Top 179 Senior document specialist Jobs in Boulder, Co

QA Product Specialist
Corden Pharma Colorado —Boulder, CO
- $100,000 - $118,000 a year
- Full-time
- Ability to walk for extended periods
- 5 years
- Mid-level
- Wellness program
- Paid parental leave
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Compliance Specialist Senior – Quality Management System Auditor
BAE Systems Inc. —Broomfield, CO
- $82,779 - $140,723 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Master's degree
- Analysis skills
- Health savings account
- Paid holidays
Manager, Total Rewards
Congruex —Boulder, CO
- $135,000 - $165,000 a year
- HIPAA
- Office
- Finance
- Paid parental leave
- Paid holidays
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Senior Quality Assurance Specialist I
Cambrex —Longmont, CO
- Full-time
- Computer literacy
- Bachelor of Science
- Writing skills
Polysomnographic Technologist/Sleep-Senior Level - FT
Pediatric Sleep Specialists —Denver, CO
- $45 - $47 an hour
- Full-time
- Background check
- PALS Certification
- BLS Certification
- Health insurance
- Dental insurance
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Sr Quality Engineer – Medical Device
Grove Technical Resources —Louisville, CO
- $55 - $65 an hour
- Contract
- Bachelor of Science
- Engineering
- Analysis skills
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Polysomnographic Technologist/Sleep-Senior Level - PRN
Pediatric Sleep Specialists —Denver, CO
- $45 - $47 an hour
- Night shift
- Background check
- PALS Certification
- BLS Certification
- Opportunities for advancement
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Compliance Specialist Senior - Quality Management System Auditor
BAE Systems —Westminster, CO
- $82,779 - $140,723 a year
- Full-time
- Bachelor of Science
- Master's degree
- Analysis skills
- Health savings account
- Paid holidays
1d
Senior Consultant - Clinical Documentation Specialist
Deloitte —Denver, CO
- $110,700 - $218,300 a year
- Full-time
- Microsoft Word
- Nursing
- RN License
Program Support Specialist
Corner Alliance —Boulder, CO
- $65,000 - $80,000 a year
- Full-time
- Writing skills
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
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AML/KYC Senior Specialist
New Direction IRA Inc. —Louisville, CO
- $65,000 - $80,000 a year
- Full-time
- Hybrid work
- Research
- Finance
- Analysis skills
- Health savings account
- Paid holidays
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3d
Supply Chain Specialist
Izzio Artisan Bakery LLC —Louisville, CO
- $65,000 - $75,000 a year
- Full-time
- Microsoft Excel
- ERP systems
- Mid-level
- Paid holidays
- Health insurance
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9d
Materials Planner
GE Vernova —Longmont, CO
- $75,400 - $113,100 a year
- Full-time
- 6 years
- Oracle
- Pass drug screening
- Paid parental leave
- Paid holidays
11d
Sr. Supplier Quality Management Specialist
Corden Pharma Colorado —Boulder, CO
- $115,000 - $125,000 a year
- Full-time
- Word processing
- Bachelor of Science
- 11+ years
- Wellness program
- Paid parental leave
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Medical Records Specialist
Denver Midtown Surgery Center —Denver, CO
- $19.84 - $29.76 an hour
- Full-time
- Entry level
- Employee stock purchase plan
- Disability insurance
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Senior Verification Operations Specialist – AI & Automation
ABC Legal Services —Boulder, CO
- $26 - $28 an hour
- Full-time
- Mid-level
- 3 years
- Java
- AD&D insurance
- Paid holidays
Quick Apply
Senior EDI Specialist Contract to hire
ThrivePass —Denver, CO
- $38 - $43 an hour
- Full-time
- Hybrid work
- Analysis skills
- Senior level
- 2 years
- Paid holidays
- Health insurance
Computer Science Online Graduate Program Specialist
University of Colorado Boulder —Boulder, CO
- $58,000 - $62,000 a year
- Weekends as needed
- Hybrid work
- Microsoft Excel
- Computer Science
- Writing skills
- Health insurance
- Dental insurance
6d
Data Operations Specialist – Head Start (Data Quality, Records & Governance)
JBS International —Denver, CO
- Mid-level
- 3 years
- Ability to lift 50 pounds
Quick Apply
Implementation Specialist
Yes Energy —Boulder, CO
- $75,000 - $115,000 a year
- Full-time
- Remote
- Computer Science
- Mid-level
- 3 years
- Health insurance
- 401(k) matching

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QA Product Specialist

Corden Pharma Colorado -
Boulder, CO

Quick Apply

Job Details

Full-time
$100,000 - $118,000 a year

Benefits

Wellness program
Paid parental leave
Health savings account
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Tuition reimbursement
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Life insurance

Qualifications

Customer communication
Presentations for conferences or internal meetings
ANOVA
Math
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Pharmaceutical manufacturing facility experience

Full Job Description

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

Provides Quality Assurance related product leadership as it relates to planning and execution of products. Responsible for the collaboration, review, and approval of GMP documents. Represents a high-level of GMP understanding and accomplishment. Responsible for providing strong Quality leadership and scientific/GMP information support as the Quality representative supporting the lifecycle of products for internal and external customers.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.

Represent QA for all Quality related customer interactions for one or more products. Responsible for clear, direct, and appropriate communication in customer interactions
Provide process support including process validation, technical transfer, and commercial activities. May include clinical development as needed
Collaborate, review, and approve product-related Change Controls, Master Batch Records, Validation Protocols and Reports, Quality Risk Assessments, Annual Product Quality Reviews, and other cGMP documentation
Collaborate, review, and approve minor and major investigations and Corrective Actions Preventative Actions (CAPAs)
Create, report, and communicate product-related quality metrics to internal and external stakeholders
Assure that manufacturing processes, packaging, and testing comply with all regulatory filings and Corden SOPs to ensure favorable quality inspections and customer satisfaction
Provide Quality leadership and decision-making on cross-functional teams that include but are not limited to Operations, Process Engineering, Quality Control, and Safety
Perform final product batch disposition
Assist in and represent Quality during internal and external audits and regulatory inspections
Perform other duties as needed to support CordenPharma initiatives and improvements

LEADERSHIP & BUDGET RESPONSIBILITIES

Responsible for providing Quality leadership throughout the lifecycle of a product. Supports training for QA Associates and other quality personnel. Carries out leadership responsibilities in accordance with Corden policies and applicable laws.

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.

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

Bachelor’s Degree in Science and 5 years of Quality Assurance experience within the Pharmaceutical Industry; or a combination of Pharmaceutical Industry within a Technical/Operations role and academic experience. Project Management experience, although not required, is beneficial to this position.

LANGUAGE SKILLS

Ability to read, analyze, and interpret common scientific and analytical journals. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to communicate information to customers and senior management. Ability to effectively present information to top management and public groups.

MATHEMATICAL SKILLS

Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.

REASONING ABILITY

Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems.

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; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific visual abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, 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 frequently exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The employee is occasionally exposed to moving mechanical parts, outside weather conditions, and risk of electrical shock. 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.

Excellent customer service skills
Knowledge of cGMP, cGLP, and FDA regulations, as well as internal quality related procedures
Practical and theoretical knowledge of the basic principle of validation and their applications
Analytical ability and ability to influence
Excellent verbal, presentation, and written communication skills
Ability to provide leadership in all aspects of QA/development processes
Analytical skills with the ability to function in an interactive interdisciplinary team environment
Proactive approach to problem solving and resolution

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 post will expire August 07, 2026

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