Silicon Valley Recruiting LLC
Quality Control Chemist
Silicon Valley Recruiting LLC, Gulfport, Mississippi, United States, 39500
Job Title:
Quality Control Laboratory Chemist Department:
Quality Control Reports To:
Quality Control Manager Employment Type:
Full-Time | On-Site Location:
Gulfport, MS Compensation:
Median $60,000-$70,000/year About the Role
Our client is seeking an experienced
Quality Control Laboratory Chemist
to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a
GMP-regulated laboratory environment . This position requires a strong background in chromatography and a proven track record of working within
cGMP
standards. Please note that you must have experience beyond a university based laboratory setting to be considered for this position. Key Responsibilities
Perform chemical analyses on raw materials, in-process products, finished products, and stability samples. Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.). Prepare reagents and samples in compliance with SOPs and regulatory requirements. Accurately document and report test results according to GMP guidelines. Contribute to method development, validation, and transfer activities. Troubleshoot and investigate testing or equipment-related issues. Collaborate with QC team members and cross-functional departments. Mentor and support junior chemists when needed. Qualifications & Requirements
3-5 years of direct hands-on experience
in a GMP-regulated QC or manufacturing laboratory. Strong background in
chromatography
(HPLC, GC, UV/VIS, FTIR). Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing. Proficiency with Empower, Microsoft Office, and laboratory data systems. Solid understanding of
cGMP , quality systems, and regulatory compliance (change control, deviations, CAPAs). Excellent attention to detail, communication, and organizational skills. Ability to multitask and prioritize in a fast-paced environment. Note:
Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most. Physical Requirements
Must be able to lift 50 lbs. or more daily. Ability to stand, walk, or sit for 8+ hours per day.
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Quality Control Laboratory Chemist Department:
Quality Control Reports To:
Quality Control Manager Employment Type:
Full-Time | On-Site Location:
Gulfport, MS Compensation:
Median $60,000-$70,000/year About the Role
Our client is seeking an experienced
Quality Control Laboratory Chemist
to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a
GMP-regulated laboratory environment . This position requires a strong background in chromatography and a proven track record of working within
cGMP
standards. Please note that you must have experience beyond a university based laboratory setting to be considered for this position. Key Responsibilities
Perform chemical analyses on raw materials, in-process products, finished products, and stability samples. Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.). Prepare reagents and samples in compliance with SOPs and regulatory requirements. Accurately document and report test results according to GMP guidelines. Contribute to method development, validation, and transfer activities. Troubleshoot and investigate testing or equipment-related issues. Collaborate with QC team members and cross-functional departments. Mentor and support junior chemists when needed. Qualifications & Requirements
3-5 years of direct hands-on experience
in a GMP-regulated QC or manufacturing laboratory. Strong background in
chromatography
(HPLC, GC, UV/VIS, FTIR). Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing. Proficiency with Empower, Microsoft Office, and laboratory data systems. Solid understanding of
cGMP , quality systems, and regulatory compliance (change control, deviations, CAPAs). Excellent attention to detail, communication, and organizational skills. Ability to multitask and prioritize in a fast-paced environment. Note:
Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most. Physical Requirements
Must be able to lift 50 lbs. or more daily. Ability to stand, walk, or sit for 8+ hours per day.
#J-18808-Ljbffr