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Rubicon Research is a specialty pharmaceutical company focused on developing high quality products using innovative technologies for the global market. We are committed to designing effective value-added formulations that enrich lives around the world. Rubicon Research has several commercial products in the U.S. market with a rich pipeline of over 70 products in development or under review. We leverage our proprietary technologies and specialized formulation development skills, along with optimization of various pharmacokinetic parameters to provide solutions to complex delivery challenges.
- Qualification:B.Sc, B.Pharm, Diploma
- Experience : 03-08+years
- Department: Packing
- Job Location: Mumbai
- Role: Technician/ officer
Time and Venue
10th December , 9.00 AM – 1.30 PM
Rubicon Research Pvt Ltd, Plot No. K 30/4 & 30/5, Additional M.I.D.C., Ambernath, Dist. Thane, Maharashtra – 421 506, India 91 251 713 9500 Ext. 582
Contact – Madhura Patil
Job description:
We have organized Walk-in Interviews for Packing Technician/ officer at Ambernath 10th Dec 2023 between 9:00-1:30 PM
1.To Perform the Packing Activity as per the SOP. to hadnle bottle line
2.Operation, Cleaning and maintenance of the Manufacturing & Packing equipments/ Instruments as per SOP.
3.Calibration of the balances and other Instruments.
4.Online recording of the activity in the BMR/BPR and Log books.
5.Checking and recording of the in process parameter during manufacturing & Packing activity.
6.To ensure environmental condition are maintained during activity and its recording in the daily logbook.
7.To ensure the safety and hygiene during manufacturing process.
8.To carry out cleaning and sanitization of the area as per the SOP
9.Follow the supervisor instructions to achieve departmental goal.
10.To report any incident or violation of GMP act to immediate supervisor
11.To carry out the activity in effective manner to achieve departmental objective
12.To maintain the cGMP environment in Manufacturing area.
Reading and understanding of the departmental SOP and be a part of the training.
13.To give BMR request to QA and ensure that BMRs are available on shop
Floor before starting the production.
14.To do the potency calculation and to dispense the correct raw material and Packaging material of correct specifications in specified quantities for specified product as per
Approved bill of material.
15.To check status label of machines and area ,Temperature, humidity, differential pressure
and on line log book entries to take line clearance for next product or next batch of same
Product.
16.To adhere to cGMP and SOPs.
17.To prepare and fill relevant documents pertaining to products, systems, equipments,
Machines and instruments.
18.To check safe handling of equipments, instruments, RM/PM and in process materials.
19.To monitor in-process control checks and record in BMR.
20.To fill on line BMR and log books during manufacturing.
21.To give daily production report and submit completed BMR to Department Head.
22.To check calibration of balances/instruments and preventive maintenance of equipments.
23.To do any other work and to follow the instruction given by superiors for achieving
department objectives
24.To give Job request to Engineering department to repair the machine or area.
25.To give technical information sheet to QA for the analysis of samples withdrawn by QA
During the process.
26.To give the Raw material requisition to warehouse as and when required.
27.To give suggestions for improving productivity, safety and economy.
28.To reduce rejection and losses during manufacturing process.
29.Reporting of the incidence, handling of the deviation and change control whenever required.
30.To prepare the Validation and Qualification documents and Execute validation and Qualification Activity
CANDIDATE MUST have experience into BOTTLE LINE WITH OSD Dosage form experience
Kindly carry your updated resume, passport size photo, last 3 months payslips
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