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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