Quality Assurance Document Supervisor- Manufacturing Industry
Quality Assurance Document Supervisor- Manufacturing Industry
Zivahh LLC
Lancaster, SC
See who Zivahh LLC has hired for this role
Job Id OOJ - 19838
Job Title Quality Assurance Document Supervisor
Industry(ies) Biotechnology/ Life Sciences,Pharmaceutical
Primary Skills Quality Assurance Professionals
Location -Lancaster, SC
Work Experience (Years) 3-15
Degree University - Bachelor's Degree/3-4 Year Degree
Pay Rate 65000-85000
Job Description
Bachelors or Associates degree with 5 years' experience in a cGMP environment
Must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control.
Job Title Quality Assurance Document Supervisor
Industry(ies) Biotechnology/ Life Sciences,Pharmaceutical
Primary Skills Quality Assurance Professionals
Location -Lancaster, SC
Work Experience (Years) 3-15
Degree University - Bachelor's Degree/3-4 Year Degree
Pay Rate 65000-85000
Job Description
- Initiating investigations, assessing NCRs to determine if they have the necessary information to be closed out.
- Oversee the Finished Product Update spreadsheets, including downloading the recently packaged batches from SAP and ensuring the laboratory sample receipt dates are accurate.
- Track individual reviewer metrics to determine if additional training or guidance is needed.
- Ensure cross training is performed and documented for individuals within the QA Document Specialist group.
- Establish and oversee an organized system for both buildings to meet turn-around time goals.
- Establish and oversee an organized system to track the change control process.
- Hold monthly team meetings to ensure both buildings are communicating and working together as a team.
- Perform other assigned duties as may be required in meeting company objectives
- Regular attendance is required.
- Communicate effectively with other departments within the organization and function within a team environment.
Bachelors or Associates degree with 5 years' experience in a cGMP environment
Must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control.
-
Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Staffing and Recruiting
Referrals increase your chances of interviewing at Zivahh LLC by 2x
See who you knowGet notified about new Quality Assurance Supervisor jobs in Lancaster, SC.
Sign in to create job alertSimilar jobs
People also viewed
-
QA Supervisor (3rd Shift) - Signing bonus
QA Supervisor (3rd Shift) - Signing bonus
-
Quality Assurance Manager I
Quality Assurance Manager I
-
Quality Control Manager
Quality Control Manager
-
Quality Assurance Manager I
Quality Assurance Manager I
-
Quality Assurance Supervisor - 3rd shift
Quality Assurance Supervisor - 3rd shift
-
Quality Control Supervisor
Quality Control Supervisor
-
Quality Supervisor
Quality Supervisor
-
Quality Manager
Quality Manager
-
Quality Assurance Manager
Quality Assurance Manager
-
Quality Manager
Quality Manager
Looking for a job?
Visit the Career Advice Hub to see tips on interviewing and resume writing.
View Career Advice Hub