Website Medreich Limited
About Medreich Limited
Medreich Limited is a fully integrated pharmaceutical company with a strong global presence. Specializing in Contract Manufacturing (CMO) and Contract Development & Manufacturing (CDMO), we cater to diverse therapeutic categories. Our state-of-the-art Research & Development center is equipped with cutting-edge technology to develop patent non-infringing and niche generic formulations for regulated markets.
We are currently seeking talented professionals for the following roles:
1. Analytical Research & Development (AR&D)
Qualification: M.Pharm / M.Sc
Experience: 2 to 6 years
Number of Positions: 07
Job Responsibilities:
- Conduct analytical method development and validation.
- Perform regular and stability sample analysis.
- Operate and maintain HPLC systems for assay, dissolution, and related substance tests for solid oral dosage forms.
- Perform particle size distribution analysis using particle sizers and microscopes.
- Ensure compliance with regulatory standards and laboratory best practices.
2. Formulation Research & Development (FR&D)
Qualification: M.Pharm
Experience: 2 to 6 years
Number of Positions: 07
Job Responsibilities:
- Conduct pre-formulation studies and R&D trials for oral solid dosage forms (tablets, capsules, etc.).
- Develop and optimize formulations to meet regulatory and quality requirements.
- Document and analyze trial data to improve formulations.
- Collaborate with cross-functional teams for technology transfer to manufacturing.
Key Requirements:
- Hands-on experience in formulation development of oral solid dosage forms.
- Knowledge of QbD, regulatory guidelines, and process optimization.
- Strong analytical and problem-solving skills.
3. Quality Control (QC)
Qualification: M.Pharm / M.Sc
Experience: 2 to 6 years
Number of Positions: 05
Job Responsibilities:
- Conduct analysis of raw materials (RM), packaging materials (PM), in-process, and finished products.
- Perform stability testing using HPLC, GC, UV, FTIR, and other QC instruments.
- Ensure compliance with GLP/GMP standards in the laboratory.
- Maintain regulatory compliance for MHRA, TGA, Health Canada, PDMA Japan, and other authorities.
Walk-In Interview Details:
📅 Date: 1st March 2025 (Saturday)
⏰ Time: 10:00 AM – 2:00 PM
📍 Location: Medreich Limited (R&D)
Plot No. 36, Bommasandra Industrial Area, Anekal Taluk, Bommasandra, Bengaluru – 560099
Join our team and contribute to groundbreaking pharmaceutical innovations! We look forward to meeting passionate and skilled professionals at the walk-in interview.
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