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.
Post : Quality Control Analyst
Job Description
POSITION SUMMARY
This position is responsible for providing reliable and expedient results from the testing and analysis of incoming materials, intermediates, finished products, swab samples, and other samples to support the commercial and development activities at the site in compliance with all regulatory requirements, company policies and procedures.
AREAS OF RESPONSIBILITY
• Responsible for testing and analyzing incoming materials, intermediates, finished products, swab samples and other samples of a moderate scope and complexity of activity.
• Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
• Responsible for supporting laboratory investigations into Out of Specification/Out of Trend results or other laboratory events.
• Responsible for performing revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
• Responsible for coordinating and sending materials for contract laboratory testing.
• Responsible for assisting with verification of compendial methods.
• Responsible for providing training to other analysts on activities for which they have developed a level of expertise.
• Responsible for assisting with activities associated with the stability program including sampling and statistical analyses.
• Responsible for executing projects of a limited to moderate scope as assigned.
• Responsible for assisting with activities related to the sampling of incoming materials as needed.
• In Microbiology – Responsible for performing microbiology testing using good ASEPTIC technique.
• Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
• Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
• Responsible for performing additional related duties as assigned.
Candidate Profile
• Requires a Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience with a minimum of two years relevant progressive experience in a Quality Control Laboratory 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).
• Prefer experience with microbiology testing.
• Solid 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 working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise and Qdocs.
• Ability to effectively document a process, explaining scientific and/or technical ideas in writing (technical writing skills).
• Ability to communicate effectively with excellent written and oral communication skills.
• Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
• Self-directed with ability to organize and prioritize work.
• Detail oriented with ability to identify errors and/or inconsistencies while performing tasks.
Additional Information:
Location: Salt Lake City, Utah, US
Qualification : Bachelor’s Degree
Industry Type: Pharma
Functional Area: QC
End Date: 15th May, 2018
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