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Quality Manager
Teva Pharmaceuticals Parsippany, NJ
$121k-152k (estimate)
Full Time | Pharmaceutical 5 Days Ago
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Teva Pharmaceuticals is Hiring a Quality Manager Near Parsippany, NJ

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Quality Manager

Date: May 6, 2024
Location:Parsippany, United States, New Jersey, 07054
Company: Teva Pharmaceuticals
Job Id: 55621
Who we are
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
The opportunity
POSITION SUMMARY
The role is accountable to deliver and responsible to manage the systems, processes, and operations in support of the quality assurance activities for Teva’s drug, biologic, medical device, and combination products produced by Teva’s Third Party External Manufacturing and Supply Operations (EMSO) partners, and ensure they meet established standards of Quality including reliability, usability, and performance. Ensures ongoing compliance with quality and industry regulatory requirements for cGMPs, 21CFR 210/211, 21CFR 820 and 21CFR Part 4.
KEY RESPONSIBILITIES
  • Assure ongoing compliance with Quality and industry regulatory requirements for cGMPs, 21CFR Parts 210/211, 21CFR Parts 600/610, 21CFR Part 820 and 21CFR Part 4, and other applicable regulations such as ISO and ICH standards.
  • Collaborate with Suppliers and Service Providers to assure the quality of their products, materials, components, operations and/or services.
  • Monitors Batch Release Cycle Time and supports efforts to develop and implement improvements for performance.
  • Follows up with suppliers on quality deviations and ensures that solutions are identified and implemented. Includes supplier audits.
  • Responsible for managing the final release activities of product manufactured and/or packaged at Teva’s EMSO Third Party Suppliers located in the U.S., as well as re-release of products from other regions to the U.S. market.
  • Provide Quality oversight for all manufacturing/packaging/testing at Teva’s EMSO Third Party Suppliers.
  • Receive and review Quality Customer Complaint investigations, Non-conformance Reports, Deviation Investigations and Laboratory Investigations ensuring all necessary components are included.
  • Review, evaluate and approve Change Controls from EMSO Third Party Suppliers and service providers and act as the point of contact for all comments between internal departments and the site.
  • Communicate to Senior Level Management any issues that may impact product currently on the market as well as any critical issues that may impact product intended for the commercial market.
  • Represent the EMSO NA Quality department and act as the primary contact for various cross functional teams involving supply chain activities.
  • Provide training, support, and guidance to EMSO and Quality employees.
Your experience and qualifications
EDUCATION
  • Bachelor’s degree in a related scientific or technical discipline.
  • Certifications such as Quality Auditor, Quality Engineer, Quality Improvement Associate and/or Six Sigma are a plus.
EXPERIENCE
  • Minimum of 5 years experience in a Pharmaceutical FDA regulated industry in Quality Assurance or related field.
  • Must have in-depth knowledge of cGMPs, CFR, ICH and applicable international regulations/guidelines.
  • Experience with Investigations, Change Controls, Product Release, CAPA, Validations, required.
  • Experience with External (Third Party/Contract) Pharmaceutical manufacturing, packaging, and testing is desired.
  • Able to resolve problems and contribute to process improvements.
  • Works independently with minimal guidance.
  • Strong technical writing skills.
  • Strong computer skills including TrackWise, Excel, and SAP is desired.
Enjoy a more rewarding choice
We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.
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. Use the following link to search and apply: Internal Career Site
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 opportunity 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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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Job Summary

JOB TYPE

Full Time

INDUSTRY

Pharmaceutical

SALARY

$121k-152k (estimate)

POST DATE

05/08/2024

EXPIRATION DATE

07/07/2024

WEBSITE

tevapharm.com

HEADQUARTERS

FAIRFIELD, NJ

SIZE

15,000 - 50,000

FOUNDED

1901

CEO

EREZ VIGODMAN

REVENUE

$200M - $500M

INDUSTRY

Pharmaceutical

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About Teva Pharmaceuticals

Teva Pharmaceuticals has been developing and producing medicines to help improve peoples lives for more than a century. We are committed to being a global leader in generic and specialty medicines with a portfolio of 3,500 products in nearly every therapeutic area. Around 200 million people around the world take a Teva medicine every day. They are served by one of the largest and most complex supply chains in the pharmaceutical industry. Along with our established presence in generics, we have significant innovative research and operations supporting our growing portfolio of specialty and biop ... harmaceutical products. Learn more at www.tevapharm.com. Please note that adverse effects for any of our products should be reported to: Safety.AE@teva.co.il Product-specific questions should be directed to Teva or Teva Group subsidiaries in your country. Contact details and Teva's Pharmacovigilance Privacy Policy may be found here: http://www.tevapharm.com/contact_us/ More
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The following is the career advancement route for Quality Manager positions, which can be used as a reference in future career path planning. As a Quality Manager, it can be promoted into senior positions as an IT Quality Assurance Director that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Manager. You can explore the career advancement for a Quality Manager below and select your interested title to get hiring information.

If you are interested in becoming a Quality Manager, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Quality Manager for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Quality Manager job description and responsibilities

Developing a quality control process to meet the needs of the business’s customer or client base.

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Checking product development and manufacturing processes to ensure quality standards are met.

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Before creating a product, the quality manager works with other management staff to brainstorm an efficient development process.

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Collaborate with an organization’s purchasing manager to ensure raw materials from external suppliers meet quality requirements.

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Propose actions required to achieve and/or maintain acceptable quality standards.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Quality Manager jobs

Quality managers must understand these standards to be sure that they are met.

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To ensure health and safety standards, quality managers must create and maintain up-to-date product or process specifications.

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Support new product launches to ensure that supplier quality meets the required standards.

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Proactively discuss audit quality matters with teams and help develop strategies to deliver high audit quality audits.

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Ensure that training plans are rolled and deployed to all departments with regards to all aspects of quality.

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