Are you a fresh or experienced B. Pharm or M. Pharm graduate looking to kickstart or advance your career in the pharmaceutical industry? Piramal Group, a global leader in pharmaceutical solutions, is hiring for the position of Trainee Executive – Quality Assurance at its Mahad, Maharashtra location. This is an excellent opportunity to join a reputed organization and contribute to ensuring the highest standards of quality in pharmaceutical manufacturing and packaging processes.
About Piramal Group
With over three decades of excellence, Piramal Group has established itself as a trusted name in the pharmaceutical and healthcare sectors. The group follows a dual strategy of organic and inorganic growth, driven by its core values of inclusivity, ethics, and innovation. As an Equal Employment Opportunity employer, Piramal Group is committed to fostering a diverse and inclusive workplace, ensuring fair treatment for all employees regardless of race, gender, age, or disability.
About Piramal Pharma Solutions (PPS)
Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) offering end-to-end solutions across the drug lifecycle. With a global network of facilities in North America, Europe, and Asia, PPS provides services ranging from drug discovery and development to commercial manufacturing of APIs and finished dosage forms. The company specializes in high-potency APIs, antibody-drug conjugates, sterile fill/finish, and biologics, making it a preferred partner for pharmaceutical innovators worldwide.
Job Description: Trainee Executive – Quality Assurance
As a Trainee Executive – Quality Assurance, you will play a critical role in maintaining the quality standards of pharmaceutical manufacturing and packaging processes. Your responsibilities will include:
- Area and Line Clearance: Ensuring clearance for manufacturing, packing, and dispensing activities.
- In-Process Checks: Monitoring and verifying manufacturing and packing activities to ensure compliance with quality standards.
- Dispensing Inspection: Conducting intermediate inspections of dispensing activities.
- Daily Verification: Performing daily checks on weighing balance calibration and environmental monitoring in raw material staging, manufacturing, and packing areas.
- Equipment and Area Cleanliness: Verifying the cleanliness of equipment and production areas during line clearance.
- Batch Manufacturing Records: Reviewing and verifying online batch manufacturing records.
- Sampling and Analysis: Collecting samples of bulk and finished goods for analysis and control.
- Non-Conformance Reporting: Documenting and reporting daily non-conformance observations.
- Training: Providing on-the-job training to new personnel in the production area.
- Statistical Process Monitoring: Implementing statistical process control to ensure consistent quality.
- CAPA Implementation: Identifying process deviations and ensuring effective Corrective and Preventive Actions (CAPA).
- Regulatory Compliance: Executing requirements for US FDA regulations (21 CFR Part 111) for dietary supplements.
- Data Integrity: Ensuring compliance with data integrity standards in all processes.
- Sanitation Program: Implementing and monitoring effective sanitation programs in the production area.
- EHS Compliance: Adhering to Environmental, Health, and Safety (EHS) norms.
Qualifications:
- B. Pharm or M. Pharm degree from a recognized institution.
- Strong attention to detail and a commitment to quality.
- Knowledge of GMP, FDA regulations, and quality assurance principles.
- Excellent communication and training skills.
Why Join Piramal Group?
- Be part of a globally recognized organization with a strong ethical foundation.
- Gain exposure to cutting-edge pharmaceutical technologies and processes.
- Enjoy a supportive work environment that promotes professional growth and development.
- Contribute to the production of life-saving drugs and healthcare products.
