Urgent requirement Qualifications-BSE, MSE

Urgent requirement

Qualifications-BSE, MSE

Experience-0 to 5 years experience in Pharma.

5 vacancy- QC, Documentation

Location- Precise Formulation Pvt ltd .Near to Ahmedabad

Preference-
FDCA APPROVED CHEMIST


Interested candidate contact
Mob no-
9723924169
Send cv to:
Kjpateld19@gmail.com

At Medreich MULTIPLE VACANCY AT BANGALORE

At Medreich, our value statement Winning Together further strengthens the winning behavior as we believe in working together as a team to scale greater heights.

Medreich facilities have received the seal of approval from leading global regulatory bodies such as -UK MHRA, Australia TGA, SA MCC, Health Canada, and French AFSSAP, GCC, PIC, regulatory bodies of various countries in the African continent and independent bodies like UNICEF and MSF.

TO APPLY ANY JOB CLICK:- http://www.naukri.com/search?xz=7_0_5&qc=11249&tem=medreich&othersrcp=14805&wExp=N

opening in our Bio analytical department for the position of Research Associate /Sr. Research Associate at Cliantha Research Ltd. ,Ahmedabad.

We have opening in our Bio analytical department for the position of Research Associate /Sr. Research Associate at Cliantha Research Ltd. ,Ahmedabad.

Please refer the job responsibilities for your reference ;
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of tasks to which the employee may be assigned.

I-STUDY RELATED ACTIVITIES:

A.Perform the extraction of samples using wet chemistry.
B.Centrifuges, evaporators, freeze specimens as required.
C.Performs aliquots of samples for wet chemistry.
D.Performs wet chemistry according to study protocol guidelines and/or SOPs.
E.Completes QC sheets and makes log book entries as required by protocol and/or SOP.
F.Operate HPLC, LC/MS/MS and ICP-OES; troubleshoots problems and performs minor repairs.

II GENERAL LAB DUTIES:

A.Prepares required reagents and solvents.
B.Under direction of the project manager, may perform some method development.

III-ADMINISTRATIVE DUTIES:

A.Conforms to training schedule for own position and maintains awareness of SOP content, according to company requirements

Best Regards,
Sonali Parmar
HR
Cliantha Research Ltd.
Contact No: 07966135625

81 QA-QC RELATED Interview QUESTIONS

Before attending interviews ready this question-answer

QA & QC DEPARTMENT

List of all questions asked in interviews of quality control and quality assurance

