• QA quality assurance manager for the pharmaceutical field
    Posted 15 hours ago

    Hot job
    Company Name: Placement achievements with results
  •   Experience: 3-4 years
  •  Location: Lod, intelligence, Petah Tikva, Rehovot, Ramla  Job type: Full-time

    Overview

    Responsible for quality assurance in a company dealing with the logistics of clinical studies. the role ...
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    Overview

    Responsible for quality assurance in a company dealing with the logistics of clinical studies. The position includes conducting investigations, handling customer complaints and following up on CAPA and validation, mapping and calibration, following up on procedures and conducting trainings Mon-Thurs 8-17 without Fridays, promotion options and a pleasant and family atmosphere

    Salary 18k

    Job requirements

    Education in the field of quality assurance / previous experience Excellent familiarity and significant experience working with Ministry of Health procedures and GMP, GDP guidelines Very high level English , very high drafting ability in English and Hebrew, ability to motivate and promote tasks, knowledge of writing and updating procedures


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    Job No. 265192

  • 1349-Quality auditor needed
    Posted 3 days ago

    Company Name: HandR
     Location: The north, Northern District, Haifa District, Nahariya, Acre  Job type: Full-time

    Overview

    Requirements for the auditor for integration:
    Reading blueprints and using measuring tools
    ...
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    Overview

    Requirements for the auditor for integration:
    Reading blueprints and using measuring tools
    Preparation of FAI

    Job requirements

    Good English
    At least two years of experience
    Availability to work 7:30-16:45 and overtime until 18:45
    Fridays and holiday evenings 7:30-12:00

    The position is for both men and women


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    Job No. 266469

  • Company Name: HandR
     Location: Or Akiva, Hod Hasharon, Hadera, Central District, Netanya  Job type: Full-time

    Overview

    Overview of the role-
    As a factory quality assurance manager, the responsibility...
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    Overview

    Overview of the role-
    As a factory quality assurance manager, your primary responsibility is to ensure that all products meet or exceed quality standards and regulatory requirements. You will be responsible for developing and implementing quality management systems, leading quality improvement initiatives, and overseeing any quality assurance process. Your role is essential in maintaining the safety, efficiency and reliability of the products manufactured in the factory.

    Key responsibilities:

    1. Development and implementation of quality management systems:
    - Establish and maintain a comprehensive quality management system in accordance with the relevant regulations and standards in the industry (for example,
    ISO 13485/ ISO 22716).
    - Plan and implement policies, procedures and quality guidelines to ensure compliance with regulatory requirements and best practices.
    – Defining key performance indicators (KPI) and metrics to evaluate and monitor the effectiveness of quality processes.

    2. Leading quality assurance processes:
    - Establish and maintain quality assurance procedures to ensure compliance with product specifications, quality standards and regulatory requirements.
    - Develop and enforce quality control measures, including test techniques, sampling procedures and test protocols.
    - Conduct internal audits to identify areas for improvement and take corrective actions to address non-conformances.

    3. Compliance with regulations:
    – Stay up-to-date with the latest regulations, standards and guidelines applicable to the production of the company's products (eg, CE, etc.).
    - Ensure compliance with regulatory requirements throughout the entire production process, including design control, documentation, labeling and packaging.
    - Prepare and coordinate external audits and inspections from regulatory agencies or notified bodies.

    4. Quality improvement initiatives:
    - Identifying opportunities to improve processes, reduce costs and improve quality.
    - Lead cross-functional teams in root cause analysis investigations and implementation of corrective and preventive actions (CAPAs).
    - Foster a culture of continuous improvement by providing training and support to employees on issues related to quality.

    5. Supplier management:
    - Collaboration with the procurement department to evaluate and select suppliers based on their quality management capabilities.
    - Establish quality agreements with suppliers and perform audits to ensure compliance with quality standards.
    - Monitor and evaluate supplier performance, address any quality issues immediately.

    6. Training and documentation:
    – Develop and deliver training programs on quality assurance principles, regulatory requirements and Good Manufacturing Practices (GMP).
    - Keep comprehensive documentation of quality processes, procedures and records, while ensuring accuracy and traceability.

