The Quality Control Specialist will perform chemical analysis for product validation samples according to approved methods, prepare documentation, and conduct analytical method validation/verification studies. Responsibilities include performing physicochemical testing, analytical transfer analysis, and training junior analysts. The role also involves reporting out-of-specification results, updating SOPs, standardization of raw materials, stability testing, and recovery studies. Adherence to HSE policies and laboratory safety procedures is crucial.
Required Skills
Engineering, Construction & Trades
○Validation○Materials
Design, Content & Media
○Usability Testing
Operations, Logistics & Supply Chain
○Lean
Other
○recovery studies○analytical transfer analysis○Chemical Analysis
Science & Research
○Physics
🎁 Benefits & Perks
HSE approval on SOPs, commitment to PPE use, adherence to HSE policy and requirements, waste segregation, calibration program for instruments, respect of Company's Values, Code of Ethics and Social Charter, respect Personal Data Protection Charter.
Requirements
Requires 3-6 years of experience in chemical analysis, analytical method validation, and quality control. Must possess a Bachelor's degree in chemical engineering, chemistry, or pharmacy. Skills in stability testing, cleaning validation, recovery studies, physicochemical testing, and analytical transfer are essential.
Description
Main ResponsibilitiesThe main purpose of this job is to perform chemical analysis for validation samples for products according to the approved method of analysis, and prepare relevant documentation as required.Perform analytical method validation/verification studies ,Protocols & final reports.Perform recovery studies & prepare cleaning validation & verification runs.Responsibilities And Tasks1- Performs all physicochemical testing of samples collected during the process validation and record the results in the validation report & Certificates of analysis required and ensures that all obtained results are within the specified approved limit, using valid method of analysis.2- Performs the analytical transfer analysis according to respective protocol.3- Perform coaching and training for junior analyst for the Analytical method validation and explain the methodology and ensure that all the junior analyst (s) understand the method validation concept and can perform full study independently .3- Immediate reporting of out of specification test results or batch deviation reports whenever needed to the Q.C manager.4- Perform analytical full method validation studies , Protocols & final reports.5- Updating of SOPs & control test methods and maintaining of relevant master files.6- Performs Standardization for Raw Materials7- Perform Stability testing & routine analysis tasks as assigned8- Perform recovery studies & prepare cleaning validation & verification runs.9- Fulfill other task(s) as assigned10- HSE & Energy ContributionEnsures HSE approval on any SOP that requires certain HSE precautions. Ensures HSE approval on any change. Follow the laboratory safety procedures Commitment to the appropriate PPE use. Follow the approved HSE policy and requirements. Following the statutory legislation concerning Health, Safety and environmental law. Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system. Implement good calibration program for all instruments.Supplementary TasksUtilizes, calibrates, maintains the QC equipment in the Chemical Lab according to the local SOP.Prepares relevant SOPs and follows up the update according to requirements.Perform other related duties as assigned.Makes sure that all activities carried on are complying with safety measurements.Updates methods of analysis.Respect of Company's Values, Code of Ethics and Social Charter.Responsible for applying the HSE related requirements for the company in all working proceduresRespect Personal Data Protection Charter. Required Years of Experience:3 to 6 years