1 Can any deviation be changed into the change control?

2 What is the difference between Humidity and Relative Humidity?

3 What should be the temperature and humidity for the tablet compression?

4 What is the difference of vacuum pressure and vapor pressure?

5 In Stability testing if significant change occurs then what will be the action plan?

6 What do you mean by MKT (Mean Kinetic Temperature) in stability?

7 What are the stability zones and stability conditions?

8 What do you mean by Bracketing andMatrixing in stability?

9 How to select HPLC column for a particular product?

10 What is the composition of a C18 column?

11 What is validation, validation protocol and validation master plan?

12 What is the process validation?

13 What is limit of cleaning validation?

14 What do you mean by MACO?

15 What is NOEL?

16 What isrecovery factor?

17 How much the minimum recovery should be in swab sampling?

18 What is the acceptance criterion fordetergentwashing?

19 What do you mean by LOD and water content?

20 What is the difference between LOD and water content?

21 What is the difference between Calibration & Validation?

22 What is the difference between Validation & Qualification?

23 What is the disintegration time of coated tablets?

24 What is the limit for friability of tablets?

25 What is disintegration time for dispersible tablets?

26 What do you mean by Q+5 in dissolution?

27 What is the disintegration time for Hard Gelatin Capsule?

28 What is limit of disintegration for Enteric coated tablets?

29 What should be the sampling point in dissolution test?

30 Which will give more drug release paddle or basket in dissolution?

31 Tablets of which drug are used in dissolution calibration?

32 What is the difference between DrugPurity and Drug Potency?

33 What should be the minimum limit of a working standard?

34 What is the storage condition for reference standard?

35 How impurity is analyzed in any tablet?

36 Why we use the placebo in analysis?

37 What is the procedure to prepare the placebo?

38 What is difference between method validation and method verification?

39 What is thetechnology transferand how is it done?

40 What are the steps for the sterilization procedure for Dry Powder injection facility (from Starting)?

41 What exepients are used in dry powder injections?

42 What should be the LOD of dry syrup?

43 How can you fix the known and unknown impurity limit for any drug substance?

44 What is the relative response factor in related substances?

45 How do we choose HPLC or Gas chromatography for a sample analysis?

46 Why 3X sampling plan are implemented in process validation?

47 What is the difference between temporary change control and deviation?

48 Why we use toluene for resolution inUV calibration?

49 What is photo stability?

50 What is pooled sample and why it isrequired in dissolution test?

51 Why we use disodium tartare for determination of factor in karl ficher titration?

52 What are closely monitor parameters in stability study?

53 What are the limits for LOD and LOQ?

54 Why should we not dispatch the reprocess material to export?

55 What is the formula for KF standardization?

56 How we fix the validity period of a volumetric solution and re-standardization due date?

57 How quantitative stability studies are done?

58 What do you mean by CAPA?

59 In KF Standardization why we use Disodium Tartarate?

60 What is the difference between Deviation and Out of Specification?

61 What is the difference between mix-up and cross-contamination?

62 What is GMP, cGMP,GDP and GLP?

63 What is thecalibration of HPLC?

64 How polarimeter is calibrated?

65 What is the difference between Analytical method validation and Analytical method transfer?

66 How melting point apparatus is calibrated?

67 What is the difference between polarimeter lamp and IR lamp?

68 What is the difference between sonication and homozinization?

69 What is the difference between uniformity of content and content uniformity as official test for all tablets?

70 What is limit of uniformity of contentas per USP?

71 How related substance method is developed for new compound which is not official in the pharmacopeia?

72 If calibration of 12 bowl dissolution apparatus does not meets single stageprocedure, how can you precede calibration?

73 What is capacity factor?

74 How will you calculate telling in any HPLC peak?

75 What do you mean by end capping?

76 What is the wave length of polarimeter lamp?

77 Which gases are used in gas chromatography?

78 Which gas is used as a mobile phase in GC?

79 What types of columns are used in GC?

80 What is stationary phase?

81 What is hold time period for swab samples?

For more information
Visit
Pjbydipakrx.blogspot.com
Regular

DR. REDDY 31 JULY AT CHNDIGHARH AND 30-31 JULY AT BANGALORE FOR VIZAG, BADDI, HEYDRABAD LOCATION FOR QA & QC

BHARAT PARENTRALS LTD VADODARA MULTIPLE VACANCY

TO APPLY ANY POST

CLICK HERE

http://bplindia.in/?page_id=4009

BHARAT PARENTARL LTD AT VADODRA

Apprenticeship Program for B.Pharm Freshers @ MYLAN

Apprenticeship Program for B.Pharm Freshers @ MYLAN

Apprenticeship program from MYLAN:

Mylan has Injectable manufacturing facilities at Bangalore and Hosur in Tamilnadu and also R&D facility at Bangalore.

We are looking for fresh B. Pharm Graduates for an Apprenticeship program. The details of program is given below

Qualification: B. Pharm

Designation: Apprentice as per Apprenticeship Act.

Duration of Apprenticeship: One year

Location: Bangalore & Hosur

Scope of Job Assignment: Selected candidates will be placed in any one of the following departments, based on candidates aptitude and suitability.

Departments: Production, Quality, Validation, Technology Transfer, Regulatory Affairs.

Career Prospects:

Candidates enrolled for Apprenticeship will get Excellent training on cGMP aspects, On the job training that enriches the Technical Skills and building technical capability, exposure to Regulatory environment, Develop high level of knowledge on Regulatory requirements, exposure to state of the art manufacturing, laboratory facilities.

Career Growth:

Candidates who successfully complete the Apprenticeship Training shall stands bright chances for a career growth at Mylan also.

Stipend:

Rs. 10,000/- per month (net cash in hand) – no deductions. Free canteen facility [Breakfast & Lunch @ our canteen].

