QC Chemist - Permanent Position

Job Description

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.

Qualifications

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.

Additional Information

For more information contact me at 732-429-1921