איש/אשת צוות הכנות | ייצור סטרילי at Teva Pharmaceutical Industries Ltd. - Israel

Kfar Saba, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

29 Jun, 26

Salary

0.0

Posted On

31 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Compliance, Process Supervision, Production Operations, Equipment Operation, Troubleshooting, Documentation Control, Data Integrity, Team Coordination, On-the-Job Training, Aseptic Preparation, Sterile Manufacturing, Analytical Instrumentation, Technical Problem Solving, Attention To Detail, Learning Agility, Organizational Skills

Industry

Pharmaceutical Manufacturing

Description

Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.The opportunity Accountable for the supervision of the production process and the relevant team in a specific medium-sized production or packaging area during the shift Areas of Impact: Production/packaging process Performs operations related to the production of single and multi-component preparations, in compliance with the prescribed procedures with the principles of GMP. Advanced operation, assembly and adjustment of simpler and more complex production equipment, device parameters setting. Deputy of supervisor in time of absence. Job Aspect: 1. Performs the full range of established procedures such as: operating machines and manipulation with material, producing and checks on daily basis necessary documentation in line with data integrity and GMP, monitoring processes in scope, keep stock adherence 2. Monitors processes parameters to ensure compliance and eliminate deviations, Coordination of production processes 3. Resolves routine issues - trouble shooting and monitors such activities for other colleagues 4. Has developed expertise, typically through a combination of job related training and considerable on-the-job experience 5. Typically acts as a lead, coordinating the work of others, but is not a supervisor (may act as supervisor deputy in time of absence) 6. Performs regular operational controls of production lines 7. Foreman - is responsible for work organization on operational basis; in case of supervisor absence performs shift handover, tracks relevant shift records, observe technology / GMP/ EHS compliance at work place 8. Provide on-the.job training to other operators 9. Works autonomously within established procedures and practices 10. Has developed a specialized level of skill to perform assigned tasks Responsibility for checking the documentation of the product series in terms of completeness of entries, confirming the compliance of the production process with the requirements of acting country law, EU law, GMP, HACCP requirements and the applicable internal documentation of the Company ; 11. Proper operation and taking care of the technical condition, immediate reporting of defects; Ongoing informing the supervisor about the progress of tasks and possible difficulties in their performance. Immediate notification of any irregularities and abuse to the detriment of the Company and events that may affect the quality of the product Competencies: Ability to follow process and procedures Attention to detail, Learning Agility, Collaboration and Communications skills, Organizational skills Basic training skills (educate and mentor other operators), GMP knowledge on the proper level Digital awareness, excellence in action, adaptation to change, good organization of own work, ability to work under time pressure Capabilities / Technical Skills: As per skills matrix per site process Areas of focus: assembly, washing processes, documentation, work with control systems (MES etc.), IPC controls,manipulation with material, stock adherence, OEE principles, GMP/EHS/FP/SOPs alignment, clean work place, daily work organization, training skills Qualifications / Trainings: GMP certification Quality / work procedures trainings EHS qualifications IT systems qualifications upon required levelHow you’ll spend your day התפקיד כולל: • הכנת פורמולציות לתרופות הסטריליות של טבע • הכנת ציוד לייצור (שטיפה ועיקור) • עבודה עם מכשור אנליטי • תפעול וביצוע תהליכים מורכבים במתקן ייצור GMP • מתן פתרונות טכניים ומקצועיים ותפעול שגרתי לתהליכי הכנה אספטיים עם רמת מורכבות גבוהה • עבודה עם ציוד אוטומטי וידני, מערכות ומכשור אנליטי מגוון ומתקדם, עבודה על פי שיטות ונהלי עבודה • עבודה מול ממשקים, גורמים טכניים ולוגיסטיים Your experience and qualifications הנדסאי/ת מכונות/אלקטרוניקה/כימיה/מדעים/ביוטכנולוגיה – חובה ניסיון בעבודה בסביבה סטרילית – יתרון ניסיון בעבודה בסביבת פארמצבטית – יתרון בעל/ת רקע טכני - יתרון משמעותי יכולת קריאה וכתיבה באנגלית ובעברית נכונות לעבודה בשלוש משמרות רמת דיוק גבוהה מוטיבציה ללמוד ולהתפתח Reports To In process of validationAlready 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. 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.

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Responsibilities

This role involves supervising the production and packaging team within a specific area during a shift, ensuring compliance with GMP procedures while performing operations for single and multi-component sterile drug preparations. Responsibilities include advanced operation and adjustment of production equipment, monitoring process parameters, and resolving routine technical issues.