Career in Pharma Manufacturing: Pharma manufacturing is one of the fastest and continuously growing Businesses across the Globe. People with right knowledge, skill and attitude will have wealth of opportunity for the career growth across country / globe. Injectable manufacturing is highly skilled, regulatory driven, niche sector in Pharma. Experience and exposure to Injectable operations will be an added advantage for career prospects.

For details contact Anil babu - 8143165066

FRESHERS:- Ajanta Pharma is a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets.

Ajanta Pharma is a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets.

Company: Ajanta Pharma Limited

Location: Dahej

Qualification: B.Pharm

Experience: Freshers

Interested candidates can send resume to deelip.sawant@ajantapharma.com⁠⁠⁠⁠ 

Walk-in Interviews @ Emcure, Pune for Quality Assurance & Quality Control Dept.s(Microbiology & Chemistry) on 30th July 2016( Saturday)

Walk-in Interviews @ Emcure, Pune for Quality Assurance & Quality Control Dept.s(Microbiology & Chemistry) on 30th July 2016( Saturday)

Dear Candidate,

Looking for stable and promising career in Pharma industry???

Join Emcure !!!

Walk-in Interviews @ Emcure, Pune for QA & QC Dept.s on 30 July 2016 (Saturday)

Quality Assurance:

Designation: Officer

Experience: 02 To 05 yrs. (Only In Pharma formulation Industry for Micro QA reviewer, Chemistry Reviewer, Qualification and validation of equipment's)

Qualification: MSc (Chemistry)/ B.Pharm/ M.Pharm

Budget : 2.50 to 5.00 CTC.

Note : Experience in Preparation of equipment qualification/ validation protocols and reports and in IPQA activities in injectable facility from Regulatory Pharmaceutical Company will be preferred

Quality Control - Chemistry

Designation: Officer/ Executive/Manager

Experience: 3 To 12 yrs. (Only In Pharma formulation Industry)

Qualification: MSc (Chemistry)/ BSc (Chemistry)/ B.Pharm/ M.Pharm

Budget:2.50 to 9.00 CTC

Note: Hands on experience on QC analytical instruments e.g. UV-Vis, Autotitrator, GC & HPLC, from Regulatory Pharmaceutical Formulation Company is mandatory, Injectable experience will be preferred.

Quality Control - Microbiology:

Designation: Microbiologist/ Officer/Asst.Manager

Experience: 2 To 7 yrs. (Only In Pharmaceutical formulation Industry, MLT, BET, Sterility validation and supervisory experience)

Qualification: MSc (Microbiology)

Budget: 2.50 to 7.00 CTC

Note: Experience from Regulatory Pharmaceutical formulation Company is mandatory.

WORK LOCATION: PUNE

Walk-In Venue:

Emcure Pharmaceuticals Ltd.

Plant III (Oncology)

Plot No. P-2, Phase II, IT-BT Park, MIDC, Hinjewadi, PUNE- 57.

Phone: 020-39821300. Ext. 1920.

Contact: HR Team- Plant III ( Oncology)

Date: 30th July 2016 ( Saturday) Time: 10.00 am to 3.00 pm

Note: Fresher's are not eligible for any of the above positions.

For all the above mentioned openings, experience in injectables will be preferred.

Contact: Candidates who may not be able to attend the interview, they may send in their resumes on sandeep.gogawale@emcure.co.in for further process.

This is a mass email, those candidates does not have relevant experience, should ignore this email.

Regards,

Sandeep Gogawale

HR Team

Emcure Pharmaceuticals

020-39821300

Pune.

Sandeep Gogawale

Emcure Pharmaceuticals Ltd.Pune

CLARIS Date : 30th July 2016, Time : 09am to 03pm Quality Control (Parenteral) - Sr. Officer/Officer/Jr Executive

Quality Control (Parenteral) - Sr. Officer/Officer/Jr Executive

Based on our preliminary assessment we invite you for a round of Interview at the below given venue and time. Kindly bring along your CV, Pass-port size photo, original mark sheets and Salary Slips for the interview.

Date : 30th July 2016, Time : 09am to 03pm

Venue: Claris Otsuka Pvt Ltd, 21st Floor, B-Block, Westgate, 

Nr. YMCA, SG Highway, Ahmedabad.

www.clarisotsuka.com

Key Responsibilities :

-To carry out the sampling of all the materials according to Standard Operating Procedure (SOP).

