Maya Biotech Private Limited Walk-in Interview 2023.Maya Biotech Private Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.Maya Biotech Pvt. Ltd. WHO-GMP Approved Company is one of the leading manufacturers and suppliers of this impeccable range of Pharmaceutical Medicines, was established in the year 2008 The range manufactured in compliance with the set FDA norms and guidelines, utilizing the finest ingredients in the best possible composition, ensure the product’s effectiveness, shelf life and precise pH level.
Vacancy details:
- Post Name: Sr. Executive (Drug & Regulatory affairs)
- Qualification: B-Pharm / M-Pharm
- Experienced: 2-4 Years
Job Description: Greeting from Maya Biotech Private Limited !!!!!
Important Details :
- Location: Chandigarh
- Post of date:15/04/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Walk-in interview Details
Date & Time and Venue
17th April – 22nd April , 11.00 AM – 5.30 PM
Plot No. 46, first floor, Industrial Area Phase 2 Chandigarh.
Contact – Shweta Nayyar ( 7696499530 )
Roles and Responsibilities
Dossier preparation, compilation and review.
Preparing of STS,STP,COA,STABILITY DATA.
Knowledge of CTD & ACTD Studying scientific and legal documents.
gathering, evaluating, organizing, managing and collating information in a variety of formats
planning, undertaking and overseeing product trials and regulatory inspections
keeping up to date with changes in regulatory legislation and guidelines
analysing complicated information, including trial data
offering advice about company policies, practices and systems
providing advice about regulations to manufacturers.
ensuring that quality standards are met and submissions meet strict deadlines
preparing documentation.
ensure that a company’s products comply with the regulations of the regions where they want to distribute them
keep up to date with national and international legislation, guidelines and customer practices
develop and write clear explanations for new product licenses and license renewals
undertake and manage regulatory inspections
review company practices and provide advice on changes to systems
liaise with, and make presentations to, regulatory authorities
undertake and manage regulatory inspections
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