APDM Pharmaceuticals Private Limited has its office in Ahmedabad with all QA and regulatory support staffs for managing CDO and CDMO projects ,vendor Audits, BA BA monitoring, project and Engg team. We are a global pharmaceutical service providers with a vast global network of CMO’s, CDMO’s and CRO’s. We have more than 100 years of CDMO, 50 years of R&D and decades of regulatory and QA experience in our company.
DATE AND TIME:
Date : 16 and 17th November 2024
Time : 09:00 am to 05:00 pm
Venue : 4th Floor, 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad 380054. Gujarat
JOB DESCRITION:
Quality Control (QC. RM/PM. Doc) (M.Sc./M.Pharm)
Post : Offi/Sr.Offi/Exe. /Sr.Exe
Req. & Location : 07 (Plant)
Experience : 2 to 5
Skills / Brief profile : Planning of AMT, AMV, API verification & Review, overall GLP maintaining & compliance, Preparation of MOA and protocols. Coordination for TT & AMV. Must have knowledge of cGMP, GLP, ALC00++ principle & GDP. MLT analysis. Culture Handling. QMS. Trend Preparation, Lab Activity support. Lab cleaning. Instrument/Equipment Cleaning
Quality Control (MV/AMT) (M.Sc / M.Pharm)
Post : AM
Req. & Location : 01 (Plant)
Experience : 8 to 10
Skills / Brief profile : Planning of AMT, AMV, API verification & Review, overall GLP maintaining & compliance. Preparation of MOA and protocols. Coordination for TT & AMV, Must have knowledge of cGMP. GLP. ALC00++ principle & GDP
Quality Assurance (M.Sc/B.Pharm/ M.Pharm)
(IPQA) Officer (03)
Req. & Location : 03 (Plant)
Experience : 2 to 3
Skills / Brief profile : Dispensing to Secondary Packing (Line Clearance. In Process checks. PV Samples. Cleaning Validation samples. Hold time samples. Online BMR/BPR Review). Should have exposure in Solid Oral Dosage Form (Tablet/Capsule/Pellets). Primary/Secondary Packing (Blister. Strip & Bottle Packing).
(QA of QC) Exe./Sr.Exe.
Req. & Location : 01 (Plant)
Experience : 5 to 7
Skills / Brief profile : Lab Exposure. Analytical Method Validation. Review of Specification. Method of Analysis Protocol Handing of 00S & 00T. Investigation & Lab event. Review & Approval of QC Documents. Knowledge of Qualification and Validation related Activities. Audit Trail Review etc
Qualification (Off ./Sr. Offi)
Req. & Location : 01 (Plant)
Experience : 2 to 3
Skills / Brief profile : Equipment & instrument qualification. HVAC/Purified Water/Compressed Air validation. Temperature Mapping. Disinfectant Validation. Transport Validation. Calculator Validation.
CSV Engineer (ITQA)
Req. & Location : 01 (Plant)
Experience : 4 to 6
Skills / Brief profile : Computer System Validation of GxP Equipment/Instrument. Inventory Management. Periodic Review of GxP Equipment/Instrument. Infrastructure Qualification etc.
FD (OSD) – Off/Sr. Off
Req. & Location : 01 (R&D)
Experience : 6 to 8
Skills / Brief profile : Development & Execution of Generic ANDA and NDA projects using QBD principle. SOP preparation and follow the SOPs as per GDP and cGMP requirements. Formulation and process development of oral solid, liquid and injection dosage forms.
FD (OSD) – Sr. Exe/AM
Req. & Location : 01 (R&D)
Experience : 7 to 9
Skills / Brief profile : Lead in Development & planning/Execution of Generic ANDA and NDA projects using QBD principle. Develop R&D plans and experimental designs for all new product development projects and processes. Analyze data to provide a relevant interpretation, draw valid conclusions and make appropriate recommendations for active projects (based on performance and costing)., training, teaching, supervising, work proactively
Job Location :
Plant (Sakodara Vill.) & R&D, Ahmedabad
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