-To perform the tests as per the specification & method of analysis and record the necessary results in prescribed documents.

-To investigate failure of finished product (FP) / In-process (IP) product, in case of any out of specification (OOS) / deviation and take corrective and preventive actions.

-To carry out the calibration of all the analysis instruments as per the schedule.

-To perform periodic chemical analysis.

-To record all the data related to the testing online, on day-to-day basis.

-To document all the testing data and related papers.

-To release Raw Material and Packing Material.

-To follow the Good Laboratory practices and Good Manufacturing practices (GMP).

(Pl Note: CANDIDATES INTERVIEWED IN LAST SIX MONTHS NEED NOT APPEAR FOR INTERVIEW. DO NOT REPLY TO HIS EMAIL. IGNORE MAIL IF NOT RELEVANT TO YOU)

FRESHER WELCOME Walk-in-interview @Emcure, Pune for Production Dept. on 31st July ( Sunday) 2016.

Walk-in-interview @Emcure, Pune for Production Dept. on 31st July ( Sunday) 2016.

We are having an urgent opening in Emcure Pharmaceuticals Ltd!!!!

-Candidates must be having relevant knowledge in Microsoft word, excel.

-Preparation of batch data.

Designation - Trainee/ Officer

Department -Production

Qualification - B.Pharm/M.Pharm

Experience - 0 to 2 years

CTC - 2.00 to 3.00 LPA

Location -Pune( Hinjewadi)

Interested candidates can send their resume to recruitment.plantIII@emcure.co.in

Or directly walk-in to our company on 31st July 2016 

Time - 9 am to 3 pm

Emcure pharmaceuticals Ltd, Plant III

Hinjewadi phase -2

Plot No - P-2 IT BT Park 

MIDC, Pune

Contact No - 02039821300 ext.- 1901

We have scheduled Walk-In for Torrent Pharmaceuticals Ltd., Indrad Plant @ Ahmedabad & Indore on 31st July, 2016 (Sunday) for Quality Control Department

We have scheduled Walk-In for Torrent Pharmaceuticals Ltd., Indrad Plant @ Ahmedabad & Indore on 31st July, 2016 (Sunday) for Quality Control Department

INTERVIEW VENUE:

1. HOTEL AMAR VILAS

CHANDRA NAGAR,

A.      B. ROAD, 

INDORE, MADHYA PRADESH

2. HOTEL NAMI RESIDENCY 

OPP. V. S. HOSPITAL,

ELLISBRIDGE, 

AHMEDABAD, GUJARAT

Date: 31st-July, 2016 - SUNDAY

TIME: 09:30 AM to 04:00 PM

Job Location: Ahmedabad (Indrad Plant)

Qualification: B.Sc. / M.Sc. / B.Pharm. / M.Pharm.

Experience: 1 - 10 years in Reputed Pharmaceutical Industry

Department: Quality Control (Formulation, Stability, API, Method Validation & Oncology)

Brief Job requirements: 

- Analysis of Finished product, Stability samples and Raw Material as per Method of Analysis

- Analytical Method Development, Verification and Validation

- Responsible for preparation of Specification and STP, Data interpretation and 

Troubleshooting

- Preparation of Method Verification Protocols and Data sheet 

- Sound knowledge of HPLC/ GC/ Dissolution Apparatus/ Particle Sizer/ AAS/ GCMS/ XRPD/ DSC/ Chemical Analysis 

Preference will be given to those who are having experience of working in Formulation/ API regulatory approved plants.

Candidates may Walk-In for an interview along with their updated Resume & Passport size photograph.

Documents required: 

Photocopy of all Marksheets, School Leaving Certificate, PAN card, Salary Slips & Bank Statement (last six months), Increment Letter

Regards,

Mayur Desai

Human Resources

Torrent Pharmaceuticals Ltd.

Office line: 9879603921/ 22/ 23/ 24/ 25

Mobile No. 990 990 54 77

E-mail: meghagupta@torrentpharma.com, mayurdesai@torrentpharma.com 

We have urgent opening for Area Business Manager (1st Line) in Pune HQ.

We have urgent opening for Area Business Manager (1st Line) in Pune HQ.

