QC

Walk in Interview in QA, Production, QC @ Acme Formulation

Walk in Interview in QA, Production, QC @ Acme Formulation

Quality Control- Officers/Executives
Exposure in Instrumental and chemical analysis i.e. RMPM/FG/Validation/Micro/ Stability and having competency on instruments like HPLC, GC.

Quality Assurance- Officers/Executives
Exposure in IPQA/QMS/ Documentation’Validation,’Qualification with thorough knowledge of cGMP norms.

Production/Packing-Officers/ Technicians
Solid Orals : Experience in Granulation, Compression, Coating,Capsules & Packing (Blister Pack & Cartonator Pack)
Injectable Experience m Vial,’Ampoule Washing Machine, Filling Machine, Lyophilizen’Autoclave & Packing Machine

Interested and eligble candidatess are advised to appear for WALK-IN along wlh updated CV, passport size photograph and salary supporting.

Note: Candidates who are ready to relocate and join us immediately will be preferred.

Timing: 9.30 am to 5.00 pm
Date : 3rd December & 4th December 2016 (Saturday & Sunday)
Venue for Walk in Interview: MEDICO Healthcare, # 501 ,Aditraj Arcade, Near Hetvi Tower, 100, Feet Ring Road, Satellite, Ahmedabad (Gujarat)

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Openings for Quality control Officer @ Cargill

Openings for Quality control Officer @ Cargill

Job Description
1. Calibration of Equipments.
2. Responsible for analysis of validation samples, stability samples, water analysis.
3. Handling and maintaining RM, FG Control samples.
4.Perform validation activitis.
5.Updation and maintenance of laboratory documents and records.
6.Conductig RM,PM,SFG&FG analysis as per test protocols.
7.Instruments and glassware calibration

Candidate Profile :
1.Adequate knowledge and understanding on the Quality Control activities.
2.Adequate knowledge in documentation ,handling of analytical instuments.
3. Prior experience in Quality Control department of pharmaceutical industry is preferred.
4. Min 2 Years experienc in QC.

Additional Information:
Experience : min 2 years
Qualification : M.Sc
Location : Karnataka
Industry Type :  Pharma / Biotech / Clinical Research
Functional Area : QC
Last date : 20th December, 2016

To apply online, Click here.

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Walk in Interview for QA, QC , Production @ Emcure

Walk in Interview for QA, QC , Production @ Emcure

Quality Control (Micro): Manager/Officers (Injectable)
M.sc (Microbiology) with 2-12 years experience in Microbial analysis, Micro method validation tike BET, MLT, Bioburden & Stenlity. Should have worked in Injectable Plant and having exposure to regulated markets. Excellent communication and people management skills are a must.

Quality Assurance : Officers (Injectable)
M.Sc/B.Pharm with 2-5 years’ experience in Pharmaceutical formulation Industry only for Micro QA reviewer, Chemistry reviewer, Qualification and validation of equipment’s. Analytical data Review. Vendor Audits, Internal Audits, Documentation QMS. hands on expenence in handling HPLCs. GC. IR, OOS, OOT. Investigations, expenence of regulated markets pharmaceutical Injectable formulation plant. Excellent communication and people management skills are must.

Engineering : Manager/Asst. Manager/Executive/Officer
B.E/Dipioma – Electrical/Instrumentation / Mechanical with 2-10 years’ expenence and having exposure to maintenance of plant equipment’s, QMS Documentation, equipment qualification. Should have worked in solid orals & Injectable formulation Plant and having exposure to regulated markets. Excellent communication and people management skills are a must.

Production : Asst. Manager/Officer/Executive
B.Pharm/M.Pharm with 3-12 years’ experience of having exposure in Sterile Injectable Facility in the following sections: Manufacturing, Vial washing. Filling area, Lyophilizer, Autoclave. Tunnel, Isolator. Should have worked in Injectable formulation Plant and having exposure to regulated markets. Excellent communication skills are a must.

WALK-IN INTERVIEWS
Date:
19th & 20th November 2016 at at Ginger Hotel, Vizag 47-10-19,2nd Lane, Dwaraka Nagar, Vlsakhapatnam – 530016, India.
Time : 9.00 am to 5.00 pm

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Opening for Freshers in QC, QA, Production @ Lini Infotech

Opening for Freshers in QC, QA, Production @ Lini Infotech




Job Description :
Qualification; BSC/MSC Frehers
Job Location : Jedcherla
Only Freshers

Candidate Profile :
BSC/MSC Chemistry freshers

Additional Information:
Experience:
Freshers
Qualification: B.Sc, M.Sc
Location: Jedcherla-Telangana
Job Type: Production.QA,QC
Industry Type: Pharma

Email your Resume : careers@liniinfo.com

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Walk in for M.Sc/B.Sc/B.Pharm/M.Pharm in Production/QC/Packing @ Macleods

Walk in for M.Sc/B.Sc/B.Pharm/M.Pharm in Production/QC/Packing @ Macleods




Vacancies for Formulation Plant
Officers / Sr.Officers – Quality Control. (Location: – Baddi/ Daman & Sikkim)
Qualification: B.Sc/M.Sc / B.Pharma / M.Pharma
Experience 2-6 years in Raw Material, Finished Product & Stability, with experience on Analytical Instrumentation – HPLC, GC, and UV IR.

Officers / Sr.Officers – Production (injectable). (Location: – Sikkim)
Qualification: B.Pharma / M.Pharma
Experience 02-08 years – Dry Powder Injection




Technical Associate Production (injectable). (Location: – Sikkim)
Qualification: ITI/ Diploma/B.Sc
Experience 02-8 years Autoclave/Filling/Sealing/Labeimg & Cartonators

Technical Associate Production (Operators)- Production /Pocking
(Location: – Baddi/Sikkim)

Qualification: ITI/ Diploma/B.Sc
Experience 02-8 years – Granulation /compression /coating / Bulk packing machine.

