Quality Control Supervisor
Aurora Pharmaceutical Aurora Pharmaceutical Northfield, MN Northfield, MN Full-time Full-time Estimated:
$59.
6K - $75.
5K a year Estimated:
$59.
6K - $75.
5K a year Aurora Pharmaceutical Inc Job title:
Quality Control Supervisor - Finished Goods Supervisor:
Quality Control Supervisor Overview:
Responsible for supervision of Quality Control Chemists.
Oversees finished product testing, raw material testing, cleaning validation, calibration, instrument qualification, and 5S programs.
Also performs analytical testing, method validation and development.
Compiles and reviews data for compliance.
Completes special projects.
Duties:
Trends and interprets statistical data Hires, trains, mentors and supervisors QC Chemists Conducts timely performance reviews for QC Chemists Coordinates reviews and approvals for QC Chemists Coordinates lab activities such as dishwashing, standard checking, reagent checking Approves analytical worksheets Releases products Ensures stability tests are conducted timely and accurately Ensures instruments are calibrated timely and accurately Completes testing projects from beginning to end Collaborates in cross-functional teams Follows all Aurora Pharmaceutical policies, procedures, regulations and the employee handbook.
Follows designated work schedule.
Assumes additional responsibilities as requested.
Accepts and acts upon supervisory directions.
Supports Manager's role.
Demonstrates flexibility, i.
e.
willingly takes on new tasks.
Performs routine sampling, analysis and documentation of pharmaceutical samples - raw materials, intermediates, drug products, package materials Generates experimental data according to written SOP, protocol, method, or work instructions Follows guidelines when recording data Uses analytical techniques such as titration, gravimetric analysis, etc.
Accurately maintains laboratory data and logs Uses analytical instrumentation such as GC, HPLC, IR and UV spectroscopy, UPLC etc.
Accurately interprets and reports results Performs method verification, method validation and method transfer Develops chromatographic methods Designs, implements and completes projects ( denotes essential job functions) Knowledge, Skills & Abilities:
Prefer candidates with interest and background in pharmaceutical testing, sampling and regulations Strong knowledge and minimum 5 years of experience with analytical chemistry and laboratory concepts and techniques Strong knowledge of computer applications Thorough knowledge of USP Education:
Bachelor's in Chemistry or Chemical Engineering Will consider:
Bachelor's in Biology, Environmental Sciences, or related degree plus a Minor in Chemistry.
Job Type:
Full-time
Benefits:
401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Vision insurance Schedule:
8 hour shift Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
$59.
6K - $75.
5K a year Estimated:
$59.
6K - $75.
5K a year Aurora Pharmaceutical Inc Job title:
Quality Control Supervisor - Finished Goods Supervisor:
Quality Control Supervisor Overview:
Responsible for supervision of Quality Control Chemists.
Oversees finished product testing, raw material testing, cleaning validation, calibration, instrument qualification, and 5S programs.
Also performs analytical testing, method validation and development.
Compiles and reviews data for compliance.
Completes special projects.
Duties:
Trends and interprets statistical data Hires, trains, mentors and supervisors QC Chemists Conducts timely performance reviews for QC Chemists Coordinates reviews and approvals for QC Chemists Coordinates lab activities such as dishwashing, standard checking, reagent checking Approves analytical worksheets Releases products Ensures stability tests are conducted timely and accurately Ensures instruments are calibrated timely and accurately Completes testing projects from beginning to end Collaborates in cross-functional teams Follows all Aurora Pharmaceutical policies, procedures, regulations and the employee handbook.
Follows designated work schedule.
Assumes additional responsibilities as requested.
Accepts and acts upon supervisory directions.
Supports Manager's role.
Demonstrates flexibility, i.
e.
willingly takes on new tasks.
Performs routine sampling, analysis and documentation of pharmaceutical samples - raw materials, intermediates, drug products, package materials Generates experimental data according to written SOP, protocol, method, or work instructions Follows guidelines when recording data Uses analytical techniques such as titration, gravimetric analysis, etc.
Accurately maintains laboratory data and logs Uses analytical instrumentation such as GC, HPLC, IR and UV spectroscopy, UPLC etc.
Accurately interprets and reports results Performs method verification, method validation and method transfer Develops chromatographic methods Designs, implements and completes projects ( denotes essential job functions) Knowledge, Skills & Abilities:
Prefer candidates with interest and background in pharmaceutical testing, sampling and regulations Strong knowledge and minimum 5 years of experience with analytical chemistry and laboratory concepts and techniques Strong knowledge of computer applications Thorough knowledge of USP Education:
Bachelor's in Chemistry or Chemical Engineering Will consider:
Bachelor's in Biology, Environmental Sciences, or related degree plus a Minor in Chemistry.
Job Type:
Full-time
Benefits:
401(k) 401(k) matching Dental insurance Employee assistance program Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Vision insurance Schedule:
8 hour shift Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
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