Qc Officer

Designation: QA Officer / Sr. Officer and QC Officer Experience: 1 to 5 Years + Education: B.SC /M.SC Location: Vadodara. JD: 1 - 5 years of experience in Formulation Division. Must have good knowledge of GMP. Fill in the details below. **Experience**: CTC: Expected CTC: Notice: **Location**: Reason for job Change: Holding any Offer?? Pay:...

From 2 to 3 year(s) of experience - ₹ 2-2.5 Lacs P.A. - Vadodara**Roles and Responsibilities** B. Pharma / M.Pharma with 2 to 3 Years of experience in QC(Pharma Formulation) for reputed Pharma Formulation company at Vadodara Location **Analysis by HPLC / GC** Calibration of sophisticated instrumentsAnalysis of F&D, PV & Stability - Role:_QA / QC...

**Department**: QC **Designation**: QC Chemist **Work Location** :Ark Golden India Pvt Ltd Block No. 238, Muval-Mobha Road, Muval, Ta.: Padra - 391430, Vadodara **Experience**:3 - 5 Years of Relevant Experience **Qualification**:MS/M.Sc.(Science)/MTech in Polymer/Organic Chemistry, Chemical Engineering & Materials Science, Chemistry **Skills**: Should...

B. Pharma / M.Pharma with 2 to 3 Years of experience in QC(Pharma Formulation) for reputed Pharma Formulation company at Vadodara Location **Analysis by HPLC / GC** Calibration of sophisticated instruments Analysis of F&D, PV & Stability **Job Types**: Full-time, Regular / Permanent **Salary**: ₹200,000.00 - ₹250,000.00 per year Schedule: -...

Job opening for B.Sc/ M.Sc - Chemistry with 2-5 years of experience in QA / QC Department in reputed Pharma API / Chemical / Intermediate manufacturing company near vadodara **Salary**: ₹200,000.00 - ₹300,000.00 per year Schedule: - Rotational shift **Speak with the employer** +91 8905012233 Application Deadline: 12/06/2023

From 1 to 3 year(s) of experience - ₹ 1,75,000 - 2,75,000 P.A. - Vadodara**Roles and Responsibilities** B. Pharma / M.Pharma with 2 to 4 Years of experience in QC(Pharma Formulation) & QA(IPQA / Documentation) for reputed Pharma Formulation company at Vadodara Location **Analysis by HPLC/ GC** - Calibration of sophisticated instruments - Analysis of F&D,...

From 1 to 3 year(s) of experience - ₹ 1,75,000 - 2,75,000 P.A. - Vadodara**Roles and Responsibilities** B. Pharma / M.Pharma with 2 to 4 Years of experience in QC(Pharma Formulation) & QA(IPQA / Documentation) for reputed Pharma Formulation company at Vadodara Location **Analysis by HPLC/ GC** - Calibration of sophisticated instruments - Analysis of F&D,...

From 2 to 3 year(s) of experience - ₹ 1,25,000 - 2,50,000 P.A. - Vadodara**Roles and Responsibilities** - Job Opening for 2-3 year Experience as a QC Officer in Pharma API and Specialty Chemical Manufacturing Company at Vadodara.- Handling and Operation HPLC, GC with HS, UV, IR, Wet Lab analysis and other lab Instruments. - Having the knowledge of GLP, GDP...

Job Description Roles and Responsibilities Preparation of BMR & SOPs, STPsIssuance of SOPs, formats / Annexures, Log Books, BMR & GMP Documents.Change control, deviation, incident, CAPA, breakdown slips etc.Responsible to inform any Non- Conformity observed in area to HODDesired Candidate Profile Handling & Maintenance of Product permissionsReview of...

From 2 to 7 year(s) of experience- ₹ Not Disclosed by Recruiter- Vadodara/ Baroda,Gujarat**Roles and Responsibilities** GLP Experience is must manage the operation and Calibration of sophisticated Instruments like HPLC, GC, UV/VIS etc., Responsibility with Sampling instructions, specification, test method Preparation and other quality control...

From 0 to 5 year(s) of experience- ₹ Not Disclosed by Recruiter- Vadodara/ Baroda,Gujarat**Roles and Responsibilities** Handling of QMS- Change control, deviation, incident & OOS & CAPA SOP preparation & SOP Reviewing. Preparation of process validation, protocol &reports/Hold time protocols & Reports Preparation of compliance reports of audit Fresher can...

JOB RESPONSIBILITIES: - Analyzing and summarizing medical records for anomalies for pre and post settlement projects. - Perform operational QC with highest accuracy and efficiency. - Interpreting clinical data in terms of medical terminology and diagnosis as per the given protocol. Adhering to company policies/ARCHER principles and hence taking good care of...

Established plastic processing unit located at Baroda, Gujarat manufacturing pharmaceutical packaging. Essential key areas with totally responsible for manufacturing activities with relevant education and experience of 0- 1.5 years. - 1. Ensure correct data input and 0 defect policy - 2. Take 4 times online shots and confirm visually & diametrically - 3....

Job description: - Receives Incoming Material Reconciles with Purchase order & making GRN. - Receipt, Inspection, Storage, Tagging of material and accounting theory. - Coordinate with QC/QA Department for sampling of RM & PM & Analysis. - To manage and implement smooth operation of inward & outward. - To Track the release status of RM, PM, And Eng. required...

Job Description: Job description: Receives Incoming Material Reconciles with Purchase order & making GRN. Receipt, Inspection, Storage, Tagging of material and accounting theory. Coordinate with QC/QA Department for sampling of RM & PM & Analysis. To manage and implement smooth operation of inward & outward. To Track the release...

Microbiologist Officer **1-2 years experience in Pharma Industry is must.** **Educational Qualification**:B.Tech. (Biotech) / M.Sc. (Micro) **Location: Vadodara (Local Preferred)** - Knowledge and understanding with regards to the significance of the presence of bacteria, yeasts, moulds, viruses and toxins in pharmaceutical raw materials, intermediates,...

Job DescriptionRoles and ResponsibilitiesMust have experience in pharma industry.To receive raw material as per PO.To prepare GRN & intimate to QC for sampling.To prepare & check the invoice with other documents.To issue the raw material as per requisition from production.Desired Candidate ProfileShould have good communication skillTo prepare monthly stock...

Job Description: Job Description: Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. ? Preparation, Compilation & Review of Registration documents that include Administrative & Technical. ? Reviewing the technical documents provided by QA, QC,...

Overseeingtesting activities and ensuring compliance with regulatoryrequirements particularly in formulationtesting.Youwill be responsible for developing and implementing microbiologicaltesting protocols ensuring their alignment with regulatorystandards and industry best practices particularly in formulationanalysis.Overseeingdaily operations you will...

Overseeingtesting activities and ensuring compliance with regulatoryrequirements particularly in formulationtesting.Youwill be responsible for developing and implementing microbiologicaltesting protocols ensuring their alignment with regulatorystandards and industry best practices particularly in formulationanalysis.Overseeingdaily operations you will...