PHARMA WISDOM

Walk-In Interviews @ Aurobindo Pharma Ltd

QA & AQA - Executive/ Senior Executive (Only For Formulations - OSD)

Openings: 10

Roles and Responsibilities:

• Ideal candidate should be a B.Pharm or M.Pharm or Msc with 03 to 09 years of experience
  from USFDA and other any regulatory plant.
• Preference will be given only to candidates who are Formulations - OSD background.
• Should have awareness about data integrity as per 21 CRF part 11 compliance.
• Should have Knowledge on QMS , LIMS and Empower 3 software.

Desired Candidate Profile:

03 - 09 years experience preferably Pharma Formulations (OSD)

Quality Assurance :

IPQA / QMS & Investigations / Validation / Documentation / Training /Equipment Qualification /

BPRR & BPAR review / Regulatory Compliance/AQA.

Should have Knowledge on QMS , LIMS and Empower 3 software.

Salary will be best and based on candidate caliber and competency.
Date : December 26, 2020 (Saturday) - UNIT 10 (Naidupeta)
Venue / Time : 9.30 AM to 2.00 PM
Aurobindo Pharma Limited, Unit X, APIIC MP SEZ, Menakur , Naidupeta , Andhra Pradesh.
Pickup will be organized from Bus stand to Naidupeta Plant - 9.30 am / 10.30 am/ 11 am
Work Location: Aurobindo Pharma Limited, Unit X, APIIC MP SEZ, Menakur , Naidupeta , Andhra Pradesh.

QC- Executive / Senior Executive (Only For Formulations - OSD)

Roles and Responsibilities:

• Ideal candidate should be a B.Pharm or M.Pharm or Msc with 3 to 8 years of experience
  from USFDA and other any regulatory plant.
• Preference will be given only to candidates who are Formulations - OSD background.
• Should have awareness about data integrity as per 21 CRF part 11 compliance.
• Should have awareness along with solution for trouble shooting of instrumentation analysis.

Desired Candidate Profile:

03 - 08 years experience preferably Pharma Formulations (OSD) Only.

Quality Control :

Having experience of Stability / Nasal / AMT / Lab Support / PM / MICRO /

In Process, Finished Product, Process Validations (Commercial & Exhibit)

Exposure to Regulatory Audits and cGMP, GLP.

Salary will be best and based on candidate caliber and competency.
Date : December 27, 2020 (Sunday)
Venue / Time : 9.30 AM to 2.00 PM
Aurobindo Pharma Ltd., Unit X, APIIC MP SEZ, Menakur , Naidupeta , Andhra Pradesh.
Pickup will be organized from Bus stand to Naidupeta Plant - 9.30 am

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COMPANY: Aurobindo Pharma Ltd

JOB LOCATION: Nayudupeta, Nellore (Dt), Andra Pradesh

DEVISON: Formulation

In subject Mention your

"Department" and "AUROBINDO"

Interest candidates send resume to globalpharmanews@gmail.com

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Aurobindo Pharma Ltd - Walk-In Interviews for Quality Assurance / AQA Departments on 12th Dec' 2020

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Dear All,

Walk in Interview for Freshers at Aurobindo Pharma Ltd, Nayudupeta on 11/12/2020.

Qualification: (2018, 2019, 2020 Pass outs)

B.Pharmacy

Diploma

B.Sc Chemistry

ITI (Electrical, Mechanical, Instrumentation, Fitter).

Experience: Fresher

Work location: Nayudupeta

Interview Date: 11/12/2020.

Venue:

Aurobindo Pharma Ltd

Nayudupeta,

Nellore District, AP.

Note :. Company Buses availabe at Nayudupeta busstand to pick up to company on 7: 45 to 8: 10 am.

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Job Vacancy for Experienced in QC and Production @Vishakhapatnam, AP.        

Greetings of the Admiron Life Sciences, (A Pranaya Group) Jobs...!!!

We have an Urgent requirement for the following departments    

Department: QC  (Bulk Drugs /API  Experience)

Position: QC CHEMIST-HPCL Analysis     

Experience -5 years

Openings: 01  

Location: Admiron Life Sciences Pvt ltd,Vishakapatnam. AP

Qualification: B.Pharm and M.Pharm-Pharmacy

Job Description: 

NOTE: Please Mention in Subject as "QC Chemist-HPCL  Analysis"

· To perform Analytical Method Validation Test assay, Degradation Products and Dissolution by HPLC.

· To perform Method Transfer and Verification activities as per SOP's and STP's.

· To prepare protocols and reports of Method Validation & Transfer.

· Handling instruments like HPLC, GC, ICP-MS, UV, FTIR, pH Meter, etc.

· To perform calibration of AMV instruments and review their documents.

· To perform cleaning validation.

