Zydus Lifesciences Walk In - GOA Zydus Group

2.0 - 10.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a Production Plant Operator/Technical Assistant at Zydus Lifesciences Ltd's SEZ 1 OSD Manufacturing Unit in Ahmedabad, you will be responsible for operating and maintaining equipment used in granulation, compression, coating, and capsule filling processes. For the Production Staff position, we are seeking individuals with a B.Pharm/M.Pharm qualification and 4-10 years of experience in market complaints handling and documentation. As a member of the Packing Staff, your role will involve managing packing operations with a focus on quality assurance. Candidates with a B.Pharm/M.Pharm qualification and 4-10 years of experience are encouraged to apply. Quality Assurance IPQA professionals with a background in B.Pharm/M.Pharm/M.Sc and 2-8 years of experience are needed to ensure compliance with IPQA, equipment qualification, and QA QMS standards. In the Engineering department, we are looking for Plant Operators/Technical Assistants with ITI/Diploma/BSc qualifications and 4-10 years of experience in process maintenance, utility operations, and electrical systems. If you meet the qualifications and have the required skills, we invite you to attend the walk-in interview at The Fern Kesarval Hotel on Verna Plateau, Kesarval Cortalim, Goa, Pincode 403710, on 03rd August 2025, from 09:00 am to 03:00 pm.,

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Quality Assurance - IPQA, QMS (Officer/Sr. Officer/ Executive) Navsari Gufic Group

2.0 - 7.0 years

2 - 6 Lacs

Navsari

Work from Office

Role & responsibilities IPQA:- Responsible for line clearance and in process checks of Production. Responsible for Sampling of in-process, Finished Product, control samples, stability samples, and Process Validation samples as per procedure. To ensure online rejection activities and environment monitoring in manufacturing and packaging areas. To conduct periodical log review. To review of batch documents (Batch Manufacturing, Batch Packaging records, and Quality Control analysis data of the batch). To ensure online documentation during manufacturing and packaging area. To prepare and review of Quality Assurance Standard Operating Procedures. To ensure Re-processing and Re-packing activity. Responsible to perform Acceptance Quality Limit and Pre Dispatch Inspection of finished product. Responsible for preparation of Annual Product Quality Review. Responsible to maintain the document as per current Good Manufacturing Practices. Responsible to initiate Change control\Deviation\Incident\Market complaint\non-conformance investigation. To assist the Head of Department for preparation of regulatory inspection. Any other responsibility assigned by Head of Department. Quality Management System:- 1. To coordinate with cross functional department for execution of training planners and maintain training record for same. 2. To master, issue and retrieve of SOPs/BMR/BPR/QC dockets and other documents in-line with the laid down procedure. 3. To maintain vendor related documents and conduct vendor audits. 4. To investigate and prepare Market Complaint investigation report. 5. To take follow up and communicate with customer/vendor regarding Complaint. 6. To handle Change control/Deviations/Incidents/NCR/CAPA. 7. Review of quality technical agreements.

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QA Executive Nutrition Shoppe

2.0 - 6.0 years

0 Lacs

punjab

On-site

As a QA Executive, you will be responsible for various quality assurance tasks including Change Control, Deviation, Out of Specification, Market Complaint, Corrective and Preventive Action (CAPA), and Annual Product Quality Review. Additionally, you will be involved in Audit Compliance Report Preparation, Label compliance, Legal Metrology (Packaged Commodities), FSSAIs Labelling and Display Regulations, and implementation of GMP/GHP requirements in the food industry. You will be required to manage Calibration activities both internally and externally, Equipment Qualification & Documentation control, Process Validation Protocol & Report Preparation, and Cleaning Validation Protocol & Report Preparation. Monitoring and compliance of Self-Inspection and Quality Audits, Technology Transfer activities, HACCP preparation and monitoring, QMS activities, Food safety-related activities, and training execution will also be part of your responsibilities. Furthermore, you will oversee the checking of Building and Facility, Equipment, HVAC System, and Process Validation. Managing GMP and Quality Documents, including CQPs & SOP's, Protocol and Reports, Formats, Logs and Log Books, and Batch Record will also be part of your duties. In this role, you will also monitor and review Reprocess and Recovery in manufacturing areas, ensure GMP Compliance in the plant on a daily basis, and coordinate with various stakeholders to maintain quality standards. This is a full-time position with benefits such as health insurance. The work schedule is during the day shift. The ideal candidate should have at least 2 years of experience in QA/QC, Quality assurance, Quality management, CGMP, Food safety, Food industry, and HACCP. Please note that the work location for this position is in person.,

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