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Job Location | Mumbai City |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | Quality (QA-QC)R&D / Product Design |
EmploymentType | Full-time |
With careers in Sales, Marketing, Manufacturing, Research and Development and various other functions we offer a wide range of opportunities. If you would like to be a part of the GUFIC Family, submit your resume for one of the positions listed below. Officer Production Planning & Inventory Control Work Responsibility a) Coordination with Production Team / Packing Team / BSR team / QA& QC team thru call & Email for GBSL & GLP b) Single Point coordinator for all third party product / Client purchase business c) R&D team for documents & licenses copy requirement as per client requirement for tender business / New product. a) Follow up : Day to day follow- up with Purchase team ( RM / PM ) for Indent & Purchase Order against shortages & requirement of RM / SPM. b) Follow up with QA & R&D team for Bill of material / Product code c) Follow up with QA for Third Party products Certificate of Analysis (COA) / Finished Goods release dates / MRP effective Batch no. d) Follow up with Production team ( GBSL & GLPL ) for Export orders packing list / packing priority. e) Follow up with Third party for party code creation data 1. Provide delivery schedule for FG to third party & own marketing team/ Gufic Stridden products. 2. Batch allocation for Generic Batches ( GBSL & GLPL) 3. Prepare monthly Lyophlisation Plan. 4. Prepare monthly SVP plan for Third Party / GS/ Own products 5. Process Sales orders in system for Third Party products. 6. Monitoring WIP report / Lyophlisation Report / packing report 7. Creating Party code / updating master of Third party code in system . 8. Book purchase bill in system for Export orders. 9. Emails to Third Parties for revision & New transfer price to third party. 10. Forwarding orders of Loan Licence party / Gufic Stridden orders to planning dept. 11. Create Rate Master for Third Party products in system. 12. Provide New / Revise MRP to Quality Assurance team 13. Provide products details for New Bill of material & Art work details to QA team / Art work team. 14. Acting as a Single Point Coordinator for all activity of production & Correspondence for any specified Business with Gufic. Candidate Profile : Any Graduate male candidate ( Preferable) with 3- 5 years experience in the planning function handling the above mentioned responsibilities in a mid sized pharma company. Exposure to injectables would be an added advantage. A post Graduate degree in Supply Chain Management would be an added advantage.Junior Graphic Designer Job Description 1) Designing Artwork for all concerned Divisions for their products 2) Handling the Art work Management System ( Software) ( Training will be provided) 3) Any other jobs as assigned by seniors Candidate Profile : Should have thorough working knowledge of Coral Draw/ Photoshop/ Illustrator. Should have 0- 2 years experience in the same handling pharma clients ( Not necessary but preferable).Any other industry experience will also do. Should have excellent communications skills Fresher s can also apply Salary : Upto Rs 10000 per month (CTC).Officer / Executive Regulatory Affairs Job Profile Compiling Product registration dossiers as per ACTD/ CTD/ Country guidelines Coordination with manufacturing sites concerned departments to source documents Relevant sample arrangement , countrywise pack designing and checking the text matter on artworks All activities pertaining to product registration query replies and registration renewal Will have to visit the sites as required candidate Profile Any Male candidate in the age group of 25- 30 . Should be a Bachelors in Pharmacy (B Pharma) . The candidate should have at least 1- 2 years experience in compiling Product Registration Dossiers of varied dosage forms mainly experience of handling Injectables ROW Salary Offered : Rs 2.50 3.00 Lakhs Per Annum (CTC)m Job Profile Compiling Product registration dossiers as per ACTD/ CTD/ Country guidelines Coordination with manufacturing sites concerned departments to source documents Relevant sample arrangement , countrywise pack designing and checking the text matter on artworks All activities pertaining to product registration query replies and registration renewal Will have to visit the sites as required Candidate Profile Any Male candidate in the age group of 28- 35 . Should be a Bachelors in Pharmacy (B Pharma) . The candidate should have at least 4- 6 years experience in compiling Product Registration Dossiers of varied dosage forms mainly experience of handling Injectables/ Finished Dosage in a mid- sized pharma company Salary Offered : Rs 4.00 5.00 Lakhs Per Annum (CTC) Please apply to hr_mgr@guficbio.com,
Keyskills :
compilation quality protocols marketing gmp validation orkmanagement finishedgoods researchdevelopment purchaseorder continuousimprovementfacilitation supplychainmanagement supplychain