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QC Document Reviewer
$1,000 SIGN-ON BONUS
Verona, WI
Job Description
POSITION OVERVIEW:
The primary purpose of the QC Document Reviewer is to perform review of all raw analytical data in laboratory notebooks, forms, worksheets, and logbooks. This review is to ensure that the various compounds and components were tested correctly according to compendial monographs, internal analytical methods, internal specifications, client procedures, and miscellaneous research procedures as required in internal SOPs.
In addition, the QC Document Reviewer may also assist in review of protocols, summary reports, SOPs, internal analytical methods and internal specifications to ensure the document is accurate and complete. The QC Document Reviewer may also be tasked with performing laboratory testing with short notice if required based on department workload/client needs.
Coating Place, Inc. pays a $1,000 Sign-On Bonus for new employees after completing one year of employment.
ESSENTIAL JOB FUNCTIONS:
EDUCATION/SKILLS/KNOWLEDGE REQUIRED:
The primary purpose of the QC Document Reviewer is to perform review of all raw analytical data in laboratory notebooks, forms, worksheets, and logbooks. This review is to ensure that the various compounds and components were tested correctly according to compendial monographs, internal analytical methods, internal specifications, client procedures, and miscellaneous research procedures as required in internal SOPs.
In addition, the QC Document Reviewer may also assist in review of protocols, summary reports, SOPs, internal analytical methods and internal specifications to ensure the document is accurate and complete. The QC Document Reviewer may also be tasked with performing laboratory testing with short notice if required based on department workload/client needs.
Coating Place, Inc. pays a $1,000 Sign-On Bonus for new employees after completing one year of employment.
ESSENTIAL JOB FUNCTIONS:
- Reviews laboratory notebooks, forms, worksheets and logbooks.
- Performs review of any internal methods, specifications and protocols to ensure compliance or accuracy.
- Assists with drafting protocols, summary reports and new or existing internal procedures or specifications.
- Performs laboratory testing following internal, compendia or client supplied methods.
- Maintains a cGMP laboratory notebook and forms.
- Follows all CPI cGMP practices, policies, and procedures.
- Follows all CPI safety practices, policies, and procedures.
- Other duties as assigned.
EDUCATION/SKILLS/KNOWLEDGE REQUIRED:
- Bachelor's degree in chemistry or related field required.
- 3+ years of experience at Coating Place, Inc. or in a cGMP pharmaceutical environment. An advanced degree may be substituted in place of experience.
- Must be detail oriented and possess strong written, organizational, and communication skills.
- Advanced time management skills to complete review of multiple documents daily with minimal supervision.
- Ability to establish and maintain effective working relationships with team members, co-workers and/or clients.
- Ability to lift object weighing up to 15 lbs. on a daily basis and up to 55 lbs. occasionally.
Job Summary
Start Date
As Soon As Possible
Employment Term and Type
Regular, Full Time
Hours per Week
40+
Work Hours (i.e. shift)
1st Shift
Salary and Benefits
Based On Experience
Required Education
Bachelor's Degree
Required Experience
Open
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