Quality Control Chemist, ANDA Projects #job

Organization
Sun Pharma
Job Location
New Brunswick, NJ
Job Description

QUALITY CONTROL CHEMIST, ANDA PROJECTS, QUALITY CONTROL 
Sun Pharma, one of the world’s largest specialty generic companies, operating in over 150 markets worldwide, has been present in the U.S. since 1996, focusing on generics, branded generics and over-the-counter (OTC) products. We are a vertically integrated company and valued supplier to the largest wholesalers, distributors, warehousing and non-warehousing chain drugstores and managed care providers. 
This position is located at OHM LABORATORIES Inc., a Sun Pharma Company; and is one of the nation’s leading manufacturer of OTC pharmaceuticals. A long standing history of superior product and a steadfast reputation for excellence has positioned OHM LABORATORIES Inc., as an integral partner of choice by many leaders in industry. Rigid quality control, quality assurance, versatility, personalized service, and the expertise of our team have continually attributed to the success of OHM LABORATORIES Inc. 
Overview: 
Accountable for the analysis of raw materials, in-process samples, finished products and stability samples. 
Essential Responsibilities: 
Ensure compliance to cGMP in the quality control laboratory. 
Development of analytical methods of new DP and API by using HPLC, GLC and UV-Vis NIR Spectrophotometer. 
Validation of analytical methods. 
Calibration of laboratory equipment and instruments. 
Analysis of raw materials, in-process samples and finished products. 
Analysis of R&D stability samples. 
Assist with the maintenance, review, reporting and verification of documents. 
Adhere to the cGLP/cGMP, safety and health programs and associate plans. 
Other responsibilities may be assigned as deemed necessary.



Requirements: 

Bachelor of Science (B.S.) degree in Chemistry is required. A Master of Science (M.S.) degree in Chemistry is preferred. 
Experience: 
Three (3) to five (5) years of experience in pharmaceutical quality control laboratory in stability department. 
Competencies: 
Technical: 
Experience in handling QC instruments to include: HPLC, GC, UV-vis/FTIR spectrophotometer, automated dissolution apparatus. 
Proficient in MS Office applications (Word, Excel). 
Behavioral: 
Must be a self-motivated, proactive team member with positive interaction with colleagues to ensure teamwork, work ethics and discipline. 
Manage with quality multiple projects and tight timelines. 
Must have excellent communication skills (verbal and written). 
Conduct oneself in a professional manner in alignment with corporate values. 
Ability to work and interact successfully in a global, diverse and dynamic environment.

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