JOB OPENINGSS TITAN LABORATORIES PVT LTD
INTERNATIONAL MARKETING ASSISTANT
MANAGER-REGULATED/EU MARKET
@GHATKOPAR
EXPERIENCE: 7-9 YEARS; GENDER:- ONLY MALE
- Handling CMO and Developments projects for Regulated Market
- Preparation of monthly, quarterly and yearly reports /presentations (Booking
Billing collection Forecast status)
- Preparing the of cost sheet (New products / Revision in prices of RM and PM)
- Responsible for sending quotations & following up with Clients for final ization
of the orders as well as for new business development through emailing, phone
or Skype.
- Coordinate with various cross-functional teams for smooth functioning of
business
- Develop and maintain business responsiveness to build customer
relationships.
has experience in finished Formulation
- International Travel exposure mandatory
Email your resumes to:
shivali.k@titanpharma.com
recruitment@titanpharma.com
JOB OPENINGS
TEAM LEADER DRUG REGULATORY AFFAIRS REGULATED/ EU MARKET
@GHATKOPAR
EXPERIENCE: 7-9 YEARSs
Team Leader Dossier preparation for eCTD market UK, EU, Australia & Newzealand
&VARIATION filing in EU/Australia market.
New project Execution, Team handled for min 2 people, Should review MFR, PDR,
BMR, PVR, SPECS MOA, STABILITY, ERA, NDMA. Should have knowledge of product
lifecycle management, RFI Response, customer queries.
Should be well versed with EMEA, TGA and ICH Guidelines. Should visit site for
required documents for dossier submission and RFl response as and when required.
Should be strong in communication and correspondence.
Desired Skills: Quality, RND (Product development), Dossier Preparation eCTD
format. Very well versed with EMEA Guidelines
Efficient Problem solving, Effective communication, creative thinking, Should be
Bold /challenge seeker, positive attitude
Email your resumes to:
shivali.k@titanpharma.com
recruitment@titanpharma.com
JOB OPENINGS
JUNIOR OFFICER QUALITY ASSURANCE
QUALIFICATION: B.PHARM/ M.PHARMA
LOCATION: MAHAD
EXPERIENCE: FRESHER
- To ensure Line Clearance during Batch/Product Change Over.
- Verification & Review of Electronic Data of Temperature & Humidity Record.
To check and monitor the training records, risk assessments.
- To handle Deviation, CAPA, incident, Change control.
Sampling of process validation Batches.
- Preparation & Compilation of Process Validation Protocol and Reports.
Issuance and Retrieval of all department controlled documents (BMR, BPR,
SOP, Protocols, Analytical worksheets)
Email your resumes to:
shivali.k@titanpharma.com
recruitment@titanpharma.com
 Opening For Quality Assurance, Regulatory Affairs,JUNIOR OFFICER , International Marketing ){kind=link}
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