March 2016 - Pharma Jobs- PJ

Pharma Jobs- PJ

A DESTINATION FOR PHARMA JOBS SEEKERS.___________PJ MOTTO:- SHARE MORE, YOU WILL GET MORE.

Wednesday, 30 March 2016

    (GC & HPLC) - Quality Control walk-in
    at Cadila Pharmaceuticals Ltd  @ Ankleshwar

    Walk-in Date : 1st April - 2016 (Friday)

    Time : 3:00 - 5.00 pm.


    Venue: Cadila Pharmaceuticals Ltd. Plot No.294 

    Opp. Atul Ltd GIDC Ankleshwar, Dist.:Bharuch, Gujarat


    Position :  Officer / Sr Officer /Executive

    Qualification: B.Sc. or M.Sc.

    Experience  : 3 to 10 Years
    (Note : Pharmaceuticals (API)  Experience preferable)


    Job Profile:

    Responsible for planning of HPLC related analysis data and analysis of data generated through LIMS & SAP systems / modules .

    To ensure that the all the analysis performed in HPLC section is as per SOP and current specification and test procedures.

    To ensure all HPLC are working satisfactory. If some problem in system then try to resolve in consultation with service engineer.

    To maintain reference / working standard/impurity standard usage records.

    Review of in-process analysis data and approval for further processing of the batch.

    To maintain instrument history record.

    Joint analysis with R&D personnel during analytical method transfer on GC.

    Preparation of stability protocols and stability reports.

    To perform analysis of stability samples as per stability schedule

    Daily monitoring and recording of temperature and humidity of refrigerator / working standard chamber and laboratory area.

    Perform holding time study of intermediates and preparation of reports.

    To prepare/ check the protocols & reports for analytical method validation and analytical method transfer

    Inform and Investigate OOS results in RM/Intermediates/APIs 
    Initiation of change control / deviations / NQI / OOT related to QC.

    Ensure CFR 21 part -11 compliance and follow good chromatography practices during analysis, integration and reviewing of on line and off  
      


    Contact Person : Mayur Dalal (8238070120) 
                               
     

    We request you to carry along with you, your latest updated Resume, One Passport Size Photographs & Salary Supporting Documents (A copy of Appointment Letter, Last Increment Letter & a copy of your Three month's salary slip) supporting your Current CTC/Package while attending the interview.

Job Description

Dr. Reddy's Laboratories Ltd. - Walk-in Drive for Quality Assurance - Injectables Plant based at Visakhapatnam
Candidates matching below criteria can Walk-in directly with their updated resume and latest increment letter.

Venue: 
Hotel Lemon Tree, 
Hosur Main Road, 
Electronics City Phase 1, 
Electronic City, 
Bengaluru

Contact person: Pulla Rao, Human Resources

Experience: 4 - 8 years

Qualification: M. Pharm / B. Pharm / M. Sc with experience in IPQA, IPQA - Packing, QMS, Analytical Assurance, Documentation

Note: M. Pharm candidates with QC reviewer experience can apply for Analytical Assurance

Computer system validation
Experience: 4 - 8 years
Qualification: M. Pharm / B. Pharm / M. Sc, BCA, MCA, B. Tech with experience in Computer system validation (CSV)

Engineering Assurance.
Experience: 4 - 8 years
Qualification: M. Pharm/B. Pharm /M. Sc/B. Tech with experience in Validation, Qualification in process area

Aggregate of 60 % marks in their highest qualification is mandatory for all the above positions.

Please refer your friends as we have multiple openings

Dr. Reddy's Laboratories Ltd. - Walk-in Drive for Quality Control - Injectables plants based at Visakhapatnam
Candidates matching below criteria can Walk-in directly with their updated resume and latest increment letter.

Venue: 
Hotel Lemon Tree, 
Hosur Main Road, 
Electronics City Phase 1, 
Electronic City, 
Bengaluru

Contact person: Pulla Rao, Human Resources

Qualification: M. Sc / B. Pharm

Experience: M.Sc / B.Pharm with 2-7 years experience in handling HPLC, GC, Dissolution and other laboratory equipments. Must have an understanding of GLP, GDP & exposure to regulatory audits.

IPFP, Stability, Lab Support, Raw materials

Aggregate of 60 % marks in their highest qualification is mandatory for all the above positions.

