Scientist - Vaccines BPR&D Clinical Supplies - Training & Critical Documentation Job

Scientist - Vaccines BPR&D Clinical Supplies - Training & Critical Documentation-BIO004951

Description

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases.

Applications are being sought for a Training and Critical Documentation Scientist position in the Merck Research Laboratories GxP Systems Group supporting Bioprocess Clinical Supplies. The individual will support pilot-scale campaigns for the GMP manufacture of bulk biologic (vaccines and therapeutic proteins) clinical supplies.

Responsibilities include:

- Coordinate and maintain SOP review and approval process

- Administering various functions within the Learning Management System (LMS)

- Working with Subject Matter Experts, develop training requirements for Standard Operating Procedures, Analytical Procedures and other training material

- Manage and facilitate instructor-led and self-paced training curricula

- Assist Area Campaign Leads with preparing GMP campaign readiness documents as they pertain to training and campaign preparedness

- Deliver New Employee Orientation training

- Manage templates for SOPs and supporting SOP documents

Qualifications

Education:

- Bachelor of Science or equivalent degree in a related field.

Required

- At least three years of experience working with cGMPs

- Working knowledge of cGMP requirements

- Demonstrated ability to manage multiple tasks and priorities

- Effective verbal and written communication skills

Preferred:

- Strong communication, interpersonal, and organizational skills, including time management.

- Candidate must have the ability to work independently and in a team environment.

Your role at Merck 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 Merck, 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:

Merck & Co., Inc. 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 Merck 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 Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

For more information about personal rights under Equal Employment Opportunity, visit:

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Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.


Job: Biological Manuf-Pilot Plant

Job Title:Scientist, Biologics Pre Manf

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Number of Openings: 1

Company Trade Name:Merck