Teva Pharmaceuticals Quality Control Auditor II (Friday, Saturday, Sunday & Monday, 8am-6pm) in Salt Lake City, Utah
Quality Control Auditor II (Friday, Saturday, Sunday & Monday, 8am-6pm)
Date: Apr 13, 2021
Location: Salt Lake City, Utah, US, 84116
Company: Teva Pharmaceuticals
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 Salt Lake City, Utah production site (s) are two 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 have 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!
Around 200 million people worldwide take one of our medicines every day. In the United States, where Teva is the leading generic pharmaceutical company, one out of every nine prescriptions is filled by a Teva product. In the both the UK and Canada, it is one out of every six. In addition, many prescription medications made by other companies include active pharmaceutical ingredients produced by Teva.
The purpose of this position is to review QC documentation, to assess compliance/validity with regulatory guidelines in the Quality Control Department, and ensure that all lab work is performed and documented accurately. The QC Auditor ensures all data generated is done in compliance of GMP. Ensures compliance with internal procedures (SOPs) and regulatory agencies. The individual should be familiar with a variety of analytical chemistry concepts, practices, and procedures. Completes tasks and goals in a timely manner. Under general supervision is expected to make decisions based on experience and technical knowledge. Ensures timely completion of all projects and batch release.
This position is Friday-Monday, 8am-6pm.
Performs peer review of chemist’s work and assembles data packets.
Performs LIMS entry and review and maintains database.
Generates Test Reports, Certificates of Compliance, and other documents using Excel and Word.
Interprets protocols and experimental design for testing plans.
Works with LIMS and Empower, and other related software systems.
Maintains appropriate documentation (records and lab notebooks) as required by SOPs.
Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.
Complies with all current Good Manufacturing Practices (cGMP) current Good Laboratory Practices (cGLP) and safety requirements, laboratory Standard Operating Procedures (SOPs) and Company policies and procedures.
2+ years laboratory experience
Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, dissolution apparatuses, FTIR, Instron operation and other techniques in testing gels, creams, lotions, oral solutions and transdermal system.
Business, scientific and personal computer hardware and software applications.
Business English usage, spelling, grammar and punctuation.
Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures.
Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines.
Performing testing accurately and precisely.
Responding to routine inquiries from management, employees and regulatory agencies.
Communicating clearly and concisely, both orally and in writing.
Managing multiple projects, duties and assignments.
Establishing and maintaining cooperative working relationships with others.
Manufacturing Quality Control
Manager Quality Control, SLC QC (US)
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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
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.
EOE including disability/veteran