Employbridge
This range is provided by Employbridge. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $70,000.00/yr - $80,000.00/yr
Direct message the job poster from Employbridge
QC Chemist We are seeking a QC Chemist to join our growing team. The QC Chemist performs routine and non‑routine chemical analyses of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance. This role supports production troubleshooting, laboratory operations, and continuous improvement activities within the Quality Control function.
Primary Responsibilities
Perform qualitative and quantitative chemical analysis using techniques such as GC‑MS, LC, FTIR, UV‑Vis, Rheology, Particle Size Analysis, Spectrophotometry, titration, wet chemistry, and basic microbiological testing.
Conduct method validations, verifications, and transfers as assigned.
Execute testing of raw materials, intermediates, finished goods, and stability samples according to established methods, SOPs, and regulatory requirements.
Review, interpret, and document analytical data clearly and accurately in laboratory notebooks and electronic data systems.
Support investigations of OOS (Out‑of‑Specification) and OOT (Out‑of‑Trend) results, including root cause analysis and CAPA activities.
Make material disposition decisions (Approve / Reject / Rework) based on analytical results.
Calibrate and maintain laboratory equipment in alignment with internal procedures.
Ensure testing activities adhere to cGMP, GLP, and applicable quality standards.
Train and mentor junior laboratory staff as required.
Assist in preparing for internal and external audits, providing data and documentation.
Support preparation and revision of SOPs, test methods, and laboratory records.
Maintain a safe, organized, and compliant laboratory environment.
Perform additional related duties as needed.
Qualifications
4–5+ years of experience in a Quality Control or Analytical Laboratory environment (required).
Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred.
Experience in cGMP‑regulated manufacturing environments (cosmetics, pharmaceuticals, chemicals, food science, or nutraceuticals).
Solid understanding of cGMP, GLP, and regulatory documentation standards.
Experience with LIMS or other electronic laboratory data systems (preferred).
Knowledge, Skills, & Abilities
Strong analytical, problem‑solving, and troubleshooting skills.
Excellent documentation accuracy and attention to detail.
Clear written and verbal communication skills.
Ability to prioritize and manage multiple tasks in a fast‑paced environment.
Collaborative work style with strong interpersonal skills.
Proficiency in Microsoft Office (Excel, Word, Outlook, Teams) and general data analysis.
Additional Details Seniority level:
Associate
Employment type:
Full‑time
Job function:
Manufacturing, Quality Assurance, and Production
Industries:
Chemical Manufacturing
Get notified about new Quality Control Chemist jobs in
Tempe, AZ .
#J-18808-Ljbffr
Base pay range $70,000.00/yr - $80,000.00/yr
Direct message the job poster from Employbridge
QC Chemist We are seeking a QC Chemist to join our growing team. The QC Chemist performs routine and non‑routine chemical analyses of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance. This role supports production troubleshooting, laboratory operations, and continuous improvement activities within the Quality Control function.
Primary Responsibilities
Perform qualitative and quantitative chemical analysis using techniques such as GC‑MS, LC, FTIR, UV‑Vis, Rheology, Particle Size Analysis, Spectrophotometry, titration, wet chemistry, and basic microbiological testing.
Conduct method validations, verifications, and transfers as assigned.
Execute testing of raw materials, intermediates, finished goods, and stability samples according to established methods, SOPs, and regulatory requirements.
Review, interpret, and document analytical data clearly and accurately in laboratory notebooks and electronic data systems.
Support investigations of OOS (Out‑of‑Specification) and OOT (Out‑of‑Trend) results, including root cause analysis and CAPA activities.
Make material disposition decisions (Approve / Reject / Rework) based on analytical results.
Calibrate and maintain laboratory equipment in alignment with internal procedures.
Ensure testing activities adhere to cGMP, GLP, and applicable quality standards.
Train and mentor junior laboratory staff as required.
Assist in preparing for internal and external audits, providing data and documentation.
Support preparation and revision of SOPs, test methods, and laboratory records.
Maintain a safe, organized, and compliant laboratory environment.
Perform additional related duties as needed.
Qualifications
4–5+ years of experience in a Quality Control or Analytical Laboratory environment (required).
Bachelor’s degree in Chemistry, Biochemistry, or related scientific field (required); Master’s degree preferred.
Experience in cGMP‑regulated manufacturing environments (cosmetics, pharmaceuticals, chemicals, food science, or nutraceuticals).
Solid understanding of cGMP, GLP, and regulatory documentation standards.
Experience with LIMS or other electronic laboratory data systems (preferred).
Knowledge, Skills, & Abilities
Strong analytical, problem‑solving, and troubleshooting skills.
Excellent documentation accuracy and attention to detail.
Clear written and verbal communication skills.
Ability to prioritize and manage multiple tasks in a fast‑paced environment.
Collaborative work style with strong interpersonal skills.
Proficiency in Microsoft Office (Excel, Word, Outlook, Teams) and general data analysis.
Additional Details Seniority level:
Associate
Employment type:
Full‑time
Job function:
Manufacturing, Quality Assurance, and Production
Industries:
Chemical Manufacturing
Get notified about new Quality Control Chemist jobs in
Tempe, AZ .
#J-18808-Ljbffr