QC Chemist

The QC Chemist works in a quality control laboratory within a pharmaceutical and specialty chemical manufacturing environment in the Milwaukee area. This role focuses on release and in-process testing of raw materials, intermediates, and finished API products using a wide range of analytical instrumentation. The QC Chemist interprets chromatography data, manages analytical documentation in compliance with GMP requirements, and contributes to method and analytical development in a growing, expansion-focused organization. Job Title: QC Chemist The QC Chemist works in a quality control laboratory within a pharmaceutical and specialty chemical manufacturing environment in the Milwaukee area. This role focuses on release and in-process testing of raw materials, intermediates, and finished API products using a wide range of analytical instrumentation. The QC Chemist interprets chromatography data, manages analytical documentation in compliance with GMP requirements, and contributes to method and analytical development in a growing, expansion-focused organization. Responsibilities Perform release and in-process testing of raw materials, intermediates, test materials, and finished API products in accordance with written methods and procedures. Follow all applicable procedures, specifications, and test methods, ensuring full compliance with internal and regulatory requirements. Execute wet chemistry and analytical chemistry techniques to support quality control activities. Operate and utilize laboratory instrumentation, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), IC, and a soon-to-be-installed ICP-MS, to perform routine and specialized analyses. Interpret chromatography data and other analytical results, using data management systems such as Chemstation or Chromeleon where applicable. Assess whether materials meet specifications for release and document decisions clearly and accurately. Perform and review critical and complex calculations to support analytical testing and data evaluation. Prepare and standardize volumetric solutions to support routine and non-routine testing. Clearly document all GMP activities accurately and legibly, maintaining complete and compliant laboratory records. Perform routine maintenance and basic troubleshooting on QC instrumentation to ensure reliable operation. Review data calculations for validation activities and ensure accuracy of analytical results. Provide information and documentation responses in cases of customer complaints or returns, supporting investigations and resolutions. Write procedures, test methods, protocols, reports, and material specifications to support laboratory operations and continuous improvement. Support a culture of consistent compliance by participating in training, providing guidance, and reviewing procedures as needed. Meet deadlines and testing schedules established by quality control leadership. Participate in a structured training process, progressing from observing tests, to performing tests under supervision, to independently executing tests. Handle laboratory supplies such as columns, liners, and septa, and ensure proper setup and use of analytical equipment. Lift up to 25 pounds as needed to handle materials, reagents, and equipment in the laboratory. Essential Skills Bachelor’s degree in a science discipline such as Chemistry, Biochemistry, or Biology. 2–3 years of experience as a chemist in an industrial setting. Hands‑on experience with HPLC and GC in a quality control or analytical laboratory environment. Proficiency with laboratory instrumentation, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), and IC. Ability to interpret and review analytical and chromatographic data accurately. Strong competency in performing and verifying critical and complex calculations. Experience working under GMP or similar regulated quality systems, with the ability to document activities clearly and legibly. At least 2 years of experience using Excel for data analysis, reporting, and documentation. Capability to prepare and standardize volumetric solutions and perform wet chemistry techniques. Ability to write clear and concise procedures, test methods, protocols, reports, and material specifications. Capacity to perform routine maintenance and basic troubleshooting on QC instrumentation. Ability to assess whether materials meet specifications for release based on analytical results. Physical ability to lift up to 25 pounds as part of laboratory duties. Additional Skills & Qualifications Experience with data management systems such as Chemstation or Chromeleon. Familiarity with NMR and broader analytical chemistry techniques. Experience with API, flavor and fragrance, or specialty chemical environments. Comfort working in smaller organizations where chemists gain exposure to a wide range of analytical equipment and responsibilities. Interest in contributing to analytical development, method development, and validation activities. Strong attention to detail and a commitment to maintaining high-quality standards in all laboratory work. Ability to work collaboratively with another chemist and cross-functional teams in both laboratory and manufacturing settings. Work Environment The QC Chemist works in a quality laboratory that supports API, flavor and fragrance, and specialty chemical manufacturing. The role involves primarily laboratory-based work with occasional visits to the manufacturing floor. The laboratory uses a broad range of analytical technologies, including HPLC, GC, FTIR, UV-Vis, Karl Fischer (KF), IC, and a soon-to-be-installed ICP-MS, providing extensive hands‑on experience with modern analytical equipment. The organization is a smaller company, which allows chemists to gain broad exposure to analytical instruments and to participate in analytical and method development, as well as validation activities. The facility is currently expanding, with an additional building being added to increase API manufacturing capabilities and enhance laboratory operations. Work is conducted on a first‑shift schedule, with initial training typically running from 8:00 a.m. to 4:30 p.m., followed by a standard shift of 7:00 a.m. to 3:30 p.m. The environment emphasizes GMP compliance, accurate documentation, and collaboration. Annual pay raises are performance‑based, with typical increases averaging around 4% of salary per year. Dress is consistent with a professional laboratory and manufacturing setting, including appropriate lab attire and any required personal protective equipment. Job Type & Location This is a Permanent position based out of St Francis, WI. Pay And Benefits The pay range for this position is $62000.00 - $62000.00/yr. Kingchem Laboratories offers a range of internal employee benefits designed to support both professional growth and personal well‑being. Employees typically have access to competitive health insurance options, retirement savings plans, and paid time off to promote work‑life balance. The company also emphasizes career development through on‑the‑job training, mentorship, and opportunities to advance within technical and quality‑focused roles. Additionally, Kingchem fosters a collaborative culture with performance incentives, recognition programs, and a strong focus on safety and compliance in the workplace. Workplace Type This is a fully onsite position in St Francis,WI. Application Deadline This position is anticipated to close on Aug 20, 2026. 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. 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