Hab Pharmaceuticals and Research Ltd Recruitment October 2020.Hab Pharmaceuticals and Research Ltd Notification full detailes below. We dedicatedly stand by our brand fundamental of Satisfaction and Growth through Customer Service, Product Quality and Innovation’ and it has helped us imbibing a sense of confidence and positive perception in the market and in the minds of our customers.
Important Vacancy details:
- Post Name: Production Planning & Inventory Control,Quality Assurance Manager
- Education:B.pharma,B.sc
- Experience:03- 12 Years
- Location:Mumbai, Vasai
- Salary:3,00,000 – 4,00,000 P.A.
- Openings: 02
Job Description: Hiring For Production Planning & Inventory Control,Quality Assurance Manager in Hab Pharmaceuticals and Research Ltd !
Production Planning & Inventory Control
Purchase , Planning and Inventory control of Packing materials for Pharma.
Preparation on indent on receipt of production program.
Tracking timely supplied of packing materials.
Follow up with the packaging development team to expedite the artworks to manufacturers.
Assisting Packing materials store manager in day to day activities.
Co ordination with production team for timely supply of packing materials.
Co-ordination between design team and QA/QC for text approval of packing materials.
Knowledge of cartons, labels, foils, PVC and all pharma packing material is a must.
Quality Assurance Manager
Quality Assurance manager for Pharmaceuticals formulation plant ( Tablets and capsules)
To maintain and control an overall quality management system documentation.
Responsible for the preparation planning, coordination and execution of QA training programme.
Assessment of other departments training
WHO-GMP documentation
Issuance of batch number, batch manufacturing record, Register, SOP’s, format, protocols, Analytical protocols to departments
To review the Analytical records, Batch manufacturing record and batch packing record
Preparation of QA-SOP’s, Validation protocol aPQR, summary reports based on the Analytical results and Batch documents data.
To coordinate for the validation activities with other department for successful completion
Submit customer questionnaire along with declarations, management of free samples.
Maintaining vendor approval process
Daily assessment of site to ensure GMP compliance level of site through round.
Management of regulatory and customer audit at site
Management of Deviation, Incident. Change control, OOS, Recall, Market complaint, Investigation, CAPA, Risk assessment etc
Interpretation of sales order and overall management of dispatch
Reviewing stability data and sharing inference with management.
Providing data to Regulatory patent or any other authorities
ABSOLUTE REQUIRMENTmust have working in QA department of a pharmaceutical company manufacturing tablets and capsules for at least 4 year
Time & Venue:29 December – 30 December , 12.00 PM – 5.30 PM 310, T.V. Industrial Estate, S.K. Ahire Marg, Behind Glaxo Lab, Worli, Mumbai 400 030 Telephone : 91-022-66261400 Fax : 66261414 Email : info@habpharma.in Contact – HAB Pharma ( 02266261400 )
Selection Process: The selection will be on the basis of Interview.
