QA 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:...

Position Vacant - QA Executive Required no of Position’s - 01 Qualification Required - MSC (Chemistry) Experience - 1 to 2 years **Preferred : Female** - **Job Location: POR**_ Working Days: Monday to Saturday **Job Description: -** - Working exposure of instruments like Viscometer, tensio-meter, particle size analyzer, karl fischer, spectro...

Position Vacant - QA Executive Required no of Position’s - 01 Qualification Required - BSC/MSC (Chemistry) Experience - 1 to 2 years Preferred : Male / Female - **Job Location: POR**_ Working Days: Monday to Saturday **Job Description: -** - Working exposure of instruments like Viscometer, tensio-meter, particle size analyzer, karl fischer, spectro...

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

Vega Biotec Pvt Ltd a fast growing pharmaceutcial manufacturing company having presence in 25+ countries is having an opening in its corporate office as follows. 1. QA executive Qualification - B. Pharma Experience - 0 to 1 year Job Profile - 1. Artwork checking and coordination. 2. Coordination with FDCA agent for FDA permissions. 3. Reporting to RA...

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 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...

**Position**: Quality Assurance Officer **Location**:Near Samlaya Railway Station, Vadodara **Experience**:1-2 Years **Jobs Description**: - 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...

From 2 to 3 year(s) of experience - ₹ 2,00,000 - 3,00,000 P.A. - Vadodara**Roles and Responsibilities** Job Opening for RA Officer having 2 to 3 Years of experience in any Pharma API Manufacturing Company near Vadodara. - To prepare and review of dossier in supervision of RA Head. - Collection, review and compilation of various QA and other department...

To perform IPQA activities at shop floor in each and every stage of manufacturing and packing. - QA overview for clean room behaviour and personnel hygiene. - Review of batch processing records. - Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. - Knowledge of APQR and CPV process. - Review of...

**Roles and Responsibilities** 1. To follow and ensure the GMP rules and regulations 2. Daily checks and review of logbooks, BMP.BPR and Environment monitoring. 3. Carry out the line clearance checks during dispensing of RM/PM/dispensing manufacturing and packaging operations. 4. Sample and Collect in process sample, finished goods sample, control sample...

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,...

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...

As a Quality Assurance Executive you will have to monitor and evaluate inbound and outbound interaction quality. Tracks issues in the quality monitoring systems or tools and analyses the results. Being a Contact Centre Quality Assurance Executive you will have to provide feedback to improve performance and develop training programs. Works with other internal...

**Roles and Responsibilities** - Preparation of process flow diagrams for products. - Preparation of mass balance & Reaction balance for new & existing product. - Raw material consumption sheet, Bar-chart preparation. - Executing validation batches for technical support & successful completion of validation. - Part of basic and detail engineering team for...

Position Regulatory Affairs Associates Location - Vadodara KRA: As a RA Sr. Officer Reviewing artwork, PRAC variations, CEP updates for EU market. Preparation of Regulatory Strategic documents for EU/UK market. Review and compilation of deficiencies response for ROW (specially MENA, LATAM market) Compilation and submission of renewal, variation for...

DescriptionSummaryWe are seeking an experienced and dynamic Lead of Quality Engineering(Automation) to lead our Quality Engineering team in India. As a lead, youwill oversee the Quality Engineering (Automation) function and play a pivotalrole in ensuring the quality of our web-based Electronic Health Record (EHR)system. You will be responsible for driving...

Description JobSummaryWeareseekingahighlyskilledandexperiencedDevelopmentManager toleadourproductdevelopmentteaminIndia.AsaDevelopmentManager,youwillberesponsibleforoverseeingthedevelopmentofourWeb-basedEHRsystem.Youwillworkcloselywith cross-functionalteams,including.NETDevelopers,DatabaseDevelopers,QA,andotherstakeholders,toensure...