Ipqa for Quality Department

As an In-Process Quality Assurance (IPQA) Specialist in a pharmaceutical company, you will be responsible for ensuring that the manufacturing processes adhere to established quality standards and comply with regulatory requirements. Your role will involve conducting real-time inspections and checks during the production of pharmaceutical products to identify any deviations or non-conformities. You will collaborate closely with manufacturing and quality control teams to maintain product quality and facilitate the smooth flow of production processes.

Key Responsibilities:
In-Process Inspections:Conduct regular and real-time inspections of production activities, including sampling, dispensing, granulation, compression, coating, and packaging, to verify compliance with standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).

Batch Record Review:Review and approve in-process batch records, logbooks, and related documentation to ensure accuracy and compliance with established procedures.
Identify and address discrepancies or deviations in real-time and initiate appropriate corrective actions, if necessary.

Process Monitoring and Control:Monitor critical process parameters during manufacturing to ensure they remain within specified limits for consistent product quality.
Collaborate with manufacturing personnel to address any process deviations and implement corrective actions promptly.

Compliance and Regulatory Support:Ensure that all manufacturing activities adhere to applicable regulatory guidelines, such as GMP, and support regulatory audits and inspections as needed.
Assist in the preparation and review of documents required for regulatory submissions.

Training and Quality Awareness:Provide training to manufacturing operators on GMP principles, quality standards, and compliance requirements to enhance their understanding and awareness of quality-related matters.

Non-Conformance Management:Investigate and document any in-process non-conformities or quality incidents, identify root causes, and propose corrective and preventive actions (CAPAs) to prevent recurrence.

Continuous Improvement:Participate in quality improvement initiatives and projects to enhance manufacturing processes, reduce defects, and optimize efficiency.

Data Management:Maintain accurate and up-to-date records of in-process inspections, non-conformances, CAPAs, and other quality-related data.

**Requirements**:

- Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
- Previous experience in pharmaceutical manufacturing or quality assurance is desirable but not always required for entry-level positions.
- Solid understanding of GMP principles and quality control practices in the pharmaceutical industry.
- Attention to detail and ability to follow procedures rigorously.
- Strong communication and interpersonal skills to work effectively with cross-functional teams.
- Analytical mindset to identify and solve problems during in-process inspections.
- Ability to work independently and make informed decisions related to quality assurance.

**Salary**: ₹15,000.00 - ₹25,000.00 per month

**Benefits**:

- Provident Fund

Schedule:

- Day shift

Supplemental pay types:

- Overtime pay

Ability to commute/relocate:

- Solan, Himachal Pradesh: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- IPQA: 1 year (preferred)

**Speak with the employer**
+91 6230929329
Expected Start Date: 07/08/2023