About Us
Teva Pharmaceuticals
has been developing and producing medicines to help improve people’s 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 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 biopharmaceutical products. Learn more
at http://www.tevapharm.com.
Teva Pharmaceutical Industries Ltd., commonly known as Teva, is an
international pharmaceutical company headquartered in Petah Tikva, Israel. It
is one of the world's largest generic drug manufacturers and develops,
manufactures, and markets a wide range of pharmaceutical products. Teva was
founded in 1901 and has since grown to become a prominent player in the global
pharmaceutical industry.
Key points
about Teva Pharmaceuticals:
- Generic Pharmaceuticals: Teva is best known for its
production of generic pharmaceuticals. Generic drugs are chemically
equivalent to brand-name drugs and are typically more affordable, making
healthcare more accessible to a larger population. Teva produces generic
versions of a variety of medications, including both prescription and
over-the-counter drugs.
- Global Presence: Teva operates on a global
scale, with a presence in over 60 countries. The company has a significant
market share in many regions, including North America, Europe, and
emerging markets.
- Branded Pharmaceuticals: In addition to its focus on
generic drugs, Teva also develops and markets branded pharmaceutical
products in various therapeutic areas. These branded products cover a
range of medical conditions, including neurological disorders, respiratory
diseases, and oncology.
- Research and Development: Teva invests in research and
development (R&D) to create new drugs and improve existing
formulations. Its R&D efforts encompass a diverse range of therapeutic
areas, and the company seeks to innovate in areas such as biosimilar
(biological products similar to existing biologics) and specialty
pharmaceuticals.
- Mergers and Acquisitions: Over the years, Teva has
engaged in various mergers and acquisitions to expand its market presence
and product portfolio. Notably, the company acquired the generic drug
business of Allergan in 2016, further solidifying its position in the
pharmaceutical industry.
- Challenges: Teva, like many
pharmaceutical companies, faces challenges related to patent expirations,
competition from other generic manufacturers, regulatory changes, and pricing
pressures. These challenges can impact the company's financial performance
and strategic decisions.
- Corporate Social
Responsibility:
Teva is also involved in various corporate social responsibility
initiatives, including efforts to increase access to affordable
healthcare, support local communities, and promote sustainability.
It's
important to note that the information provided here is based on my knowledge
as of September 2021, and there may have been developments or changes since
that time. If you're looking for the most up-to-date information about Teva
Pharmaceutical Industries, I recommend checking their official website or
recent news sources.
Role: Sr. Manager
Department: QA- Plant, API
Location: Gwalior, MP
Experience: 15+ years
Main
Responsibilities:
1. Ensure Review of all documentation (i.e. batch records, test results,
deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) and perform
disposition (release or rejection) of the batch.
2. Ensure Review of step-by-step performance and compliance to batch
manufacturing and packaging record requirements and resolution of any
errors/deviations identified.
3. Development of corrective and preventive actions (review, approval, and on-time
closure of the CAPA) to resolve an event. Ensuring
Process/documentation (i.e. Protocol/report) of reviewing effectiveness to
determine the effectiveness of a corrective or preventive action.
4. Ensuring and performing an investigation into a product quality complaint
with resolution including corrective and preventive actions and closure of the
investigation.
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