Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree * 2 + years in the biotechnology, device, or pharmaceutical industry * Qualified ...
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree * 2 + years in the biotechnology, device, or pharmaceutical industry * Qualified ...
Associate Director, Global Labeling
$170K - $231K/yr
... to labeling of pharmaceutical products. Keep up to date on emerging clinical and other data ... Must be detail-oriented and able to multi-task and manage multiple projects. Skilled in written and ...
Associate Director, Global Labeling
$170K - $231K/yr
... to labeling of pharmaceutical products. Keep up to date on emerging clinical and other data ... Must be detail-oriented and able to multi-task and manage multiple projects. Skilled in written and ...
Associate Director, Global Labeling Strategy Lead
Billerica, MA · On-site
$134K - $202K/yr
Manage the creation and maintenance, review and approval of US and EU PIs ensuring consistency with ... Bachelor's degree in science or health-related discipline * 5+ years of relevant pharmaceutical ...
Associate Director, Global Labeling Strategy Lead
Billerica, MA · On-site
$134K - $202K/yr
Manage the creation and maintenance, review and approval of US and EU PIs ensuring consistency with ... Bachelor's degree in science or health-related discipline * 5+ years of relevant pharmaceutical ...
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree * 3-5 years in the biotechnology or pharmaceutical industry * Qualified ...
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree * 3-5 years in the biotechnology or pharmaceutical industry * Qualified ...
Associate Director, Global Labeling Strategy Lead
Billerica, MA · On-site
$134K - $202K/yr
Manage the creation and maintenance, review and approval of US and EU PIs ensuring consistency with ... Bachelor's degree in science or health-related discipline * 5+ years of relevant pharmaceutical ...
Associate Director, Global Labeling Strategy Lead
Billerica, MA · On-site
$134K - $202K/yr
Manage the creation and maintenance, review and approval of US and EU PIs ensuring consistency with ... Bachelor's degree in science or health-related discipline * 5+ years of relevant pharmaceutical ...
This position is to support the Global Labeling Centre of Excellence (GL COE) Global Labeling ... environment (pharmaceutical, etc.) required. Prior change control management experience (i.e ...
This position is to support the Global Labeling Centre of Excellence (GL COE) Global Labeling ... environment (pharmaceutical, etc.) required. Prior change control management experience (i.e ...
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree 3-5 years in the biotechnology or pharmaceutical industry * Qualified applicants ...
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy ... Bachelor's degree 3-5 years in the biotechnology or pharmaceutical industry * Qualified applicants ...
Job Responsibilities: * Assist Director of Project Management with client project requirements * Liaison between client and internal production team managing daily client communications * Maintain ...
Job Responsibilities: * Assist Director of Project Management with client project requirements * Liaison between client and internal production team managing daily client communications * Maintain ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Pharmaceutical/Biotech industry a plus Exposure or familiarity with evaluating clinical trials ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Pharmaceutical/Biotech industry a plus Exposure or familiarity with evaluating clinical trials ...
$26.36 - $36.38/hr
Quality Documentation and Labeling Associate Full Time Clerical Plymouth, MN, US 2 days ago ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
$26.36 - $36.38/hr
Quality Documentation and Labeling Associate Full Time Clerical Plymouth, MN, US 2 days ago ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
Quality Documentation and Labeling Associate
Plymouth, MN · On-site
$26.36 - $36.38/hr
Quality Documentation and Labeling Associate Full Time Clerical Plymouth, MN, US 2 days ago ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
Quality Documentation and Labeling Associate
Plymouth, MN · On-site
$26.36 - $36.38/hr
Quality Documentation and Labeling Associate Full Time Clerical Plymouth, MN, US 2 days ago ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
The Importance of the Role The Associate Director, Regulatory Labeling and Disclosures, will be ... Manage process for individual participant data (IPD) report generation at the end of clinical ...
The Importance of the Role The Associate Director, Regulatory Labeling and Disclosures, will be ... Manage process for individual participant data (IPD) report generation at the end of clinical ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and ... Apply labeling software and technical tools to manage translation workflows and documentation ...
Position Description The Associate Labeling Specialist supports regulatory labeling strategy and ... Apply labeling software and technical tools to manage translation workflows and documentation ...
The Importance of the Role The Associate Director, Regulatory Labeling and Disclosures, will be ... Manage process for individual participant data (IPD) report generation at the end of clinical ...
The Importance of the Role The Associate Director, Regulatory Labeling and Disclosures, will be ... Manage process for individual participant data (IPD) report generation at the end of clinical ...
Quality Documentation and Labeling Associate
Plymouth, MN · On-site
$26.36 - $36.38/hr
The Quality Documentation and Labeling Associate supports ProMed's mission and values by applying ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
Quality Documentation and Labeling Associate
Plymouth, MN · On-site
$26.36 - $36.38/hr
The Quality Documentation and Labeling Associate supports ProMed's mission and values by applying ... Maintain the document management system to ensure accuracy, accessibility, and version integrity of ...
Labeling and Packaging Associate
Chattanooga, TN · On-site
$26.09/hr
Join the team supported by Adecco in Swiftwater, PA, as a Labeling and Packaging Associate--an ... Record basic production data to monitor performance and output. * Assist with inventory management ...
Quick apply
Labeling and Packaging Associate
Chattanooga, TN · On-site
$26.09/hr
Join the team supported by Adecco in Swiftwater, PA, as a Labeling and Packaging Associate--an ... Record basic production data to monitor performance and output. * Assist with inventory management ...
