1476 Capa Jobs - Page 20

As a Qualified Person (QP) at PCI, you will play a crucial role in certifying investigational medicinal products in compliance with the requirements of the Investigational Medicinal Product Dossier (IMPD) and Product Specification File (PSF). Your responsibilities include ensuring the compliance of all batches to EU Directives, Annex 16, and Detailed Commission Guidelines related to Investigational Medicinal Products (IMPs). You will provide direct support and guidance to the Quality management team to ensure that Quality operations meet the necessary site safety, quality, and cGMP requirements. Additionally, you will participate in cross-functional teams to offer consultative support on qua...

The role of Senior Engineer - Electrical Design requires a candidate with a Diploma / B.Tech/B.E. in Electrical engineering with a minimum of 3 years of experience in a similar role. The preferred work location for this position is Vadodara. As a Senior Engineer - Electrical Design, your responsibilities will include working on solenoid assembly & its components design, modelling, drafting, BOM preparation, SAP activities, and testing troubleshooting. You will be expected to understand the basic function & configuration rules of all SOV, Coil, and Valve products. Additionally, you will create product string building rules for standard catalog products, NCPs, and ETOs, and modify Mrktg. & Pro...

As a Quality Control Reviewer at TAPI, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your primary responsibilities will include reviewing various documents such as batch records, test results, deviations, and corrective actions to determine the disposition of batches. You will also be responsible for monitoring manufacturing and packaging processes, investigating any errors or deviations, and implementing corrective and preventive actions as necessary. Your role will involve collaborating with internal and external stakeholders to address quality and compliance issues, facilitate batch reviews, and ensure the timely shipment and receipt o...

The ideal candidate will be responsible for ensuring the implementation of Client and JLL HSE Procedures at the Client location. You will be in charge of conducting HSE trainings, Mock drills, and Tool box talks. It will be your duty to ensure that the site and facility operations are in compliance with the relevant HSE regulations. Timely reporting of incidents, as well as managing RCA and CAPA, will be part of your responsibilities. You will conduct HSE audits for the site and submit reports to the admin team. It will also be your responsibility to ensure that both external and internal HSE audit points are closed and take measures to prevent the recurrence of these audit points. You will ...

You will be responsible for quality control activities at the leading FMCG Company. Your role will include conducting process audits, ensuring system awareness, inspecting raw materials, in-process and finished goods, as per established SOPs. You will also be required to inspect processes as per the defined frequency, address internal complaints using Root cause analysis and CAPA, and review the effectiveness of actions taken. Additionally, you will track the daily productivity of machines, plan productivity improvement actions, maintain communication with the Quality team, and manage daily and monthly dashboards related to PQCDS (Productivity, Quality, Cost, Delivery & Safety). The ideal ca...

You will be responsible for preparing and reviewing the master documents of sterile manufacturing for the parenteral facility. Additionally, you will prepare and review protocols and reports based on the specified requirements. Document management and preparation tasks such as BMRs, BPRs, and master SOPs will also fall under your responsibilities. Handling change control, deviations, CAPA, investigations, and providing training to subordinates, technicians, and operators within the department are key aspects of this role. You will also be accountable for audit and compliance on the manufacturing shop floor. The ideal candidate for this position should hold a B.Pharm/M.Pharm degree and posses...

As a Manager, Senior Central Testing Analyst within the Clinical Data Sciences (CDS) group of the Clinical Development & Operations (CD&O) organization at Pfizer, your primary responsibility is to oversee and ensure the successful delivery of User Acceptance Testing (UAT) activities for assigned studies. You will collaborate closely with various teams including Clinical Data Scientists, Data Managers, Clinical Database Management, Data Management Reporting and Analytics (DMRA), and other groups within CDS to ensure timely and high-quality deliverables that support the Pfizer portfolio. Your role encompasses a range of key responsibilities, including testing CRF design, database building, acq...

