may occasionally work in the manufacturing area to support production-related analytical needs. The position is on third shift, Monday through Friday, typically 11:00 pm-7:30 am, or 3:00-11:00pm with potential flexibility for a 4x10 schedule. Initial training is conducted on an evening schedule, either 7:00 p.m. to 3:30 a.m. (5x8s) or 7:00 p.m. to 5:30 a.m. (4x10s) for the first few months. Work involves regular use of laboratory equipment and analytical technologies, including wet chemistry apparatus, balances for standard weighing, and, with training, HPLC and GC systems. The environment emphasizes collaboration, internal promotion, and ample opportunities for growth and upward mobility following a recent organizational restructuring. Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Application Deadline This position is anticipated to close on Nov 6, 2026. Workplace Type This is a fully onsite position in Columbus, OH. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email View email address on click.appcast.io for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools. Actalent