Teva Pharmaceuticals Jobs – Quality Analyst III Job Vacancies in West Chester, PA

Teva Pharmaceuticals Jobs – Quality Analyst III Jobs in Pennsylvania Careers Employment Opportunity. Get Teva Pharmaceuticals Quality Analyst III Jobs in Pennsylvania. Teva Pharmaceuticals Careers. Job seekers who are looking for job search at Teva Pharmaceuticals. There is news related to Jobs Pennsylvania. We looked at this information of Teva Pharmaceuticals Quality Analyst III Jobs in Pennsylvania at the Teva Pharmaceuticals Careers Employment page. Job seekers who are trying to get the latest news related to Teva Pharmaceuticals Quality Analyst III Jobs can take advantage of these new Jobs in Teva Pharmaceuticals. Check State of Pennsylvania Jobs.


Teva Pharmaceuticals Jobs – Quality Analyst III Jobs in Pennsylvania

Teva Pharmaceuticals Quality Analyst III Jobs:- As per the Teva Pharmaceuticals Careers employment page, current time Teva Pharmaceuticals hiring for Quality Analyst III Jobs in Teva Pharmaceuticals. Candidates who have a Desire qualification according to this Jobs at Pennsylvania can apply online through Teva Pharmaceuticals’s official career page. Quality Analyst III Jobs Pennsylvania Salary $ 123,960.00 Per Year.

After the Announcement of this Teva Pharmaceuticals Jobs you have a few questions related to this Teva Pharmaceuticals employment like as What is the Qualification of this Teva Pharmaceuticals Quality Analyst III Jobs?, What is the minimum/maximum age requirement ?, How I can apply for this Teva Pharmaceuticals recruitment? and what will be applying dates for jobs at Teva Pharmaceuticals?  All answers to these questions you can get in the below section.

Disclaimer:- Governmentjobs24.com team recommends all jobseekers to read the notification issued on the Teva Pharmaceuticals official site before applying for any job. Governmentjobs24.com team always tries to provide correct information. This information is taken from the Teva Pharmaceuticals official website. GovernmentJobs24.com’s team will not be responsible for any errors in this Teva Pharmaceuticals Job Post.

Information Table: Quality Analyst III Jobs Teva Pharmaceuticals

Name of Employer Agency Teva Pharmaceuticals
Job Profile Quality Analyst III
Salary Offer by Department $ 123,960.00 Per Year
Job Type Jobs in West Chester
This Profile Hiring for  Jobs in Pennsylvania
Timing Full Time

Required Qualification:- Teva Pharmaceuticals Jobs 

Job aspirants should be Bachelor’s or Master’s Degree or relevant experience holders can apply for this Teva Pharmaceuticals Jobs.

Quality Analyst III at Teva Pharmaceuticals Job Description

Who are we?

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!

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, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance.

The Quality Analyst III is responsible for supporting biologics manufacturing compliance, which includes the Internal Audit and Vendor/Supplier Management Programs, Quality Council, and Regulatory Inspections Readiness.

This position is not remote.

Essential Responsibilities

  • Assist in the planning and execution and internal audits
  • Follow up on internal audit CAPA to ensure timely closure
  • Support regulatory agency filings and inspections
  • Participate in regulatory inspections
  • Participate in routine vendor monitoring and requalification
  • Support GMP compliance and inspection readiness
  • Generate and manager quality agreements
  • Assist in preparation and/or participate in vendor audits
  • Issue and track completion of vendor complaints
  • Assist in the preparation and presentation of site Quality Council
  • Ensure Supplier Change Notifications are reviewed and addressed by the proper site functions
  • Utilize Quality Systems to review and approve change controls, deviations, laboratory investigations, CAPAs, and CAPA Effectiveness checks
  • Perform gap assessments of local SOPs to corporate standards; draft SOPs as needed
  • Review and approve SOPs, work instructions, and controlled forms
  • Understanding of gowning and aseptic techniques for controlled environments
  • Support cross-functional department customers in a manner which is clear in approach, communication, and action
  • Review and approve Controlled Material Specifications
  • Control material disposition and release
  • Support area room clearances and product changeover activities
  • Review and approve environmental and utilities monitoring data
  • Participate in the QA On-The-Floor Program in the production facility
  • Review and approve master and executed batch records, validation protocols/reports, method transfer protocols/reports, and Controlled Material Specifications
  • Provide communication to customers to ensure timely escalation and resolution of issues