Job Description For Manager Quality - Product DLF Unit Roles and Responsibilities 1. Root cause of quality issues from field 2. Prepare CAPA to OEMs based on root cause 3. Discuss with customer to solve these issues 4. Track CAPA implementation within company From Internal Test bench:- 1. Measurement of items in Machine Shop 2. Vendor complaint quality- outsourced 3. Vendor complaint quality- Bought out 4. Submit MIS to Management- Daily/ Weekly Monitor 5. Visit customers site to understand issues in details 6. Host customer teams during their factory visit 7. Implement new methods to avoid quality issues

As a member of the ACG Capsules team based in Shirwal, your primary responsibilities will include: - Checking the allocated post production (ATS/Printing/camera) line(s) during each shift according to the CTQ (Critical to Quality) / CTP (Critical to Productivity) checklist. - Following the plan outlined in the color change note to minimize change over time at each sub-section. - Adhering to instructions from the shift lead to ensure timely change over by making sure roller(s)/ink are available. - Performing In-Process Quality Checks (IPQC) after every roller cleaning and checking camera rejections hourly to achieve zero defects. - Operating cameras according to the Standard Operating Procedu...

As a part of this role in the pharmaceutical industry, you will be responsible for handling CAPA (Corrective and Preventive Actions), OOS (Out of Specification) incidents, and deviations effectively. Your duties will also include the generation of Standard Operating Procedures (SOPs) to ensure smooth operations within the organization. Additionally, you will be involved in validation processes and maintaining compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). This is a full-time position with a day shift schedule. The ideal candidate should have a total work experience of 1 year in a similar role within the pharmaceutical sector. The work location for ...

Deliver site IT services in line with quality, reliability and cost expectations. Responsible for Margin Improvement Projects delivery. Monitor site incidents and request tickets to ensure they are resolved within SLA and that root cause is identified and addressed while coordinating with AMS partner. Ensure that critical site applications are available, patched and backed up and enabled by business and system owners. Own the roadmap for site reliability improvements and synchronize upgrades, patching and project efforts with site downtime windows. Collaborate with supporting partners and IT teams including onsite support, remote desktop support, IT outsourcing partner to maintain IT site re...

As a Quality Control Analyst at Piramal Enterprises Limited in Digwal, Medak, Telangana, your main responsibility will be to complete assigned tasks and undergo training on activities provided by the supervisor/HOD-QC before execution. You will be required to review packing materials, raw materials, stability samples, in-process and finished products data. Additionally, you will need to review Qualification, Validation, Calibration data, Procedure, Audit Trail in a timely manner. It will also be your duty to identify any unsafe conditions/acts within the laboratory, report them to the supervisor/HOD-QC, and ensure their resolution. Handling the receipt and inward of analysis samples, includi...

As the QA Head at Sun Pharma's Panoli location, you will be responsible for managing overall quality assurance oversight and site activities related to quality systems, including documentation review, SOP updates, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget management, continuous improvement of quality systems, RA support, monitoring of pest control, and retention sample management in accordance with Good Manufacturing Practices requirements. You will ensure individual compliance with all regulatory requirements, GxPs, and applicable departmen...

As a Senior Executive in the Quality Assurance team at Dishman Carbogen Amcis Limited, located in Bavla, Gujarat, you will be responsible for ensuring manufacturing compliance through activities such as In-Process Quality Assurance (IPQA). You will also oversee Quality Management System (QMS) documents including Corrective and Preventive Actions (CAPA), Out of Specification (OOS) investigations, and Change Control procedures. Additionally, you will be involved in Annual Product Quality Review (APQR) processes and Batch Release activities. The ideal candidate for this role should possess strong communication skills and have experience in handling audits. This position offers exposure to vario...

Role & Responsibilities Study part drawings and learn inspection methods Inspect critical parts for competency improvement Supplier entry warehouse entry (if required) Issue confirmation/review @ TFF RQA & M/c shop QA Rejection quantity confirmation/block in SAP Issue communication to supplier representative/supplier Suspected parts - Stock status review (all divisions, W/H, transit) Discuss with SQE, supplier representative & finalize Containment - Audit for marking/adequacy containment plan for transit material Containment form submission & Q-note modifications in SAP Deviation query (if required) Segregation status close looping Sorting support in urgency/supplier representative not avail...

You will be responsible for activities related to Quality control, Finished Goods and Raw Material approvals, Leading Packaging Projects trials and validation, quality engineering, and Integrated Pest Management program governance. Additionally, you will drive continual improvements and review/ implement initiatives in Product Packaging, Quality testings, approvals, and executing policies and guidelines issued from Support Center. Your role will involve working with the team on Corrective and Preventive Actions (CAPA) against Non-conformance and their effectiveness. You will participate in the Monthly Quality system Meet with Plant senior leadership team, lead Packaging initiatives, trials, ...

