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
-
Supervisor, Production
Supervisor, Production
-
Production Supervisor
Production Supervisor
-
Production Supervisor
Production Supervisor
-
Production Supervisor - 2nd Shift
Production Supervisor - 2nd Shift
-
Production Supervisor
Production Supervisor
-
IPQA Specialist
IPQA Specialist
-
Housekeeper Teammate
Housekeeper Teammate
-
Night Shift Field/Diesel Technician/Mechanic
Night Shift Field/Diesel Technician/Mechanic
-
Mine Site Heavy/Diesel Technician
Mine Site Heavy/Diesel Technician
Similar Searches
Explore collaborative articles
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
Explore More