Charles City, IA
QC Chemist I
Overview
Reporting to the Quality Control Supervisor, the Quality Control Chemist I will be responsible for daily laboratory testing of raw materials, in process and finished goods.
Responsibilities
- Perform a wide variety of chemical analyses for release of raw materials, intermediates and finished - Recommend, develop and maintain laboratory programs,including stability, calibration, preventive maintenance,reduced testing, check sample, IQ/OQ,etc., to comply with cGMP regulationsand audits. - Write controlled documents such as stability reports, test procedures,SOPs, SAPs,et - Evaluate performance of instrumentation and validity of test results - Perform instrument maintenance and troubleshoot equipment as - Perform and document method transfer from Analytical Development - Perform method development including instrument parameters,new instruments and method improvement - Handle,analyze and dispose of hazardous samples and - Perform statistical evaluation of date including SPC,expiration dating of stability data,system suitability, instrument and method linearity - Adhere to all EPA, FDA,cGMP, cGLP DEA regulations and internal SOP'sas they relate to the operation of the Quality Control lab and general operation of the chemical production - Follow all OSHA and company safety rules and practices. - Review and enter data for Inventory Control - Provide on-call coverage for non-scheduled work - Maintain laboratory solutions, inventory and notebooks. - Responsible for coverage of all job duties for QC Analyst. All employees are required to adhere to EPA, DEA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
Qualifications
- BS in Chemistry - Experience in a laboratory environment preferred - Knowledge of analytical instrumentation - Strong chemistry theory - Proven ability to handle various project load is beneficial Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the ‘Arthur I. Mendolia Scholarship Program.’ Relocation assistance will be offered for this position. #CB #LI-MI1
Reporting to the Quality Control Supervisor, the Quality Control Chemist I will be responsible for daily laboratory testing of raw materials, in process and finished goods.
Responsibilities
- Perform a wide variety of chemical analyses for release of raw materials, intermediates and finished - Recommend, develop and maintain laboratory programs,including stability, calibration, preventive maintenance,reduced testing, check sample, IQ/OQ,etc., to comply with cGMP regulationsand audits. - Write controlled documents such as stability reports, test procedures,SOPs, SAPs,et - Evaluate performance of instrumentation and validity of test results - Perform instrument maintenance and troubleshoot equipment as - Perform and document method transfer from Analytical Development - Perform method development including instrument parameters,new instruments and method improvement - Handle,analyze and dispose of hazardous samples and - Perform statistical evaluation of date including SPC,expiration dating of stability data,system suitability, instrument and method linearity - Adhere to all EPA, FDA,cGMP, cGLP DEA regulations and internal SOP'sas they relate to the operation of the Quality Control lab and general operation of the chemical production - Follow all OSHA and company safety rules and practices. - Review and enter data for Inventory Control - Provide on-call coverage for non-scheduled work - Maintain laboratory solutions, inventory and notebooks. - Responsible for coverage of all job duties for QC Analyst. All employees are required to adhere to EPA, DEA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
Qualifications
- BS in Chemistry - Experience in a laboratory environment preferred - Knowledge of analytical instrumentation - Strong chemistry theory - Proven ability to handle various project load is beneficial Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the ‘Arthur I. Mendolia Scholarship Program.’ Relocation assistance will be offered for this position. #CB #LI-MI1
Recommended Skills
- Analytical Chemistry
- Auditing
- Calibration
- Chemistry
- Finished Good
- Instrumentation
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