· Exposure of Labware software (Empower 3, UV Pro)

INTERESTED CANDIDATES PLEASE SHARE RESUMES TO hr.corporate@pranayagroup.com and samhitha.hr@pranayagroup.com

Department: QC  (Bulk Drugs /API  Experience)

Position: QC Chemist- GC Analysis        

Experience -5 years

Openings: 04

Location: Admiron Life Sciences Pvt ltd, Vishakapatnam.AP

Qualification: B.Pharm and M.Pharm-Pharmacy

Job Description: 

NOTE: Please Mention in Subject as "QC Chemist- GC Analysis"

Operates and maintains laboratory equipment and instrumentation required for cGMP analysis of samples.

Prepares chemical solutions following standard operating procedures and appropriate testing methods.

Operates and maintains Gas Chromatography and/or High Pressure Liquid Chromatograph.

Keeps an inventory of laboratory chemicals and disposable equipment necessary for the daily functioning of the laboratory.

Performs wet chemistry and raw material analysis as requested.

Perform testing in accordance with specified methods.

Document activities in accordance with cGMP.

Maintains orderly work area.

Department: QC  (Bulk Drugs /API  Experience)

Position: QC Chemist -WET Analysis 

Experience -5 years

Openings: 04  

Location: Admiron Life Sciences Pvt ltd,Vishakapatnam,AP.

Qualification: B.Pharm and M.Pharm-Pharmacy

Job Description: 

NOTE: Please Mention in Subject as "QC Chemist- Intermediate and API WET Analysis"

Analysis of samples by chemical method and online reporting of in process and intermediate samples and analysis of in process validation samples.

Analysis of samples by methods using HPLC,.

Thorough knowledge on handling Validation & calibration of HPLC.

Knowledge on handling of OOS, Deviations, Incidents. Should have Knowledge on Wet chemistry.

Exposure to regulatory audits. Should have the knowledge of cGMP and Good documentation practices.

INTERESTED CANDIDATES PLEASE SHARE RESUMES TO hr.corporate@pranayagroup.com and samhitha.hr@pranayagroup.com

Department: Production (Bulk Drugs /API  Experience)

Position: Deputy Manager/Manager     Experience -8-10 years

Openings: 04                 

Location: Admiron Life Sciences Pvt ltd,Vishakapatnam,AP.

Qualification: Organic Chemistry MSC

- Preparing and reviewing of Batch Manufacturing Records and Standard Operating Procedures related to various products applicable to the facility.

- To ensure on-line filing of Batch Manufacturing Records at the time of performance of activity. All other API manufacturing related work as mandated.

- Daily work allocation as per requirement and arrangement of manpower.

- Handled unit operations like Filtration, Distillation, Extraction and Drying.

- Handle equipments reactors (S.S Reactor, GLR Reactor, MSGL Reactor) , Centrifuge (Top Discharge & Piller type) Vacuum tray dryer, Vibratory Sifter, Sparkler filter, Cartridge filter.

- Must handle Solvent recovery plant like column operation & D.C.S. Handled production Activities of all active pharmaceutical ingredient and drugs Intermediate per cGMP.

- Ensure all raw materials are procured as per production plan and analyzed in-time.

- Ensure all customer targets are met as per agreed plan.

- Participate in trouble shooting and investigation meetings, while deviation is raised.

- Ensure to close deviations, change controls and implement CAPAs as per the targeted timelines.

- Ensure smooth transfer of product technology from Pilot Plant/Kilo Lab to production department in coordination with R&D and monitoring the trial and validation batches in production block, whenever necessary.

- Reviewing the BMRs, SOPs, validation reports and related documents.

- Calculate, review & monitor product manufacturing costs to meet pre-determined targets.    

Department: R&D (Bulk Drugs /API  Experience)

Position: Deputy Manager/Manager     Experience -8-10 years

Openings: 04                 

Location: Admiron Life Sciences Pvt ltd,Vishakapatnam,AP.

Qualification: Any degree.

- Lead the team to screen, validate and execute routes for APIs Identify challenges and propose alternatives that are cost-effective, efficient and preferably green RoS

- Generate final route selection document and product strategy report

 - Perform literature studies and evaluate data to summarise the route selection strategy and identify challenges

 - Identify the cost effective routes and IP compliant routes Process development and optimisation 

 - Develop scalable and robust processes integrating chemistry and unit operations

Monitor and review the progress of the project

 - Collaborate with the team to synthesise challenging impurities and to prepare degradation pathways

Regards,
Samhitha K

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Urgent Requirements of Fresher- Microbiology

Qualification: M.Sc or B.Sc (Microbiology)

No. of Positions: 01

Only male candidates, from Andhra Pradesh or Telangana,

Contact 9963474092,

Mail I'd: hr@kekulelife.com

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