Technical Aspects of Packing Coordination (Pharmaceuticals)
1. Artwork Management;
Management of artwork creation, revision & approval as per regulatory guidelines (EMA, WHO, CDSCO).
Checking legibility, font size, barcodes, Braille text (where applicable).
Ensuring compliance of carton, foil, label information with approved dossier (MA File).
Control on master packing record (MPR) & batch packing record (BPR).
2. Packing Material Specifications
Defining & maintaining specifications for primary, secondary & tertiary packaging:
Primary: Blister foil, alu-alu foil, PVC/PVDC, bottles, caps, induction seals etc.
Secondary: Cartons, labels, leaflets, shrink wraps etc.
Tertiary: Shippers, stretch film, pallets etc.
Verification of DMF (Drug Master File)/COA of packing materials.
Compatibility check of registered packing with respect to existing formulation machine suitability.
3. GMP & Regulatory Compliance
Packing operations to be executed as per cGMP (EU-GMP, MHRA & Schedule M).
Experience
4 - 8 Years
No. of Openings
01
Education
Post Graduate (Post Graduate Diploma)
Role
Executive Packaging Development
Industry Type
Manufacturing / Production / Quality
Gender
Male
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office
Face interview location
Village : Thana, Baddi, Teshil: Baddi, Dist. Solan, Himachal Pradesh, India