Schedule:

3:30 PM - 11:30 PM Job Overview CMIC is seeking a motivated and detail-oriented Junior QC Chemist to join our Quality Control laboratory on 2nd shift (3:30 PM - 11:30 PM) . This is an excellent opportunity for a recent college graduate or early-career scientist interested in building a career in pharmaceutical Quality Control. The Junior QC Chemist will receive training to perform routine analytical testing in support of pharmaceutical manufacturing, batch release, and stability programs. The position is a hands-on, laboratory-based role working with pharmaceutical products, including solid oral dosage forms such as tablets and capsules. The ideal candidate will have a strong educational foundation in chemistry or a related scientific discipline, good laboratory skills, strong attention to detail, and an interest in working in a regulated pharmaceutical manufacturing environment. Key Responsibilities QC Laboratory Testing Perform routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products under the guidance of experienced QC personnel. Support batch release and stability testing of pharmaceutical products, including tablets and capsules. Perform testing such as assay, dissolution, and impurity testing using established analytical methods and procedures. Prepare samples, standards, reagents, and solutions according to approved laboratory procedures. Follow established test methods, specifications, SOPs, and laboratory procedures. Laboratory Instrumentation Learn to operate analytical laboratory equipment including HPLC/UPLC, dissolution, GC, UV-Vis, and FT-IR . Perform routine instrument setup, system suitability, calibration checks, and basic equipment maintenance as assigned. Develop proficiency with chromatography and laboratory data systems such as Empower and LIMS . Documentation & Data Integrity Accurately document laboratory activities, calculations, observations, and analytical results. Maintain complete and accurate laboratory records in accordance with cGMP and ALCOA+ data integrity principles . Enter and maintain analytical data in applicable laboratory systems. Ensure laboratory documentation is complete, accurate, and audit-ready. Quality & Compliance Follow all applicable cGMP, FDA, ICH, company SOP, safety, and laboratory requirements . Promptly report unexpected or questionable analytical results to QC supervision. Assist experienced QC personnel with OOS, OOT, deviation, and laboratory investigations as appropriate. Participate in required laboratory, safety, GMP, and technical training. Support internal and external audits as needed. Collaboration Work closely with other members of the Quality Control team to support laboratory priorities and production timelines. Collaborate with Quality Assurance, Manufacturing, and other departments as needed. Communicate testing status, laboratory issues, and potential delays to QC supervision. Maintain a clean, organized, and safe laboratory work environment.

QUALIFICATIONS

Education Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline required. Recent college graduates are encouraged to apply. Experience 1-2 years of chemistry laboratory experience. Previous pharmaceutical, cGMP, QC, internship, co-op, or academic laboratory experience is preferred but not required. Hands-on laboratory experience obtained through undergraduate coursework, research, internships, or employment will be considered. Training will be provided on CMIC's pharmaceutical QC procedures, analytical methods, instrumentation, and cGMP requirements. Technical Skills Basic understanding of analytical chemistry and laboratory techniques. Academic or hands-on exposure to HPLC or other chromatography techniques is preferred. Exposure to analytical instrumentation such as HPLC/UPLC, GC, UV-Vis, FT-IR, or dissolution equipment is a plus. Ability to accurately perform laboratory calculations, dilutions, solution preparation, and sample preparation. Basic computer skills and ability to learn laboratory software systems such as LIMS and Empower . Familiarity with cGMP, pharmaceutical Quality Control, or data integrity principles is a plus but not required. Experience Previous laboratory experience in a pharmaceutical or biochemical setting is preferred but not required; relevant internships or academic projects are also valuable. Strong knowledge of analytical chemistry techniques including chromatography (HPLC, GC), spectroscopic analysis (FTIR, UV-Vis), mass spectrometry (LC-MS, GC-MS), and microscopy. Familiarity with laboratory instruments such as spectrophotometers, Fourier-transform infrared (FTIR) spectrometers, high-performance liquid chromatography systems, gas chromatographs, and mass spectrometers. Experience with laboratory information management systems (LIMS) for data entry and record keeping. Understanding of

GLP, CGMP, FDA

regulations, and pharmaceutical quality standards is highly desirable. Ability to follow detailed protocols accurately while maintaining a high level of attention to detail in a fast-paced environment. Strong communication skills for documenting results clearly and collaborating effectively with team members. Join us to be part of a dedicated team committed to excellence in pharmaceutical quality control! Core Competencies Strong attention to detail and commitment to accurate documentation. Ability and willingness to learn pharmaceutical QC laboratory procedures and instrumentation. Good organizational and time-management skills. Ability to follow written procedures and established analytical methods. Strong scientific curiosity and problem-solving skills. Effective verbal and written communication skills. Ability to work collaboratively as part of a laboratory team. Dependable and able to consistently work the assigned 2nd shift schedule of 3:30 PM - 11:30 PM . Working Conditions Laboratory-based environment with exposure to chemicals and specialized analytical equipment. Ability to stand for extended periods and lift up to 25 lbs. Must be able to work 2nd shift, 3:30 PM - 11:30 PM . Flexibility to support production schedules, including occasional overtime, may be required. This job description is not intended to be all-inclusive. Employees may be required to perform other duties as assigned by management.

Pay:

$45,000.00 - $50,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Disability insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance

Work Location:

In person