Walk In drive for Analytical Research & Development – Department – API ( AR&D – API ) Analytical Method Development & Analytical Method Validation ) MSN R&D Center Pashamylaram on 03.09.2022 ( Saturday )
- Experience :- 2 to 8 Years AR&D LCMSMS analysis with Peptides analysis, sequencing
- Qualification : BSc Chemistry / B Pharma / M Pharma / MSc Chemistry
- Department : Analytical Research & Development – API( Analytical Method Development &
- Validation ) LCMSMS analysis with Peptides analysis, sequencing
- Position : Junior Executive / Executive / Senior Executive / Junior Manager
- Work Location :- MSN R&D Center Pashamylaram.
- Openings: 50
Date Of Interview :- 03.09.2022 ( Saturday )
Timings:- 09:00 AM to 1:00 PM
Only Male Candidates
Venue :- MSN Laboratories Pvt. Ltd.,
R&D Center, plot no.12, Phase-IV, Sy.no.119, IDA Pashamylaram, ptancherru, sangareddy, 502307.
Phone :- +91-8452304702/4789
Walk- In Drive for Formulation Analytical Research & Development (FAR&D) Department .in MSN R&D Center, Saturday 03-09-2022 at MSN R&D Center Pashamylaram.
JOB DESCRIPTION:
- Position : Junior Executive / Executive / Senior Executive / Junior Management /Assistant Manager
- Qualification : BSc / B Pharma / M Pharma / MSc
- Department : Formulation Analytical Research & Development (FAR&D)
- Experience : Minimum 1 to 13 Years experience in Formulation AR&D ( FAR&D ) Department.
- Openings: 100
Analytical Method Development , Analytical Method Validation , HPLC, GC-MS , LC MS, Complex Injectable , OSD , Liquids, oncology, Formulation Analytical Quarries, analytical documentation, analytical support,
- Should have 2-10 years of adequate hands on experience in performing analysis of special oral dosage forms such as Suspensions, Solutions/Syrups, and Powders/granules for Oral suspensions.
- Should have experience in Method development and method validation along with support and stability studies of suspensions and Solutions.
- Should have hands on experience in handling analytical instruments such as, not limited to Dissolution, High Performance chromatography, Gas Chromatography, Karl-Fischer Instrument, IR spectroscopy, Viscometer.
- Should possess adequate analytical skills to perform tests like Assay, Dissolution, Related substances, Residual solvents, pH and specific gravity measurements, Suspendability and redispersibility, Sedimentation velocity, Pourability, Viscosity, flocculation and de-flocculation etc.
- Should have strong desire for analytical research-orientated work and assignments.
- Should have technical knowledge and capability in interpreting analytical data and results
- Should be able to work collectively and collaboratively with in team and analytical department.
- Should able to work and adhere strictly to quality and compliance policies of company by following SOP and STP.
Date of Interview : 03.09.2022 ( Saturday )
Interview Time : 9.00 AM to 1.00 PM
Work Location : MSN R&D Center, Pashamylaram.
Venue Details :
MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana
Walk In drive for Formulation Research & Development – Department FR&D – Oral Solid Dosage / Liquids Oral Dosage – MSN R&D Center Pashamylaram. on 03.09.2022 (Saturday)
Formulation R&D Department ( Formulations R&D) in Formulation Division – R&D Center.
1 ) Candidate Should have minimum 0 to 8 Years of experience in formulation development of solid oral dosage form for regulated market such as USA and Europe. Candidate should have exposure in handling various dosage forms such as tablets and capsules with exposure of scale up activities. Exposure to preparation documents such as MFR, BMR, PDR are consider as added advantage.
2 ) Candidate should have 0 to 8 Years of experience in solid oral dosage forms for regulated market such as USA, Europe, Australia, etc.. He should have exposure in handling various dosage forms like tablets and capsules (ER/SR, IR). Experience in handling MUPS project is an added advantage. He should have exposure in designing strategies, DOE/QbD based development, data compilation and interpretation, basic knowledge about bio study evaluation, etc. Should have scale up exposure for regulated markets and should have appropriate knowledge about regulated market requirement. Should have exposure in preparing and reviewing documents like PDR, MFR, BMR, etc. Supervising and knowledge about handling regulatory queries will be an added advantage
3 ) should have 0 – 8 years experience in FR&D (solids) should have knowledge in QbD & DoE & its application in Formulation Development. should have knowledge on regulatory guidance.
