11 Manufacturing Compliance Jobs

This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients. What You Will Achieve In this role, you will: Investigate quality issues w...

Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients. What You Will Achieve In this role, you will: Investigate quality issues within manufacturing. Examine deviations, and atypical investigations Identify root causes and suggest effective corrective action plans Ensure all reports comply with regulatory re...

Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients. What You Will Achieve In this role, you will: Investigate quality issues within manufacturing and quality laboratories Examine deviations, out-of-specification results, and atypical investigations Identify root causes and suggest effective corrective act...

Be responsible to lead downstream manufacturing compliance. Ensure quality management systems in line with cGMP and regulatory requirements and handling training requirements Handling Change control management system including CCF impact assessment, preapproval, cross functional CCF evaluation, monitoring of closure of change controls and change control action item. Coordinate with investigator in identifying appropriate CAPA and tracking for closure of the CAPA. Responsible for the review and approval of Master manufacturing records for the commercial batches. Responsible for review and approval of scale up, exhibit, intended and Process validation master manufacturing records. To review an...

As a Veeva Vault Safety Configuration Analyst at our organization, you will be instrumental in developing innovative health solutions by leveraging your expertise on the Veeva Vault platform. Your role will involve collaborating with cross-functional teams, configuring and maintaining Veeva Vault Safety applications, and ensuring seamless system integration. **Key Responsibilities:** - **Requirements Gathering** - Collaborate with product management, engineering, and marketing teams to gather and document product requirements. - Facilitate workshops and meetings to ensure a clear understanding of business needs. - **Product Development Support** - Provide analytical support during the produc...

You will be joining Biocon Biologics, a subsidiary of Biocon Ltd, a global biopharmaceuticals company dedicated to developing high-quality, affordable biosimilars to provide advanced therapies to patients worldwide. As a QMS Compliance Team Member, you will play a crucial role in ensuring manufacturing compliance for biosimilars in the following key responsibilities: **Role 1 Manufacturing Compliance (Biosimilars Compliance):** - Investigate microbial excursions for facility, utility, and process. - Prepare contamination control and strategy documents. - Conduct product quality assessments for microbial contaminations. - Develop risk assessment protocols and reports. - Harmonize procedures a...

You will be responsible for the following tasks as Officer - API at Dishman Carbogen Amcis Limited in Bavla, Gujarat, IN: - Handling Manufacturing Compliance activities such as IPQA Activity - Managing QMS Documents including CAPA, OOS, and Change control - Handling APQR processes - Managing Batch release activities - Demonstrating strong communication skills - Having exposure to Regulatory audits If you possess the necessary qualifications and experience for this role, you are encouraged to apply.,

Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients. What You Will Achieve In this role, you will: Investigate quality issues within manufacturing and quality laboratories Examine deviations, out-of-specification results, and atypical investigations Identify root causes and suggest effective corrective act...

Key Responsibilities: Oversee and manage the entire production process of electronics components manufacturing. Ensure production targets are met, maintaining quality standards and meeting deadlines. Handle day-to-day production operations and resolve any production-related issues. Develop and implement efficient production plans to optimize productivity and minimize costs. Supervise and lead the production team to achieve production goals while ensuring adherence to safety and quality standards. Coordinate with other departments (quality control, maintenance, etc.) to ensure seamless production flow. Maintain inventory control and ensure the availability of required materials for uninterrup...

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...