    Job requirements

    Qualifications and requirements:

    - Bachelor's degree in engineering, life sciences or a related field. Master's degree is an advantage.
    - Extensive experience (usually 5+ years) in quality assurance, preferably in the pharmaceutical or toiletries industry.
    - In-depth knowledge of quality management systems, regulatory requirements (such as FDA, ISO 13485/ ISO 22716) and relevant industry standards.
    - Strong understanding of manufacturing processes, quality control methods, and statistical techniques.
    - Experience in leading cross-functional teams and implementing quality improvement initiatives.
    - Excellent problem solving skills and ability to perform root cause analysis and implement corrective actions.
    - Strong organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.
    - Excellent communication skills, both written and oral, with the ability to communicate effectively with employees at all levels of the organization.
    - Attention to details and commitment to maintaining high quality standards.
    - Professional certifications in quality management (eg, certified quality manager, certified quality auditor) are highly desirable.

    The position is intended for both men and women!


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    Job No. 266462

  • Company Name: HandR
     Location: Or Akiva, Hod Hasharon, Hadera, Netanya, Ramat Hasharon  Job type: Full-time

    Overview

    To Cosmopharm, a proud Israeli industry, one of the leading manufacturing companies in the country To view the job details 

    Overview

    To Cosmopharm, a proud Israeli industry, one of the leading manufacturing companies in the country
    In the field of cosmetics, toiletries and medicinal products, our factory needs:
    Quality auditor.
    job description:
    • Performing quality control according to standards, specifications and work procedures.
    • Release of packaging materials for work according to test specifications
    • Performing an inspection and approving the opening of a workstation; Filling and packaging lines.
    • Performing in-process tests for products in filling lines according to specifications (in process control
    • Documentation of results in computer systems
    • Be part of the quality assurance team at the factory.

    Job requirements

    Requirements:
    • Relevant education in the field of quality control - an advantage
    • Industry experience - mandatory
    and ISO 9001 • Background and work experience in accordance with GMP rules
    • Motivation to succeed, prevent errors and bring the department to a high level.
    • Broad understanding of the quality policy.
    • Service approach and work in cooperation with colleagues and employees.
    • critical thinking
    • Languages: Hebrew - mandatory
    English - good level
    In particular Excel - and Office - • Understanding of computer programs
    Advantage -Priority • Knowledge and experience in software
    • Ability to work in a team, big head, assertiveness, raising a flag and driving processes.
    • Willingness to work shifts
    Work in the Emek Hafer industrial area
    *This position applies to both women and men


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    Job No. 266461

  •  Location: Southern Region  Job type: Full-time

    Overview

    1. Education - at least a bachelor's degree in biotechnology / pharmacy / chemistry / science...
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    Overview

    1. Education - at least a bachelor's degree in biotechnology / pharmacy / chemistry / life sciences / chemical engineering / pharmaceutical engineering - mandatory
    2. Experience in quality assurance in a pharmaceutical company
    3. Order and organization skills, punctuality, "big head", excellent human relations, ability to work with interfaces.
    4. Controlling OFFICE
    5. Experience and knowledge of working with Adobe reader
    6. English at a very high level

    * Job # 270055 is for men and women alike

    Job requirements

    A pharmaceutical company needs a technical reporter.
    Job Summary:
    1. Writing procedures, quality documents, organizational quality policy documents and risk assessments
    2. Preparation of quality contracts with service providers, suppliers and subcontractors
    3. Support in writing summaries of investigations and anomalies
    4. Writing annual quality summaries for BTG products
    5. Reviewing the Guidelines of the regulatory bodies concerning the pharmaceutical industry and implementing their requirements in the organization

    י


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    Job No. 266349

  • Company Name: Adam-Mazor placement services
  •   Experience: 1-2 years
  •  Location: Hod Hasharon, Hadera, Kfar Saba, Netanya, Petah Tikva, Ra'anana  Job type: Full-time

    Overview

    A leading company in the food sector from the Netanya area needs a quality auditor.

    B...
    To view the job details 

    Overview

    A leading company in the food sector from the Netanya area needs a quality auditor.

    As part of the job:

    Accompanying and controlling processes, updating and implementing procedures and work instructions.
    Carrying out sampling training and control of microbial and chemical tests.
    Working with suppliers, performing quality checks, preventing and analyzing non-quality events.
    Finding solutions for faults that arise in production and leading corrective actions and improvement processes, etc.

    We suggest:
    - Direct absorption into the company starting from the first day.
    – Round trip transportation.
    – A dining room that provides subsidized meals.
    - 30% employee discount in chain stores.

    - "A bank account for the company's employee" (after a year) in which a sum of money is deposited by the employer and thus you can buy the chain's products free of charge.
    - High-quality and advanced work environment.
    - Long-term employment stability.
    – A variety of promotion options.

