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Stability Senior Specialist Job - United States  

MSD (company)

Posted on : 16 April 2017

Project Description

Stability Senior Specialist-QUA005690


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. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

Responsible for supervising the development and implementation of stability protocols, evaluation of stability data, and investigation of atypical and out of specification stability results, primarily for an immuno-oncology biological product. Manages the activities of the Stability Unit personnel in the execution of day-to-day responsibilities consistent with the department’s requirements and objectives. Maintains clear and effective communication with internal and external customers, participates in cross-functional teams related to stability issues for products, methods, and/or procedures, and represents stability on site and divisional initiatives. Maintains forward thinking attitude for constant improvements to increase efficiencies within the department.



- B.S., M.S., or Ph.D. in chemistry, biological science, pharmacy or related science or engineering field.

Required :

- Minimum 5 years of experience in a laboratory, technical services, and/or quality analyst position with leadership responsibilities.

- Demonstrated effective leadership and communication, interpersonal and negotiating skills, and advanced knowledge of analytical and/or statistical methods as well as GMP Compliance.

Preferred :

- Experience supporting the stability program of a global product with various manufacturing and testing locations.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. If you need an accommodation for the application process please email us at

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.

Visa sponsorship is not available for this position.

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

EEOC Poster

EEOC GINA Supplement​

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

Job: Quality Operations

Job Title:Sr. Spclst, Quality

Primary Location: NA-US-PA-West Point

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): N/A

Company Trade Name:Merck

Nearest Major Market: Philadelphia

Job Segment: Oncology, Engineer, Pharmacy, Laboratory, Animal Health, Healthcare, Engineering, Science, Veterinary