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Resident Engineer

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1 وظيفة شاغرة
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الخبرة

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1 - 1 سنوات

موقع الوظيفة

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دبي - الامارات

الراتب الشهري

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لم يكشف

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الجنسية

أي جنسية

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عدد الوظائف الشاغرة

1 وظيفة شاغرة

الوصف الوظيفي

رقم الوظيفة : 2267347

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.

Our goal is to skyrocket our clients success, and you can be a part of our team s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.

The Experience

With operations spanning the globe and featuring a multi-cultural team, PSC Biotech is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At PSC Biotech , it s about more than just a job it s about your career and your future.

Your Role
  • Responsible for supporting qualification activities associated with formulation equipment and processes.
  • This includes developing validation plans with minimum supervision, preparing protocols independently, performing executions, analyzing test results, and preparing summary reports.
  • Coordinates validation and execution activities with, and seeks team supports from, Validation, Development, Manufacturing, Engineering, Quality, third Parties, and other groups on validation projects to ensure validation projects are carried out on time and on budget.
  • Perform qualification data collection and analysis against acceptance criteria.
  • Perform documentation updates (SOPs, Forms, etc.).
  • Perform or conduct meeting attendance and project coordination.
  • Represents the department on cross-functional project teams.
  • Additional duties as assigned.


Requirements

  • Bachelor degree from accredited institution in Science or Engineering
  • 3-5 years of Pharmaceutical and/or Facilities Engineering experience
  • Strong experience with the commissioning and qualification of utilities
  • Experience in a pharmaceutical/manufacturing environment
  • Strong knowledge of cGMP guidelines
  • Experience with Protocol Writing and Execution
  • Excellent communication skills to effectively work with cross-functional teams for documentation review and approval.
    Experience with utilities (WFI, CDA, Pure Steam, AHU, etc) is a plus.
  • Excellent analytical and problem solving skills.
  • Willingness to travel is preferred.


Benefits

Offering a full suite of benefits, PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.


  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more.
  • 401(k) and 401(k) matching - PSC matches, dollar for dollar, employees investment into the 401(k) plan up to 6%.
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Discounted rate at Anytime Fitness
  • Financial Perks and Discounts


Annual Salary Range (dependent on experience) $84,200 - $88,900

Equal Opportunity Employment Statement:
PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in 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 of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant s, employee s, or intern s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

#LI-AS1

Bachelor degree from accredited institution in Science or Engineering 3-5 years of Pharmaceutical and/or Facilities Engineering experience Strong experience with the commissioning and qualification of utilities Experience in a pharmaceutical/manufacturing environment Strong knowledge of cGMP guidelines Experience with Protocol Writing and Execution Excellent communication skills to effectively work with cross-functional teams for documentation review and approval. Experience with utilities (WFI, CDA, Pure Steam, AHU, etc) is a plus. Excellent analytical and problem solving skills. Willingness to travel is preferred.

نوع التوظيف

دوام كامل

القسم / المجال المهني

الهندسة

المهارات المطلوبة

نبذة عن الشركة

الإبلاغ عن هذه الوظيفة
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