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Merck & Co. Inc. Work Values
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Daily Duties at Merck & Co. Inc.:
Coordinate and manage all aspects of regulatory inspections by US FDA and international agencies. Manage responses to regulatory observations - coordinate review, and contribute as technical writer. Prepare other regulatory communications for FDA and international agencies as needed. Revise and maintain Site Master File per PIC/S guidance. Author and revise departmental SOPs. Review and approve regulatory commitments for Quality.
What they like about Merck & Co. Inc.:
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
Quality Assurance, Specialist, Pharmaceutical, Laboratory, Supervisor, Documentation, Coordinator, SAP, Documentum, Microsoft Office, Audits, Regulatory, Compliance, cGMP, PIC/S, ICH, ISO, Stability
Information about Merck & Co. Inc.
Company Rank: Not Available
Average length of employment : 16 years
Average salary of employees: $57,500
These are some of the questions we asked our climbers about their experiences with Merck & Co. Inc.:
05| | ||
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 |
Climbers who worked at Merck & Co. Inc. had these interests:
Books | |
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Gaia's Garden |
Home-scale Permaculture |
This Organic Life |
Organic Gardening & Food Sustainability |
Websites | |
PIC/S http://www.picscheme.org/ |
Pharmaceutical Inspection Cooperation Scheme |
FDA http://www.fda.gov |
FDA home page |
ICH http://ICH.org |
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use |
EMA http://www.ema.europa.eu/ema/ |
Eurpean Medicines Agency home page |
