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    radio officer - Doha, دولة قطر - RIGZONE PETROLEUM COMPANY

    RIGZONE PETROLEUM COMPANY
    RIGZONE PETROLEUM COMPANY Doha, دولة قطر

    منذ أسبوع

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    وصف
    PSCBiotech provides the life sciences with essential services toensure that health care products are developed, manufactured, anddistributed to the highest standards, in compliance with allapplicable regulatory requirements.

    Ourgoal is to skyrocket our clients success, and you can be a part ofour team s achievements. Employing a global team of skilledprofessionals and experts that span across strategically locatedoffices in North America, Europe, Asia and the Middle East, we areproud of the roles we have fulfilled to help our clients achievesuccess.

    TheExperience

    Withoperations spanning the globe and featuring a multi-cultural team,PSC Biotech is passionate about bringing the best and brightesttogether in an effort to form something truly special. When youmake the decision to join our team, you will be offered the abilityto feel inspired in your career, explore your professionalpassions, and work alongside a group of people who will value andnurture yourtalents.

    Weare firm believers in coaching and developing the next generationof industry leaders and influencers. As such, you will not only beoffered compensation and benefits structure that rewards you, butalso be provided with the tools that will help you grow andlearn.

    AtPSC Biotech , it s about more than just a job it s about yourcareer and yourfuture.

    YourRole
    • Leadthe coordination for required quality events - responsible for thedesign history file remediation project for specific medicaldevice.
    • Responsiblefor writing, analyzing, and executing quality requirements whileverifying, validating, and making relevant changes to currentdesign requirements.
    • Supportall backlog and remediationtasks.
    • Makeappropriate updates to current procedures andspecifications.
    • Designquality standards and control systems (inspect materials,equipment, processes) and determine corrective actions/solutions.
    • Analyzequality performance and determine any foreseeable risks andimplement process improvement.
    • Ensurethat processes and specifications comply with required qualitystandards and regulations.
    • Otherduties asassigned.


    Requirements

    • Collegedegree in engineering or related sciences (medical device, design,quality, etc.)
    • 7-10years of experience in the medical device industry with a strongbackground in design verification and design validation.
    • Extensiveexperience writing design qualityrequirements.
    • Advancedunderstanding of regulatory requirements regarding designquality.
    • Knoweldgeof risk management and corrective action.
    • Experiencewith various quality management systems.
    • Strongknowledge of risk analysis tools.
    • Excellentattention to detail and problem-solvingskills.
    • Goaloriented and task driven.
    • Abilityand willingness to travel is preferred.


    Benefits

    Offeringa full suite of benefits, PSC Biotech is firmly focused ondiligently investing in our employees who enable our company tofulfill our mission and achieve success. We want to promotebalance, so you not only enjoy your work, but also have the timeand resources to live your life happy and healthy.

    Medical,Dental, and Vision - PSC pays 100% of all qualifying employeemedical premiums and 50% for qualifyingdependents
    Insuranceoptions for Employee Assistance Programs, Basic Life Insurance,Short/Long Term Disability andmore.
    401(k)and 401(k)matching
    PTO,Sick Time, and PaidHolidays
    EducationAssistance
    PetInsurance
    Discountedrate at AnytimeFitness
    FinancialPerks andDiscounts

    AnnualSalary Range (dependent on experience)$109,000-$173,000

    EqualOpportunity EmploymentStatement:
    PSCis committed to is committed to a policy of Equal EmploymentOpportunity with respect to all employees, interns, and applicantsfor employment. Consistent with this commitment, our policy is tocomply with all applicable federal, state and local laws concerningemployment discrimination. Accordingly, the Company prohibitsdiscrimination against qualified employees, interns and applicantsin all aspects of employment including, but not limited to:recruitment, interviewing, hiring (or failure or refusal to hire),evaluation, compensation, promotion, job assignment, transfer,demotion, training, leaves of absence, layoff, benefits, use offacilities, working conditions, termination and employer-sponsoredactivities and programs, including wellness, social andrecreational programs. Employment decisions will be made withoutregard to an applicant s, employee s, or intern s actual orperceived: race, color, religion, sex (including pregnancy, genderidentity, and sexual orientation), national origin, age (40 orolder), disability, genetic information, or any other statusprotected bylaw.

    #LI-TW1

    Minimum requirement College Degree with Science background.Extensive experience writing design quality requirements.Verifying, validating, and changing design requirements. Goodunderstanding of regulatory requirements around design quality. Hasquality management system experience. Task-driven and has a"go-getter" personality.
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