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SENIOR QC CHEMIST

LGM Pharma, LLC
Posted 4 months ago, valid for 14 days
Location

Rosenberg, TX 77471, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position involves performing routine and non-routine chemical analysis of raw materials and products using validated methods.
  • Candidates are required to have a Bachelor’s degree in chemistry or a related scientific field, with a minimum of 5+ years of experience in a pharmaceutical or GMP-regulated laboratory.
  • The role includes operating laboratory instrumentation such as HPLC and GC, troubleshooting analytical methods, and ensuring compliance with regulatory requirements.
  • Additionally, the successful candidate will be responsible for training junior staff, preparing laboratory documentation, and collaborating with cross-functional teams.
  • The salary for this position is competitive and commensurate with experience, reflecting the importance of the role within the organization.

 

PRIMARY DUTIES AND RESPONSIBILITIES:

  • Perform routine and non-routine chemical analysis of raw materials, in-process samples, and finished products using validated analytical methods. 
  • Operate and maintain laboratory instrumentation such as HPLC, GC, UV-Vis, FTIR, and other analytical equipment. 
  • Review and interpret analytical data to ensure compliance with specifications and regulatory requirements. 
  • Troubleshoot analytical methods, instrumentation issues, and laboratory processes. 
  • Develop, validate, and transfer analytical methods in accordance with industry standards (e.g., USP, ICH, FDA guidelines). 
  • Prepare and review laboratory documentation, including test methods, protocols, reports, and SOPs. 
  • Ensure all laboratory activities comply with cGMP, safety, and company policies. 
  • Train and mentor junior chemists and laboratory technicians. 
  • Support internal and external audits and inspections. 
  • Maintain accurate and timely documentation in laboratory systems (e.g., LIMS, notebooks). 
  • Collaborate with cross-functional teams, including Quality Assurance, Production, and R&D. 
  • Assist with investigations related to out-of-specification (OOS) and out-of-trend (OOT) results. 


QUALIFICATIONS: 

  • Bachelor’s degree in chemistry or related scientific field required; Master’s degree preferred. 
  • Minimum of 5+ years of experience in a pharmaceutical or GMP-regulated laboratory. 
  • Strong knowledge of analytical techniques such as HPLC, GC, and spectroscopy. 
  • Familiarity with cGMP, FDA, USP, and ICH guidelines. 
  • Strong analytical, problem-solving, and organizational skills. 
  • Ability to work independently and manage multiple priorities. 
  • Excellent written and verbal communication skills. 


At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.




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