5 Capa Implementation Jobs

As a Sr. Executive / Assistant Manager Quality Assurance (QA) at SAVA Healthcare Limited, Surendranagar Plant, your primary responsibility is to ensure the implementation and maintenance of cGMP practices, quality systems, and compliance with regulatory requirements. You will oversee QA activities including documentation, validations, audits, and shop floor compliance to uphold product quality and regulatory adherence. Your key responsibilities will include ensuring compliance with cGMP, SOPs, and regulatory requirements on the manufacturing floor, reviewing and approving batch manufacturing records (BMRs) and batch packing records (BPRs), handling deviations, change controls, CAPA, and quality risk management activities, conducting self-inspections, and supporting external/internal audits. You will review and approve SOPs, protocols, and reports related to validation, qualification, and quality systems, monitor and support validation activities, oversee document control, ensure timely closure of audit observations and CAPA implementation, and coordinate with various departments to ensure overall GMP compliance. Additionally, you will participate in training programs and provide QA training to cross-functional teams. SAVA Healthcare Limited (SHL) is a diversified pharmaceutical company committed to delivering quality-driven pharmaceutical solutions globally. Established in 2003, SHL has a strong presence in International Business, Animal Healthcare, Herbal Products, and Contract Research & Manufacturing Services (CRAMS). The ideal candidate for this role should have a B.Pharm / M.Pharm / M.Sc. degree with 4 to 7 years of experience in QA in a regulated pharmaceutical formulation plant. You should possess a strong understanding of GMP guidelines, quality systems, validation practices, and regulatory audits. If you are passionate about maintaining high-quality standards, ensuring regulatory compliance, and contributing to the success of a leading pharmaceutical company, we encourage you to apply for this exciting opportunity at SAVA Healthcare Limited, Surendranagar Plant, Gujarat.,

As the Manager Quality in the Spinning Unit located in Edlapadu, your primary responsibility will be to oversee and lead the quality function of a large spinning unit with 100,000 spindles. Your role will be crucial in ensuring the consistent delivery of high-quality yarn for both local and export markets while focusing on achieving superior yarn quality, addressing customer feedback, and upholding compliance with social and sustainability standards. Your key responsibilities will include ensuring adherence to specified quality parameters for various types of yarn such as combed warp, hosiery counts, dyed packages, core-spandex, slub yarns, and export-grade yarns. You will be required to monitor and analyze daily quality test results, promptly identify deviations, and implement necessary corrective actions to maintain optimal yarn realization and minimize wastage through effective process control. Collaboration with production and maintenance teams will be essential to uphold the required quality standards and develop suitable cotton mixing parameters based on product requirements. Your role will demand a comprehensive understanding of medium and fine cotton yarn counts, hands-on experience with machinery such as KTTM, Trtzschler, and LMW, as well as the ability to comprehend key maintenance schedules and their impact on product quality. Efficiently handling customer feedback, implementing Corrective and Preventive Actions (CAPA), and ensuring customer satisfaction by meeting product quality expectations will be integral to your duties. You will also lead social and sustainability compliance audits including GOTS, OCS, BCI, Regenagri, Oeko-Tex, Inditex, and GCC, maintaining all necessary records and documentation for certifications and audits. In terms of skills and competencies, you should possess strong analytical and problem-solving abilities, excellent interpersonal and team coordination skills, proficiency in computer applications like Excel and ERP systems, in-depth knowledge of cotton yarn manufacturing and quality systems, and the capability to collaborate effectively with cross-functional teams. The ideal candidate for this role should hold a Diploma/Degree in Textile Technology or a relevant field and have a minimum of 10-15 years of experience in managing quality in large spinning units with a minimum of 100,000 spindles. Familiarity with both domestic and export yarn quality standards will be advantageous. If you believe you possess the requisite qualifications and experience for this role, please share your resume at jigisha.m@nsltextiles.com.,

