Hiring Company: Merck
Location: Elkton,
Virginia
Job Type: Full Time
Salary: Not Specified
Experience Desired: 3 - 5 Years
Last Update: Jul 19, 2018 11:56:42 AM
Full Job Description:
Responsibilities:
• Position carries out a variety of activities covering the various shifts to support 24/7 operations becoming familiar with site processes, procedures, and policies assuring alignment with cGMPs (current Good Manufacturing Processes) and Health Authority regulations.
• Conducts batch record reviews, audits, investigations, and helps with internal audits / external inspections.
• Supports sampling requirements for several areas.
• Performs quarantine functions and accountability reviews.
• Supports special projects as assigned.
• Follow cGMP and routinely makes decisions using cGMP/process knowledge.
• Works with customers to resolve problems and to satisfy quality and production needs.
• Performs regulatory document reviews and prepare regulatory or other required documents per local and divisional guidance.
• Follows site safety requirements.
• Authors, reviews, and or approves data and documents such as methods, procedures, and protocols.
• Completes assigned projects.
• Performs all work in a timely manner and is an active member of 1 or more teams.
• Tracks/reports metrics.
Qualifications
Minimum Requirements:
• Bachelor's degree in a Scientific discipline (biology, engineering, or other science)
• 2 years experience in pharmaceutical industry or quality assurance/control
• Must be willing to work a rotating shift including nights and weekends
Preferred Experience and Skills:
• Demonstrated verbal/written communication and decision making skills
• Experience with GMP/compliance requirements for food or pharmaceutical industry; technical writing skills; understanding of computer system SAP and Office products; basic statistical understanding
Your role at our Manufacturing division is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At our Manufacturing division, we’re inventing for life.
If you need an accommodation for the application process please email us at staffingaadar@merck.com.
Search Firm Representatives Please Read Carefully:
Our Manufacturing division is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at our Manufacturing division via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of our Manufacturing division. No fee will be paid in the event the candidate is hired by our Manufacturing division as a result of the referral or through other means.
Visa sponsorship is not available for this position.
Apply online at:
https://jobs.merck.com/job/Elkton-Specialist%2C-Quality-Assurance-VA-22827/445950900/
Company Type: Direct Employer
Contact Name : Sharie Pace
Contact Phone: (None)
Contact Email : (None)
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