1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
Not Disclosed by Recruiter
Canteen Management – Manage overall canteen services for employees.
Cafeteria Operations – Monitor breakfast, lunch, dinner and tea services.
Canteen Committee – Arrange meetings, prepare MOMs and ensure follow-ups.
Inventory Management – Manage cafeteria, guest house items and consumables.
Asset Management – Plan and manage cafeteria and guest house assets.
Horticulture – Monitor plants, greenery ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
Not Disclosed by Recruiter
Experience in handling Import Registration with CDSCO
Knowledge of European regulation for Export Purpose.
Knowledge of MoCRA
Knowledge of Regulatory requirement of Fragrances and its Alleergen.
Knowledge of ISO16128 ISO 16128-1:2016 Guidelines.
Knowledge of Prop 65, Sephora Clean.
Knowledge of BIS.
Regulatory Compliance
Ensure compliance of cosmetic products with applicable Indian regulations, including Cosmetics Rules, 2020 and ...
1 Opening(s)
0 To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Executive - QA
Location: Silvassa
Experience: 0 - 5 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, SOPs, and quality standards.
Perform line clearance and in-process quality checks.
Review BMR/BPR and QA documentation.
Monitor production activities for quality compliance.
Handle deviations, CAPA, and change control activities.
Conduct QA inspections and internal audits.
Ensure ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsibilities: QA Executive
To assign control number of Change control, Deviation, CAPA, OOS, OOT etc.
To handle QMS related documents and its applicable Quality trends.
To review investigation reports for deviation, OOS, OOT, OOE & Market Complaint.
To coordinate for Internal Audit.
To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for ...
5 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
๐ Documentation & Compliance
Preparation, review, and control of SOPs, BMRs, BPRs, and other GMP documents
Ensure proper documentation practices (GDP compliance)
Handling change control, deviation, and CAPA
๐ญ Shop Floor QA Activities
Line clearance before batch initiation
In-process checks and verification
Monitoring of manufacturing and packing activities
๐งช Validation & Qualification
Support in process validation, cleaning validation
Equipment qualification ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are hiring an experienced QC professional to lead and manage quality control operations in our API manufacturing unit. The Assistant Manager will be responsible for supervising analytical activities, ensuring regulatory compliance, handling audits, and supporting continuous improvement initiatives.
Key Responsibilities:
Supervise routine analysis of raw materials, intermediates, and finished APIs
Review ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle.
Key Responsibilities:
Perform in-process checks during various stages of API ...
1 Opening(s)
5.0 Year(s) To 9.0 Year(s)
3.00 LPA TO 7.00 LPA
PRODUCTION EXECUTIVE
Job Responsibilities• Responsible to maintain an optimum level of manpower and over time• Responsible to ensure all operation of production adherence to cGMP compliance• Responsible on manpower development (training) for quality, productivity and cost consciousness• To train the production personnel on cGMP Trend & regulatory requirement.• Monitor the work ...
1 Opening(s)
0 To 1.0 Year(s)
1.50 LPA TO 2.30 LPA
To perform all the activities of Quality assurance departments.
Ensure that SOPs are available for all quality related activities and they are current.
Prepare and review all quality assurance related documents such as SOPs, log book, format, etc.
Responsible for the Release of the final products.
Review batch sheet, packing sheet and final product ...