37 Capa Implementation Jobs - Page 2

As a Procurement Manager at a leading CDMO of active pharmaceutical ingredients (APIs) and an end-to-end solution provider for the pharmaceutical industry, your primary responsibilities will include: - Submitting RFQs, compiling quotation comparisons, conducting negotiations, issuing purchase orders, and actively tracking all material deliveries. - Reviewing with the planning team and monitoring purchase requests to ensure 100% On-Time In-Full deliveries. - Managing Contract Manufacturing Operations End-to-End to ensure completion of Regular as well as development campaigns. - Coordinating with all stakeholders to ensure CMO Projects are carried out smoothly without any delay, including Sale...

Oversee lab ops for raw/in-process/finished goods. Maintain HPLC/GC, ensure calibration/validation, GMP/GLP, audits, CAPA, SOPs, and ISO compliance. Skilled in QA, validation, and regulatory in chemical/agrochemical manufacturing.

You will be responsible for resolving technical issues for SGRE & Vestas fleet, providing training to Asset Management & Self O&M team, and implementing RCA & CAPA processes. Your duties will include tracking software implementation, ensuring technical clearance of major components, and conducting Factory Acceptance Tests for construction and engineering projects. You will also be tasked with finding alternative components for key parts, writing technical documentation, and implementing maintenance strategies. Additionally, you will focus on team building and mentoring to enhance technical skills for handling SGRE and Vestas turbines. You will be involved in initiating, developing, and monit...

As a member of the ACG Packaging Materials team, your primary responsibilities will include strategic planning and analysis of customer complaints to recommend appropriate corrective and preventive actions. You will ensure compliance for updating CTQ requirements in ZMIC (SAP) to eliminate repeat complaints from critical customers, thus contributing to the avoidance of re-occurrence. Your role will also involve resolving technical issues at the customer end by providing guidance during trials and ensuring the effectiveness of action plans to avoid rejection and help in Cost of Poor Quality (COPQ) reduction. In your core functional duties, you will collect all necessary information related to...

We are seeking skilled and dedicated individuals to join our Quality Assurance (QA) department at Fido Pharma Private Limited, an esteemed pharmaceutical company located at Plot No: 108-109, Global Industrial Park, Mauli, Barwala, Panchkula, Haryana. If you have a background in B.Pharm / M.Pharm / M.Sc. and a passion for ensuring quality in pharmaceutical products, we have the following positions available: QA Manager: As a QA Manager, you will lead our Quality Assurance department, overseeing adherence to GMP and regulatory guidelines such as EU-GMP and WHO-GMP. Your responsibilities will include managing document control, validations, change control, Vendor Qualification, CAPA, deviations,...

As a Lead - Safety, Health & Environment (SHE) based in Hyderabad, your main responsibility will be to drive safety initiatives, ensure compliance with regulations, and promote environmental sustainability at our site operations. Your leadership is crucial in upholding our commitment to zero accidents and fostering a strong safety culture within the facility. In this role, you will be expected to lead the implementation of safety measures, including conducting Job Safety Analysis (JSA) for high-risk operations, promoting a near-miss reporting culture, and conducting regular safety inspections and toolbox talks to enhance accident prevention awareness. Your goal will be to achieve zero accide...

The responsibilities for this role include reviewing raw and finished product specifications, ensuring good laboratory practices in the Quality Control department, reviewing audit trial records, analyzing analytical records, reviewing instrument calibration and equipment qualification documents related to QC, validating analytical methods, verifying samples, handling reserve sample room, ensuring analyst qualification, reviewing working standards, managing deviations, change control, OOT, OOS, laboratory incidents, investigations, and annual trends, coordinating CAPA implementation verification and closure, reviewing instrument and equipment preventive maintenance, monitoring and recording t...

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 qual...

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 mon...

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 certi...

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 polyuretha...

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...