M. Pharm need not apply

Please refer your friends or collegues as we have multiple positions

    Designation : Project Coordinator
    Department : Formulation Technology Transfer
    Qualification : B.Pharm & MBA

    Female Candidates having minimum 1 year experience in project management in pharma industry.

    Candidate have to coordinate among different sites of tech. transfer / plants.

    Good communication & follow up skill

    Able to manage day to day work pressure & quick in reporting about the developments to concerned authority.

    Interested candidates can send their resume on mitalkhambhati@torrentpharma.com

    Contact No. 75674 33366 / 02764 233671 (Ext. No. 210)

    Job Title  : Packaging Tech. Asst. / Executive
    Qualification : M.Pharm / B. Pharm / M.Sc. / B.Sc.
    Experience : 1 - 5 yrs
    Location : Indrad (50 Kms. away from Ahmedabad)

    Job Description :

    Packaging Instrument qualification 
    IQ / OQ / PQ
    Candidates who had exposure to production instrument qualification can also apply

    Interested candidate candidate can send their resume on mitalkhambhati@torrentpharma.com

    Contact No. 75674 33366 / 02764 233671 (Ext. No. 210)

DesignationOfficer/ Executive - ADL Validation
Job Description-To perform the sample analysis by using High performance liquid chromatograph. with diffent detector (s).
-To perform Dissolution test using Dissolution Appratus and UV Visible Spectrophotometer.
-To perform thin layer chromatography,infra-red spectroscopy and titration analysis by using Autotitraor
-To follow the Good Laboratory Practices.
-To perform disinegration test friability test and hardness test.
-To perform the physical parameters of Samples as per requirements.
-To check the availability of analytical resources like chemicals/reagents / columns / standards etc. before start the analysis.
-To maintain the column history card, instrument log book, chemicals / reagents / standards etc. used as per Standard Testing Procedure or method validation protocol.

Desired ProfileWorking knowledge of HPLC, GC, Dissolution apparatus, Karl Fisher , pH meter etc. is must.
System oriented and go getter approach
Good communication & interpersonal skills
Computer knowledge is must.
To improve and maintain interpersonal relationship.
To keep the things and his work area clean and tidy.

Experience3 - 6 Years
Industry TypePharma / Biotech / Clinical Research
RoleResearch Scientist
Functional AreaMedical, Healthcare, R&D, Pharmaceuticals, Biotechnology
EducationUG - B.Sc - Any Specialization, B.Pharma - Pharmacy
PG - M.Sc - Any Specialization, M.Pharma - Pharmacy
Doctorate - Doctorate Not Required
Compensation: Not disclosed
LocationAhmedabad
KeywordsHPLC Chemical Analysis Method Validation method testing process validation
ContactMs. Bhumija Marfatia
Cadila Healthcare Limited 
Telephone02717-666-560
Emailbhumija.marfatia@zyduscadila.com

Experience: 2 -7 Years
Officer / Executive - R&D Zydus Cadila API Dabhasa Cadila Healthcare Limited 2 - 7 yrs Vadodara/Baroda  

Qualification: M Sc (Organic Chemistry) / Ph. D. - Chemistry 

Job Profile: 

Good experience in handling multistage reactions with knowledge of analytical data interpretation; 

literature search, 

non-infringing route of synthesis

In depth knowledge of organic chemistry. 

Job Location : Vadodara 


Candidates must have experience of working in regulatory approved plants, exposure to GMP , and SAP Environment will be preferred.

Interested Candidate may send their resume on
pooja.thakkar@zyduscadila.com

Contact No.  0266 2679767

Regards,
Team HR
Cadila Hrealthcare Ltd. 

    Walk-in for Quality Assurance on 02nd April 2016 at Ankleshwar

    Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.

    Key Responsibilities are mentioned as below:

    QUALITY ASSURANCE : Sr.Executive / Executive : M.Sc./ B.Sc Chemistry with 4 - 8 year , must be familiar with cGMP requirements, Data Integrity, Document Cell, Batch release process, Trending APR shop floor Operation in API / Bulk Drug
    Manufacturing.

    a) Data Integrity - Responsible to review of HPLC and GC , QC Sop Compliances, Investigation activities , OOS and OOT and quality control instruments.

    b) Document Cell -Review of documents before DMF submissions, distribution / Issuance of BMRs, Master Formulae, SOPs and Formats to the respective departments and controlling all master documents.

    c) Batch Release 
    - Knowledge of ICH guidelines and should review of BMRs and Validation documents and to give usage decision and dispatch of all APIs and salable intermediates in LIMS and SAP.

    d) Technology transfer documents - Review R&D process & TTD, evaluation of CPP & CQA and comparison with batch record , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.

    e) Trending and APR - Knowledge of Market complaint, Deviation, Incident, Change control for trending of Systems, Review of Master SOPs, BMRs, PCRs, validation Protocols and reports and Annual Review reports.