Vacancies for Formulation Plant

Research Associate – Bio-analytical department
Qualification: M.Sc/M.Pharm
Experience 1-7 years experience in Bio-analytical department

WALK IN interview 9.30 -18.00 Hrs with CV and Salary proof on following date & Places. Walk-In Date: 13th November, 2016
Venue : Hotel Amrutha Castle 5-9-U. ODD, Secretariat. Saiabod. Hvdarobod. Telanaana 500063

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Opening for Officer/Sr.Officer/Executives – Quality Control in Glenmark Pharmaceuticals Ltd

Opening for Officer/Sr.Officer/Executives – Quality Control in Glenmark Pharmaceuticals Ltd




Job Description:
Qualification: M.Sc/B.Sc (Chemistry)

Experience: 2-8 years’ experience in Pharmaceuticals /Fine Chemicals Job Profile : Hands on advanced instruments like HPLC /GC /UV/IR /auto titrates along with wet analysis, Raw material /packing material analysis as per cGMP requirements, knowledge and work experience in stability study management / QC compliance system /Calibrations/working standard qualifications. Work experience on Advanced instruments XRD /DSC /Particle size analyser.




Additional Information:
Experience: 2-8 years
Location: Madhya Pradesh
Education: B.Sc-Chemistry, M.Sc-Chemistry
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QC

Date & Time : 13th November 2016 From 9:00 A.M to 5:30 P.M
Location : Radission Blu Hotel 12,Scheme No. 94C,Ring Road,Indore, Madhya Pradesh – 452010

Those unable to attend the Personal Interview may send their resume through e-mail: payal.shastri@glenmarkpharma.com

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Work for QA / QC / Production / Engineering Departments of Hetero Drugs | B.Pharm

Work for QA / QC / Production / Engineering Departments of Hetero Drugs | B.Pharm




Quality Control :
Positions : Jr. Officer – Asst. Manager
Exp. :  2 to 10 years of Experience in QC Dept.

Quality Assurance
Positions : Jr. Officer – Asst. Manager
Exp. :  2 to 12 years of Experience in QA Dept.

Production:
Exp. 2 to 6 years of Experience in Production dept.




Engineering:
Exp. 10 to 25 years of experience in Maintenance department

Interested candidates with experience in Pharma Industry can send profiles to raju.ch@heterodrugs.com

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Opening for Manager/Assistant Manager @ Titan Laboratories for – Quality Control (formulation)

Opening for Manager/Assistant Manager @ Titan Laboratories for – Quality Control (formulation)




No of Posts: 02

Job description :
1. Sampling, Analysis, Reporting / Review / in shift wise.
2. Instrument handling like, HPLC/UV/IR/GC etc.
3. Good experience in audits like WHO/MHRA/EU/WHO.
4. Stability Samples Review/Updating Documents.
5. Follow up procedures, rules and regulation according to SOP.
6. Preparation and Checking of COA and analysis report.
7. Preparation of calibration schedule.
8. Formulation Routine analysis (Tablets / Capsules / Pellets).
9. To maintain documents as per WHO-GMP, c GMP & ISO norms.
10. GMP/GLP activities Implementation of SOP and GMP
11. To involve actively in regulatory audits.
12. Other allotted work time to time.




Candidate Profile :
Candidates should have faced the audits like EU MHRA USFDA GMP FDA etc

Additional Information:
Experience: 3-8 years
Qualification: B.Sc, M.Sc
Location: Mahad
Functional Area: QC
Industry Type: Pharmaceutical (Formulation)
Salary: 3- 8 lacs

Mail your resume at hrd2@titanpharma.com.




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Stabicon Life Sciences Pvt. Ltd – Walk-in Interviews for QC / AR&D on 10th -12th November, 2016 @ Bangalore

Stabicon Life Sciences Pvt. Ltd – Walk-in Interviews for QC / AR&D on 10th -12th November, 2016 @ Bangalore

Company: Stabicon Life Sciences Pvt. Ltd

Department: QC / AR&D

Job Title: Executive

Experience: 2 – 5 years

Location: Bengaluru

Walk In date: 10 November-12th November
Job Description:

-Having knowledge in current GLP requirements. -Having adequate knowledge in handling of analytical instruments like HPLC, UPLC, GC and Dissolution testers.

-Having technical exposure on testing of various dosage forms for Assay, Related substances/compounds, Dissolution, Content Uniformity & etc as per Good Documentation practices

-Experience in method validations, method verification and method transfer for analytical methods of drug products for Assay, Related substances/compounds, Dissolution, Content Uniformity and residual solvents by using HPLC, GC and UV-Visible Spectrophotometer as per current ICH guidelines and Pharmacopoeia.

-Experience in calibration / Qualification of analytical instruments like HPLC, UPLC, GC, Dissolution tester, UV-Visible Spectrophotometer, etc.

-Having adequate knowledge in Preparation and review of analytical method validation/ method verification protocols, Method transfer/Routine/Stability documents for drug products for Assay, Related compounds, Dissolution, Content Uniformity & residual solvents.

-Having adequate knowledge in review of analytical raw data & trends of stability samples.
-Ability to work in a multi-task environment. -Ability to produce high quality outputs.

Venue Details:

Stabicon Life Sdences Pvt. Ltd.

Plot No. 28,

Bommasandra Industrial Area,

4th Phase, Jigani hobli, Anekal Taluk,

Bangalore 560 100
Interested candidate can send confirmation either by mail to hrd@stabicon.com or call at 91 80 27839259/9260 between 9.00 AM to 5.00 PM.

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