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Quality Assurance Associate Job
Eingestellt von Yoh
Gesuchte Skills: Marketing, Client
Projektbeschreibung
QUALITY ASSURANCE ASSOCIATE needed for a CONTRACT opportunity with Yoh's client located in Cedar Knolls, NJ.
What You'll Be Doing:
- Maintains documentation filing systems for security, confidentiality and ease of use. Files, tracks and/or retrieves archived information on a routine basis.
- Maintains the archive system for off-site storage so that documents, records and files can be easily retrieved for audit and review purposes.
- Conducts QA review of various types of files, records and batch records for completeness and accuracy according to SOP. Notes and sets activities for all required follow-up. Follows-up to verify completion of activities.
- Updates logs, databases and catalogs including, but not limited to, SOP Manuals, Training Records and SOP History Files.
- Completes and provides data for Continuous Quality Improvement for all records reviewed per SOP.
- Provides assistance to other QA staff members as needed.
What You Need to Bring to the Table:
- Bachelor's degree in a Life Science
- Minimum of two (2) years of work experience in a GxP regulated field.
- Basic understanding of medical terminology and information
- Detail oriented with high degree of focus Able to interpret and follow set policies and procedures.
- Able to perform with minimal supervision and contribute in a team environment.
- Able to communicate results and issues effectively, both written and orally.
- Basic knowledge in MS Word and Excel with applications in data entry and management
Bonus Points! Otherwise Known As Preferred Qualifications:
- Pharmaceutical/Biotech Industry Experience
What's In It for You?
- This is your chance to shine while supporting our client's dynamic Product Marketing, drug development and Research teams.
GET HIRED, APPLY NOW!
RECRUITER: Sidra Chaudhry
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: CLINICAL
MONJOBJ2WNECLIN
Ref:
SFSF: LS
What You'll Be Doing:
- Maintains documentation filing systems for security, confidentiality and ease of use. Files, tracks and/or retrieves archived information on a routine basis.
- Maintains the archive system for off-site storage so that documents, records and files can be easily retrieved for audit and review purposes.
- Conducts QA review of various types of files, records and batch records for completeness and accuracy according to SOP. Notes and sets activities for all required follow-up. Follows-up to verify completion of activities.
- Updates logs, databases and catalogs including, but not limited to, SOP Manuals, Training Records and SOP History Files.
- Completes and provides data for Continuous Quality Improvement for all records reviewed per SOP.
- Provides assistance to other QA staff members as needed.
What You Need to Bring to the Table:
- Bachelor's degree in a Life Science
- Minimum of two (2) years of work experience in a GxP regulated field.
- Basic understanding of medical terminology and information
- Detail oriented with high degree of focus Able to interpret and follow set policies and procedures.
- Able to perform with minimal supervision and contribute in a team environment.
- Able to communicate results and issues effectively, both written and orally.
- Basic knowledge in MS Word and Excel with applications in data entry and management
Bonus Points! Otherwise Known As Preferred Qualifications:
- Pharmaceutical/Biotech Industry Experience
What's In It for You?
- This is your chance to shine while supporting our client's dynamic Product Marketing, drug development and Research teams.
GET HIRED, APPLY NOW!
RECRUITER: Sidra Chaudhry
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.
J2W: CLINICAL
MONJOBJ2WNECLIN
Ref:
SFSF: LS
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Marketing/Vertrieb