    Investigation Positions for Production / QC / Process engineering / Process development : Sr.Executive / Executive 
    Should have knowledge of investigation tools and technics. , Flow chart, Parato chart, Fishbone tech., Brain storming, 5 Why tech 
    Should be well versed with statistical analysis technics and data evaluation, ANOVA, Regression, Correlation, Minitab software. 
    Should be competent in Quality Risk Assessment technics, FMEA, Fault tree analysis. 
    Should have through knowledge of pharmaceutical manufacturing processes, unit operation and unit processes, Mixing, Blending, Type of reactor and agitators etc.
    Should have experience in handling of failure investigations i.e OOS, OOT, market complain, deviations. 
    Should have experience / knowledge of working principles of quality control instruments, HPLC, GC, XRD etc. 
    Should have handled Phase-I investigations. 
    Should be conversant for utilization of Minitab software and Microsoft excel for data evaluation.
    Should have knowledge of report writing, technical writing and presentation skill. 
    Should have knowledge of relevant regulatory guidelines, ICH-Q7, ICH-Q9, 
    USFDA OOS investigation etc.

    Interested candidate may Walk-In for Interview along with their CVs and relevant documents at

    Date: 02nd April 2016 (Saturday) 

    Time: 09:30 AM to 05:00 PM

    Venue: Cadila Healthcare Ltd
                   Plot No 291, GIDC
                   Industrial Estate
                  Gujarat

    Contact No of HR representative: 02646-660408 / 660507

    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 ank.hr@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.

Currently we are handling an assignment into different pharmaceutical sector for one of our esteem client.

The details of the position are as given below:-
Bio- Clinical (Required - Clinical Research Associate)
Qualification: M.SC / M Pharma
Experience 2-8 years experience with QC Background.

Bio- Clinical - QC (Required - Clinical Research Associate)
Qualification: B.SC/M.SC /B.Pharma / M Pharma
Experience 2-8 years experience with QC Background.


Regards
Kavita Ruia 
97024 43322


We have an Urgent opening with a Reputed Pharma Company (USFDA Approved)

(I) Position:- Research Associate / Research Scientist - Bio- Analytical
Location:- Andheri, Mumbai
Experience & exposure to Bio Analytical having equipment knowledge of LC-MS/MS, developing method on LCMS.

(II) Position:- Clinical Research Associate- Bio- Clinical 
Location:- Andheri, Mumbai
Experience with QC Background can apply

(III) Position:- Clinical Research Associate- Bio- Clinical QC
Location:- Andheri, Mumbai.
Experience with QC Background can apply

Note:- 
1) Interviews will be conducted at Ahemdabad on 3rd April 2016 (Sunday). If interested for above mention positions, call back immediately on 9773551311

Kindly let me know whether you will be interested in this opening, If Yes then please forward your updated C.V. in Word Doc File & current gross salary immediately. 

We assure you that your CV will not be posted to any of our clients, without your prior consent for every assignment. This way we also ensure the confidentiality of your candidature. 

Please do not delete the title of the mail while reverting CV 

Please mention the ' Hierarchy in your department.' (Reporting to) 

Note:- 
This is a System generated mail, Kindly ignore if your profile does not match. 

Thanks and Regards,
Ms. Shrutika Sawant 
shrutika@aspiremgs.co.in

ASPIRE MANAGEMENT SOLUTIONS PVT.LTD
022 - 29671972/73/74
Mob:- 9773551311
Web: - www.aspiremgs.co.in

At present we have following Opening regarding your job profile with our reputed client company. 


Qualification : M.Pharma,B.Pharma,M.Sc
 
Experience : 1 - 9 Years
 
Job Locations : bharuch, Gujrat

Company Profile:
 

* Our client company is API Manufacturing Pharma Company.
 