Qualifications

  • Bachelor’s or Master’s Degree in Life Science discipline required
  • Knowledge in quality compliance (cGMP, ICH, FDA, EMA, USP/EP policies and guidelines) required
  • Minimum of 5 years QA experience in development of Biopharmaceutical products required
  • Experience leading internal audits required
  • Experience performing supplier audits required
  • Project Management skills and/or auditing certification a plus
  • Experience managing CMO/CROs preferred
  • Experience with analytical assay and process qualification/validation from the QA perspective preferred
  • Experience with Regulatory inspections preferred
  • Experience with review of Regulatory inspections preferred
  • TrackWise experience a plus

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.

Function

Quality

Sub Function

R&D Quality

Reports To

Quality Head of Compliance

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:

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.

Inclusion & Diversity at Teva

Empowering our diverse employee base and creating an inclusive culture is both a business imperative and an opportunity to bring us closer to our patients, our partners and our communities. Teva employees respect and embrace a diverse range of experiences, capabilities and perspectives that connect us to new insights and opportunities, while building a more inclusive culture for all. We strive to enable a work environment where all employees can feel engaged and know they are making an important contribution to improving health and making people feel better.

How to Apply for Jobs in Teva Pharmaceuticals?

  • Applicants go through official website of Teva Pharmaceuticals.
  • Check first official announcement notice published by Teva Pharmaceuticals.
  • Now read the Teva Pharmaceuticals jobs employment notification details.
  • After read this notification your educational profile matching with Teva Pharmaceuticals Quality Analyst III jobs.
  • Then you should apply for Teva Pharmaceuticals Jobs as per details given in next paragraph.

Candidates who really interested and wanted to apply for Teva Pharmaceuticals Jobs should submit a cover letter, resume, and three professional references and apply online.

Apply Online at Teva Pharmaceuticals Jobs Site

Read Carefully Before Apply

FAQ: Related to Teva Pharmaceuticals Jobs

After announcement of this Teva Pharmaceuticals Jobs you have few question related to this Teva Pharmaceuticals employment like as What is Qualification of this Teva Pharmaceuticals Quality Analyst III Jobs?, What is minimum/maximum age requirement ?, How i can apply for this Teva Pharmaceuticals recruitment? and what will be applying dates for jobs Teva Pharmaceuticals.

  • Teva Pharmaceuticals has issued a notification for which post?

Answer: Currently Teva Pharmaceuticals has published notification for Quality Analyst III Jobs.


  • Teva Pharmaceuticals has issued notifications for how many posts?

Answer: The Teva Pharmaceuticals has published notification for many Quality Analyst III Jobs.


  • Who can apply of this Teva Pharmaceuticals Quality Analyst III Jobs?

Answer: The aspirant who have a High school diploma/equivalency required, Bachelor’s degree are eligible for Recruitment in Teva Pharmaceuticals .


  • How I can apply for this Teva Pharmaceuticals recruitment?

Answer: Applicants who are Interested to apply for Teva Pharmaceuticals Jobs should submit a cover letter, resume, and three professional references and apply online.


  • Other Eligibility to Get This Job

Answer: The effective up-and-comer must be coordinated, adaptable, simple and have great agreement, astounding client support and relational aptitudes, and function admirably with a wide assortment of individuals. Must be dependable, can take care of the issue, and work freely. Must have PC aptitudes, including capacity to investigate specialized issues. Past experience and utilization of CWMARS and Evergreen ILS liked.


