AMNEAL PHARMACEUTICALS WALK IN INTERVIEW FOR QUALITY CONTROL / QUALITY ASSURANCE | B.PHARM /M.PHARM / M.SC CANDIDATES CAN APPLY
Amneal
Pharmaceuticals LLC American publicly traded
generics and specialty pharmaceutical company. The company is headquartered in
Bridgewater, New Jersey. Amneal Pharmaceuticals LLC manufactures and
supplies generic pharmaceuticals. The Company offers prescription
pharmaceutical products in various forms including hormonal, potency
formulations, soft gelatin capsules, tablets, liquids, and oral solids.
Amneal
Pharmaceuticals looking for competent, dynamic and
motivated candidates for suitable positions for Injectable unit for Ahmedabad
SEZ Matoda Plant. Interested
and eligible candidates can attend interview on scheduled time and venue.
JOB DETAILS:
COMPANY NAME: Amneal Pharmaceuticals
1. DEPARTMENTS: Quality Assurance (IPQA/Validation/EM/QMS) - Injectable unit
/Parenteral Unit)
POST: Officer/Sr.
Officer/ Executive
NO OF POST: 12
QUALIFICATION: B.Pharm/M. Pharm/ M.sc
EXPERIENCE: 2 to 7 years
NOTE: Candidate should have 02 to 07 years of
relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21
CFR compliance) organization.
SALARY: Details not provided by
recruiter
JOB DESCRIPTION: IPQA, Line Clearance, Environment monitoring, Validation,
qualification, Quality Management System, Change control, Deviation, CAPA, etc.
LOCATION: Ahmedabad (Bavla, Moraiya,
Changodar )
JOB DESCRIPTION/SKILLS REQUIRED.
1. Responsible for preparation,
review and implementation of Standard Operating Procedures of Quality Assurance
department.
2. Should have sound knowledge
and experience in Environmental Monitoring (Air Sampling, Settle Plate, Surface
Monitoring, Personnel Monitoring)
3. Responsible for stage wise
line clearance activity before commencing the operations like dispensing,
manufacturing, filling, Lyophilization, sealing, labelling and packing
operations.
4. Supervision of sampling
activity for in process and finished samples for analysis and other samples
requirement as per protocols (Process Validation, Cleaning Validation etc.)
5. To review test results
comparison report of API/ Excipients against manufacturer’s certificate of
analysis and Amneal’s certificate of analysis for vendor qualification.
6. Review and implementation of
vendor notification/declaration provided by SSSM from respective vendor at
site.
7. To prepare standard
operating procedures of Quality Assurance Department and review the SOPs of
cross functional departments.
8. To handle the changes
carried out in the location by assessing the risks associated with it as per
the change control procedure.
9. Supervision of sampling
activity for in process and finished samples for analysis and other samples
requirement as per protocols (Process Validation, Cleaning Validation etc.)
2. DEPARTMENTS: Quality Control - (Injectable unit
/Parenteral Unit)
POST: Officer/Sr.
Officer/ Executive
NO OF POST: 20
QUALIFICATION: B.Pharm/M. Pharm/ M.sc
EXPERIENCE: 2 to 7 years
NOTE: Candidate should have 02 to 07 years of
relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21
CFR compliance) organization.
AREA: GLP, Calibration, HPLC, QC-QMS, LIMS, Stability, RM,
PM, FP, IP, Stability, Analysis, Testing, reviewer etc.
LOCATION: Ahmedabad ( Bavla, Moraiya, Changodar )
SALARY: Details not provided by
recruiter
JOB DESCRIPTION/SKILLS REQUIRED:
1. Testing of raw material, packing material,
in-process, finished product and stability samples (as per stability protocol).
2. To keep neat and cleanliness at work place and
follow the Good laboratory practices in the laboratory.
3. To keep update of instrument slog-books and to
record the data in LNB during testing. To attain and complete self-training
record.
4. To initiate and review of A) Deviation B)Out of
specification/Out of trend C)Change control
5. To ensure in and out of stability samples from
stability chambers.
6. Charging of stability samples as per stability
protocol.
7. To perform water analysis as per specification,
SOP and GTP.
8. To co-ordinate QA for documentation for issuance
and retrievals.
9. Review and monitoring of USP, EP, BP and other
pharmacopeia monographs for changes/ revision.
10. To prepare COA of various product/material as
per requirement whenever required.
11. LIMS master preparation for various product /
material/ instruments/ Volumetric solutions etc.
12. Registration of reference standard, working
standard, column, instrument etc. in LIMS
13. Preparation/updating of calibration schedule in
LIMS
14. Updating of LIMS master as and when required
15. Preparation of configured Test plan.
16. Trouble shooting in LIMS, Involve in
Qualification of LIMS module/ Instrument, Preparation of LIMS related protocol
study and execution.
Candidate with good communication & interpersonal skills,
computer knowledge, exposure to cGMP/ GLP and understanding of regulatory
requirement will be preferred.
You have to walk in for interview with 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 1 passport size photograph.
If you are unable to attend interview you can share CV on
neha.modi@amnealindia.com
BELOW THINGS NEED TO FOLLOW:
·
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.
WALK IN DETAILS:
DATE OF INTERVIEW: 21st March 2021
TIME OF INTERVIEW: 9.00
AM – 3.00 PM
VENUE: Amneal Pharmaceuticals Pvt. Ltd. Plot No 15, 16,
17 Pharmez Village: Matoda Sarkhej Bavla Road, Ahmedabad – 382213 (view
on Map)
Email: neha.modi@amnealindia.com
 AT AMNEAL PHARMACEUTICALS.){kind=link}
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