Job Description:

* Experience must be in API Pharma Company ,
* Candidate must have experience with different type of project.


Salary is not constraint for right candidate.
 

If you are interested please revert with your updated resume do mention your Complete detail of Company, designation, duration, current and expected CTC, Detailed Job Profile, Latest Contact nos. & mail ID.

If the profile mentioned in this E-mail does not match your profile kindly forward this e-mail to the people who look for the similar openings in your connections & favour them.

We have some more openings in other fields too so if you know who is searching a job, kindly tell to send updated CV to us to our e-mail ID shubham@skynetplacements.com


Thanks & Regards
Shubham J.
09033068854 (Work)
09911590055(per)
Emal ID : subham@skynetplacements.com
Web Site : www.skynetplacements.com


We are currently looking for below position for one of our client.

COMPANY: One of the Leading pharmaceutical Company

LOCATION: Pune

POSITION:
1.            Officer/Sr. Officer-QA
2.            Officer/Sr. Officer-QC

Department: Formulation

Responsibilities:

*             Should be work in pilot plant.
*             Formulation Plant

Exp: 1 to 3 Years

CTC: Best in the Industry

Education: M.Sc, M.pharma

If you are looking for a change do revert us back on jobs.pharma@evokehr.com


Saturday, 26 March 2016

we are having the following vacancies for our new branches at INDORE, AHMEDABAD, BANGALORE.

1) Analyst-pesticide residues(1-6 years exp.)
2) Analyst foods(1-6 years exp.)
3) Analyst microbiology(1-6 years exp.)
4) Group Leader Pesticide residue analysis(7-9 years exp.)
5) Manager food labs(10-15 years exp.)
NOTE: Candidates shud have experience working in a testing laboratory who is well versed with ISO/IEC 17025 standards.

Interested candidates shud send their cv to suryavamsi.vasireddy@vimta.com before 24th march 2016 before 5pm


Personal interview will be scheduled at hyderabad on 29th march 2016 at 10am (THIS IS NOT A WALK-IN).


REFERENCE :- RATHORE DIPAK

Thursday, 24 March 2016

Requirement on urgent basis

Assistant Professor ( 03 )
Pharmacology-1
Qualitative Analysis-1
Medicinal Chemistry-1
NOTE: M.Pharm in the above mentioned respected subjects. M.Pharm in the above subjects is the minimum qualification required.
Send ur cv to : contact.samanvay@gmail.com
Mob. 9624377302

Opportunity to work with Claris Otsuka (Gujarat- Ahmedabad) in Quality
Control Department as an Q.C Officer or Sr.Officer.

Qualification:-  B.pharm, Bsc(Chemistry) or Msc (Organic chemistry)

Experience:- 6months to 4 year
                                      Candidate should have sound
knowledge of HPLC,GC, UV, Titration, Calibration and relevant
experience in Pharmaceutical Industry.
                                        Interview Date:
25thMarch(Friday).

 Reference Rathore dipak

Regards:-                 Rishikesh(HRM) -Claris otsuka pvt
ltd.                                        

   Mail I'd:-
rishikesh.dharkar@clarisotsuka.com

Wednesday, 23 March 2016

PJ JOB UPDATES:-  SHARE MORE , GET MORE

BLOG LINK:-  http://pjbydipakrx.blogspot.in/
1.
INDUSTRY NAME
Tata consulting services, Mumbai
2.
INTERVIEW DATE
31st March 2016
3.
EDUCATION
M.Pharm Second year passed in 2016
4.
VENUE
BharatiVidyapeeth College of Pharmacy, Kolhapur
5.
JOB LOCATION
Mumbai/Pune
6.
EXPERIENCE
--
7.
FRESHER
Yes
8.
OPENINGS FOR DEPT
Pharmacovigilence
9.
POSITION
Garde-II
10.
CONTACT PERSON
Dr. Anilkumar J Shinde
11.
CONTACT DETAILS
Dr. Anilkumar J. Shinde
Training & Placement Officer
Mobile: 09823866196
E mail: tpo.bvcopk@gmail.com 
ajshinde07@rediffmail.com
12.
SEND CV TO
Pool- campus Interview for Shivaji University, Kolhapur affiliated Pharmacy Colleges.
13.
REMARKS IF ANY




REFERENCE :- RATHORE DIPAK




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