Please find below the job details & interested candidates please share your resume at nirmal.kher@erislifesciences.com

To accomplish the sales objectives assigned by the company

To maintain proper coverage and call average for self and team.

Implement the strategies and practices assigned, with proper feedback to HO

Identify the areas of improvement among team members and report the same to RBMs and SMs on periodic basis

Keep HO informed with the promotional activities of competitors

Induct, counsel and coach and manage BEs.

Thanks & Regards

HR Team

Eris Lifesciences Pvt. Ltd.

GLENMARK GOA FOR PRODUCTION

urgent requirement of Production Sr. Officer with our client GLENMARK PHARMACEUTICALS LTD, GOA having approvals like US-FDA, MHRA etc.

If you possess the following qualification pls send us your latest resume on consultancydisha@yahoo.co.in

POSITION : Production Sr.Officer
Company :- Glenmark Pharmaceuticals Ltd, Goa
JOB LOCATION : Goa
EXPERIENCE REQUIRED : MINIMUM 2 to 5 YEARS
Qualifications :- B.Pharm/Mpharm
CTC: Max. Upto 4.50 LPA depends upon last CTC & experience.
Interview Process: By Telephonic Interview

Candidate should be from any reputed US-FDA/MHRA approved plant.
Candidate should have knowledge of Pallet Coating/Wooster Coating.

Pls mention following details in your resume :-
Current CTC :
Expected CTC :
Current Location :
Notice Period :
Total Work Experience :

Note :- If you are not interested for this position kindly refer to any of your friend having similar expertise.

Thanks
Nitin Jain
9302526235 / 7389919235 / 7389903235

Intas 7 august indore MP

Glenmark 24 July pithampur

ZYDUS CADILA FOR FRESHER 22-23 JULY

Ajanta Pharma, QC JOB

Urgent requirement of Ajanta Pharma,so We are pleased to inform you that if you are suitable and interested, reply on gayatri@uppl.in and call 8488863098 and also share to your friends also.

We have opening for the position of Formulation Officer/Executive QC in Pharma company
Location:Dahej (Bharuch)

CTC: 1,000,00 to 4,00,000p.a.

Requirement: candidate should be BSC / MSC/ BPharm/ Mpharm with minimum 1yr experience in formulation-tab and capsule ( with HPLC )

If you are interested then pls send your latest c.v. on this mail ID:- gayatri@uppl.in

With Warm Regards,

Gayatri Agrawal
Utkarsh Placement Pvt. Ltd.
Baroda
Phone: 0265 - 3316370
MOB: 8488863098

We have an opening for the position of '' Sr. Executive / Asst. Manager Production'' Location : Pune

We have an opening for the position of '' Sr. Executive / Asst. Manager Production''

Location : Pune ( periphery of 30 / 40 km)

Qualification : B.Pharma / M.Pharma

Experience : 6 to 8 years ( in Formulation of ointment / cream/ lotion : Must)

Sr. Executive / Asst. Manager Production . : Production Experience in Cream / ointment /lotion is Must.

FDA approval will be preferred.

If intersted pls send CV atrakshat@epharmafocus.com

Walk In Interview @ MORAIYA, 23rd July, 2016 Time : 9:00 p.m. to 3:00 p.m.

Walk In Interview @ MORAIYA, 23rd July, 2016

Time : 9:00 p.m. to 3:00 p.m.

DEPARTMENT : CORPORATE QUALITY ASSURANCE - STABILITY LAB.

DESIGNATION :- OFFICER/EXECUTIVE/SENIOR EXECUTIVE/ ASSISTANT MANAGER/ DEPUTY MANAGER

Qualification: M.Sc. / B.Sc. / B.Pharm./M.Pharm.

Experience: 02 to 10 years

Job Location : Magnet Park, Opp. Zydus Hospital, Ahmedabad 

Preference will be given ONLY to the candidates who match with the following criteria 

Knowledge and experience of stability protocol registration to sample destruction 

Investigating OOS/OOT/incidents reported in QC department and to plan, execute the work for testing 

Analysis of finished product in process samples & stability samples of various dosage form

Candidates having experience of working in regulatory approved plants and SAP Environment will be preferred.

