The National Agriculture Commission (NAC) recommended establishment of Forest Development Corporations in each State to accelerate progress and development of forestry sector. Gujarat State Forest Development Corporation Limited ( GSFDC ) was established in August 1976 and registered under the Companies Act 1956.
In 1979 the Minor Forest Produce (MFP) trade came to be nationalized in Gujarat. The Corporation was entrusted with the task of its execution. This meant translating on the ground the State Policy of protecting economic interest of STs, SCs and other weaker sections, while justifying its corporate status. This corporation gets no grants and budgetary support from the Government.
Gujarat State Forest Development Corporation Ltd. urgently requires for its Ayurvedic Formulations Manufacturing Unit "DHANVANTRI" at GIDC, Ramangamdi, Por, Dist. Vadodara. Following two person purely on CONTRACT:-
Post: Production Incharge, Quality control Incharge
The Minimum Qualification, Period of contract, total Emoluments, Last date of submission of application, whom to address and send are given as under:
(1) Minimum Qualification:
(i) Production Incharge
Minimum Post graduation in Botany/ Chemistry/ Ayurvedic Pharmacy/ Ayurvedic Medicine
(ii) Quality Control Incharge
Minimum Post graduation Botany/ Chemistry/ Ayurvedic Pharmacy/ Ayurvedic Medicine
(2) Preference:
(i) For Production Incharge
Good Knowledge/ Experience in manufacturing of Drugs pertaining to Ayurvedic system of medicine.
(ii) For Quality Control Incharge
Good Knowledge/ Experience in carrying out Tests and Analysis such as Phyto-chemical, pharmcognosical as per Ayurvedic Pharmacopeia.
(3) Duties & Responsibility: Given in last pages for the vacancies separately.
(4) Other details for the vacancies:
1) Period of Contract: 11 Months
2) Total Emoluments: Rs. 25,000/- Month or Negotiable
3) Last Date of receiving application: 19-02-2015
4) Application is to be addressed to Managing Director
5) Application is to be submitted on line our web site.
6) Selection Procedure: Through personal interview. Weightage will be given to knowledge, experience and Performance in personal interview
Find More Info Go to Next Page...
Subscribe to Pharmatutor Job Alerts by Email
Duties for Production Incharge (PI)
1. Supervision of production process, drawing up a production schedule.
2. Ensuring that the production is cost effective.
3. Making sure that products are produced on time and are of good quality.
4. Estimating cost and setting the quality standards.
5. Being responsible for the selection and maintenance of Equipments/ Machineries.
6. Monitoring products standards and implementing quality control programmes.
7. Ensuring health and safety guidelines are followed.
8. Supervising & motivating a team of workers.
9. Reviewing workers performance and identifying training needs.
10. Working with managers to implement the company's policies and goals.
11. Also involved in the pre-production (Planning) stage as well as the production (Control and supervision)
12. To maintain manufacturing records related to Foods and Drug administration.
13. To suggest new formulations (Both classical and patent).
In addition to this, you will have to carry out such other duties as may be assigned to you by your higher authorities from time to time.
Duties for Quality Control Incharge (QC)
1. Analysis of herbal raw material, packing material and finished products testing.
2. Analysis of Raw material, In process and Finished Products like Churna/ Tablets/ Oil/ Capsule/ Liquid syrup etc. as per Ayurvedic Pharmacopeia of India (API) and In House Specification.
3. Operating instruments like TLC, UV-Visible Spectrophotometer, Refracto meter, pH meter, Karl-fisher, Friability, Moisture Balance, Centrifuge, Microscope and Weighing Balance etc.
4. Responsible for in process quality control/ quality assurance testing.
5. Implementation of sampling and quality control procedure.
6. Instruments calibration, SOP & STP preparation and insure the availability of QC consumables.
7. To issue, collect and keep Batch Manufacturing Record.
8. Implement the quality management system as per WHO-GMP guidelines.
9. Submission of duly sigh report of each product tested to Sub-Divisional Manager and copy of it send to with duly sign of both quality control incharge and Sub-Divisional Manager to Sr. Manager Vadodara Project.
10. Initiation of batch recalls and its investigation thereof.
11. Approval of master documents such as specifications and test procedures, production and control records, standard operating procedures validation of protocols and reports.
12. Line clearance at every stage from dispensing of raw material to dispatching of finished Products.
In addition to this, you will have to carry out such duties as may be assigned to you by your higher authorities from time to time.
See All Gujarat Alerts B.Pharm Alerts M.Pharm Alerts
See All Other Jobs in our Database
.png)
