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MasterControl Administrator at CordenPharma

CordenPharma · Boulder, United States Of America · Onsite

$35,000.00  -  $45,000.00

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CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people’s lives.

 

Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.

 

Our People Vision

We strive for excellence. We share our passion. Together, we make a difference in patients' lives.

 

SUMMARY

This role will be responsible for coordination of the Document Control System at Corden Pharma Colorado sites. 

 

ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.

 

  • Administers MasterControl from a Quality Management System perspective
  • Represents Quality regarding MasterControl in internal meetings
  • Handles the definition of MasterControl and ensures the electronic workflows/lifecycle are appropriate to approved SOPs
  • Maintains the MasterControl configuration for Quality Management System documents, to ensure documents are kept well organized and available for use by appropriate personnel/roles
  • Provides MasterControl support for user needs to ensure life cycle movement per needs of internal customers
  • Supports projects to implement continuous improvement in the MasterControl environment
  • Supports document requests during client audits and regulatory inspections
  • Provides reports, as directed by Quality management
  • Audits training, as needed to ensure conformance with site requirements

 

LEADERSHIP & BUDGET RESPONSIBILITIES

None.

 

SAFETY & ENVIRONMENTAL RESPONSIBILITIES

Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.

 

QUALITY RESPONSIBILITIES

Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC’s Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. 

 

cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado.

 

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

EDUCATION and/or EXPERIENCE

High school diploma or General Education Degree (GED). Associate Degree in business or science. Five years of experience in a cGMP Document Control environment with electronic document management systems; or equivalent combination of education and experience. 

 

Experience with electronic document management systems, such as MasterControl, is required.

 

LANGUAGE SKILLS

Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, regulatory agencies, and/or board of directors.

 

MATHEMATICAL SKILLS

Competence in mathematical skills including metric analysis, trending, and reporting.

 

REASONING ABILITY

Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form.

 

CERTIFICATES, LICENSES, REGISTRATIONS

None.

 

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to work with hands; reach above shoulder height; climb or balance; and stoop, kneel, or crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, and ability to adjust focus.

 

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

While performing the duties of this job, the employee is occasionally exposed to wet and/or humid conditions, moving mechanical parts, and outside weather conditions. The noise level in the work environment is usually moderate.

 

CORE COMPETENCIES

These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.

 

  • Strong interpersonal skills, high motivation, and energy to coordinate a number of functions across an organization
  • Organized, flexible, responsive, and proactive
  • Ability to work efficiently and accurately with details and numbers
  • Ability to become the subject matter expert and to master computerized systems such as MasterControl
  • Functional competency in Microsoft Word and Excel
  • Ability to create and deliver training materials for MasterControl end users
  • Ability to apply creativity and innovation to identify new approaches and solve existing problems
  • Ability to forecast work, identify potential conflicts, and develop and communicate potential solutions 
  • Ability to understand and execute company policies and practices, including regulatory compliance
  • High level of attention to detail and ability to identify errors or changes needed to take corrective actions

 

SALARY

Actual pay will be based on your skills and experience.

 

BENEFITS

  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service 
  • Accident Plan
  • Critical Illness Insurance
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Paid Parental Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation – Three Weeks 1st Year
  • Vision Insurance

EQUAL OPPORTUNITY EMPLOYER

Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.


This posting with expire on November 3, 2025


 



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