Associate Principal Scientist - Residue Chemist Job
- Employer
- Merck
- Location
- Madison NJ
- Closing date
- Jun 21, 2017
View more
- Sector
- Science, Physical Sciences and Engineering, Chemistry, Biochemistry, Veterinary Medicine, Law
- Organization Type
- Corporate
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Job Details
Associate Principal Scientist - Residue Chemist-PHA001379
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 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
Merck’s Animal Health (MAH) division works to improve the health of animals around the world through collaborative partnerships and a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. This team of energetic, independent thinkers offers one of the industry’s most innovative portfolios of products, services, and technologies that serve to prevent, treat, and control diseases across all major farm and companion animal species both domestically and internationally.
The candidate should be knowledgeable in the conduct of residue, metabolism and bioanalytical studies to support veterinary drug development in food producing animals. Specific roles and tasks include, but are not limited to, study director, study monitor, study design, the preparation and the review of study protocols, study data, final reports, and responses to questions from regualtory agencies.
Qualifications
Education Minimum Requirement:
- Ph.D with at least two years of experience in analytical chemistry, biochemistry, or a closely-related discipline
Required Experience and Skills:
- Knowledge of US-FDA and EU-CVMP guidelines on veterinary drug development for food producing animals
- Knowledge in conducting residue chemistry, metabolism and bioanalytical studies to support domestic and international registration of pharmaceuticals in food producing animals
- Familiarity with guidelines that govern the use of animals to conduct residue studies
- Experience with quantitative and/or qualitative chromatographic techniques, in particular LC-MS/MS, HPLC-UV/VIS/FL and computerized automation of laboratory equipment as it pertains to residue chemistry and bioanalytical studies
- Knowledge of Good Laboratory Practice (GLP) regulations and regulations on electronic records
- Proficient in written communications and in the preparation of study documents for submission to regulatory agencies
- Excellent verbal communication and presentation skills required; team player required to represent the group in internal meetings, in meetings with regulatory officials and in scientific meetings
- Working knowledge of standard computer software applications for general office work use and for laboratory equipment
- Domestic travel required
Preferred Experience and Skills:
- Experience with US-FDA and EU-CVMP guidelines for conducting metabolism and residue chemistry studies for veterinary pharmaceuticals in food producing animals
- Experience with conducting and supervising method validation, residue depletion and pharmacokinetics studies to support drug development for food producing animals
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.
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: Pharmacokinetics/Drug Metab
Job Title:Assoc Prin. Scientist, Pharmacokinetics
Primary Location: NA-US-NJ-Madison
Employee Status: Regular
Travel: Yes, 10 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Company Trade Name:Merck
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 125-year legacy. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
Merck’s Animal Health (MAH) division works to improve the health of animals around the world through collaborative partnerships and a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. This team of energetic, independent thinkers offers one of the industry’s most innovative portfolios of products, services, and technologies that serve to prevent, treat, and control diseases across all major farm and companion animal species both domestically and internationally.
The candidate should be knowledgeable in the conduct of residue, metabolism and bioanalytical studies to support veterinary drug development in food producing animals. Specific roles and tasks include, but are not limited to, study director, study monitor, study design, the preparation and the review of study protocols, study data, final reports, and responses to questions from regualtory agencies.
Qualifications
Education Minimum Requirement:
- Ph.D with at least two years of experience in analytical chemistry, biochemistry, or a closely-related discipline
Required Experience and Skills:
- Knowledge of US-FDA and EU-CVMP guidelines on veterinary drug development for food producing animals
- Knowledge in conducting residue chemistry, metabolism and bioanalytical studies to support domestic and international registration of pharmaceuticals in food producing animals
- Familiarity with guidelines that govern the use of animals to conduct residue studies
- Experience with quantitative and/or qualitative chromatographic techniques, in particular LC-MS/MS, HPLC-UV/VIS/FL and computerized automation of laboratory equipment as it pertains to residue chemistry and bioanalytical studies
- Knowledge of Good Laboratory Practice (GLP) regulations and regulations on electronic records
- Proficient in written communications and in the preparation of study documents for submission to regulatory agencies
- Excellent verbal communication and presentation skills required; team player required to represent the group in internal meetings, in meetings with regulatory officials and in scientific meetings
- Working knowledge of standard computer software applications for general office work use and for laboratory equipment
- Domestic travel required
Preferred Experience and Skills:
- Experience with US-FDA and EU-CVMP guidelines for conducting metabolism and residue chemistry studies for veterinary pharmaceuticals in food producing animals
- Experience with conducting and supervising method validation, residue depletion and pharmacokinetics studies to support drug development for food producing animals
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.
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: Pharmacokinetics/Drug Metab
Job Title:Assoc Prin. Scientist, Pharmacokinetics
Primary Location: NA-US-NJ-Madison
Employee Status: Regular
Travel: Yes, 10 % of the Time
Number of Openings: 1
Shift (if applicable): 1st
Company Trade Name:Merck
Company
Our vision is to make a difference in the lives of people globally through our innovative medicines, vaccines, biologic therapies, consumer health and animal products. We aspire to be the best healthcare company in the world and are dedicated to providing leading innovations and solutions for tomorrow.
We have made it our mission to provide innovative, distinctive products and services that save and improve lives, satisfy customer needs and to be recognized as a great place to work
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