Friday, November 19, 2021

MSN Laboratories Pvt. Ltd – Walk-In Drive for Regulatory Affairs / FR and D / Kilo Lab on 20th Nov’ 2021

 MSN Laboratories Pvt. Ltd (MSN Group) is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs) and Finished dosages in India. Established in the year 2003, MSN Group comprises of eight API manufacturing plants ( including one for Oncology), two finished dosage facility ( one more for Oncology being built) and a dedicated R&D Center and is growing 30-40% every year. Our plants are ISO 9001-2000 certified, WHO: GMP, EU:GMP and USFDA approved. Our manufacturing units are designed to confirm to the principles of Quality, Safety and sound Environment.

Walk- In Drive For FR&D Dept- Formulation Division- R&D Center

Formulation R&D Department ( Formulations R&D) in Formulation Division – R&D Center.

1 ) Candidate Should have minimum 2 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 2 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 2 – 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 / Senior Executive / Junior Manager – FR&D-Department : FR&D – OSD / Injectable / Liquids.

  • Qualification : M Pharma Pharmaceutics
  • Work Location : R&D Center
  • Male Candidate Only
  • Position : Executive / Senior Executive / Junior Manager
  • Department : Formulation Research & Development -( FR&D – )
  • Experience : 2 to 8 Years

Date of Interview : 20.11.2021 ( Saturday)

Interview Time : 9.00 AM to 11.00 AM

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 – R&D Center.

On Saturday 20-11-2021.

  • Regulatory Affairs API RA Dept . . in API Division ,
  • Job Description: ( Regulatory Affairs – API Division )
  • Should have minimum of 2 to 15 years of experience in API Regulatory Affairs
  • Job Title: Executive / Senior Executive Experience: 1 to 8 years in API RA field
  • Education: B Pharma / M Pharma / MSc
  • Department: Regulatory Affairs

Job Title: Executive – Manager Experience: 2 to 15 years in API RA field Education: M Sc / B Pharma / M Pharma

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 : 20-11-2021

  • Department : Drug Regulatory Affairs API RA Dept.
  • Experience : 2 to 15 Years
  • Position: Executive to Manager

Work Location : R&D Center

Venue: MSN Laboratories Pvt. Ltd,

R&D Center, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana

91-8452304799/4899 & 040-30438786

 

 

Walk- In Drive for  B Tech Chemical Engineering /   Kilo Lab  / Pilot plant Dept  .in API  Division- R&D Center.

B Tech Chemical Engineering-  Kilo lab  / Pilot Plant  Dept . . in API Division-R&D Center.

Positions Vacancies :

  • 1.B Tech Chemical Engineering- with 1 – 4 year experience
  • B Tech Chemical Engineering

Department : B Tech Chemical Engineering   kilo Lab / Pilot plant Department , API

  • Eligibility Criteria : B Tech Chemical Engineering
  • Male Candidates Preferable .
  • Position :  Executive

 

Date of Interview : 20.11.2021 ( Saturday )

Interview Time : 9.00 AM to 1.00 PM

Department : Kilo Lab / Production

Venue Details :

MSN Laboratories Pvt.Ltd.,

R&D Center, Pashamylaram

Ph No : +91-8452304799/4899

040-30438786

Work Location : R&D Center

 

Walk- In Drive for  BSc Chemistry –   Kilo Lab  / Pilot plant Department in API  Division- R&D Center.

Positions Vacancies :

  • 1.BSc Chemistry – with 0 – 3 year experience
  • BSc Chemistry Fresher’s Passed out candidates 2018, 2019 & 2020
  • Department : BSc Chemistry –   kilo Lab / Pilot plant Dept , API
  • Eligibility Criteria : BSc Chemistry Fresher’s
  • Male Candidates Preferable .
  • Position :  Junior Executive Trainee / Junior Executive

Date of Interview : 20.11.2021 ( Saturday )

Interview Time : 9.00 AM to 1.00 PM

Department : Kilo Lab / Production

Venue Details :

MSN Laboratories Pvt.Ltd.,

R&D Center, Pashamylaram

Ph No : +91-8452304799/4899

040-30438786

Work Location : R&D Center

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