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PHARMA JOBS POST > Vapi > Amneal Walk-in interviews at Vapi for OSD & Injectable Manufacturing on 5th March – 6th March 2022
VapiB.PharmB.ScDiplomaITIM.PharmM.ScWalk In Interview

Amneal Walk-in interviews at Vapi for OSD & Injectable Manufacturing on 5th March – 6th March 2022

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Last updated: February 27, 2022 5:39 am
ADMIN 3 years ago 316 Views
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Amneal Walk-in interviews at Vapi for OSD & Injectable Manufacturing on 5th March – 6th March 2022
We are looking for competent, dynamic and motivated candidates for suitable positions for OSD & Injectable unit for our Rajoda and SEZ Matoda Plant.

INJECTABLE REQUIREMENT

  1. Sterile Manufacturing (Injectable/Parenteral Unit)
    Designation: Operator/Officer/ Sr. Officer /Executive/ Sr. Executive
    Qualification: ITI/ B.Sc/ Diploma / B. Pharm / M.Sc/ M. Pharm
    Total Experience: 02 to 06 years
    Area: Aseptic & Controlled area operation (Filling, Sealing, filtration, intervention, Production QMS, Autoclave, Batch Manufacturing, terminal sterilization etc.)

Line: Ophthalmic, PFS, Lyo and Vial

Machine Exposure: Three piece sterile eye drop machine (Groninger), nenomil, isolator, Trucking, Bosch, fedegree & Optima

Desired Profile:

To observe & follow all rules and regulations of the production department.
Must be from Parenteral background & exposure to filling process is desirable.
To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures.
Sound technical knowledge of Aseptic area & Controlled area related activities.
Technical exposure and expertise on filling & Autoclave machine.
Knowledge of Regulatory guidelines and exposure of USFDA audits.
Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
Expertise in batch manufacturing and preparation related activities.
Knowledge of equipment validation and qualifications in injectable.
Preparation & review of BMR-BPR
Preferred Exposure for Ophthalmic line: Three piece sterile eye drop filling machine operation (Groninger), Nanomill Operation, autoclave (Fedegari) Manufacturing and Filtration vessel operation, CIP and SIP processing
Knowledge of packing area operation and visual inspection

  1. Oral Solid REQUIREMENT

Designation: Operator/Officer/ Sr. Officer /Executive/ Sr. Executive
Qualification: ITI/ B.Sc/ Diploma / B. Pharm / M.Sc/ M. Pharm
Total Experience: 02 to 06 years

Area: Coating (Wruster Coater), Granulation, Compression, Capsulation, Packing and QMS

Machine Exposure: FBE, pam glatt and Blister
Desired Profile:

Candidates should have hands on experience along with knowledge of 21 CFR compliance in equipment’s like RMG, FBE, Glatt, Co-Mill, V-Blender, Bosch capsule Filling machine, Fette compression machine, Auto coater, CVC Line and Blister packaging line equipment with Track and Trace system.
Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing/Packaging area of OSD.
Able to understand & have relevant knowledge of fluid bed equipment
To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.
To maintain the areas and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition.
To impart training of operation and cleaning related SOP to all subordinates and operators
Co-ordination for IQ / OQ for any new equipment / system
To perform PQ for any new equipment / system
To follow all concern departmental SOP’s for day to day operation and cleaning
To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record
Able to understand &operate fluid Bed equipment
To have knowledge of 21 CFR and audit trails etc.
To perform online documentation with respect to departmental procedures as per good documentation
Maintaining the change parts for all equipment at manufacturing

Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP/ GLP and understanding of regulatory requirement will be preferred.

Note : Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization.

Kindly carry your updated CV along with copies of CTC proof, Appointment letter, Increment letter, last 3 months salary slips, Bank statement, Education certificates & Marksheets, Aadhar & PAN card and passport size photograph, at the interview venue.
If you are unable to attend interview you can share CV on [email protected] & [email protected]

Below points need to be followed:

All precautions pertaining to Covid 19 pandemic will be strictly followed.
Please do not attend interview if you are suffering from any health issue (cold, cough, fever or sore throat). We can conduct a telephonic or video meeting with you later.
Face Mask is mandatory all the time you are in the premises.
Social distance will be followed strictly.
Kindly co-operate with security personnel.

Time and Venue
5th March – 6th March , 9.00 AM – 4.00 PM
HOTEL SILVER LEAF, opp. VIA Cricket Ground, Ajit Nagar, Phase 2, GIDC, Vapi, Gujarat 396191
Contact – Neha Modi & Aarti Gadhavi

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