Amneal Pharmaceuticals Walk in Interview on 22nd
December(Sunday) for Injectable & OSD @ VAPI
We are looking for competent, dynamic and motivated
candidates for suitable positions for Injectable & OSD (oral solid dosage)
unit for our Ahmedabad SEZ Matoda Plant.
Date: 22nd December, 2019 (Sunday)
Timing: 9:00 AM to 12:00 PM
Venue :
Hotel Silver Leaf
Plot No.CM-14 & 15, Raghuvir Complex
Opp Vapi Industries Association Ground GIDC, Vapi 396195.
Openings: 60
INJECTABLE REQUIREMENT
1. Sterile Manufacturing (Injectable unit /Parenteral Unit)
Designation: Officer/ Sr. Officer/ Operators
Qualification: B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/
ITI
Total Experience: 02 to 07 years
Area: Aseptic & Controlled area, Vial, PFS, LYO,
Sealing, Filling, capping
Position: 50
Desired Profile:
· To observe
& follow all rules and regulations of the production department.
· Must be from
Parenteral background
· To be aware
and responsible for achieving quality objective and fulfilling the requirements
of the quality of the company's service by means of applicable quality
procedures.
· Sound
technical knowledge of Aseptic area and controlled are related activities.
· Technical
exposure and expertise on vial filling, sealing, Autoclave, Lyophilizer, PFS
filling, cartridge filling machine.
· Knowledge of
Regulatory guidelines and exposure of USFDA audits.
· Knowledge of
Eye drop filling machine and related batch mfg. process.
· 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.
OSD REQUIREMENT
1. Quality Control (QC - OSD) & Quality Control
(Technology Transfer)
Designation: Officer/ Sr. Officer/ Executive
Qualification: B.Sc/ M.Sc /B.Pharm/ M.Pharm
Total experience: 02 to 07 years
Position: 10
Area: Technology Transfer, RM, FP, Stability, LIMS
Desired Profile:
· Able to
perform sampling of raw-materials and packing materials within the specified
time frame to support manufacturing activities.
· Should have
experience to perform analysis & documentation of Raw-materials,
In-process, Finished products, stability & validation samples by using
Caliber LIMS software
· Exposure to
for management of working/reference standards on Caliber LIMS
· Should have
exposure to perform analytical method transfer, method verification and method
validation activities as per ICH guideline and as per SOP's
· Exposure to
prepare and standardization of volumetric solutions/reagents
· Responsible
to perform all activities in laboratory in GLP compliance manner
· Caliber LIMS
knowledge is preferable
· Responsible
for the analysis & documentation of Raw-materials, In-process and Finished
products, stability & validation samples.
· Responsible
for the operation & calibration of balances in Sampling room & to
maintain its record.
· Responsible
for receiving of samples and making entry in the respective sample inward
register.
· Responsible
for the preparation, handling & management of working/reference standards.
· Responsible
for the preparation and standardization of volumetric solutions/reagents and to
maintain related documents.
Required Candidate profile
The candidate with good communication and inter personal
skills, computer knowledge and exposure to cGMP/ GLP Knowledge and
understanding of regulatory requirement is essential.
Note : Candidate should have 02 to 07 years of relevant
experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation.
Who You may walk in for interview with current CV along with CTC proof
Appointment letter, Increment letter & last 3 months salary slip & Bank
statement, Aadhar & PAN card and 2 passport size photograph.
Those who have already attended interview in last 6 month
need not appear again for interview
If you are unable to attend interview you can share cv on
FOR MORE JOB UPDATES
No comments:
Post a Comment