1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.00 LPA TO 2.00 LPA
Receive, inspect, and store incoming materials and verify against purchase orders.Maintain stock registers, and records of incoming/outgoing materials.Ensure proper tagging, stacking, and storage of materials as per safety norms.Conduct regular stock audits and reconcile discrepancies.Inventory Control:
Monitor inventory levels and initiate purchase requisitions.Minimize overstocking and understocking situations.Maintain minimum and maximum stock ...
1 Opening(s)
3.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Job SummaryWe are looking for a responsible and organized Store In-Charge to manage day-to-day storeand warehouse operations. The candidate will be responsible for receiving, storing, issuing,and maintaining inventory, ensuring proper documentation, stock accuracy, and timelyavailability of materials for production and other departments.Key Responsibilitiesīˇ Manage day-to-day activities of the stores and ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 16.00 LPA
AM - Costing (Accountant)
Location: Haridwar, UttarakhandDepartment: Finance & Accounts / CostingDesignation: Assistant Manager – Costing (Accountant)Experience: 5–8 YearsQualification: B.Com / M.Com / CA Inter / CMA Inter or CMA preferredIndustry Preference: Cosmetics, FMCG, Manufacturing, Personal Care, Pharma or similar manufacturing industry
Job Purpose
We are looking for an experienced AM - Costing ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
9.00 LPA TO 9.00 LPA
Job Description COCO (Company Owned Company Operated) Manager
Experience: 5–8 YearsBase Location: Delhi NCR (Travel to all COCO Showrooms)Employment Type: Full-Time
About the Role We are looking for a highly energetic and execution-focused COCO Manager to lead the operations, sales and profitability of our Company Owned Company Operated (COCO) showrooms. The role is ...
1 Opening(s)
0 To 1.0 Year(s)
1.20 LPA TO 1.80 LPA
The Asst Production Chemist is responsible for planning, supervising, and executing manufacturing activities to ensure products are produced safely, efficiently, and in compliance with cGMP, ISO 13485 (where applicable), Medical Device Rules (MDR) 2017, approved procedures, and company quality standards. The role includes manpower supervision, production planning, documentation, equipment utilization, ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
20.00 LPA TO 22.00 LPA
Position: Asst. Manager/Manager - RA
Location: Daman
Experience: 15 - 20 Years
Industries: Pharma
Responsibilities:
Lead the Regulatory Affairs function and manage regulatory submissions for domestic and international markets.
Prepare, review and submit CTD/eCTD dossiers, variations, renewals and regulatory responses.
Coordinate with R&D, QA, QC, Production and other departments for regulatory documentation.
Handle regulatory ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: QA Executive
Location: Daman
Experience: 8 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with cGMP, GLP, SOPs and regulatory requirements.
Review and approve BMR/BPR, SOPs, specifications and quality documents.
Handle Deviations, OOS/OOT, CAPA, Change Control and investigations.
Monitor QA activities across manufacturing and ensure GMP compliance.
Conduct and support internal, customer and ...
1 Opening(s)
18.0 Year(s) To 20.0 Year(s)
16.00 LPA TO 18.00 LPA
Position: QC Head
Location: Daman
Experience: 18 - 20 Years
Industries: Pharma
Responsibilities:
Lead and manage the overall Quality Control function and QC laboratory.
Ensure compliance with cGMP, GLP, ICH, WHO and regulatory requirements.
Oversee testing and release of raw materials, packing materials, in-process and finished products.
Review and approve specifications, analytical reports, SOPs, ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities
Manage receipt, storage, and issue of raw materials, packing materials, and finished goods.
Ensure proper identification, labeling, segregation, and storage of materials as per GMP guidelines.
Maintain warehouse records, stock registers, and inventory documentation.
Handle material inward/outward activities and coordinate with Production, QC, and QA departments.
Follow FIFO/FEFO practices and ensure proper stock ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Perform testing of raw materials, intermediates, APIs and finished products
Handle routine analysis using HPLC, GC, UV, IR, pH meter, KF, etc.
Prepare and maintain COA, analytical reports, worksheets and laboratory records
Follow GMP, GLP, SOP and data integrity requirements
Ensure proper sampling, testing and documentation as per specifications
Investigate OOS/OOT results and support ...