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Senior Packaging Engineer at Teva Pharmaceuticals

Senior Packaging Engineer

Teva Pharmaceuticals Fort Lauderdale, FL Full-Time

Who are we?


Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds.


Working here means working for the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.


The Opportunity


We have an opportunity for an experienced Senior Packaging Engineer to join our team. As part of our Solids Manufacturing & Supply Ops team, and reporting to the Senior Director of MS&T, you’ll play an essential role in improving the overall quality of our business here at Teva.


How you’ll spend your day


In this role, the Senior Packaging Engineer is responsible for package engineering and packaging validation activities for solid oral dosage forms. Responsibilities include participation in cross-functional teams or leading cross-functional teams for validation, leading cost improvement projects in packaging, and leading relevant packaging changes.


Day to day, you will:


• Leading package engineering projects in packaging facilities area for oral solid dosage forms. The focus is on primary package design through the identification of selecting and recommending solutions

• Skilled in Project Management tools, techniques, and decision-making

• Conduct & evaluate complex packaging design & development to test, prove or modify new package components for new products

• Manage package qualification testing, packaging equipment performance qualification, and packaging validation per site procedures

• Support & troubleshoot commercial packaging operations

• Author, execute and close out qualification and or validation documents, gap/risk assessment, and relevant VMP

• Support process optimization teams with broad knowledge of process and cleaning needs

• Aid R&D in transferring technology gained from Product development or external source

• Author, review, or approve (as needed) investigation reports, protocols batch records, and CMC documentation

• Knowledge of current and advanced validation strategies, current regulatory landscape and agency expectations for pre-validation, PPQ validation of oral solid dosage forms using novel manufacturing technologies

• Support compliance activities (e.g. CAPA, deviations, change controls, assessments, etc.)

• Support artwork review, container closure optimization, consolidation, line optimization, etc.

• Provide technical training and assistance to others

• Responsible for completing all training requirements and maintaining 100% compliance with all assignments

• Responsible to comply with company goals based on departmental assigned goals

• Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMPs), and Standard Operating Procedures (SOPs) instructions

• Responsible for performing additional related duties as assigned



Your experience and qualifications


Any equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.


Education/Certification/Experience:

• A Master of Science degree with 5 years or a Bachelor’s degree with 7 years (in Packaging Engineering, Pharmaceutical Engineering, Pharmaceutical Manufacturing, or Pharmaceutical Technology) is required

• Proficiency with statistics (use of Minitab or JMP) and project management tools is required (PMI certification preferred)

• Experience using Excel for data mining and analysis is required

• Experience in package engineering or qualification and or validation of packaging processes including risk management (preferably for oral solids)


Skills/Knowledge/Abilities:

• Excellent verbal, written, and interpersonal skills required

• Comply with FDA regulations at all times

• Skill levels in MS Office including proficiency in Word, PowerPoint, Excel, and SharePoint; JMP or Minitab and other relevant software



Enjoy a more rewarding choice


While we take great pride in helping millions around the world enjoy healthier lives every day, looking after our people is our priority. This is why we offer a highly competitive benefits package, including medical, dental, vision, and prescription coverage starting on the first day on the job. We also offer a top-tier 401(k) plan with a 6% match and a defined contribution,

disability and life insurance, paid time off, employee stock purchase plan, tuition assistance, and ongoing career development opportunities.


We also offer a dedicated Wellbeing Community Platform, containing global content, activities, and resources to aid your overall wellbeing. Additionally, our Employee Assistance Program is focused on sharing resources and support specific to mental health.


Find your purpose with Teva

To find out more about us, visit [ Link removed ] - Click here to apply to Senior Packaging Engineer />

If you want to be involved in purposeful work that helps improve the lives of millions of people around the world, join us.

Apply Now!



Function

Manufacturing


Sub Function

Technical Transfer


Reports To

Senior Director MS&T



Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.


Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunities be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.






Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.

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