Tuesday, 27 June 2017

Multiple Vacancies in F&D / RA / Q.A / A&D / API / HR / BD / Projects / Accounts for India & China Locations @ Menovo Pharmaceuticals Co., Limited

Multiple Vacancies for Menovo Pharmaceutical Co., Limited.
Head Office - China
Departments: F&D/RA/QA/AD/API/HR/BD/Projects/Accounts for India & China Locations
Kindly Contact Sonali: 022 61409696, Mail id- sonali@menovopharm.com
Reference – Asim Kumar
Analytical Development Manager (R&D)
Experience -8 to 12 years
Post- 03
Location- India/China
Qualification: M. Pharma/ M. Sc Organic/Analytical/Applied chemistry
Candidates should have 8 to 12 years of experience in reviewing AD related Documents for ANDA/EU. Should have hands working on instruments like HPLC, GC, FTIR, UV, Particle size distribution, XRD etc, 
(Understanding on 21 CFR P-11 compliance is required)
Analytical Development Scientist- (R&D)
Experience -3 to 6 years
Post- 03
Location- China
Qualification: M.Pharm / M. Sc Organic/Analytical/Applied chemistry
Candidates should have relevant experience of 3 to 6 years handling HPLC/GC/Dissolution and worked for ANDA/EU should be preferred.
(Awareness on 21 CFR P-11 compliance is required)
Formulation Development Manager (R&D)
Experience -8 to 12 years
Post- 01
Location- China
Qualification: M. Pharma Pharmaceutics/Industrial Pharmacy
Candidates should have 8 to 12 years of experience in development for ANDA/EU market. Knowledge on PDR preparation, review and familiar with regulatory requirement / guidance and procedures of ANDA development and filing.
Formulation Development Scientist (R&D)
Experience - 4 to 7 years
Post- 01
Location- China
Qualification: M. Pharma Pharmaceutics/Industrial Pharmacy
Candidates should have 4 to 7 years of experience in development for ANDA/EU market. Knowledge on PDR preparation, review and familiar with regulatory requirement / guidance and procedures of ANDA development and filing.
Quality Assurance Manager (R&D)
Experience -8 to 12 years
Post- 01
Location- China
Qualification: M.Pharm-Quality Assurance
Candidates should have relevant experience of 8 to 12 years experience for GMP management of US formulation, Responsible for formulation quality monitoring; Responsible for reviewing quality management documentations and audit of formulation plants; Responsible for organizing group risk evaluation and regulation training for formulation personnel, ensuring the company meets related formulation regulation requirements.
Regulatory Affairs Manager (API - R&D)
Experience -7 to 12 years
Post- 01
Location- China
Qualification: M.Pharm / B.Pharm / M.Sc
Candidate should have more than 7 years experience in Registered post, with a background of chemical related professional; have ECTD file preparation and submit experience, and well-known the FDA's newest API review requirements; cumulatively complete and successfully register more than 30 USDMFs.
Regulatory Affairs Manager (R&D)
Experience -7 to 12 years
Post- 02
Location- India / China
Qualification: M.Pharm /B.Pharm
Candidate should have more than 7 years experience in Registered post, have ECTD file preparation and submit experience, and well-known the FDA's newest review requirements; cumulatively complete and successfully filed more than 10 ANDAs.
Project Manager (R&D)
Experience -8 to 12 years
Post- 01
Location- China
Qualification: M. Pharm / B.Pharm / MBA
Candidates should have 8 to 12 years of experience in development for ANDA/EU market. Responsible for writing the Project  report of ANDA  project, Writing the research plans and implementing programs of ANDA Knowledge and review and familiar with regulatory requirement / guidance and procedures of ANDA development and filing.
International Registration Manager (R&D)
Experience -8 to 12 years
Post- 01
Location- China
Qualification: M. Pharm /B.Pharm / M.Sc
Candidates should have 8 to 12 years of experience in ANDA/EU market, Collecting the drugs registration requirements, familiar with the laws and regulations; Tracking change of FDA registration regulations, analysis the consequences of the policy change, and give the feasible Suggestions; Timely grasp the procedure of registration and patent application, follow the registration process, ensure the smooth progress of every section. Guarantee the submitted registration dossier compliance with the policies and regulations; Comprehensive understanding of the registered product information: including production, QC, and shelf life information, packaging materials, etc; 6)Provide reference opinions that relevant to laws and regulations, policy to the researcher, to ensure the implementation of product development goals; Translating, editing registration documents; Management registration data;
Medical Specialist (R&D)
Experience -8 to 12 years
Post- 01
Location- China
Qualification: M. Pharm / B.Pharm
Candidate should have bachelor degree or above of Clinical or Medical with 1-2 years experiences of NDA, ANDA clinical trial conducting and monitoring should be familiar with Learning ability and adaptability, strong communication skill, team cooperation ability, Have responsibility, Independent working  ability and execution force 5)Good ability of plan, organization and problem  solving, Adapt to long-term business trip.
Analytical Scientist for API (R&D)
Experience -4 to 6 years
Post- 02
Location- China
Qualification: M. Pharma /B.Pharm /M.Sc/B.Sc
Candidate should have 4 to 6 year of experience in analytical method development and method validation by GC, HPLC. Training regarding ICH guidelines, Knowledge for US / EU market.
Project Director - API
Experience – More than 15 years
Post- 01
Location- India
Candidate should be Master of Chemistry. Worked in Prominent API companies for more than 15 years with experience of working in regulated markets, travel experience and working with know pharmaceuticals customers.  KPI: Liscense USDMF or EMDF site transfer to Menovo. Capable of being the clients to the menovo site for such products, create the business revenue on that. CMO formulation. Bring clients for Menovo existing API & Intermediate list
Business Development Head – Finished Product International
Experience – More than 15 years
Post- 01
Location- India
Candidates have More than 15 yrs of experience. Have the experience of FDA product technology transfer and Business management, got the latest project experience is preferred, know Indian pharmaceutical market, have the abundant pharmaceutical resources, know regulated markets laws and regulations in Pharma industry. KPI: License existing ANDA or Europe dossier site transfer to Menovo. Bring Business to Menovo for such products. CMO formulation. Sell Menovo existing dossier to emerging market.
HR Manager
Experience – At least 6 years
Post- 01
Location- India
Candidate should have at least 6 yrs experience. BS / MS in Human Resources Management. bachelors degree or equivalent, Recruiting experience of at least 5 yrs. Knowledge of general principles of recruiting & staffing systems and tools, Should be from Pharmaceutical Background
Account Assistant Manager
Experience – At least 5 years
Post- 01
Location- India
Candidate should have at least 5 yrs experience. B.Com/M.Com. Knowledge of accounting, taxation and knowledge on Tally.
Kindly Contact Sonali: 022 61409696, Mail id- sonali@menovopharm.com
Reference – Asim Kumar
Salary based on company norms.

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