Quality Control Senior Chemist #job
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. Actively participates in the development of QC Chemists (train, mentor, and guide).
Essential Responsibilities:
Analyze laboratory samples (raw material, in-process, finished product, stability, etc.).
Legibly document the data and report the results associated with each analysis.
Participate in laboratory investigations.
Service laboratory equipment (calibrations, preventative maintenance, etc.).
Compliance with all applicable OSHA safety and health programs.
Adhere to applicable cGXP regulations.
Diligently follow written laboratory protocols, guidelines, procedures and methods.
Initiate and investigate the Out-of-Specifications and Analytical Deviations of quality control laboratory investigations.
Ensure that products are being teste strictly under cGMP conditions and disposition is taken on time as per the committed production plan for every month (C to A, >95%) and or procedural requirements.
Troubleshoot laboratory equipment and methods.
Assist group leaders in various aspects when required.
Order and maintain all laboratory chemicals and other needs of the laboratory.
Diligently perform laboratory analysis correctly first time, every time.
Other responsibilities may be assigned as deemed necessary.
Requirements:
Bachelor of Science (B.S.) degree in Chemistry, Pharmacy, Biochemistry or related field is required. A Master of Science (M.S.) in Chemistry, Pharmacy, Biochemistry or related field is preferred.
Experience:
Three (3) years of experience in pharmaceutical quality control laboratory in stability department.
Competencies:
Technical:
Hands on experience in handling and troubleshooting and maintaining analytical instruments to include: HPLC, Dissolution, GC, IR, UV, AAS, DSC, TGA, Malvern particle size, etc.
Proficient in MS Office applications (Word, Excel).
Behavioral:
People management and development skills.
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.