    Job requirements

    Experience as a quality auditor in a food/pharma factory - a significant advantage.
    ability to drive processes, assertiveness,
    - Attention to detail and thoroughness, patience and good human relations. Ability to work independently and under pressure.

    Tagged as: , ,


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    Job No. 266024

  • Company Name: Adam-Mazor placement services
  •   Experience: 5-6 years
  •  Location: Hod Hasharon, Hadera, Kfar Saba, Netanya, Petah Tikva, Ra'anana  Job type: Full-time

    Overview

    For a large and high-quality high-tech company in the field of multi-system technology development...
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    Overview

    A large and high-quality high-tech company in the field of multi-system technology development for high-tech companies, automobiles, consumer products and more needs an experienced quality controller for a permanent long-term job:

    As part of the job:
    - Performing quality audits for items and assemblies at the suppliers or in the company and producing reports.
    - Auditing the supplier's subcontractors as needed
    - Performing audits in the process and producing reports
    - Performing an ATP audit at the supplier according to documented test plans and producing reports
    - Opening a complaint for an abnormal product and placing it in quarantine.
    We suggest:
    - Direct absorption to a leading company in the economy.
    - A high-quality long-term job with a variety of promotion and growth options.
    – Subsidized meals.
    - Solid employment stability.
    - Adequate salary and conditions!

    Job requirements

    - At least 5 years of experience as a quality auditor
    - Knowledge and experience in reading mechanical drawings
    - Extensive knowledge and experience in all measuring tools required at work
    - Ability to organize and order, attention to details
    - Good human relations and willingness to work as a team
    - Hebrew and English at a high level
    - Good familiarity with Office software, priority
    - Familiarity with SolidWorks software - an advantage
    - Driver's license - mandatory!
    - PT and the seats in the vicinity or self-arrival - a must!

    Tagged as: , , , ,


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    Job No. 266026

  • Company Name: Tal Hel Yaske
  •   Experience: inexperienced
  •  Location: Ashdod, Ashkelon, Yavne, Lod, Qiryat Gat, Kiryat Malachi  Job type: Full-time

    Overview

    A quality inspector is needed for a food factory in Be'er Tovia.
    Possible without miracles...
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    Overview

    A quality inspector is needed for a food factory in Be'er Tovia.
    Possible without experience - with a desire to learn.

    Filling and handling of forms and supervision of the production departments, responsibility for product integrity, dealing with the quality assurance manager.
    The job is full time
    Excellent conditions for suitable candidates.

    Job requirements

    Responsibility, ability to work in a stressful environment and meet goals.
    The position is intended for both women and men.

    Tagged as: ,


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    Job No. 242991

  •  Location: Haifa, Haifa District  Job type: Full-time

    Overview

    A leading global company, in the Haifa area, is looking for an expert consultant with a deep understanding...
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    Overview

    A leading global company, in the Haifa area, is looking for an expert consultant with a deep understanding of hazardous materials and environmental quality regulation for a significant position with responsibility for the management of the HMS system, including storage and transportation.
    The position combines field and office.

    As part of the job:
    • Strategic leadership for environmental quality and safety and implementation of plans and work routines while complying with internal and external inspections in accordance with the requirements of the law and environmental regulation and the 14001ISO standard, preparation of inspection and control reports.
    • Working with relevant regulatory bodies.
    • Carrying out trainings in the fields of environmental quality and implementing management routines.
    • Participation in meetings, tours with clients and regulatory representatives.

    Requirements:
    Bachelor's degree in the fields of environmental quality / chemistry / other relevant
    4+ years of experience in managing environmental regulation and hazardous materials.
    Proven experience in leading safety / environmental quality systems and working with authorities. (planners, authorities and consulting companies).
    Ability to motivate people and charisma
    Readiness for combined field and office work.
    * Job # 279050 is for men and women alike


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    Job No. 265157

  • Company Name: LR - JOB
     Location: Or Akiva, The north, Hadera, Yokneam Illith, Haifa District  Job type: Full-time

    Overview

    Role includes:
    Weighing of raw materials, sampling of raw materials
    To view the job details 

    Overview

    Role includes:
    Weighing of raw materials, sampling of raw materials
    Receiving and issuing raw materials and packaging.
    Contact with internal and external parties
    Work according to exact procedures.
    Maintaining order and cleanliness in warehouses
    Working in front of a computer - receiving materials, issuing certificates, etc.

