Yoh, A Day & Zimmermann Company
Quality Control Technician (Full Time)
Yoh, A Day & Zimmermann Company, Noblesville, Indiana, United States
Yoh is hiring for a
Quality Control Specialist for our pharmaceutical client in Noblesville, Indiana. The Quality Control Specialist role is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance. Hours:
Monday - Friday, 8AM - 5PM Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, ICP-MS etc. Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs. Review and interpret analytical data; Maintain laboratory equipment, including calibration, qualification, and troubleshooting. Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards. Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation. Participate in audits and inspections and support documentation requests from regulatory authorities. Bachelor of Science in Biology, Chemistry or related field required. ~Solid knowledge of analytical techniques and instrumentation (HPLC, GC, etc.). ~ Familiarity with cGMP, GLP, and regulatory guidelines. ~ Must be able to resolve problems, handle conflict and make effective decisions under pressure, and conduct Root Cause Analysis ~ Ability to do simple to complex math calculations, input data into the computer and analyze data as required. ~ Ability to multitask projects. ~ Must be proficient in use of Microsoft suite office products. ~ Good computer skills, including utilizing personal computers and data entry programs Good hands on, analytical, and problem solving and decision making skills. ~ Excellent writing and verbal communications skills. ~ Verifiable working knowledge of cGMP guidelines and their application in a pharmaceutical manufacturing environment.
#Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) ~ Health Savings Account (HSA) (for employees working 20+ hours per week) ~ Life & Disability Insurance (for employees working 20+ hours per week) ~ Employee Assistance Program (EAP) ~401K Retirement Savings Plan ~ Direct Deposit & weekly epayroll ~ Referral Bonus Programs ~ Certification and training opportunities
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit
to contact us if you are an individual with a disability and require accommodation in the application process. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Quality Control Specialist for our pharmaceutical client in Noblesville, Indiana. The Quality Control Specialist role is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance. Hours:
Monday - Friday, 8AM - 5PM Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, ICP-MS etc. Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs. Review and interpret analytical data; Maintain laboratory equipment, including calibration, qualification, and troubleshooting. Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards. Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation. Participate in audits and inspections and support documentation requests from regulatory authorities. Bachelor of Science in Biology, Chemistry or related field required. ~Solid knowledge of analytical techniques and instrumentation (HPLC, GC, etc.). ~ Familiarity with cGMP, GLP, and regulatory guidelines. ~ Must be able to resolve problems, handle conflict and make effective decisions under pressure, and conduct Root Cause Analysis ~ Ability to do simple to complex math calculations, input data into the computer and analyze data as required. ~ Ability to multitask projects. ~ Must be proficient in use of Microsoft suite office products. ~ Good computer skills, including utilizing personal computers and data entry programs Good hands on, analytical, and problem solving and decision making skills. ~ Excellent writing and verbal communications skills. ~ Verifiable working knowledge of cGMP guidelines and their application in a pharmaceutical manufacturing environment.
#Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) ~ Health Savings Account (HSA) (for employees working 20+ hours per week) ~ Life & Disability Insurance (for employees working 20+ hours per week) ~ Employee Assistance Program (EAP) ~401K Retirement Savings Plan ~ Direct Deposit & weekly epayroll ~ Referral Bonus Programs ~ Certification and training opportunities
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit
to contact us if you are an individual with a disability and require accommodation in the application process. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.