Warm Regards,

Virendrasinh Jadeja,

Human Resources,

Cadila Healthcare Limited ,

Sarkhej-Bavla NH-8A, Moraiya, Sanand, 

Ahmedabad - 382210,

Walk-in Interviews @ Emcure, Pune for Quality Assurance & Quality Control Dept.s(Microbiology & Chemistry) on 30th July 2016( Saturday)

Walk-in Interviews @ Emcure, Pune for Quality Assurance & Quality Control Dept.s(Microbiology & Chemistry) on 30th July 2016( Saturday)

Dear Candidate,
Looking for stable and promising career in Pharma industry???

Join Emcure !!!

Walk-in Interviews @ Emcure, Pune for QA & QC Dept.s on 30 July 2016 (Saturday)

Quality Assurance:

Designation: Officer
Experience: 02 To 05 yrs. (Only In Pharma formulation Industry for Micro QA reviewer, Chemistry Reviewer, Qualification and validation of equipment's)
Qualification: MSc (Chemistry)/ B.Pharm/ M.Pharm
Budget : 2.50 to 5.00 CTC.
Note : Experience in Preparation of equipment qualification/ validation protocols and reports and in IPQA activities in injectable facility from Regulatory Pharmaceutical Company will be preferred


Quality Control - Chemistry

Designation: Officer/ Executive/Manager
Experience: 3 To 12 yrs. (Only In Pharma formulation Industry)
Qualification: MSc (Chemistry)/ BSc (Chemistry)/ B.Pharm/ M.Pharm
Budget:2.50 to 9.00 CTC
Note: Hands on experience on QC analytical instruments e.g. UV-Vis, Autotitrator, GC & HPLC, from Regulatory Pharmaceutical Formulation Company is mandatory, Injectable experience will be preferred.


Quality Control - Microbiology:

Designation: Microbiologist/ Officer/Asst.Manager
Experience: 2 To 7 yrs. (Only In Pharmaceutical formulation Industry, MLT, BET, Sterility validation and supervisory experience)
Qualification: MSc (Microbiology)
Budget: 2.50 to 7.00 CTC
Note: Experience from Regulatory Pharmaceutical formulation Company is mandatory.

WORK LOCATION: PUNE

Walk-In Venue:
Emcure Pharmaceuticals Ltd.
Plant III (Oncology)
Plot No. P-2, Phase II, IT-BT Park, MIDC, Hinjewadi, PUNE- 57.
Phone: 020-39821300. Ext. 1920.

Contact: HR Team- Plant III ( Oncology)

Date: 30th July 2016 ( Saturday) Time: 10.00 am to 3.00 pm

Note: Fresher's are not eligible for any of the above positions.
For all the above mentioned openings, experience in injectables will be preferred.

Contact: Candidates who may not be able to attend the interview, they may send in their resumes on sandeep.gogawale@emcure.co.in for further process.

This is a mass email, those candidates does not have relevant experience, should ignore this email.

Regards,
Sandeep Gogawale
HR Team
Emcure Pharmaceuticals
020-39821300
Pune.


Sandeep Gogawale
Emcure Pharmaceuticals Ltd.Pune

LUPIN 22 JULY AT DOMBIVLI , TARATPUR, MH

Walk-in for Quality Control on 22nd July 2016 at ZYDUS Cadila Healthcare Ltd, API Ankleshwar Multi Product Plant

Walk-in for Quality Control on 22nd July 2016 at Cadila Healthcare Ltd, API Ankleshwar Multi Product Plant
  
Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.


Candidates having experience of 3 to 8 years in Quality Control API pharma can Walk-In for Interview along with their CVs and relevant documents at

Date : 22nd July 2016 (Friday)

Time: 09:30 AM to 04:00 PM

Venue : Plot No 291, Cadila Healthcare Ltd,
Industrial Estate , GIDC  
Dist :Bharuch, 
Ankleshwar, 
Gujarat
 
Contact No of HR representative: 02646-660408 / 660507
Key Responsibilities are mentioned as below:


QUALITY CONTROL : Sr.Executive / Executive : M.Sc /B.Sc (Chemistry / Microbiology) with 3 - 8 years of hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab, micro lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.


Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.

Those who are unable to attend the Personal Interview may send their resume through e-mail at reema.patel@zydusmail.com

Please mention the position applying for on the top of envelope or subject in case of e-mail.

