What are the responsibilities and job description for the Document Control Specialist position at IFF?
Job Summary
Collect, maintain, and distribute all quality documents necessary to define receiving, manufacturing, and distribution processes, along with documents covering quality and safety systems within the organization that ensure conformance to customer and regulatory requirements. Develop and maintain a comprehensive filing system and revision control for documents throughout the organization, including quality control, manufacturing, account management, human resources, and safety. Maintain revision control and document issuance to ensure that all users have the current revision of appropriate documentation in a timely manner. Other responsibilities may include helping to generate documents such as policies, procedures, forms, logs, and more within a team environment. Serve as a technical resource for the maintenance and control of hard-copy and electronic documents within the organization
SHIFT
Monday - Friday
Qualifications
A. A.S. degree in English or Communications preferred
B. Minimum 2 years’ experience in a FDA/cGMP manufacturing environment preferred
C. Proficient with Microsoft applications such as MS Office and SharePoint
D. Experience with online documentation management and computer-based learning
E. Exceptional attention to detail with excellent writing and communication skills in English
F. Excellent communication and interpersonal skills with proven ability to take initiative and build strong productive relationships
G. Self-directed with the ability to work independently and prioritize responsibilities
H. Strong organizational and multi-tasking abilities
I. Must be able to work in a fast-paced, dynamic, team environment, while staying focused and carrying out tasks in a timely and accurate manner
Requirements
It is essential for all employees to adhere to Company policies.
Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more
Salary Ranges:
$58400- $73000
Collect, maintain, and distribute all quality documents necessary to define receiving, manufacturing, and distribution processes, along with documents covering quality and safety systems within the organization that ensure conformance to customer and regulatory requirements. Develop and maintain a comprehensive filing system and revision control for documents throughout the organization, including quality control, manufacturing, account management, human resources, and safety. Maintain revision control and document issuance to ensure that all users have the current revision of appropriate documentation in a timely manner. Other responsibilities may include helping to generate documents such as policies, procedures, forms, logs, and more within a team environment. Serve as a technical resource for the maintenance and control of hard-copy and electronic documents within the organization
SHIFT
Monday - Friday
Qualifications
A. A.S. degree in English or Communications preferred
B. Minimum 2 years’ experience in a FDA/cGMP manufacturing environment preferred
C. Proficient with Microsoft applications such as MS Office and SharePoint
D. Experience with online documentation management and computer-based learning
E. Exceptional attention to detail with excellent writing and communication skills in English
F. Excellent communication and interpersonal skills with proven ability to take initiative and build strong productive relationships
G. Self-directed with the ability to work independently and prioritize responsibilities
H. Strong organizational and multi-tasking abilities
I. Must be able to work in a fast-paced, dynamic, team environment, while staying focused and carrying out tasks in a timely and accurate manner
Requirements
- A legal right to work in the United States
- Must pass pre-employment drug screen and background check
- For those applying out of the area We love working for such an awesome company within the beautiful Pacific NW and understand your motivation is to do the same! Please recognize that relocation packages are not being offered at this time.
It is essential for all employees to adhere to Company policies.
- Maintain and continuously improve existing document control system to accurately track controlled documents through the organization
- Assign document identification numbers and maintain a list of all current, obsolete, pending, and archived documents
- Ensure only current approved document revisions are available at point of use and on the SharePoint site
- Route documents for review and approval through Sign-Easy document system
- Maintain records, as needed for the organization
- Ensure organization is audit-ready with respect to published controlled documents, specific equipment, test method, and other records, as needed
- Notify training department of newly released documents
- Track and measure organizational adherence to document review cycle
- Ability to be at the physical location of the job for the designated work schedule
- Will be asked to train someone and/or participate in a task force to improve company procedures or operations.
- Ability to effectively problem-solve
- Ability to work collaboratively and maintain effective working relationships with co-workers.
- Must be able to successfully pass all job-related tests and certifications required for working in a cGMP, quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job. Must re-qualify every year on all job-related tests and certifications as job or qualifications require.
- Performs other duties as assigned
Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more
Salary Ranges:
$58400- $73000
Salary : $58,400 - $73,000
