Titan Laboratories Pvt. Ltd Hiring 2022.Titan Laboratories Pvt. Ltd Notification full details below..Interested and eligible candidates can Send Resume.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.
- Vacancy details:
- Post Name: QC Officer/Assistant Manager QA/GM / DGM / AGM – QA/QA (IPQA)/Senior Executive To Assistant Manager CQA/Executive QA
- Qualification:M. pharm / B. pharm , MSC / BSC
- Experienced:01 t0 24 years
Job Description: Greeting from Titan Laboratories Pvt. Ltd !!!!
- Important Details :
- Location: Mahad
- Post of date: 13/12/2022
- Selection Process: The selection will be on the basis of Interview.
Job Description:
HPLC Operators
From Finished Formulations
1 – 4 Years Experience Must- (Only Male candidate Preferred Pharma Background) )
1. HPLC 21 CFR Compliance System Handle
2. Instrument handling like, HPLC / Dissolution / UV / IR / GC etc.
3. Maintain the Reserve samples and their quality review.
4. Handling of General SOP’s and Operating procedures of Analytical Instruments, Calibrations of Instruments.
5. To maintain documents as per EUGMP, WHO-GMP, c GMP. MHRA, USFDA, TGA, TPD etc.
6. Candidate should have good understanding of subject matter.
7. Candidate should face the audit like EUGMP, MHRA, USDFA, TGA etc
8. Candidate Should have good communication skills.
We request you to please visit our companies web site and social media site to
know more about Titan Laboratories Pvt Ltd
http://www.titan-lab.com
https://www.facebook.com/TitanLaboratoriesPvtLtd/
https://www.instagram.com/titanlaboratoriespvtltd/
https://www.linkedin.com/company/titanlabindia
https://twitter.com/pvt_titan
Kindly send your resumes on recruitment@titanpharma.com
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
http://www.titan-lab.com
https://www.facebook.com/TitanLaboratoriesPvtLtd/
https://www.instagram.com/titanlaboratoriespvtltd/
https://www.linkedin.com/company/titanlabindia
https://twitter.com/pvt_titan
Kindly send your resumes on recruitment@titanpharma.com
Opening For Assistant Management QA for Mahad location from Pharma Industry Only
Job description :
- Vendor Management
- Audit Compliance
- Self Inspection
- TRAMMS
- Quality Management Review
- Elemental Impurity RA
- NDMA RA
- Excipients RA
- Technical Agreements Management
Desired Candidate Profile
Coordination, Communication Skills , Audits Handling
We request you to please visit our companies web site and social media site to know more about Titan Laboratories Pvt Ltd
https://www.facebook.com/TitanLaboratoriesPvtLtd/ https://www.instagram.com/titanlaboratoriespvtltd/ https://www.linkedin.com/company/titanlabindia https://twitter.com/pvt_titan
Interested candidates kindly send us your CV’s on recruitment@titanpharma.com
JOB PROFILE:-GM / DGM / AGM – Quality Assurance
Job location: Mahad, Raigad
Job Description –
- Design of Quality Systems.
- Implementation and monitoring of Quality Systems in Plant.
- Audits (customer audits and regulatory audits) and compliances.
- Investigation of Market complaints.
- Implementation and monitoring of CAPA.
- Deviation and Change Control Management.
- Imparting GMP training to workmen and staff. On the job training to sub-ordinates.
- Ensuring compliances of manufacturing documents (Batch Manufacturing Record and Validation protocols) as per registered dossier of Customer.
- Communication with customer and resolving customer queries.
- Self-Inspections.
- Management of operational QA functions – IPQA , Documentation , Validation and Batch Records review sections
- Management of IPQA functions Line clearances, In-process checks, Sampling of semi-finished and finished product and implementation of GMP in manufacturing and packing areas.
- Documentation Control of MFR, Specifications, SOPs, BMRs, BPRs, Quality documents and Validation protocols and records.
- Management and monitoring of validation activities – Process Validation and Equipment Qualification.
- Responsible for Batch Release. Review and approval of batch records.
- Management of Retention samples.
- Development of sub-ordinates.
Area of expertise :-
- Handling – IPQA , Validation , Batch Record Review and Documentation Control section
- Implementation and Monitoring of Quality Systems.
- Documentation Control
- Deviation Control Management
- Change Control Management
- Self Inspections
- Validations – Process Validation , Equipment Qualifications and Hold time Studies
- Training
- Market complaint and Batch Failure investigations
- Customer audit and compliances
We request you to please visit our companies web site and social media site to
know more about Titan Laboratories Pvt Ltd
http://www.titan-lab.com
https://www.facebook.com/TitanLaboratoriesPvtLtd/
https://www.instagram.com/titanlaboratoriespvtltd/
https://www.linkedin.com/company/titanlabindia
https://twitter.com/pvt_titan
Interested candidates kindly send your CV’s on jyoti@titanpharma.com, recruitment@titanpharma.com or suchita.b@titanpharma.com
SHOULD HAVE WORKED FOR US FDA APPROVED COMPANY (MUST)
- Effective implementation and monitoring of Quality Management System.
