The Regulatory Labeling Associate provides support to the Global Regulatory Affairs Labeling Center ... Managing complexity/Technical accountability Demonstrates technical competency to perform job ...
The Regulatory Labeling Associate provides support to the Global Regulatory Affairs Labeling Center ... Managing complexity/Technical accountability Demonstrates technical competency to perform job ...
... Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global ... managed within PDT BU's Global Labeling function, pertaining to pharmaceutical drug and device.
... Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global ... managed within PDT BU's Global Labeling function, pertaining to pharmaceutical drug and device.
T his 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 ...
T his 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 ...
Labeling Specialist
Jersey City, NJ · On-site
Assisting labeling managers with overall labeling process of brand prescription products ... Logistics and work of the pharmaceutical industry. Current Company policies, practices and ...
Labeling Specialist
Jersey City, NJ · On-site
Assisting labeling managers with overall labeling process of brand prescription products ... Logistics and work of the pharmaceutical industry. Current Company policies, practices and ...
Associate, Regulatory Affairs- Labeling
Princeton, NJ · On-site
$94K - $105K/yr
Princeton, NJ Company: Sun Pharmaceutical Industries, Inc (USA) Job purpose This role is ... Maintain documents on approved and newly filed products and also Life Cycle Management. * Assist ...
Associate, Regulatory Affairs- Labeling
Princeton, NJ · On-site
$94K - $105K/yr
Princeton, NJ Company: Sun Pharmaceutical Industries, Inc (USA) Job purpose This role is ... Maintain documents on approved and newly filed products and also Life Cycle Management. * Assist ...
This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to ... Demonstrated experience with biopharmaceuticals and management capability Business Certification ...
This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to ... Demonstrated experience with biopharmaceuticals and management capability Business Certification ...
... pharmaceutical drug/device labeling. * Contribute labeling strategy to regulatory strategies ... Drive CCDS/US/EU labeling strategy and lifecycle management; lead development and maintenance of ...
... pharmaceutical drug/device labeling. * Contribute labeling strategy to regulatory strategies ... Drive CCDS/US/EU labeling strategy and lifecycle management; lead development and maintenance of ...
Associate Director, Global RA Labeling Lead
Cambridge, MA · On-site
$115.62 - $146.62/hr
The Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies ... managed within PDT BU's Global Labeling function, pertaining to pharmaceutical drug and device.
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Associate Director, Global RA Labeling Lead
Cambridge, MA · On-site
$115.62 - $146.62/hr
The Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies ... managed within PDT BU's Global Labeling function, pertaining to pharmaceutical drug and device.
New
Relevant experience in the pharmaceutical industry (e.g., Regulatory Affairs, Clinical, Medical ... Experience working with document management systems is required. * Experience effectively ...
New
Relevant experience in the pharmaceutical industry (e.g., Regulatory Affairs, Clinical, Medical ... Experience working with document management systems is required. * Experience effectively ...
New
Associate, Regulatory Affairs- Labeling
Princeton, NJ · On-site
$94K - $105K/yr
Maintain documents on approved and newly filed products and also Life Cycle Management. * Assist ... generic pharmaceutical industry. * Advanced computer skills required. * Solid writing and ...
Associate, Regulatory Affairs- Labeling
Princeton, NJ · On-site
$94K - $105K/yr
Maintain documents on approved and newly filed products and also Life Cycle Management. * Assist ... generic pharmaceutical industry. * Advanced computer skills required. * Solid writing and ...
Associate Labeling Strategy Director
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
Associate Labeling Strategy Director
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
Support labeling negotiations with FDA and manage implementation of approved labeling updates ... Strong desire to grow career in the pharmaceutical industry, willingness to learn, and ...
Support labeling negotiations with FDA and manage implementation of approved labeling updates ... Strong desire to grow career in the pharmaceutical industry, willingness to learn, and ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus
Associate Director, Global Labeling
Philadelphia, PA · On-site
$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
Philadelphia, PA · On-site
$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 ...
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus
Clinical Operations & Program Management * Clinical Sciences * Regulatory Strategy * Regulatory ... Prior Internship or rotational experience within the Pharmaceutical/Biotech industry a plus
Associate Labeling Strategy Director
Durham, NC · On-site
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
Associate Labeling Strategy Director
Durham, NC · On-site
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
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 ...
Associate Director, Global Labeling
Cambridge, MA · On-site
$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 ...
