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File Coordinator Jobs in Iowa (NOW HIRING)

Label coordination/management-design, etc. * Order labels for Production, check in labels ... Filing of SOPs, Product specs, RM specs and other miscellaneous filing as needed * Log book updates ...

The Project Coordinator will maintain open communication between all personnel to ensure all ... File and distribute construction drawings * Assist in preparation of owner pay applications ...

Human Resources Coordinator Driven by integrity and united by the people-and-pet bond, we find ... Responsibilities include maintaining payroll processing, employee files, administering employee ...

New

Project Coordinator

Council Bluffs, IA · On-site

$46K - $50K/yr

If you enjoy solving problems, coordinating teams, tracking details and helping projects succeed ... Maintain organized project files and documentation in accordance with company standards. Prepare ...

The Operations Support Department is looking to add an Operations Coordinator to support numerous ... Other responsibilities include handling multiple phone lines, maintaining concise files, reviewing ...

Showing results 41-60

File Coordinator information

What is a file coordinator?

File Coordinators are administrative professionals responsible for organizing, managing, and maintaining files and records within an organization. They ensure that documents are accurately filed, easily accessible, and securely stored, whether in physical or digital formats. File Coordinators often handle data entry, retrieval requests, and may implement or improve filing systems to enhance efficiency. Their role is critical in ensuring compliance with organizational policies and legal requirements for document retention and confidentiality.

What are the key skills and qualifications needed to thrive as a file coordinator, and why are they important?

To thrive as a File Coordinator, you need strong organizational skills, attention to detail, and a high school diploma or equivalent. Familiarity with electronic filing systems, document management software, and office productivity tools like Microsoft Office is typically required. Excellent communication, time management, and problem-solving abilities help you excel in managing and retrieving records efficiently. These skills ensure files are accurately maintained, easily accessible, and securely handled, which is critical for operational efficiency and regulatory compliance.

What are some common challenges faced by file coordinators, and how can they be effectively managed?

File Coordinators often face challenges such as managing large volumes of documents, maintaining data accuracy, and ensuring timely retrieval and distribution of files. These challenges can be effectively managed by utilizing robust file management systems, establishing clear organizational protocols, and maintaining strong attention to detail. Consistent communication with team members and regular audits of filing systems also help prevent misplacement and ensure compliance with company policies.
What are the most commonly searched types of File jobs in Iowa? The most popular types of File jobs in Iowa are:
What are popular job titles related to File Coordinator jobs in Iowa? For File Coordinator jobs in Iowa, the most frequently searched job titles are:
What job categories do people searching File Coordinator jobs in Iowa look for? The top searched job categories for File Coordinator jobs in Iowa are:
What cities in Iowa are hiring for File Coordinator jobs? Cities in Iowa with the most File Coordinator job openings:

QA Data Coordinator

Cambrex

Charles City, IA

Full-time

Medical, Life, Retirement

Posted 24 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!


Job Overview

This position provides critical administrative and documentation support for pharmaceutical manufacturing operations by managing batch records, labels, training documentation, and controlled records in compliance with cGMP, FDA, DEA, and EPA requirements. The role ensures production documentation is accurate, organized, and available to support daily manufacturing activities while maintaining filing systems, logbooks, and compliance records. Working closely with Production and other departments, this individual coordinates documentation, tracks training and supplements, and provides backup support for operational administrative functions. Success in this role requires strong organizational skills, attention to detail, computer proficiency, and the ability to thrive in a regulated manufacturing environment.


Responsibilities
  • Issue requested batch records for next day’s production and attach necessary stamped labels 
  • Label coordination/management-design, etc. 
  • Order labels for Production, check in labels, maintenance of label storage according to cGMP regulations. 
  • Issue and track training records for all records, including batch records, SOPs and other miscellaneous required training 
  • Maintain MSDS Sheets 
  • WFI auditing and document maintenance 
  • Filing of SOPs, Product specs, RM specs and other miscellaneous filing as needed 
  • Log book updates and auditing 
  • Maintain work center logs and equipment logs in an orderly manner 
  • Track supplements and ensure proper closure and follow up 
  • Back  up Admin Assistant as needed on batch record entry and other miscellaneous operations assignments 
  • File completed batch records and other filing as necessary.  Maintain tight control of batch record files  

Qualifications/Skills
  • Strong computer skills 
  • Manufacturing office background preferred 

Education, Experience & Licensing Requirements
  • 3 or more years of office experience  
  • Associates Degree in Adminstration/ Business or related degree prefered

Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration. 

All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law.

 

Qualifications:
  • 3 or more years of office experience  
  • Associates Degree in Adminstration/ Business or related degree prefered
Education:UNAVAILABLEEmployment Type: FULL_TIME

What Cambrex employees say

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Benefits

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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