Associate Food Labeling Certifications Specialist
Omaha, NE · On-site
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Associate Food Labeling Certifications Specialist
Omaha, NE · On-site
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Associate Food Labeling Certifications Specialist
Omaha, NE · Hybrid
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Associate Food Labeling Certifications Specialist
Omaha, NE · Hybrid
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Join the team supported by Adecco in Swiftwater, PA, as a Labeling and Packaging Associate--an ... Record basic production data to monitor performance and output. * Assist with inventory management ...
Quick apply
Join the team supported by Adecco in Swiftwater, PA, as a Labeling and Packaging Associate--an ... Record basic production data to monitor performance and output. * Assist with inventory management ...
Associate Food Labeling Certifications Specialist
Omaha, NE · On-site
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Associate Food Labeling Certifications Specialist
Omaha, NE · On-site
$59K - $79K/yr
Reporting to the Labeling Certifications Manager, you will support food labeling, certification ... Number of Days in Office: 3 #LI-Hybrid #LI-MH1 #LI-Associate Compensation Pay Range:$59,000-$79,000 ...
Pharmaceutical Labeling Associate Manager information
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1% of jobs
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0% of jobs
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1% of jobs
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1% of jobs
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Associate - Labeling Implementation - North America
Indianapolis, IN • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 10 days ago
Eli Lilly and Company rating
8.9
Based on 64 frontline employees who took The Breakroom Quiz
Job description
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Organization Overview
At Lilly, we serve an extraordinary purpose.We make a difference for peoplearound the globeby discovering,developingand delivering medicines that helpthemlive longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Purpose
The Associate - Global Regulatory Affairs (GRA) Labeling Implementation -North America drives the timely and high-quality implementation and maintenance of product labeling in the assigned country/region. This role develops collegial, mutually positive relationships across Regulatory, Printed Packaging Development (PPD), Manufacturing/Supply Chain, Global Packaging, Development, and other business partners. The Global Regulatory Affairs (GRA) Labeling Implementation utilizes regulatory labeling process expertise across the organization and geographies to drive consistency and influence effective change management.
Responsibilities
Labeling Implementation Leadership
Lead, partner, and influence labeling-related activities throughout the product lifecycle to drive timely and efficient implementation of labeling changes ensuring regulator and internal timelines are met.
Function as a delegate for Affiliate labeling implementation responsibilities outlined in the Labeling Development and Maintenance standard.
Lead and monitor the implementation of updated or new labeling components into the market.
Advise affiliates on responsibility for managing control and integrity of affiliate truth copy documents.
Liaise with cross functional partners to handle multiple changes occurring simultaneously (e.g., GRA-CMC or site technical changes impacting labeling).
Provide oversight for the proof copy approval process and interactions with PPD.
Train and assist affiliates on the use of systems, tools, and processes.
Act as a power user for key labeling systems such as BLUE, RIM, etc.
Assist with deviations, escalations, and audits related to labeling implementation.
Monitor new regulations and guidances for assigned country/region, assess impact with input from Regional Regulatory Scientists, Device Regulatory Scientists, and Labeling Process Owner, and track progress.
Functional and Technical Expertise
Maintain an understanding and expertise on local requirements, laws, and regulations related to labeling implementation.
Act as a subject matter authority and resource for other GRA colleagues (e.g., Regional Regulatory Scientists, Device Regulatory Scientists, Product Communication reviewers) on labeling processes.
Educate customers on regulatory requirements, roles / responsibilities, labeling best practices and the process to ensure timely implementation of new or revised labeling.
Decision Making/Influence/Problem Solving
Serve as a labeling resource for regulatory to develop and gain support for strategies and concepts that will deliver timely labeling for marketed products.
Apply knowledge of business processes and labeling to gain alignment with partners on standardized processes and labeling deliverables.
Process information and team dynamics and adapt a style when negotiating with cross functional partners to enable effective decision making and timely completion of deliverables.
Impact
Drive timely implementation of labeling changes ensuring regulatory and internal timelines are met.
Demonstrate understanding of labeling implementation process and understand impact. Communicate impact of labeling changes to cross-functional partners.
Collaborate with Regulatory team on submission and implementation plans to capitalize upon opportunities for bundling changes for more efficient implementation, when applicable.
Customer / External Focus
Routinely share labeling knowledge with key customers. Participate in internal working groups to make recommendations that may shape regulatory labeling environment.
Identify appropriate customers and partners to communicate impact of labeling changes. Anticipate questions and proactively communicate possible impact to labeling.
Basic Qualifications
Bachelor's degree
2 + years in the biotechnology, device, or pharmaceutical industry
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1
Additional Preferences/Other Information
Scientific or health sciences degree field preferred (or equivalent work experience)
Knowledge of local regulatory procedures and practices and awareness of evolving regulatory reform
Understanding of manufacturing and supply chain practices
Knowledge of drug development
Project management experience
Demonstrated ability to lead, influence and partner cross-functionally
Demonstrated capability for contributing on complex projects with accelerated timelines
Demonstrated strong communication skills: writing, presenting, listening.
Shown flexibility to handle multiple tasks simultaneously
Proven competence of computer skills (e.g., Word, Excel, PowerPoint)
Demonstrated agility to learn new computer systems and tools, attention to detail and organizational skills, and ability to work independently
Demonstrated effective teamwork abilities, adaptability to diverse interpersonal styles, and problem-solving skills
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$63,000 - $149,600Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly
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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Indianapolis, IN, US
Year founded
1876