Astrix Technology
Document Control Specialist
Astrix Technology, Indianapolis, Indiana, us, 46262
Document Control Specialist
Quality Assurance
Indianapolis, IN, US
Added - 25/10/2024
Apply for Job
Our client is seeking a Document Control Specialist at a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals.
Why Us?
Competitive wages and comprehensive health benefits
Positive and safe work environments
Opportunities for growth and development for all the stages of your career
Schedule
M-F
1 st shift
Pay
$55k-65k/yr
Key Tasks:
Manage the document control process, including the creation, review, approval, distribution, and archiving documents.
Ensure that all documents comply with company policies and regulatory requirements.
Maintain and update the document management system to ensure easy retrieval and reference.
Collaborate with various departments to gather and prepare documentation for projects, audits, and inspections.
Conduct regular audits of document control processes to identify areas for improvement.
Provide training and support to staff on document control procedures and tools.
Assist in the development and maintenance of document control procedures and best practices.
Generate reports on document status and compliance for management review.
Facilitate the flow of information between teams and stakeholders regarding document updates and revisions.
Experience/Education:
High School Diploma required
Minimum of 4 years of experience with QA in a GMP environment with Document Control
Pharmaceutical experience preferred
INDBH
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Quality Assurance
Indianapolis, IN, US
Added - 25/10/2024
Apply for Job
Our client is seeking a Document Control Specialist at a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals.
Why Us?
Competitive wages and comprehensive health benefits
Positive and safe work environments
Opportunities for growth and development for all the stages of your career
Schedule
M-F
1 st shift
Pay
$55k-65k/yr
Key Tasks:
Manage the document control process, including the creation, review, approval, distribution, and archiving documents.
Ensure that all documents comply with company policies and regulatory requirements.
Maintain and update the document management system to ensure easy retrieval and reference.
Collaborate with various departments to gather and prepare documentation for projects, audits, and inspections.
Conduct regular audits of document control processes to identify areas for improvement.
Provide training and support to staff on document control procedures and tools.
Assist in the development and maintenance of document control procedures and best practices.
Generate reports on document status and compliance for management review.
Facilitate the flow of information between teams and stakeholders regarding document updates and revisions.
Experience/Education:
High School Diploma required
Minimum of 4 years of experience with QA in a GMP environment with Document Control
Pharmaceutical experience preferred
INDBH
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.