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Qs Pharma Work Values
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Daily Duties at Qs Pharma:
All Validation documentation (including computer validation documents), change controls, calibrations, utility monitoring, and all construction, expansion and renovation projects.
What they like about Qs Pharma:
Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.
Tags
Validation, Commissioing, Engineering, Computer Validation, Cleaning Validation, Change controls, 21CFR Part 11 Compliance, Clean rooms, Controlled environments, Construction Management
Skills
Writing IQ/OQ/PQ Protocols, Reviewing IQ/OQ/PQ Protocols, Personel Supervision, Temperature and humidity Mapping, Writing and Reviewing Master Validation Plans, 21 CFR Part 11 Compliance, Construction Management, Design of Pharmaceutical Manufacturing Areas, Utility Monitoring, Managing Calibration Program, Managing Change Control Program, Managing an Equipment/Facility cleaning program
Information about Qs Pharma
Company Rank: Not Available
Average length of employment : 11 years
Average salary of employees: $130,000
These are some of the questions we asked our climbers about their experiences with Qs Pharma:
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| Were your performance expectations clearly communicated? | 0.0 |
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| Were you recognized for meeting or exceeding expectations? | 0.0 |
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| Did you feel like your personal contribution was important? | 0.0 |
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| Was your career path clearly outlined and discussed? | 0.0 |
| 03| | ||
| I would recommend this as a place of employment. | 0.0 | |
| I believe in the purpose of this organization. | 0.0 | |
| I would work for this organization again. | 0.0 | |
| I feel employees are fairly compensated. | 0.0 |