As a Validation Specialist at Piramal Pharma Solutions, your primary responsibility will involve preparing and updating various validation documents to ensure compliance with regulatory requirements. This includes developing Validation Master Plans (VMP), Process Validation protocols, Computer System Validation protocols, and reports. You will also be responsible for creating product matrices, Cleaning Validation/Verification protocols, qualification/requalification protocols for equipment/instruments, utilities, and facilities, as well as area validation protocols and reports. In addition to validation activities, you will be involved in quality risk assessments, review of calibration certificates, issuance and archival of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR), preparation of Annual Product Quality Review (APQR), line clearance for manufacturing, packing, and dispensing activities, sampling of bulk and finished goods, and review of production records. Furthermore, you will play a key role in managing change controls, deviations, and CAPA (Corrective and Preventive Actions), conducting complaint handling, updating departmental SOPs, providing training as per schedule, coordinating training programs with HR, and ensuring documentation management as per SOP. You will also be responsible for providing necessary documents/data to meet internal and external quality, environmental, health, and safety requirements. Moreover, you will be involved in compliance monitoring through self-inspection programs, audit compliance coordination, preparation of responses to audit reports, and execution of food/dietary supplements regulations for export markets. You will also oversee the implementation of sanitation programs, adherence to EHS norms, and various corporate initiatives. Piramal Group values equal employment opportunity, ensuring that all applicants and employees are treated fairly based on merit, qualifications, skills, and performance. As part of a globally integrated network of facilities, Piramal Pharma Solutions offers a wide range of services across the drug life cycle, making it a trusted partner for innovators and generic companies worldwide.,

You are dedicated to enhancing daily living through innovative, ergonomic solutions that promote comfort and well-being. Your mission is to design the next generation of products to empower people to walk, sit, and sleep better. Each product you create is fueled by the same passion that drove you to innovate from day one: to give people the freedom to do more. Join the mission to transform everyday struggles into freedom and joy. Discover Frido and experience the freedom to live life your way. You are seeking a skilled and experienced Production Engineer to oversee the manufacturing process of polyurethane memory foam products. The ideal candidate will have a deep understanding of polyurethane foam production techniques, quality control measures, and operational efficiency. You will be responsible for leading a team, optimizing production schedules, and ensuring product quality meets or exceeds industry standards. Responsibilities include: - Production Oversight: Manage day-to-day operations of the polyurethane foam production facility, ensuring production targets are met while maintaining high standards of quality and safety. Implement strategies to optimize production processes, minimize waste, monitor production metrics, and report on KPIs. - Team Leadership: Lead and motivate a team of production staff, including supervisors and operators. Provide training and guidance to all team members, foster a culture of continuous improvement and teamwork. - Inventory Management: Coordinate with the supply chain and procurement teams to ensure adequate inventory of raw materials and supplies. Optimize inventory levels to minimize stockouts and excess inventory. - Safety Compliance: Enforce safety protocols and procedures to ensure a safe working environment for all employees. Conduct regular safety inspections and training sessions. Investigate and report any accidents or incidents and implement preventive measures. - Budget Management: Develop and manage the production budget, including labor, materials, and overhead costs. Identify opportunities to reduce costs and improve efficiency without compromising quality. - Continuous Improvement: Drive continuous improvement initiatives to enhance productivity and quality. Collaborate with cross-functional teams to implement best practices and innovative solutions. Qualifications: - Bachelor's degree in Engineering, Manufacturing, or a related field (preferred). - Proven experience in polyurethane foam production, expertise in memory foam production is desirable. - Strong leadership and management skills with the ability to inspire and motivate teams. - Excellent problem-solving abilities and attention to detail. - Sound knowledge of production planning, scheduling, and inventory management. - Familiarity with quality management systems and regulatory standards. - Proficiency in MS Office and CAPA implementation. Experience in the Audit of ISO 9001:2015. - Effective communication and interpersonal skills. If you are interested in this position, please send your CV to ruchi.c@myfrido.com along with details of your Current CTC and Notice Period.,

Job Description: As a member of the team, you will be responsible for identifying, reviewing, and implementing Pharmacopeial updates on a global scale. This will involve conducting activities related to the revision of product specifications and methods through a change management process. You will also be required to assess the impact of changes and review updates to ISO Guidelines. Additionally, you will collaborate with various departments to ensure compliance with USP/NF or other Pharmacopeial standards and ISO Guidelines. Regular reporting of work completion status to the reporting manager and coordination with them for updates to the management will be essential tasks. You will also be involved in preparing quality metrics, conducting risk assessments related to the Compendial Review Team, and ensuring compliance with the QMS system. Furthermore, your role will include the preparation, review, and implementation of common SOPs, procedures, and policies. Your educational background should include an M.Pharmacy/M.Sc degree, along with a minimum of 6 to 8 years of experience in QC/QC reviewer/QA (GMP). This position requires strong attention to detail, excellent communication skills, and the ability to work effectively in a dynamic and regulated environment. If you are passionate about ensuring quality and compliance in pharmaceutical processes, this role will provide you with the opportunity to make a significant impact in the industry.,