Job Description:

Position: IPQA Officer
Department: In-Process Quality Assurance (IPQA)
Experience Required: 4-6 years
Location: [Client Location]

Overview:

Our client, a renowned pharmaceutical company, is seeking a dedicated IPQA Officer with 4-6 years of experience to join their quality assurance team. The ideal candidate will be responsible for overseeing in-process quality assurance activities, ensuring compliance with GMP standards, and maintaining the highest levels of product quality throughout the production process.

Key Responsibilities:

• In-Process Quality Assurance (IPQA): Conduct IPQA activities including batch record review, logbook review, line clearance, and sampling withdrawal to ensure compliance with established quality standards.
• Batch Record Review: Perform thorough reviews of batch records to ensure accuracy and completeness, identifying any deviations or issues that may affect product quality.
• Logbook Review: Maintain and review logbooks to ensure all entries are accurate, complete, and comply with GMP requirements.
• Line Clearance: Ensure line clearance is properly conducted at every stage of production to prevent cross-contamination and ensure a clean, safe manufacturing environment.
• Sampling Withdrawal: Oversee the withdrawal of samples during production to ensure that they meet required specifications for quality testing.
• Validation: Participate in validation activities, ensuring that all processes, equipment, and systems are operating according to approved protocols.
• Quality Management Systems (QMS): Support the implementation and maintenance of QMS, including handling deviations, change controls, CAPA, and other quality-related documentation.

Key Requirements:

• Experience: 4-6 years of experience in IPQA within the pharmaceutical industry.
• Technical Expertise: Proficiency in IPQA activities, including batch record review, logbook review, line clearance, sampling, and validation.
• Regulatory Knowledge: Strong understanding of GMP, QMS, and other regulatory standards relevant to pharmaceutical manufacturing.
• Attention to Detail: Meticulous attention to detail, ensuring that all quality assurance activities are performed to the highest standard.
• Communication Skills: Excellent communication and interpersonal skills to work effectively with cross-functional teams.

Why Join Us?

• Leading Pharmaceutical Company: Be part of a company that is committed to innovation and excellence in the pharmaceutical industry.
• Career Growth: Opportunities for professional development and career advancement within the quality assurance field.
• Quality-Driven Culture: Join a team that values quality and compliance at every stage of production.

Apply Now:
If you have 4-6 years of experience in IPQA and are passionate about ensuring the highest standards of quality in pharmaceutical manufacturing, we encourage you to apply.