Quality Assurance Data Reviewer - Lincolnshire, IL
Company Name:
SGS AUTOMOTIVE
#### Primary Responsibilities
The Quality Assurance Data Reviewer is responsible for the second person review of selected data generated in the laboratory. The QA Data Reviewer must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory. The QA Data Reviewer also works closely with Analytical and Microbiology Management. This job also requires the ability to demonstrate a high commitment to interpersonal relations.
#### Reporting to
SGS Life Science Services QA Manager
SGS is the world's leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 80,000 employees, SGS operates a network of over 1,650 offices and laboratories around the world.
#### Specific responsibilities
SERVICE RESPONSIBILITIES TO CLIENTS:
Perform data review following staff performance of client test requests in a timely and effective manner.
Ensure that all client requests for information pertaining to testing (or any other services) are met in a timely and effective manner.
Ensure that routine testing submitted by clients is completed within established parameters governing Company quality and regulatory compliance specifications.
Ensure that data recorded attendant to client requests pertaining to the development and completion of specialized studies is reviewed in a timely and effective manner.
Ensure initiation of client contact for issues concerning USP Purified Water testing.
SERVICE RESPONSIBILITIES TO INTERNAL CUSTOMERS:
Ensure that all reasonable requests from Quality Assurance or Management pertaining to review of laboratory data supporting a given test or group of tests are met in a timely and effective manner.
Provide Departmental staff with appropriate notification of any special requests regarding log-in, reporting, and billing activities.
Play a role in Departmental or company-wide projects designed to improve the internal efficiency and overall quality of work performed at the laboratory.
Play a role in creating and maintaining an atmosphere of teamwork throughout the laboratory.
Provide support in the development of Guidelines, Technical Advisories, and Corrective/ Preventive Action plans.
TECHNICAL
Responsibilities:
Maintain thorough knowledge and understanding of all general SOPs pertaining to the laboratory.
Maintain thorough knowledge and understanding of GMP/GLP/ISO requirements as these pertain to work performed in the laboratory.
May be invited to participate in the preparation and review process for appropriate department SOPs, worksheets and data forms.
ADMINISTRATIVE
Responsibilities:
Adherence to relevant SOPs governing documentation and reporting.
Compliance with applicable SOPs related to the handling of client complaints.
Adherence to applicable personnel policies regarding time clock, telephones, sick days, vacation days, etc.
Participation in general staff training sessions as these are scheduled.
Approve and issue Certificate of Analysis
#### Profile
Bachelor''s of Science in Chemistry, Biology, Microbiology or equivalent experience required
Thorough knowledge of scientific principles required
Experience with GMP preferred
#### Skills
Familiarity with all of the laboratory techniques and equipment applicable to the tasks performed in the laboratory.
Highest commitment to Good Manufacturing Practices (GMP''s) with regard to the recording of laboratory data for testing of pharmaceuticals and medical devices.
Excellent language and communication skills required.
Must be able to clearly communicate responsibilities of solid documentation needs on a daily basis.
Good listening skills are essential, must be detail oriented.
Must be able to work with a diverse group of individuals performing bench testing.
Must have a solid grasp of the fundamentals and importance of teamwork in the contemporary business world.
#### Additional information
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skill, and/or ability required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
SGS is an EOE AA M/F/Vet/Disability employer.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, protected veteran status or disability.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call for assistance and leave a message. You will be called back shortly. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Industry or Theme: Chemical,Life Sciences
Functional Area: Laboratories
Contract Type:
Reference Number: US04488
Listing Date: 13.05.2014 00
Closing Date: 31.08.2014 00Estimated Salary: $20 to $28 per hour based on qualifications.
SGS AUTOMOTIVE
#### Primary Responsibilities
The Quality Assurance Data Reviewer is responsible for the second person review of selected data generated in the laboratory. The QA Data Reviewer must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory. The QA Data Reviewer also works closely with Analytical and Microbiology Management. This job also requires the ability to demonstrate a high commitment to interpersonal relations.
#### Reporting to
SGS Life Science Services QA Manager
SGS is the world's leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 80,000 employees, SGS operates a network of over 1,650 offices and laboratories around the world.
#### Specific responsibilities
SERVICE RESPONSIBILITIES TO CLIENTS:
Perform data review following staff performance of client test requests in a timely and effective manner.
Ensure that all client requests for information pertaining to testing (or any other services) are met in a timely and effective manner.
Ensure that routine testing submitted by clients is completed within established parameters governing Company quality and regulatory compliance specifications.
Ensure that data recorded attendant to client requests pertaining to the development and completion of specialized studies is reviewed in a timely and effective manner.
Ensure initiation of client contact for issues concerning USP Purified Water testing.
SERVICE RESPONSIBILITIES TO INTERNAL CUSTOMERS:
Ensure that all reasonable requests from Quality Assurance or Management pertaining to review of laboratory data supporting a given test or group of tests are met in a timely and effective manner.
Provide Departmental staff with appropriate notification of any special requests regarding log-in, reporting, and billing activities.
Play a role in Departmental or company-wide projects designed to improve the internal efficiency and overall quality of work performed at the laboratory.
Play a role in creating and maintaining an atmosphere of teamwork throughout the laboratory.
Provide support in the development of Guidelines, Technical Advisories, and Corrective/ Preventive Action plans.
TECHNICAL
Responsibilities:
Maintain thorough knowledge and understanding of all general SOPs pertaining to the laboratory.
Maintain thorough knowledge and understanding of GMP/GLP/ISO requirements as these pertain to work performed in the laboratory.
May be invited to participate in the preparation and review process for appropriate department SOPs, worksheets and data forms.
ADMINISTRATIVE
Responsibilities:
Adherence to relevant SOPs governing documentation and reporting.
Compliance with applicable SOPs related to the handling of client complaints.
Adherence to applicable personnel policies regarding time clock, telephones, sick days, vacation days, etc.
Participation in general staff training sessions as these are scheduled.
Approve and issue Certificate of Analysis
#### Profile
Bachelor''s of Science in Chemistry, Biology, Microbiology or equivalent experience required
Thorough knowledge of scientific principles required
Experience with GMP preferred
#### Skills
Familiarity with all of the laboratory techniques and equipment applicable to the tasks performed in the laboratory.
Highest commitment to Good Manufacturing Practices (GMP''s) with regard to the recording of laboratory data for testing of pharmaceuticals and medical devices.
Excellent language and communication skills required.
Must be able to clearly communicate responsibilities of solid documentation needs on a daily basis.
Good listening skills are essential, must be detail oriented.
Must be able to work with a diverse group of individuals performing bench testing.
Must have a solid grasp of the fundamentals and importance of teamwork in the contemporary business world.
#### Additional information
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skill, and/or ability required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
SGS is an EOE AA M/F/Vet/Disability employer.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, protected veteran status or disability.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call for assistance and leave a message. You will be called back shortly. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Industry or Theme: Chemical,Life Sciences
Functional Area: Laboratories
Contract Type:
Reference Number: US04488
Listing Date: 13.05.2014 00
Closing Date: 31.08.2014 00Estimated Salary: $20 to $28 per hour based on qualifications.
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