At Ascent Meditech , quality isnt just a checkpoint its a commitment stitched into every support belt, sealed into every wound-care product, and engineered into every mobility aid we craft. As the custodians of Flamingo , one of Indias most trusted medical device brands, were looking for a Head Quality Control who believes defects are not errors they are missed opportunities to protect trust. Whats the Mission To lead from the front in our journey toward zero-defect manufacturing , robust supplier performance, and world-class product reliability across orthopaedic supports, healthcare essentials, wound & injury care, and mobility solutions. Your Toolbox Should Include: 1.1218 years in Medica...

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,...

The Manager Quality Assurance position involves collecting, analyzing, and presenting data related to goods receipt rejection, line rejection, and rework to generate action points for continual PPM reduction. You will be required to prepare CAPA (Corrective and Preventive Action) 8D, Why-Why Analysis, and Cause and Effect Diagrams. Additionally, you will assess the implementation of Quality Plans and Quality Control Plans. Your responsibilities will include reducing in-house rejection/rework and developing action plans if defined goals are not met. Motivating employees to maintain high-quality work and ensuring safety protocols for operators will be crucial. You will also implement correctiv...

You will be responsible for supervising and guiding the IPQA team to conduct real-time monitoring during manufacturing and packing processes. Your role will involve ensuring compliance with BMR/BPR review and approvals at each stage, as well as overseeing line clearance before manufacturing and packaging activities. It will be essential to monitor critical process parameters, in-process checks, and control sampling activities including IPC, stability, validation, etc. You will be expected to ensure timely review and approval of executed batch records and logbooks, review and ensure compliance of standard operating procedures (SOPs), and maintain and control GMP documentation related to IPQA ...

You will be responsible for managing the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory. Your role includes ensuring testing of stability samples within the structure of timelines identified in relevant SOPs, maintaining laboratory activities on par with compliance expectations, and providing top-notch inter- and intra-department customer service. With at least 8 years of experience in a laboratory related to a cGMP/Pharmaceutical environment, including a minimum of 4 years in a Supervisor capacity, you will manage the day-to-day operations of the Quality Control laboratory. This ...

POSITION REPORTS TO: SENIOR MANAGER OE DEPARTMENT: QUALITY POSITION LOCATION: VADODARA, GUJARAT, INDIA (ON-SITE) BUDGET: 4,00,000 - 5,00,000 PA. POSITION SUMMARY The BK QC Associate plays a critical role in reviewing and ensuring quality standards, processing accuracy and compliance as per predefined checklist. This position requires an understanding of legal documentation, including but not limited to court orders, retainer agreement, affidavits, and BK filings, which are essential for Company to deliver its services. The BK QC Associate will collaborate closely with the BK Coordinators from both US and IND businesses to execute daily responsibilities. JOB RESPONSIBILITIES Collaborate with ...

As a Senior Manager of Manufacturing Excellence, Digitalization & Quality Management System (QMS) at Sun Pharmaceutical Industries Ltd in Dewas SGO - Operations Block P, your role will be crucial in driving operational efficiency improvements and fostering a culture of continuous improvement across the site. With a focus on operational management, continuous improvement, QMS oversight, and digitalization transformation, you will work closely with the site leadership team to identify opportunities for enhancement in quality, cost, productivity, and delivery. Your responsibilities will include identifying root causes of gaps between demand, commitment, and supply, and collaborating with the le...

The Executive Cell Leader position at RK INDUSTRIES CHENNAI is a full-time on-site role that requires expertise in New Product Developments, CNC Programming, and Quality Managements (CAPA). As an Executive Cell Leader, your responsibilities will include leading new product development initiatives, programming CNC machines, and overseeing quality control processes, specifically Corrective and Preventive Actions (CAPA). You will be tasked with coordinating daily cell activities to ensure production targets and quality standards are achieved while working closely with cross-functional teams to drive continuous improvement. The ideal candidate for this role should possess the following qualifica...

The position of OBA Quality Engineer at Factory is a contract role (3rd Party) with Xiaomi, where you will be required to work in rotational shifts, six days a week. As the Xiaomi Factory Quality Onsite Manager, your primary responsibility will be to conduct inspections of TVs in accordance with Xiaomi standards. Your roles and responsibilities will include having a basic knowledge of electronics parts, ESD, and Line Audit. You should be familiar with product inspection processes such as IQC, OQC, OBA, and PDI. It is essential to have knowledge of the 7QC tools, Quality Standards, and First article inspection. You will be responsible for checking the TVs before shipment to ensure they meet t...