Fermenta Biotech Ltd Walk In Interview For QA Dept
1) Executive- Quality Assurance
Candidates with 5 to 8 years of experience from Pharma/API industries accompanied with good academic pedigree
Qualification: B.Sc./M.Sc. (Chemistry)
Job Profile Executive:
Responsibilities:
(1) To handle QMS like Change control, Deviation, CAPA, OOS, OOT etc. (2) To perform vendor evaluation for Raw materials, packing materials etc.
(3) To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for all finished product and intermediates. (4) To issue finished product label to production and maintain reconciliation record for the same.
(5) To issue protocols for analysis of raw material, intermediates, and finished products.
(6) Take facility round and check in process sample, online monitoring of plant activity and its compliance as per GMP.
(7) To perform dispatch related activity with co-ordination of QC, production, warehouse.
(8) To prepare and review of all SOP's.
(9) To review filled batch production record and equipment cleaning records of finished products and intermediates.
(10) To review filled analytical protocols of finished products and intermediates.
(11) To distribute approved standard operating procedures and standard testing procedures to all concerned departments and retrievals.
(12) To Prepare/Review product labels in bartender application software. To keep all the master files and Logbooks on their dedicated place.
(13) To aware about food safety, Feed safety, legality, and quality in related to all activities.
(14) To perform activity assigned by QA head in timely manner.
Preference will be given to candidates with API & Pharma industries experience with proven record of facing regulatory audits.
2) Assistant Manager - Quality Assurance
Candidates with 8 to 12 years of experience from Pharma/API industries accompanied with good academic pedigree
Qualification: B.Sc./M.Sc. (Chemistry)
Job Profile Assistant Manager:
Responsibilities:
(1) Preparation and Review of SOPs, BPRs, Specifications and STPs, Protocols, Quality manual, MSDS.
(2) Document control activities.
(3) Review of stability data provided by QC.
(4) Initiation/Review of change control, impact assessment and management of change control records.
(5) Preparation of Annual Product Quality Review & MRM record.
(6) Review of Vendor questionnaire and related documents.
(7) Updating of Master Formats, Master document Index and Master Format List.
(8) Review of analysis data of finished product before release.
(9)Handling of deviation, market complaints, out of specification and CAPA.
(10) Conduction Internal Audit.
(11) Release of API in absence of Manager-QA.
(12) Conduct GMP/Regulatory Training.
(13) Review of Investigation of Deviation, OOS & Other Non-Conformities.
(14) Review Of Validation, Qualification CSV Document.
Preference will be given to candidates with API & Pharma industries experience with proven record of facing regulatory audits.
Walk In Interview Details
Date: 9:30 AM to 04:00 PM,
Time : 28th Sep 2024 (Saturday)
Venue: 68, Patel Society, Near Shital Circle, Dist.: Bharuch-392001, Gujarat, India.
 |
Fermenta Biotech Ltd Walk In Interview For QA Dept |
Post a Comment