- Responsible for Authorization of SOPs as per the procedure.
- Responsible for approval of master documents for example Batch manufacturing record, validation and qualification protocols, Site Master File, validation master plan, Product Specification including their revision.
- Responsible for approval of process validation, cleaning validation and qualification protocol and Report and executed validation activities.
- Responsible for release / dispatches of Finished Product as per the SOP.
- Responsible for department and cross functional department training.
- Responsible for review of Quality Manual.
- Approval of the vendor or supplier of the materials as per the SOP.
- Approval and monitoring of contract service providers of GMP related outsourced activities. •
- Responsible for storage, archival and retention of documents and records as per SOP.
- Monitoring of compliance with the requirements of current Good Manufacturing Practice.
- Ensuring that a timely and effective communication and escalation process exist to raise quality issues to the management.
- Participation in the Quality Management Reviews of process performance, Product Quality and of the quality management system.
- To ensure timely completion, review and approval of APQR as per the procedure and recommend CAPA if any.
- Responsible for approval of Deviation, Change Control, Market Complaints, OOS, OOT, Product
- Recall, Quality Risk Assessment, Manufacturing Incidents and laboratory incidents as per
- procedure.
- To conduct investigation and Root Cause Analysis to design the CAPA for the failures occurred in the plant.
- To Conduct self-inspection as a lead auditor as per the procedure. Monitor the effective execution of self-inspection and suggest the CAPA to the audit findings.
- Responsible for regulatory and customer audit compliance and verification of CAPA.
- To ensure timely review and revision of SOPs of all the departments and its issuance and retrieval as well maintenance of master SOPs, to ensure effective compliance of SOP management.
- Responsible for audit of manufacturer and supplier of Raw material and packing material as per the vendor approval SOP.
- Responsible for rejection of Raw material, Packing material and finished product as per the SOP.
Kindly share your resumes on
Education – M. pharm / B. pharm , MSC / BSC
From Pharmaceutical Industry Only
Location – Ghatkopar East (Mumbai)
Opening For Senior Executive to Assistant Manager
Job Description
1. Responsible for overseeing the controls and quality standards for Quality Management Systems, CAPA, NC, Document Management software systems through self inspection.
2. Responsible and having sound knowledge of Change Control, Deviation, Quality Risk Management, Market Complaints.
3. Responsible for Root Cause Analysis and Investigations Perform final review and provide disposition of investigations in case of deviation/CAPA.
4. Knowledge of site transfer activity including but not limited to review of batch documents, documentation for site variation filling and cross functional activity
5. API Vendor Audit and compliance : Minimum Vendor audits performed 25. Audits and Knowledge of Vendor management related activities.
6. Time to time updates and guide the team for regulatory requirements
7. Sound knowledge of GMP guidelines specifically in PIC/s, EU GMP
8. Sustain and support the complaints management system as needed
9. To manage workload effectively in order to achieve personal and departmental objectives
10. To show initiative in problem solving by identifying and recommending solutions to problems encountered
11. Knowledge of process validation, analytical method validation.
12. Knowledge of quality control function added advantage & Self Inspection
13. APQR Preparation & Review
14. QMS Documentation
Desired Candidate Profile
QMS, Vendor Management, Audit & Compliance, Regulatory Guidelines. Risk assessment, Validation
We request you to please visit our companies web site and social media site to
know more about Titan Laboratories Pvt Ltd
http://www.titan-lab.com
https://www.facebook.com/TitanLaboratoriesPvtLtd/
https://www.instagram.com/titanlaboratoriespvtltd/
https://www.linkedin.com/company/titanlabindia
https://twitter.com/pvt_titan
Interested candidates kindly send your CV’s on recruitment@titanpharma.com or suchita.b@titanpharma.com
Designation – Officer to Executive
Education – MSC/BSC/BPHARM/MPHARM
Location – Mahad
Roles and Responsibilities
JD
- IPQA
- Line clearance ,
- Sampling,
- online review of BMR / BPR ,
- In process checks,
- GMP monitoring
Desired Skills – Vigilant, GMP Knowledge, Experience in IPQA in OSD, Semi solids, Regulated Markets with Eu, MHRA, USFDA approved companies
JD
- QMS
- Handling of change control ,
- Deviations,
- Incidents,
- CAPA
- Handling of market complaints / Integration
- Trending of QMS data
- Updating of SOP’S
Desired Skills – Experience in QMS section in regulated market – EU, MDRA, USFDA
Send your updated resumes on – recruitment@titanpharma.com
CANDIDATES WILLING TO RELOCATE TO MAHAD LOCATION & FROM PHARMACEUTICAL INDUSTRY ONLY
We request you to please visit our companies web site and social media site to
know more about Titan Laboratories Pvt Ltd
http://www.titan-lab.com
https://www.facebook.com/TitanLaboratoriesPvtLtd/
https://www.instagram.com/titanlaboratoriespvtltd/
https://www.linkedin.com/company/titanlabindia
https://twitter.com/pvt_titan
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