Medreich Limited, a pharmaceutical company established in 1976, is a renowned manufacturer of generic and branded drugs across multiple therapeutic areas. With a workforce of over 2,900 employees globally and an extensive client base spanning 54 countries, Medreich Limited is known for maintaining exceptional quality standards and product excellence.
Position: Development Quality Assurance Professionals
Department: Development Quality Assurance
Experience Required: 5-7 years
Location: Bengaluru (Bommasandra)
Note: Freshers are not eligible to apply.
Preferred Skill Set:
- Documentation Review: Experience in reviewing Formulation LNB, Pre-formulation study reports, Master formula cards, scale-up reports, and product development reports.
- Process Validation: Adequate knowledge of process validation concepts, with experience in preparing/reviewing process validation protocols and reports, hold time study protocols, and reports.
- Production Documentation: Experience in the preparation and review of Master Production documents (BMR, BPR).
- Quality Management Systems (QMS): Proficiency in QMS activities, including Change Control, Deviation, CAPA, CAPA effectiveness, risk assessment, Out of Specification (OOS), Out of Trend (OOT), Incidents, and Internal Audits.
- Equipment Qualification: Knowledge of equipment qualification procedures.
- Systems Knowledge: Familiarity with Document Management System (DMS), Learning Management System (LMS), and SAP.
- Regulatory Guidelines: Knowledge of regulatory guidelines, including ICH, EU-GMP, and Health Canada standards.
Application Process
Email: Submit your resume to vineeta.k@medreich.com
Position: Analytical Research & Development Professionals
Roles Available: Officer, Executive, Research Scientist
Department: Research & Development
Experience Required: 1-4 years
Education:
- Required Degree: M.Pharm in Pharmaceutical Analysis or M.Sc. in General Chemistry/Applied Chemistry
Location: Bengaluru (Bommasandra)
Note: Freshers are not eligible to apply.
Key Skills:
- Analytical Development: Experience in Analytical Development (AD), Analytical Development Laboratory (ADL), and Quality Control (QC) validation for formulations in Oral Solid Dosage (OSD) forms.
- LCMS/MS Operations: Proficiency in handling LCMS/MS for genotoxic impurities, method validation, and routine R&D support.
- Nitrosamine Analysis: Expertise in analytical method validation, development, and transfer for nitrosamines in drug products/substances.
- Stability Analysis: Ability to conduct stability analysis for nitrosamines in drug products/substances.
- Calibration & Method Equivalency: Experience in LCMS/MS calibration and method equivalency.
Application Process
Email: Submit your resume to vineeta.k@medreich.com
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