    Job requirements

     

    Education: full matriculation preferred for an engineer 
    Experience in a GMP environment / orderly work environment with rules

    and defined and precise work procedures

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    Job No. 208481

  •  Location: Hod Hasharon, Herzliya, Kfar Saba, Ra'anana  Job type: Full-time

    Overview

    A regulatory manager is needed for an interesting and leading medical company in its field.

    ...
    To view the job details 

    Overview

    A regulatory manager is needed for an interesting and leading medical company in its field.

    As part of the job:
    Leading the regulatory field in the development and implementation of regulatory strategies to support the approval of the company's products in the US and European Union markets.
    Testing and preparation of regulatory submissions, including 510(k), IDE and CE submissions.
    Preparation of technical files, ensuring completeness, accuracy and compliance with regulatory requirements.
    Ongoing collaboration and interfaces with R&D, Quality Assurance, Clinical Affairs and other departments to ensure regulatory requirements are integrated into product development processes.
    Provide regulatory guidance and support to internal stakeholders on product-related issues: development, labeling, advertising and market surveillance.
    Regular updates on changes in FDA and EU regulations, industry guidelines and trends, and communicating possible impacts on the organization.
    Managing interactions with regulatory agencies, including responding to inquiries, preparing for meetings, and leading inspections and audits.

    Requirements:
    Bachelor's degree in a scientific or engineering field - advanced degree preferred.
    At least 10 years of experience in regulatory affairs in the medical device industry.
    Proven expertise in FDA and CE regulatory submissions, including 510(k), IDE and CE Technical File
    High familiarity with medical device regulations in the USA and the European Union, including FDA regulations (21 parts CFR
    800-1299) and the EU Medical Device Regulation (MDR).
    Proven track record of successful interactions with regulatory agencies, including the FDA and aligned entities.
    Excellent communication, negotiation and interpersonal skills.
    Regulatory Affairs Certification (RAC) - an advantage.
    * Job # 276658 is for men and women alike


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    Job No. 264718

  •  Location: Netanya  Job type: Full-time

    Overview

    For a leading energy company, a quality safety engineer is needed for the Netanya area,
    ...
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    Overview

    For a leading energy company, a quality safety engineer is needed for the Netanya area,
    As part of the job -
    1. Managing a quality assurance system.
    2. Training and development of professional knowledge in the company (training programs, information sheets, etc.).
    3. Maintaining contact with the institutions responsible for the gas industry and distributing instructions in accordance with those established by the above-mentioned institutions: the Standards Institute, the Oil Institute, the Association of Manufacturers.
    4. Answering technical questions from the field (for technicians and engineers).
    5. Representing the company in front of the gas manager (audits, complaints, etc.).
    6. Investigating events and drawing lessons.
    7. Editing technical work procedures and safety procedures
    8. Management of field audits, audits in branches, agencies, contractors. Matrix management of the company's engineers in this field.
    9. Follow-up of reviews and drawing lessons in the company.
    10. Management and participation in the company's safety committees.
    11. Participation in safety committees of other facilities in the company.
    12. Participation and safety exercises in the company's facilities.
    13. Preparation of professional and technical conferences.
    14. Leading and supervising the field of safety in the company's projects.
    15. Additional duties to be assigned from time to time by the superiors.

    Requirements -
    1. Proven experience of two years as a safety supervisor - mandatory.
    2. Education - degree in engineering (fields: mechanical, chemical, agricultural and aeronautics) / or an engineer with 4 years of experience - + certified safety officer - mandatory.
    3. Previous experience in an energy company - an advantage.
    * Job # 272070 is for men and women alike


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    Job No. 264384

  •  Location: Migdal Haemek  Job type: Full-time

    Overview

    For a manufacturing plant in the Migdal HaEmek area, a quality leader is needed,
    As part of the production ...
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    Overview

    For a manufacturing plant in the Migdal HaEmek area, a quality leader is needed,
    As part of the job -
    Presentation of quality plans and indicators for improvement (inside plants and in front of the customer)
    -Handling customer complaints (investigation and prevention for the future)
    - Collection and concentration of quality data and production of reports
    -Implementation of work practices
    - Performing tests
    - Investigation of supplier failures

     

    Job requirements

    Engineers/Industrial and Management Engineers/Electronics/Mechanics,
    High command of English
    There is a standard without experience - but with an affinity to the field of quality
    There is a standard with experience - 2-4 years of experience - mandatory in the field of quality (quality leader / quality engineer and more)
    * Job # 272032 is for men and women alike


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    Job No. 263863

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