Loading...
Share this Job

Quality Control Analyst, Chemist

Date: Oct 9, 2021

Location: Irvine, California, US, 92618

Company: Teva Pharmaceuticals

Company Info

 

If you’re like people at Teva, you dare to be different. We’re making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.


Teva’s Irvine, CA production site is one of our complex manufacturing and supply chain operations.


We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!


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


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!

 

Relocation may be available. 

 

Job Description

 

The position requires proficiency with authoring and executing analytical method validation protocols and reports, compendia verifications and method transfers.  Provides technical support for complex investigations and junior staff.  Performs analytical testing of raw or finished dosage pharmaceutical products, may perform trouble-shooting and minor maintenance of analytical instruments and perform laboratory analysis.

 

• Authors and/or executes protocols and reports for method validation, method transfer and USP verifications
• Provides support for complex technical investigations and projects
• Working knowledge of analytical instrumentation
• Complete Investigation and Deviations (Capa effectiveness) in Trackwise
• Ability to mentor team members
• Participate in cross-functional project teams, internal and external to Irvine
• Participates in troubleshooting of analytical test methods
• Complies with all company policies and procedures, including safety rules and regulations
• Carries out responsibilities in accordance with the organization’s policies, procedures, and state, Federal and local laws
• Performs related duties as assigned

Qualifications

 

Education/Certification/Experience:
• Requires a Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience with a minimum of 10 years relevant progressive experience in a Quality Control / Quality Assurance environment.
• Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
• Prefer experience with Laboratory Information Management Systems (Labware LIMS and/or Empower preferred).


Skills/Knowledge/Abilities:
• Understanding of method validation requirements.
• Understanding of compendia.
• Understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other general analytical techniques.
• Computer proficiency with comprehensive knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise.
• Ability to effectively document a process, explaining scientific and/or technical ideas in writing (technical writing skills). 
• Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
• Detail oriented with ability to identify errors and/or inconsistencies while performing tasks.

Function

Quality

Sub Function

Manufacturing Quality Control

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.

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.

 


Nearest Major Market: Irvine California
Nearest Secondary Market: Los Angeles