About Teva Pharmaceuticals:

Teva Pharmaceutical Industries Ltd. is an Israeli multinational pharmaceutical company with headquarters in Petah Tikva, Israel. It specializes primarily in generic drugs, but other business interests include active pharmaceutical ingredients and, to a lesser extent, proprietary pharmaceuticals.


Teva Pharmaceuticals Jobs – Associate Director Formulation Jobs in Pennsylvania

Teva Pharmaceuticals Associate Director Formulation Jobs:- As per the Teva Pharmaceuticals Careers employment page, current time Teva Pharmaceuticals hiring for Associate Director Formulation Jobs in Teva Pharmaceuticals. Candidates who have a Desire qualification according to this Jobs at Pennsylvania can apply online through Teva Pharmaceuticals’s official career page. Associate Director Formulation Jobs Pennsylvania Salary $ 176,619.00 Per Year.

After the Announcement of this Teva Pharmaceuticals Jobs you have a few questions related to this Teva Pharmaceuticals employment like as What is the Qualification of this Teva Pharmaceuticals Associate Director Formulation Jobs?, What is the minimum/maximum age requirement ?, How I can apply for this Teva Pharmaceuticals recruitment? and what will be applying dates for jobs at Teva Pharmaceuticals?  All answers to these questions you can get in the below section.

Disclaimer:- Governmentjobs24.com team recommends all jobseekers to read the notification issued on the Teva Pharmaceuticals official site before applying for any job. Governmentjobs24.com team always tries to provide correct information. This information is taken from the Teva Pharmaceuticals official website. GovernmentJobs24.com’s team will not be responsible for any errors in this Teva Pharmaceuticals Job Post.

Information Table: Associate Director Formulation Jobs Teva Pharmaceuticals

Name of Employer Agency Teva Pharmaceuticals
Job Profile Associate Director Formulation
Salary Offer by Department $ 176,619.00 Per Year
Job Type Jobs in West Chester
This Profile Hiring for  Jobs in Pennsylvania
Timing Full Time

Required Qualification:- Teva Pharmaceuticals Jobs 

Job aspirants should be Required Qualification or relevant experience holders can apply for this Teva Pharmaceuticals Jobs.

Associate Director Formulation at Teva Pharmaceuticals Job Description

Who are we?

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!

This Associate Director position will be a key leadership role in DPDO to support the development of Teva innovative and biosimilar product pipeline reporting into the head of the DPDO department.  The incumbent will be responsible for formulation development including representing DPDO on matrix teams, writing relevant sections of submissions and managing a team of scientist with project leadership responsibilities to ensure project deliverables are met.  In addition, the incumbent will be responsible for innovative formulation technology evaluation and development.

Responsibilities 

  • Responsible for formulation development and/or review of all associated protocols and technical reports for biosimilar and innovative biologic programs.
  • Bring to implementation high-through-put formulation development platform.
  • Evaluate new formulation technology to enable high concentration of proteins.
  • Represent DPDO on matrix team to progress the pipeline including interfacing with regulatory and nonclinical and clinical organization to develop appropriate regulatory submissions and respond to agency questions and develop appropriate in-use studies.
  • Collaborate with partner functional groups for the progression of Combination Drug Product in devices (i.e. PFS, NSD, AI), providing knowledge of the characteristics of the drug product and expertise to any collaborative study design for products delivered via devices.
  • Contribute to relevant Drug Product formulation sections in regulatory submission and response to questions as DPDO line reviewer or author, if needed.
  • Contribute to resource planning, objective setting and any other business related processes as appropriate.
  • Provide leadership in cross department initiatives.
  • Manage direct reports with various experiences.  Including providing opportunities for development, advising, coaching and mentoring.