Position : Executive Trainee / Executive / Senior Executive – FR&D-Department : FR&D – Oral Solid Dosage / Liquids Oral Dosage
- Qualification : M Pharma Pharmaceutics Fresher’s – 2020/2021 Passed out.
- Work Location : MSN R&D Center, Pashamylaram.
- Position : Executive Trainee / Executive / Senior Executive
- Department : Formulation Research & Development – ( FR&D )
- Experience : 0 to 8 Years ( Preferable Male Candidates )
- Openings: 30
Date of Interview : 03.09.2022 ( Friday)
Interview Time : 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt. Ltd.,
MSN R&D center, Pashamylaram, Isnapur, Patancheru, Sangareddy
040-30438786
Work Location : MSN R&D Center , Pashamylaram.
Walk-In Drive For for API -Regulatory Affairs -Department in API Division – MSN R&D Center Pashamylaram, On Saturday 03-09-2022.
- Should have minimum of 2 to 15 years of experience in API Regulatory Affairs
- Job Title: Executive / Senior Executive / Junior Manager :- Experience: 2 to 10 years in API RA field
- Education: MSc – Chemistry Should have minimum of 2 to 15 Years
- Job Title: Executive – Manager Experience: 2 to 15 years in API RA field Education:
Department: Regulatory Affairs – API
Job Profile:
1. Collecting and reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies.
2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc]..
3. Hands on experience on preparation of drug master files, Applicants Parts, Tech Pack, life cycle management [updates and amendments] and drafting of response to deficiencies and customer DMF review comments for all global regions.
4. Should have hands on experience on eCTD regulatory submission tools.
5. Should have knowledge on the requirements to respond to the deficiencies.
6. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
Job Title: Junior Manager / Assistant Manager Experience: 6 to 10 years in API RA field Education: M Sc
Department: Regulatory Affairs
Job Profile:
1. Good scientific conceptual background to the level to evaluate the processes and procedures in the area of Quality, R&D, AR&D and Production.
2. Manageable communication in English [should be able to manage regulatory and scientific discussions in the internal and external meetings and one to one interactions within the organization and with customers]
3. Manageable knowledge on the regulatory and quality guidelines from various regulatory agencies ICH, FDA, EMA, Health Canada, ANVISA, PMDA, MFDS, CFDA etc.
4. Thorough knowledge and hands on experience on the DMF registration and marketing authorization application systems in the major regulatory regions [US, Canada, Europe etc]..
5. Hands on experience on preparation of drug master files, life cycle management and drafting of response to deficiencies and customer DMF review comments for all global regions.
6. Should have knowledge on product developmental and the quality systems to ensure the regulatory compliance.
7. Should have hands on experience on eCTD regulatory submission tools.
8. Conducting meetings for the deficiencies received from various regulatory agencies and should have knowledge on the requirements to respond to the deficiencies. Ensuring that the accurate and adequate responses are sent to the authorities within the timelines defined by agencies.
9. Thorough review and ensuring that the regulatory submissions are adequate and error free with minimum open issues and closing of open issues before filing or before the receipt of deficiencies.
10. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
11. Reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies.
12. Review and assessment of change controls and providing guidance to the team on proposed changes.
13. Ensuring that the regulatory databases are properly maintained and updated on time to time for each regulatory activity.
Interview Date : 03-09-2022
- Department : Drug Regulatory Affairs API RA Dept.
- Experience : 2 to 15 Years
- Position: Executive / Senior Executive / Junior Manager / Assistant Manger / Deputy Manager / Manager
- Work Location : MSN R&D Center, Pashamylaram.
Venue: MSN Laboratories Pvt. Ltd,
R&D Center, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana
91-8452304799/4899 & 040-30438786
