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Science Jobs in New Brunswick, NJ

QC Chemist- Permanent Position

Integrated Resources, Inc

New Brunswick, New Jersey

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Biochemistry, Biotech and Pharmaceutical, Capsules, Chemistry, Clinical Research, Current Good Manufacturing Practice (cGMP), Documentation, GCP (Good Clinical Practices), GxP, High Performance Liquid Chromatography (HPLC), IR (Infrared), Identify Issues, Information Technology & Information Systems, Laboratory Analysis, Laboratory Equipment, Laboratory Management, Mentoring, OSHA, Pharmaceutical Analysis, Pharmacy, Preventative Maintenance, Product Testing, Production Planning, Quality Assurance, Quality Control, Rehabilitation Nursing, Safety/Work Safety, Specimens/Samples, Team Lead/Manager, Time Management
LOCATION
New Brunswick, New Jersey
POSTED
1 day ago
QC Chemist- Permanent PositionA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob ResponsibilitiesAnalyze laboratory samples (raw material, in-process, finished product, stability, etc.)Legibly document the data and report the results associated with each analysisParticipate in laboratory investigations when requiredService laboratory equipment (calibrations, preventative maintenances, etc.)Laboratory responsibilities can be assigned as deemed necessaryActively participates in the development of lower level Chemists (train, mentor & guide)Comply with all applicable OSHA Safety and Health ProgramsAdhere to all applicable cGXP regulationsFollow protocols, guidelines, procedures and methods as writtenObey all corporate systems and policiesInitiate and takes the lead role in Out-of-Specifications and Analytical Deviations of Quality Control Laboratory Investigations.Ensure that products are being tested strictly under cGMP conditions and disposition is taken on time as per the committed Production Plan of every month (C to A, > 95%) and or procedural requirementsTroubleshoot laboratory equipment and methodsHelping to the Group Leaders in various aspects as and when needed.Order and maintain all the Laboratory Chemicals and other needs of the Laboratory.Hands on experience in handling analytical instruments like HPLC, GC, IR, UV, AAS, DSC, TGA, Malvern particle sizeKnowledge on trouble shooting the Analytical EquipmentPerformance of laboratory analyses correctly at the first timeMaintenance of the Analytical Equipment, the Analytical Columns and all other necessary things.QualificationsEDUCATION & EXPERIENCE:2- 4 years analytical experience in Pharmaceutical companies within the Quality Control / Quality Assurance environmentBS/MS in Chemistry, Pharmacy, Biochemistry or related field.Experience in Generic Pharma. And Solid oral Dosage tablets / capsule highly desirable.Job LocationI'm interested

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