Lannett Company

  • Contractor
  • Full-Time
  • Carmel, NY
  • Splintpharma
  • Prefferd visa: OPT, CPT, F1, H4, L2, Have H1 Visa, Need H1 Visa, EAD, TN Permit Holder, Green Card Holder, US Citizen
  • Posted 1 year ago – Accepting applications
Job Detail
  • Offerd Salary $ 30 - $ 45
  • Required Position 2-4 hires
  • Experience 0-5 Years Required
Job Description

Senior Quality Control Auditor

 

 

Scientific Search client has an immediate need for a Senior Quality Control Auditor. This is a 6+ month contract engagement with a potential transition to perm. The Senior Quality Control Auditor reports directly to the Quality Control Manager and is responsible for performing the review of laboratory notebooks and data generated from the testing of routine tests on active pharmaceutical ingredients, excipients, in-process and finished products using wet chemical, physical and instruments.  The Senior Quality Control Auditor works independently in addition to acting as a reviewer on test procedures, SOPs, technical documents and other record types as required.  Assists with special projects and other tasks as deemed necessary.

 

Responsibilities:

  • Work within a team environment of <25 individuals performing day-to-day laboratory activities.  Tasks are guided by management. This role has limited scheduling responsibilities, it does not have management or budget responsibilities
  • Perform accurate and timely review of analytical testing for components, supplies, raw materials, finished and intermediate products, manufacturing equipment cleaning samples for both Operations and Development groups
  • Perform review of laboratory equipment calibration/verification and preventative maintenance.
  • Perform the review of method validation and method transfer testing data for components, supplies, raw materials, finished and intermediate products, manufacturing equipment cleaning samples for both Operations and Development group
  • Review SOPs and other technical documents
  • Assist with development of laboratory work instructions
  • Assist with the performance of laboratory method troubleshooting and OOS/OOT investigations
  • Keep abreast of all compendial changes and regulatory requirements
  • Train and Mentor other auditors
  • Document all laboratory data reviews and legible notebooks records
  • Entry of all necessary information into the appropriate database in a timely manner for trending and capacity modeling purposes

 

Qualifications:

  • Bachelor’s degree in Chemistry and 10+ years of laboratory experience ora master’s degree in Chemistry and 8+ years of experience, preferably within a pharmaceutical or manufacturing environment
  • Knowledge of cGMP and other regulatory requirements
  • Thorough understanding of pharmaceutical development and manufacturing
  • SME of laboratory testing procedures and instruments, especially HPLC & GC
  • SME for Method Development and Validation procedures
  • Knowledge of USP/NF methodology and relevant requirements
  • Ability to wear PPE, gown up for analytical lab testing area
  • Ability to perform general office tasks
Job Requirement

Senior Quality Control Auditor

 

 

Scientific Search client has an immediate need for a Senior Quality Control Auditor. This is a 6+ month contract engagement with a potential transition to perm. The Senior Quality Control Auditor reports directly to the Quality Control Manager and is responsible for performing the review of laboratory notebooks and data generated from the testing of routine tests on active pharmaceutical ingredients, excipients, in-process and finished products using wet chemical, physical and instruments.  The Senior Quality Control Auditor works independently in addition to acting as a reviewer on test procedures, SOPs, technical documents and other record types as required.  Assists with special projects and other tasks as deemed necessary.

 

Responsibilities:

  • Work within a team environment of <25 individuals performing day-to-day laboratory activities.  Tasks are guided by management. This role has limited scheduling responsibilities, it does not have management or budget responsibilities
  • Perform accurate and timely review of analytical testing for components, supplies, raw materials, finished and intermediate products, manufacturing equipment cleaning samples for both Operations and Development groups
  • Perform review of laboratory equipment calibration/verification and preventative maintenance.
  • Perform the review of method validation and method transfer testing data for components, supplies, raw materials, finished and intermediate products, manufacturing equipment cleaning samples for both Operations and Development group
  • Review SOPs and other technical documents
  • Assist with development of laboratory work instructions
  • Assist with the performance of laboratory method troubleshooting and OOS/OOT investigations
  • Keep abreast of all compendial changes and regulatory requirements
  • Train and Mentor other auditors
  • Document all laboratory data reviews and legible notebooks records
  • Entry of all necessary information into the appropriate database in a timely manner for trending and capacity modeling purposes

 

Qualifications:

  • Bachelor’s degree in Chemistry and 10+ years of laboratory experience ora master’s degree in Chemistry and 8+ years of experience, preferably within a pharmaceutical or manufacturing environment
  • Knowledge of cGMP and other regulatory requirements
  • Thorough understanding of pharmaceutical development and manufacturing
  • SME of laboratory testing procedures and instruments, especially HPLC & GC
  • SME for Method Development and Validation procedures
  • Knowledge of USP/NF methodology and relevant requirements
  • Ability to wear PPE, gown up for analytical lab testing area
  • Ability to perform general office tasks
Required skills