QC Chemist- Permanent Position
Job 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 when required
• Service laboratory equipment (calibrations, preventative maintenances, etc.)
• Laboratory responsibilities can be assigned as deemed necessary
• actively participates in the development of lower level Chemists (train, mentor & guide)
• Comply with all applicable OSHA Safety and Health Programs
• Adhere to all applicable cGXP regulations
• Follow protocols, guidelines, procedures and methods as written
• Obey all corporate systems and policies
• Initiate 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 requirements
• Troubleshoot laboratory equipment and methods
• Helping 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 size
• Knowledge on trouble shooting the Analytical Equipment
• Performance of laboratory analyses correctly at the first time
• Maintenance of the Analytical Equipment, the Analytical Columns and all other necessary things.
EDUCATION & EXPERIENCE:
• 2- 4 years analytical experience in Pharmaceutical companies within the Quality Control / Quality Assurance environment
• BS/MS in Chemistry, Pharmacy, Biochemistry or related field.
• Experience in Generic Pharma. And Solid oral Dosage tablets / capsule highly desirable.
For more information contact me at 732-429-1921