Medreich R&D Hiring Regulatory Affairs Professionals: Formulation Background Only
- Regulatory Affairs Job Vacancies
- Medreich R&D (a Meiji Group Company) Recruitment Notification
- Job Highlights
- Key Responsibilities
- Candidate Profile
- Application Process
Regulatory Affairs Job Vacancies
Medreich R&D (a Meiji Group Company) Recruitment Notification
Medreich R&D, a prestigious division of the Meiji Group, is seeking qualified professionals for its Regulatory Affairs Team in Bengaluru (Bommasandra). This opportunity is ideal for candidates with expertise in formulation and a passion for excelling in the pharmaceutical sector.
Job Highlights
- Location: Bengaluru (Bommasandra)
- Experience Required: 1–3 years in core Regulatory Affairs with a formulation background.
- Qualification: M.Pharm (Pharmaceutics).
- Availability: Candidates who can join within 30 days are preferred.
- Note: Freshers are not eligible for this role.
Key Responsibilities
- Experience in technical review and compilation of registration dossiers for regulated markets.
- Review of master documents (Specifications, MFR, BMR, BPR, PVP, PVR, HTSP, HTSR, PDR, elemental impurity risk assessment, nitrosamine risk assessment, stability protocols), DMF.
- Deficiency management for products filed to regulated markets
Candidate Profile
- Strong knowledge and experience in Regulatory Affairs related to formulations.
- Familiarity with regulated markets and their compliance requirements.
- Ability to work independently and handle technical documentation with precision.
- Excellent communication skills for effective collaboration with cross-functional teams.
Application Process
Interested candidates can apply by submitting their resume to:
vineeta.k@medreich.com
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📱 Get More DetailsDeadline: Candidates must ensure their availability to join within 30 days of selection.
