Analytical Development Chemist IV

Teva Pharmaceuticals

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Analytical Improvement Chemist IV

Date: Nov 8, 2023

Location: 

Toronto, Canada, Ontario, M1B 2K9

Firm: Teva Prescribed drugs

Job Id: 51286

Who we’re

Collectively, we’re on a mission to make good well being extra reasonably priced and accessible, to assist hundreds of thousands all over the world get pleasure from more healthy lives. It’s a mission that bonds our individuals throughout almost 60 international locations and a wealthy, various number of nationalities and backgrounds. Working right here means working with the world’s main producer of generic medicines, and the proud producer of lots of the merchandise on the World Well being Group’s Important Medicines Checklist. Immediately, at the very least 200 million individuals all over the world take one in every of our medicines each single day. A tremendous quantity, however we’re at all times in search of new methods to proceed making a distinction, and new individuals to make a distinction with.

The chance

on this place, the Analytical Improvement Chemist IV will develop, revise and validate strategies of superior stage of complexity utilizing widespread analytical laboratory devices, akin to HPLC, UPLC, GC, Dissolution, Particle measurement analyzer, FTIR, UV, Raman, ICP-MS and auto titrators and so on.; With steerage from Senior group member, the Analytical Improvement Chemist IV will performs complicated materials characterization testing to help provider pushed materials adjustments, Various API sourcing, crucial product investigation and QA requested investigation in accordance with the suitable SOP’s; Have in depth data of compendia publication and DMF, performs crucial assessment of compendia and DMF updates. 

  • Plans and performs analytical technique growth, validation and technique switch for varied analytical methods for bodily and chemical evaluation of pharmaceutical supplies.
  • Develops and validates, in compliance with all present SOP’s and regulatory necessities, analytical strategies of an superior stage of complexity with little help from the senior group member. 
  • Prepares technique validation experiences summarizing analytical information in concise write-ups of top of the range in a well timed method.
  • Plans and absolutely co-ordinates most points of labor in a logical trend and performs in an correct and well timed method that is price efficient.
  • Shows wonderful downside fixing expertise and exhibits innovation on an on-going foundation.

The way you’ll spend your day

  • Operates and troubleshoots analytical laboratory devices akin to HPLC, UPLC, GC, Malvern Particle Dimension Analyzer, 
  • UV, FTIR, ICP-MS, SEM, Picture analyzer and Dissolution Equipment.
  • Shows wonderful written and verbal communication expertise.
  • With steerage from Senior group member, performs complicated materials characterization testing to help provider pushed materials adjustments, Various API sourcing and significant product investigation.
  • Conducts materials characterization evaluation and information interpretation with varied methods akin to Malvern PSD analyzer, FTIR, Picture analyzer, SEM, LC-MS and so on. 
  • Opinions API suppliers’ technical packages or open half Drug Grasp Recordsdata. 
  • Evaluates the bodily and chemical properties of the API and determines the suitability of the alternate API for use within the drug product. 
  • Plans and performs required experiments together with extra technique growth/validation when required. 
  • Proposes and justifies the adjustments to the present specs.
  • With steerage from Senior group member, performs QA investigations and solves complicated issues to help QA’s CAPA dedication.
  • Makes use of good problem-solving expertise to resolve complicated and tough issues that require complete inquiry or analysis. 
  • Performs QA investigations together with identification of overseas matter (black specks), buyer complaints investigations, 
  • QDR or OOS investigations and industrial product failure investigations. 
  • Assists the QC lab supervisors/managers on an ongoing foundation to sort out issues that always require modern strategy to discovering options.
  • Supporting Tech Providers actions.
  • Performs and if wanted recommends analytical testing together with dissolution, disintegration, assay, impurities and CU/BU and so on., to help any formulation and course of adjustments in addition to know-how switch tasks. 
  • Conducts crucial evaluations of the analytical information to establish and resolve product chemistry, uniformity and drug dissolution associated points. 
  • Gives suggestions and strategies to Tech Providers.
  • Contributes to the participation of the QC-AD group within the High quality Management Laboratory.
  • Ensures the environment friendly well timed completion of labor in accordance with the established priorities.
  • Actively participates in conferences with supervisor and friends to make sure collaboration and knowledge is collected to make knowledgeable choices as a way to resolve points.
  • Collaborates with different QC Lab teams to assist seize synergies, arrange, and prioritize necessities meet established objectives. 
  • Participates within the implementation of processes within the High quality Management Laboratory to expedite analytical testing, enhance customer support, scale back operational prices and enhance laboratory security.
  • Successfully communicates, displays the corporate values, maintains priorities and displays coaching to make sure a excessive commonplace of efficiency. 
  • Adheres to, protected operational practices to stop accidents and keep away from hazard to others within the office.
  • Assists in supervision of Junior QC-AD Chemists.

Your expertise and {qualifications}

Schooling:

Required – College Diploma or Faculty Diploma in Chemistry or associated science.

Most well-liked – MSc or PhD in Chemistry or a associated science is helpful.

Expertise:

  • Minimal 5 (5) years of expertise in associated discipline. 
  • Technique growth/validation fundamentals and necessities
  • Chemical and bodily characterization of pharmaceutical elements.
  • Analytical laboratory gear widespread in QC Lab setting (HPLC, UPLC, GC, Dissolution, Particle Dimension Analyzer, UV, FTIR, SEM, Picture analyzer and ICP-MS and so on.). 
  • Technical necessities as per compendia (USP/NF,BP/EP), in- home strategies and common QC laboratory 
  • procedures
  • ICH pointers, GMP/cGMP laws as they apply to the laboratories.
  • Interpret analytical information and talk about the problems/issues with the supervisor and friends if required.
  • Write in a lucid format, technical analysis experiences, Basic lab procedures, SOPs, validation/technique switch experiences and different related QC paperwork. 
  • Good laptop expertise with proficiency in Microsoft Workplace and Labware LIMS, SAP navigating on-line compendia publications.
  • Good data of QA enterprise processes & RA enterprise processes. Good understanding of: 
  • Analytical strategies and methods widespread to QC Lab
  • GMP, cGMP and different regulatory necessities
  • Key measurements to help enterprise associated to customer support.
  • Arrange self and make good use of time to finish duties and tasks.
  • Skill to deal with duties concurrently.
  • Develop work plans contemplating the departmental goals, tasks, accountabilities, timelines and sources.
  • Hold acceptable people knowledgeable on progress of duties/tasks.

Already Working @TEVA?

If you’re a present Teva worker, please apply utilizing the interior profession web site out there on “Worker Central”. By doing so, your utility will probably be handled with precedence. Additionally, you will have the ability to see alternatives which can be open solely to Teva staff. Use the next hyperlink to go looking and apply: Inside Profession Website

The inner profession web site is obtainable from your house community as nicely. If in case you have bother accessing your EC account, please contact your native HR/IT accomplice.

Teva’s Equal Employment Alternative Dedication

Teva Prescribed drugs is dedicated to equal alternative in employment. It’s Teva’s international coverage that equal employment alternative be offered with out regard to age, race, creed, shade, faith, intercourse, incapacity, being pregnant, medical situation, sexual orientation, gender identification or expression, ancestry, veteran standing, nationwide or ethnic origin or another legally acknowledged standing entitled to safety beneath relevant legal guidelines. We’re dedicated to a various and inclusive office for all. If you’re contacted for a job alternative, please advise us of any lodging wanted to help you all through the recruitment and choice course of. All lodging info offered will probably be handled as confidential and used just for the aim of offering an accessible candidate expertise.

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