Preference will be given to candidates having API - Pharmaceutical Industries experience.

Cipla requires for its Sterile formulation at Indore, Goa & Sikkim 24 JULY

Cipla 
requires 
for its Sterile formulation at Indore, Goa & Sikkim


We are looking for appropriately qualified candidates as 
MANAGERS/ EXECUTIVES/ OFFICERS/ASSOCIATES
with 1 to 7 years of experience in Sterile Manufacturing/Packing & Quality Control with regulatory exposure


Interested candidates may meet Mr. Ajit Gupta with an updated copy of their resume, a colour photograph and CTC (salary) details. 


Date : July 24, 2016 (Sunday) Time : 9:00 am to 5:00 pm 
Venue: 
Hotel Solitaire
SCO : 902-903, NAC, Housing Board Chowk, Manimajra
CHANDIGARH


Candidates who are unable to attend the interview on the above mentioned date may send their applications to 


hrdindore@cipla.com | hrdgoa@cipla.com | hrdskm@cipla.com | hrdblr@Cipla.com | 

CIPLA Walk-in for Production & ADL on 23.07.2016 at Cipla, Virgonagar Cipla Ltd 1 - 6 yrs Bengaluru/Bangalore

Walk-in for Production & ADL on 23.07.2016 at Cipla, Virgonagar

Cipla Ltd

1 - 6 yrs 

Bengaluru/Bangalore

Note : Only for experienced candidates


Cipla invites candidates for its API Plant in Virgonagar Bangalore.


Job profile for Production includes:
1. Handling all the production related equipment
2. Knowledge on SOPs related to API production
3. Shop floor activities
4. Documentation


Job Profile for ADL includes:
1. HPLC Routine Analysis
2. Analysis by GC & Potentiometric Techniques
3. Stability Sample Incubation
4. Good Knowledge on Wet Analysis
5. Method Development
6. Pre-Validation
Interested candidates can Walk-in with their updated CV, CTC /Salary Break-up and one photograph between 09.00 am to 02.00 pm on Saturday 23.07.2016 at below mentioned address:


Cipla Limited
Virgonagar Post
Old Madras Road
K R Puram
Bangalore : 560 049

IND-SWIFT LAB CHANDIGARH ON 22-23 GWALIOR & 24-25 INDORE

BIOCON 24 JULY @ BANAGLORE

This is to Inform you that we are conducting a Walk-in to be held on 24th July 2016 , Sunday at 9:00 AM in the morning, we will be having Interviews across Injectable Production, Engineering & Maintenance and Instrumentation.
· To Apply in Production , the Candidate should be B.Sc. / B. Pharm/M. Pharm with 1-6 years of technical skills, regulations, qualifications/validations in sterile formulation facilities. Should have regulatory audits exposure. Should have experience in handling process like Vial Filling/ Vial Washing/ Autoclave/ Lyophilisation/Vial Sealing.

· To Apply in Engineering & Maintenance , the Candidate should be B Tech/ Diploma in Electrical/ Mechanical with 1-6 years of technical skills. Should have experience in handling Equipment like HVAC and Boilers , Clean Room , Black Utilities , Water Systems and Calibrations.

Request you all to inform to the candidates who are Interested in Joining Biocon there along want to pursue their career within.

Venue details :
Biocon Campus
20th Km,
Electronic City,
Bangalore – 5600100.

Kindly ask them to carry along the educational as well as Employment documents with them.

Reputed MNC pharma company Located at Ahmedabad (Gujarat)-job opening for Executive-QC

We have job opening for
Executive-QC (Formulation/sod/solid/osd/tablets/capsules/OTC)

Reputed MNC pharma company Located at Ahmedabad (Gujarat)

CCTC:
ExpCTC:
Notice Period:
Total Yrs Exp:

Note: Must have Exp in Formulation/SOD/Solids

Please kindly send me updated CVs to : mallesh.formulahrc.com
or call :04044670003

