WELZO Research & Development – Walk-In Drive for QC / F&D / ADL Roles
Date: November 24, 2024
Location: [Exact venue details as per the provided link]
Departments Hiring: Quality Control (QC), Formulation & Development (F&D), Analytical Development Laboratory (ADL)
About WELZO Research & Development
WELZO Research & Development is a leading organization in the pharmaceutical sector, specializing in innovative drug development, cutting-edge analytical research, and ensuring stringent quality control standards. The company is recognized for its commitment to innovation, compliance, and excellence in creating pharmaceutical products.
Opportunities in the Walk-In Drive
WELZO is conducting a walk-in recruitment drive, targeting qualified professionals in QC, F&D, and ADL departments. Here’s a breakdown of the roles and responsibilities:
1. Quality Control (QC):
Responsibilities:
Performing quality checks on raw materials, intermediates, and finished products.
Ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
Using advanced analytical instruments like HPLC, GC, UV, and FTIR for product analysis.
Managing documentation and adhering to Standard Operating Procedures (SOPs).
Requirements:
Experience in QC for pharmaceutical manufacturing units.
Proficiency in analytical techniques and quality standards.
2. Formulation & Development (F&D):
Responsibilities:
Designing and developing new formulations for solid, liquid, and semi-solid dosage forms.
Conducting feasibility studies and scaling up formulations for commercialization.
Collaborating with cross-functional teams to optimize processes.
Ensuring regulatory compliance in formulation designs.
Requirements:
Hands-on experience in formulation development.
Expertise in product stability and process validation.
3. Analytical Development Laboratory (ADL):
Responsibilities:
Developing and validating analytical methods for pharmaceutical products.
Conducting stability studies to ensure product efficacy over time.
Troubleshooting and refining analytical procedures.
Documenting findings in compliance with regulatory guidelines.
Requirements:
Knowledge of regulatory requirements like ICH and USFDA guidelines.
Advanced proficiency in chromatographic and spectroscopic techniques.
Eligibility Criteria
Education: B.Pharm/M.Pharm/M.Sc. in relevant disciplines.
Experience: Minimum 2–6 years of experience in the pharmaceutical industry.
Skillset: Knowledge of cGMP, analytical instruments, regulatory norms, and excellent documentation practices.
Walk-In Details
Date: November 24, 2024
Time: 9:30 AM to 4:30 PM
