VACANCY IN CIRON DRUGS & PHARMACEUTICALS PVT. LTD @ MUMBAI

REFERENCE

Srinivasulu Tirumalasetty

Global pharma News

Dear Candidate,

Greeting from Ciron Drugs & Pharmaceuticals Pvt. Ltd.

Ciron Drugs & Pharmaceuticals Ltd is the fastest growing company, engaged in the production of sterile dosage forms like injectable in ampoules and vials, lyophilized injections, pre filled syringe and eye drops. We are upcoming with the new Plant with state of the art equipment's for regulated markets like Europe, Pic's countries, South Africa, Australia and USA at Tarapur region, extended suburb of Mumbai, within a two hours' drive from downtown with all the possible facilities in the city, 

Ciron is looking after bright, smart, sincere, experienced people who can be a dedicated team with us to achieve the goals of Regulatory approval.

For more information, you are also invited to browse our website: http://www.cironpharma.com/

Location - Mumbai at Tarapur [Boiser]

We are looking for candidate for our QA department for below mentioned Role & Responsibility also we looking for a candidates from Regulatory Market.

1) Area/ Section - Facility, Equipment and Utility Qualification
Role and Responsibility - Preapration of Installation Qualification, Operational Qualification and Performance qualification protocol and compilation of the report
Experience in the relevant area - 3- 4 Years in Validation and Qualification of Sterile formulation

2) Area/ Section - Facility, Equipment and Utility Qualification
Role and Responsibility - Preapration of Installation Qualification, Operational Qualification and Performance qualification protocol and compilation of the report
Experience in the relevant area - 6-10 Years in management of Validation and Qualification of Sterile formulations

3) Area/ Section - Media fill and Process Validation

Role and Responsibility - Preparation of process validation protocol and sampling plan, co-ordination of process validation and compilation of report
Experience in the relevant area - 3- 4 Years in Process Validation of Sterile formulation

4) Area/ Section - Training
Role and Responsibility - Training of Validation and qualification protocols, SOPs etc
Experience in the relevant area - 3-5 Years of Management of training in pharmaceutical industries

5) Area/ Section - Quality Management System (Change Control, Deviation and Investigations)
Role and Responsibility - Change control inititation, followup, closer and verification of change implementation
Experience in the relevant area - 6-10 Years in Quality Management Systems of Sterile formulations

6) Area/ Section - Cleaning Validation
Role and Responsibility - Assessment of Cleaning validation, preparation of protocol and report for cleaning validation, surface area calculation of equipments, MACO calculations, Sampling rinse
Experience in the relevant area - 3- 4 Years in Cleaning Validation of Sterile formulation

If you are Interested kindly share your updated profile on hr@cironpharma.com

If you find this profile not suitable to your profile feel free to help us with reference or you can forward this mail to your colleague or friend who looking for changes and interested in this profile.

Thanks & Regards,
Prajakta
HR
Ciron Pharma

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