Qualifications

Minimum Qualifications

  • Bachelor’s in chemistry, biology, pharmaceutical sciences, biochemistry, chemical engineering or other related discipline with 15 years of experience in biologics that includes formulation and analytical characterization of mAbs, or Master’s in a related discipline with 10 years, or Ph.D. in a similar discipline with 7 years of experience.
  • At least 3 years of people management experience.
  • Understanding with hands on experience of analytical techniques as it relates to formulation development for biological products using physical and biochemical characterization methods, such as general appearance, opalescence, osmolality, particulate analysis (MFI and HIAC), HPLC and other biophysical characterization methods.
  • Experience authoring and reviewing regulatory submissions related to CMC activities.
  • Current knowledge of regulatory guidelines related to biologic pharmaceutical development, characterization, and comparability including ICH guidance and cGMP.

Preferred Qualifications

  • Experience writing guidance documents for technical processes as it related to biological drug product.
  • Experience in the creation and implementation of high-through-put formulation development.
  • Experience with extractable and leachable programs as it relates to drug product.
  • Experience working in a matrix team to progress biologic products.
  • Experience collaborating with process development, analytical and other relevant organizations for the progression of biologics to commercial.
  • Ability to develop plans and deliver results in a dynamic changing environment.
  • Ability to manage multiple partners and interfaces to progress project objectives.
  • Highly motivated individual, with ability to work in a team environment and build productive relationships within and across departments.
  • Excellent project management, verbal/written communication, and interpersonal skills.

Function

Research & Development

Sub Function

Drug Development and Preclinical Studies

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:

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.

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.

How to Apply for Jobs in Teva Pharmaceuticals?

  • Applicants go through official website of Teva Pharmaceuticals.
  • Check first official announcement notice published by Teva Pharmaceuticals.
  • Now read the Teva Pharmaceuticals jobs employment notification details.
  • After read this notification your educational profile matching with Teva Pharmaceuticals Associate Director Formulation jobs.
  • Then you should apply for Teva Pharmaceuticals Jobs as per details given in next paragraph.

Candidates who really interested and wanted to apply for Teva Pharmaceuticals Jobs should submit a cover letter, resume, and three professional references and apply online.

Apply Online at Teva Pharmaceuticals Jobs Site

Read Carefully Before Apply

FAQ: Related to Teva Pharmaceuticals Jobs

After announcement of this Teva Pharmaceuticals Jobs you have few question related to this Teva Pharmaceuticals employment like as What is Qualification of this Teva Pharmaceuticals Associate Director Formulation Jobs?, What is minimum/maximum age requirement ?, How i can apply for this Teva Pharmaceuticals recruitment? and what will be applying dates for jobs Teva Pharmaceuticals.

  • Teva Pharmaceuticals has issued a notification for which post?

Answer: Currently Teva Pharmaceuticals has published notification for Associate Director Formulation Jobs.


  • Teva Pharmaceuticals has issued notifications for how many posts?

Answer: The Teva Pharmaceuticals has published notification for many Associate Director Formulation Jobs.


  • Who can apply of this Teva Pharmaceuticals Associate Director Formulation Jobs?

Answer: The aspirant who have a High school diploma/equivalency required, Bachelor’s degree are eligible for Recruitment in Teva Pharmaceuticals .


  • How I can apply for this Teva Pharmaceuticals recruitment?

Answer: Applicants who are Interested to apply for Teva Pharmaceuticals Jobs should submit a cover letter, resume, and three professional references and apply online.


  • Other Eligibility to Get This Job

Answer: The effective up-and-comer must be coordinated, adaptable, simple and have great agreement, astounding client support and relational aptitudes, and function admirably with a wide assortment of individuals. Must be dependable, can take care of the issue, and work freely. Must have PC aptitudes, including capacity to investigate specialized issues. Past experience and utilization of CWMARS and Evergreen ILS liked.


About Teva Pharmaceuticals:

Teva Pharmaceutical Industries Ltd. is an Israeli multinational pharmaceutical company with headquarters in Petah Tikva, Israel. It specializes primarily in generic drugs, but other business interests include active pharmaceutical ingredients and, to a lesser extent, proprietary pharmaceuticals.

 

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