Titan Laboratories Walk In Interview 2023.Titan Laboratories Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue. Titan Laboratories Pvt.Ltd. is the one of select few Company in india with dedicated state of art WHO GMP facility for producing high quality Sustained and Modified Release Pellets, DC Granules& Taste Masked Granules. The plant is located in green belt of mahad industrial zone about 180Kms from mumbai.
Vacancy details:
- Post Name: DQA Executive / Senior Executive – R&D/QC Officer’s
- Department: DQA/R&D/QC
- Qualification: Bpharm,Mpharm,Bsc,Msc
- Experienced: 2 to 8 years
Job Description: Greeting from Titan Laboratories !!!!!!
Important Details :
- Location: Mumbai (All Areas)
- Post of date:18/08/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To face
- Interview Rounds of Interview: HR
Roles and Responsibilities
In Section FP /Val
JD
Instrumental analysis and reporting of In-process, F.P., Validation samples.
• Chemical as well as instrumental analysis and reporting of raw material samples.
• To perform In-Process / Finished Product / Validation samples physical parameters as per
Specifications.
• Mobile phase preparation as per method of analysis.
• Maintenance, Operation of Analytical Balance.
• Maintenance, Operation of pH meter
• Maintenance, Operation of Karl fischer Apparatus.
• Maintenance, Operation of UV Visible Spectrometers.
• Maintenance, Operation of Dissolution test apparatus.
• Preparation of Reagents and solutions. Preparation and Standardization of Volumetric
solutions.
• Maintain documentation as per cGMP norms.
• Additional work assigned by HOD.
In Stability Section
JD
Responsible for checking and verifying Charging, pullout of stability samples.
• Responsible for checking daily printouts of Temperature and Humidity recording of Stability
chambers and Data Logger print of Control sample room.
• Responsible as a Shift In charge for review of Chromatograms, Raw data, Metadata, Protocols.
Trouble shooting of instruments and to guide the analysts.
• Responsible for preparation of Stability trends.
• Responsible for review of Stability study protocol, Stability reports.
• Responsible for the investigation of OOS/OOT/Incident/Laboratory errors.
• Maintain Documentation as per cGMP norms.
• Maintain Working Area and Documents as per GLP.
• Additional work assigned by Section Head or QC Head.
• Responsible to promote Safety in Premises.
We request you to please visit our companies web site and social media site to
know more about Titan Laboratories Pvt Ltd
Kindly send your resumes on jyoti.g@titanpharma.com
Roles and Responsibilities
- Monitoring of R&D trials and overall activities
- Review of lab notes
- Review of PDR
- Issuance of logbooks
- Review of MFR
Desired Candidate Profile
RND (Product development), QA Exposure, Hands on experience in development of products. Knowledge of QBD and requirements. Good auditing skills and observatory skills.
We request you to please visit our companies web site and social media site to know more about Titan Laboratories Pvt Ltd
Interested candidates kindly send your CV’s on recruitment@titanpharma.com
