Amneal Pharmaceuticals Pvt. Ltd. Looking for Injectable & OSD (oral solid dosage) unit for our Ahmedabad SEZ Matoda Plant
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:
15th December, 2019 (Sunday)
Timing:
9:00 AM to 12:00 PM
Venue:
Amneal
Pharmaceuticals Pvt. Ltd.
Plot
No 15,16,17 Pharmez
Village:
Matoda
Sarkhej
Bavla Road, Abad
Please
find the Job details below:
1.
Sterile Manufacturing ( Injectable unit /Parenteral Unit)
Designation:
Officer /Sr. Officer/Operators
Qualification:
B.Pharm/M.Sc/ITI/Diploma
Total
Experience: 0 to 05 years
Position:
50
Desired
Profile :
1.
To observe & follow all rules and regulations of the production department.
2.
Must be from Parenteral background
3.
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.
4.
Sound technical knowledge of Aseptic area and controlled are related
activities.
5.
Technical exposure and expertise on vial filling, sealing, Autoclave,
Lyophilizer, PFS filling, cartridge filling machine.
6.
Knowledge of Regulatory guidelines and exposure of USFDA audits.
7.
Knowledge of Eye drop filling machine and related batch mfg. process.
8.
Knowledge of Quality Management System (QMS) i.e. change control, Deviation,
CAPA, and documentation in manufacturing area of injectable.
9.
Expertise in batch manufacturing and preparation related activities.
10.
Knowledge of equipment validation and qualifications in injectable.
2.
Quality Control (QC - OSD)
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 :
1.
Able to perform sampling of raw-materials and packing materials within the
specified time frame to support manufacturing activities.
2.
Should have experience to perform analysis & documentation of
Raw-materials, In-process, Finished products, stability & validation
samples by using Caliber LIMS software
3.
Exposure to for management of working/reference standards on Caliber LIMS
4.
Should have exposure to perform analytical method transfer, method verification
and method validation activities as per ICH guideline and as per SOP's
5.
Exposure to prepare and standardization of volumetric solutions/reagents
6.
Responsible to perform all activities in laboratory in GLP compliance manner
7.
Caliber LIMS knowledge is preferable
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.
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.
If
you are unable to attend interview you can share cv on
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