89 Job openings found

Authorization of all procedures and standard instructions of process, controls etc Investigation and closure of all deviations, OOS and complaints Conducting self inspections. Conducting vendor evaluation of raw materials. Should have sound knowledge of Process validation. Should be familiar with preparation of process validation protocol and report. Should have sound knowledge of QMS System and ...

We are looking for an experienced person will oversee the end to end supply chain process for our R&D and manufacturing requirements encompassing safety, sourcing, product selection, demand planning, quality, inventory, warehousing and transport for group companies . The candidate will develop world-class partnerships with suppliers and other organizations. It’s ...

experience in QC, R&D, Public Testing Laboratories. A strong TESTING LAB business abilities with strategic outlook, yet very hands on approach with successful record of contribution. Expertise in building team there by streamlining operations using procedures to facilitate robust quality management system. Excellent conceptual & analytical skills to provide the ...

Candidate should have experience around 3 years to 7 years in Pharma intermediates & Specialty Chemical.  Manage and evaluate machine resources to ensure productivity and minimal downtime Oversee a workforce in the manufacturing department Strive to reduce expenses and increase productivity across all product lines Ensure all employees follow industry standard health and safety ...

Preparation of Certificate of Pharmaceutical Product. Expertise in liaising, coordinating inspections with regulatory agencies (FDA ISO    9000) Knowledge of Microsoft Office, Microsoft Excel, ERP etc. Goal Oriented and Results Driven Team Leader. Expertise in writing, reviewing & approving lab procedures / documentations, Out off   Specification                     reports, batch records, protocols, etc. Review of QC related ...

HPLC (Operation and Troubleshooting) stability study as per ICH Guideline. Dissolution apparatus operation and method development. AMV analytical method validation  analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.   To perform the daily calibration of Instruments/Equipments. To review raw materials, in process, intermediate, finished products, packing material, stability, ...

HPLC (Operation and Troubleshooting) stability study as per ICH Guideline. Dissolution apparatus operation and method development. AMV analytical method validation  analyze the Raw materials, In-process and intermediates finished product and stability samples as per respective test procedures.   To perform the daily calibration of Instruments/Equipments. To review raw materials, in process, intermediate, finished products, packing material, stability, ...

A Sr. Chemist QC (Quality Control) analyzes raw materials, in-process samples, and finished products using advanced techniques (HPLC, GC) to ensure quality, consistency, and regulatory compliance (GMP, ISO), requiring strong analytical skills, documentation, equipment management, and leadership to mentor junior staff and resolve complex quality issues. Key duties involve developing SOPs, ...

Department - QA Job Locaion - ambernath Willingness should be there to work in all shifts Job Description Experience in issuing of line clearance at every step of Batch Manufacturing Hands on performing In-process quality assurance checks for Tablets, Capsules and Intermediates. Stability Sample Handling as well as Stability Chamber. Monitoring and Executing Process Validation and Sampling of the same. Carry out In-house Calibration and External Calibration of Balance, Instrument, Equipments, LAF and HVAC validation. Periodic checking of Retention Sample and Handling of the same. Documentation of Records. BMR and BPR Preparation and reviewing. Carry out Destruction Activities for Rejected and Expired Raw and Packing Materials. Preparation of PQR & APQR.