
Caring for the world, one person at a time.
RA Professional Artwork Management EMEA - 1-year contract at Johnson & Johnson
About the role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Regulatory Affairs Group:
Job Sub Function:
Regulatory Product Submissions and Registration:
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description: About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for an RA Professional C-ROSS Artwork Management to be in Warsaw, Poland; This is a 1-year fixed term contract.Responsibilities:
-
Use of Artwork management System to initiate artwork for new labelling or changes to current labelling into production and/or generation of mock-up needed for regulatory submissions
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Complete review of the artwork (using electronic tool, where possible) and co-ordinate the final approval of the artwork with Local Operating Companies driven by the agreed deadlines.
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Entering data and using tools to monitor metrics for tracking of implementation of packaging material
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Liaise with Local Operating Companies Regulatory Affairs, quality, Product Artwork, supply chain, packaging sites internal/external to meet both Health Authorities implementation timelines and minimize current stock /component write off costs
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Performing and/or co-ordination of Quality Check (QC) of local Product Information
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Communication with local stakeholders of the Local Operating Companies in scope during the review process
Requirements:
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Previous experience of 2 years in Regulatory Affairs and artwork management
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Experience of working in a virtual team and/or global organization would be an asset
-
Experience in working with limited supervision and able to make independent decisions is of advantage
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Cultural sensitivity and ability to work and thrive in a multi-cultural environment
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Experience with computer systems usage (MS office, excel)
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Proficient level of English
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Knowledge of multiple languages would be an asset
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Accuracy, precision and respect of timelines is mandatory
Required Skills: Preferred Skills:The anticipated base pay range for this position is:
zł94,500.00 - zł151,800.00
Benefits:
In addition to base pay, we offer the following benefits: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.
This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
Required skills
Regulatory affairs
Artwork management
Documentation
Compliance
Cross-functional collaboration
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About Johnson & Johnson

Johnson & Johnson
PublicJohnson & Johnson (J&J) is an American multinational pharmaceutical, biotechnology, and medical technologies corporation headquartered in New Brunswick, New Jersey, and publicly traded on the New York Stock Exchange.
10,001+
Employees
New Brunswick
Headquarters
$400B
Valuation
Reviews
2 reviews
3.3
2 reviews
Work-life balance
4.0
Compensation
2.5
Culture
2.5
Career
2.0
Management
2.0
65%
Recommend to a friend
Pros
Good work-life balance
Strong R&D environment
Potential for fulfilling work
Cons
Significant pay cuts
Employees feel unimportant
Unclear role expectations
Salary Ranges
2,250 data points
Senior/L5
Senior/L5 · SENIOR COUNSEL
1 reports
$258,000
total per year
Base
$224,300
Stock
-
Bonus
-
$258,000
$258,000
Interview experience
6 interviews
Difficulty
3.0
/ 5
Duration
14-28 weeks
Interview process
1
Application Review
2
HR Screen
3
Personality/Assessment Test
4
Virtual/Video Interview
5
Hiring Manager Interview
6
Offer
Common questions
Behavioral/STAR
Technical Knowledge
Culture Fit
Past Experience
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