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Laboratory Supervisor - Finished & Stability Job - Puerto Rico  

Company managed [?] Still accepting applications

Posted on : 12 April 2017

Project Description

Laboratory Supervisor - Finished & Stability-QUA005719

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. 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.


This position is responsible for the supervision, technical support and testing coordination of the different duties on the Finished Product/Stability Laboratory. Is responsible for the training of the laboratory employees on Merck, LPO analytical techniques and regulatory rules applicable to the laboratory. Reports to the IPT Analytical Laboratory Lead. Responsible for the department in the absence of the IPT Analytical Laboratory Lead.

In addition, directly supervises employees in the Finished Product/Stability Laboratory Department. Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws.

The position is based in Merck Las Piedras and does not include relocation assistance.

Shifts within the following schedules: Monday to Wednesday: Second Shift, and Saturday and Sunday: First Shift.

Qualifications

Requirements:

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Bachelor degree in Natural Sciences with concentration in Chemistry.

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PR Chemist license, required.

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Minimum of five (5) years experience in an analytical laboratory.

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Must have ability to evaluate analytical results in order to determine possible failures and assure product purity, strength and quality.

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Computer skills, analytical abilities and analytical instrumentation knowledge a must.

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Extensive knowledge of cGMP’s and laboratory operations required.

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Must be fully bilingual (English and Spanish, oral and written).

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Explosive License, preferred.

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Able to work different shifts.

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 staffingaadar@merck.com.

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 Lab Related

Job Title:Mgr, Quality Control

Primary Location: NA-PR-East-Las Piedras

Employee Status: Regular

Travel: No

Number of Openings: 1

Shift (if applicable): Other (see Work Schedule)

Company Trade Name:MSD


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