AMNEAL 23rd Jul'16 (SATURDAY) Timing: 9:30 AM to 2 PM MULTIPLE POSITION IN ALL DEPT

Dear Candidate, Greetings from Amneal!! We have arranged Walkin Interview for our Multiple Open Positions, please come along with your Updated CV, Salary Proof & Passport Size Photograph at below: Date: 23rd Jul'16 (SATURDAY) Timing: 9:30 AM to 2 PM Venue: Amneal Pharmaceuticals Pvt. Ltd. 508-514, 5th Floor,  Venus Atlantis Corporate Park Near Shell Petrol Pump, Prahladnagar, Ahmedabad Please find below the details of Open positions: Quality Assurance-OSD:  Experience: 02-10 Yrs Qualification: B. Pharma / M. Pharma Description:  Should be from Solid Oral background Opening is for different sections in QA like IPQA / QMS / Documentation etc. Candidates working in USFDA plant are more preferable. 2. QUALITY CONTROL-OSD: Experience: 2-10 Yrs Designation: Officer to Sr. Executive Qualification: M. Sc / B. Sc / B. Pharma Description:  Should be from Solid Oral Background only. Please do not come if your current exposure are into API background. Candidates working in USFDA plant are more preferable. 3. Analytical R&D - Injectable: Exp: 03 to 08 Yrs Designation: Officer to Asst Manager Description:  Candidate must be from Injectable background. Should have exposure of Method Development and Validation of Injectable dosage form. Should be from USFDA plant. 4. QUALITY CONTROL-CHEMICAL (INJECTABLE) Experience: 02-07 Yrs Desig: Officer to Sr. Executive Qualification: B.Sc / M.Sc / B. Pharma / M. Pharma Description:  Must be from Parentral background only. Should have exp in testing & documentation of injectable formulations. Must have exp in handling sophisticated instruments like: HPLC, FTIR, TOC, GC etc. 5. QUALITY CONTROL-MICROBIOLOGY (INJECTABLE) Experience: 02-07 Yrs Desig: Officer to Sr. Executive Qualification: M.Sc - Microbiology Description: Responsible to perform full range of Microbiology testings. (Parentral Exp is must) Should have exp in Environmental Monitoring. (Air Sampling, Settle Plate, Surface Monitoring, Personnel Monitoring) Must have exposure of Validation of method, equipments i.e. Autoclave, LAF, Area, Water System, Sterility Testing Etc. 6. QUALITY ASSURANCE - INJECTABLE (QMS) Experience: 02 to 08 Yrs Desig: Officer to Sr Executive Qualification: B. Pharma / M. Pharma Description:  Drafting of Deviation Handling of CAPA Handling of Change Control Handling of Quality Risk Assessment documents 7. Sterile Manufacturing: Exp: 0 to 08 Yrs (ITI & D. Pharma freshers may apply) Desig: Operators / Officer to Sr Exe Desired Profile:  Should have good exposure in Parentral Production BMR completion of filing, LYO Loading & unloading & sealing of vials. Check of pH of bulks & Assay before filtration start. Preference will be given to candidates having exp into USFDA  Plant. 8. For Analytical R&D - OSD Exp: 01-07 Yrs  Desig: Officer to Sr Exe Qualification: M.Sc (Analytical Chemistry) / B. Pharma / M. Pharma Description: Opening for various groups in ARD like, Stability / GLP / Method Validation only. 9. Formulation & Development - OSD Exp: 01 to 07 Yrs Desig: Officer to Sr Exe Qualification: M.Sc (Analytical Chemistry) / B. Pharma / M. Pharma Description: Should have exposure in F&D for USA market into solid oral dosage form. 10. Manufacturing - OSD  Exp: 02 to 08 Yrs Designation: Operator / Officer to Sr. Exe Qualification: B. Pharma / M. Pharma / ITI Description:  Should have exposure of Solid Oral Granulation, Compression, Coating, Bulk Packaging, well versed with cGMP norms. Note: Only ITI / D. Pharma Freshers can apply if interested for Production (Injectable) Job. Candidates having working experience of API are not allowed. Only candidates having Pharma background are eligible. B. Pharma / M. Pharma freshers can drop your CV at manojm@amnealindia.com / chandanid@amnealindia.com / aartig@amnealindia.com for future requirements. Please drop your CV at pujas@amnealindia.com if looking for job in F&D-Injectable. Please share this mail with your friends and colleagues those who are looking for job change. Regards, Team HR