Associate Director, Global Labeling
Cambridge, MA · On-site
$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 ...
Associate Labeling Strategy Director
Durham, NC · On-site
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
Associate Labeling Strategy Director
Durham, NC · On-site
$103K - $288K/yr
Ability to lead and manage labeling team meetings, driving strategic discussions and managing ... pharmaceutical industry * 7+ years of experience in Regulatory labeling * Strong knowledge of ...
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 ...
Pharmaceutical Labeling Associate Manager information
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$15.82 is the 25th percentile. Wages below this are outliers.
$12.98 - $20.48
66% of jobs
$20.48 - $27.97
6% of jobs
$31.10 is the 75th percentile. Wages above this are outliers.
$27.97 - $35.47
6% of jobs
$35.47 - $42.96
7% of jobs
$42.96 - $50.46
5% of jobs
$50.46 - $57.95
5% of jobs
$57.95 - $65.45
1% of jobs
$65.45 - $72.95
0% of jobs
$72.95 - $80.44
0% of jobs
$80.44 - $87.94
1% of jobs
$87.94 - $95.43
1% of jobs
$12
$30
$95
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Regulatory Labeling Associate
Jacksonville, FL • On-site
Full-time
Re-posted 14 days ago
Job description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
The Regulatory Labeling Associate provides support to the Global Regulatory Affairs Labeling Center of Excellence (LCoE) team by supporting labeling content and artwork development activities for new products as well as updates to existing product labeling.
The Regulatory Labeling Associate will:
Master Complexity
Autonomy
Works independently on routine tasks;
Requires some supervision on non-routine tasks.
Managing complexity/Technical accountability
Demonstrates technical competency to perform job function;
Demonstrates compliance with departmental operations;
Demonstrates knowledge of current regulations and standards.
Innovation
Continuous Learning/Managing Risk
Demonstrates a systematic approach to solving problems.
Fueling Business Growth/Impact on Systems & Practices
Identifies and implements improvements on work assignments.
Customer Focus
Delivery of results/Customer value
Is proactive in fulfilling customer requirements.
Interdependent Partnering
Team Contribution
Completes technical tasks on work teams.
Relationship skills
Interacts effectively with peers and supervisors.
Organizational & People Development
Developing Others
Responsible for individual development
Creating the environment
Contributes to day-to-day harmony within the group;
Adapts to changing priorities.
CREDO
Adheres to environmental policy and procedures and supports department environmental objectives.
ESSENTIAL FUNCTIONS / RESPONSIBILITIES
Assists in reviewing, analyzing, and evaluating proposed worldwide labeling including, but not limited to, packaging, instructions for use, and investigational/clinical labeling for accuracy against established standards.
Conducting required research including part number and copy clearance verification, historical submission information, competitive labeling intelligence, etc.
Document/artwork formatting to support copy clearance, review, and submission documentation.
Facilitating and tracking electronic document and artwork submissions in internal systems.
Gathering and analyzing data related to labeling processes, errors, and efficiencies and preparing associated metrics reports.
Other activities and tasks to support the LCoE or Global Regulatory Affairs department, as assigned by management.
QUALIFICATIONS
High school diploma required, Bachelor's degree preferred.
Minimum experience (number of month/years and type of work experience beyond formal education) required for competent performance:
0 years with bachelor's degree or 3 years of prior operations, RA, QA or R&D experience preferred.
Past labeling or artwork development experience preferred.
Flexibility to work on multiple projects; ability to collect and analyze published material; familiarity with regulatory submissions, ability to develop innovative solutions to problems with limited complexity; keen attention to detail; very good organizational, communication and interpersonal skills; ability to work in a cross-functional team environment and provide quality customer service.
Familiarity/working knowledge of the following software programs (Required):
Microsoft Outlook
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Adobe Acrobat Professional
Additional preferred software program experience includes:
Adobe InDesign
Adobe Illustrator
SUPERVISION / AUTHORITY
Give no supervision to others.
Have lead responsibilities for one or more employees.
Responsible for work flow production, training of new employees on covered jobs, answering job-related questions in one or more areas.
In addition, assist in reporting on performance, recommending advancements, implementing new or changed procedures. Generally recognized as Group Leader or Assistant Supervisor.
Have full, direct supervisory responsibilities for a department or function.
Feel free to forward my email to your friends/colleagues who might be available.
For more information contact me at (732) 4291635
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996