What are the responsibilities and job description for the Analytical Chemist I position at KVK Tech, Inc.?
KVK Tech is seeking an Analytical Chemist I to join our team in Newtown, PA.
The Analytical Chemist I will perform analytical testing to support product development, validation, and routine quality operations within a cGMP-regulated laboratory environment. This role operates analytical instrumentation—including HPLC/UPLC, GC, UV-Vis, and dissolution systems—while maintaining rigorous documentation, data integrity, and adherence to laboratory procedures. The ideal candidate will demonstrate strong foundational laboratory skills, an ability to follow detailed methods, and a commitment to generating accurate, reliable analytical data in support of oral solid dosage development.
This position’s responsibilities will include, but not be limited to the following:
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position
The Analytical Chemist I will perform analytical testing to support product development, validation, and routine quality operations within a cGMP-regulated laboratory environment. This role operates analytical instrumentation—including HPLC/UPLC, GC, UV-Vis, and dissolution systems—while maintaining rigorous documentation, data integrity, and adherence to laboratory procedures. The ideal candidate will demonstrate strong foundational laboratory skills, an ability to follow detailed methods, and a commitment to generating accurate, reliable analytical data in support of oral solid dosage development.
This position’s responsibilities will include, but not be limited to the following:
- Perform analytical testing of raw materials, in-process samples, stability samples, and finished products using chromatographic and spectroscopic techniques.
- Operate, calibrate, and troubleshoot analytical instruments such as HPLC/UPLC, GC, UV-Vis, and dissolution systems.
- Document all analytical work clearly and accurately in compliance with cGMP, FDA, USP, and ICH requirements.
- Execute method verifications, transfers, and validations under supervision to ensure method reliability and regulatory alignment.
- Prepare reagents, standards, solutions, and mobile phases according to approved methods.
- Participate in laboratory investigations, including instrument- or method-related deviations and root cause analysis.
- Maintain laboratory cleanliness, equipment readiness, and adherence to safety standards.
- Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
- 0–2 years of analytical laboratory experience in a pharmaceutical, biotechnology, or academic setting.
- Hands-on experience with chromatographic techniques (HPLC/UPLC or GC) and wet-chemistry practices.
- Working knowledge of cGMP, GLP, data integrity expectations, and laboratory documentation standards.
- Strong technical, analytical, and problem-solving skills with proficiency in Microsoft Excel and Word; experience with Empower or other CDS is preferred.
- 401(k) with company match
- Health, vision, and dental Insurance
- Childcare expense reimbursement
- Tuition reimbursement
- Annual bonus eligibility
- Annual merit increases
- Paid Time Off and Flexible Holidays
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
Apply for this position