1459 Capa Jobs - Page 2

Level: L2+L3 L2 (Experience 3-5 Years, Incase not explicitly mentioned) Log and manage Problem Management (PM) tickets with end-to-end ownership in SNOW. Coordinate initial problem records with relevant SMEs and CUSTOMER SPOCs. Automate PM workflows and dashboards in SNOW. Lead weekly and monthly governance meetings to analyze trends and recurring issues. Identify potential problems through trend analysis, incident patterns, and RCA. Drive RCA and CAPA submissions within defined timelines. Coordinate change management for deploying permanent fixes. Continuously improve PM processes based on lessons learned. Publish monthly PM reports and dashboards, and weekly reports to resolver groups. Mai...

Level: L2+L3 L2 (Experience 3-5 Years, Incase not explicitly mentioned) Log and manage Problem Management (PM) tickets with end-to-end ownership in SNOW. Coordinate initial problem records with relevant SMEs and CUSTOMER SPOCs. Automate PM workflows and dashboards in SNOW. Lead weekly and monthly governance meetings to analyze trends and recurring issues. Identify potential problems through trend analysis, incident patterns, and RCA. Drive RCA and CAPA submissions within defined timelines. Coordinate change management for deploying permanent fixes. Continuously improve PM processes based on lessons learned. Publish monthly PM reports and dashboards, and weekly reports to resolver groups. Mai...

As a Material Management Specialist, your role involves planning and controlling inventories of raw materials and packaging materials to meet production requirements. You will coordinate with Purchase and Quality Control teams to ensure timely availability and release of materials. Additionally, you will oversee the receipt, storage, and dispensing of materials in compliance with SOPs, MSDS, and safety requirements. It will be your responsibility to manage the return, rejection, and destruction of non-conforming materials following established procedures. Your key responsibilities include: - Planning and controlling inventories of raw materials and packaging materials - Coordinating with Pur...

As the Site QA Head at Sun Pharmaceutical Industries Ltd, your role will involve managing overall quality assurance oversight and site activities related to quality systems. This includes documentation review, SOP updates, in-process quality assurance, sampling and batch release, preventive maintenance, calibration, qualification, validation, internal audits, compliance, quality oversight of electronic systems, budget management, continuous improvement of quality systems, RA support, monitoring of pest control, and retention sample management as per Good Manufacturing Practices requirements. Your key responsibilities will include: - Defining operational strategy and road map for quality assu...

Quality assessments on all incoming materials from vendors and outgoing products shipping. Reject all product materials that fail meet quality expectations. Read blueprints, plans, and specifications to understand requirements products and services.

Job Track Description: Performs business support or technical work, using data organizing and coordination skills. Performs tasks based on established procedures. In some areas, requires vocational training, certifications, licensures, or equivalent experience. General Profile Expands skills within an analytical or operational process. Maintains appropriate licenses, training, and certifications. Applies experience and skills to complete assigned work. Works within established procedures and practices. Establishes the appropriate approach for new assignments. Works with a limited degree of supervision. Functional Knowledge Has developed skillset in a range of processes, procedures, and syste...

Long Description IMS Development & Implementation: Collaborate with cross-functional teams to design and implement the IMS, ensuring alignment with industry standards (e.g., ISO 9001, ISO 45001 & ISO 14001), relevant regulatory and customer requirements. Develop IMS documentation, including policies, procedures, work instructions, forms, and templates, to establish a clear framework for processes and practices. Compliance & Auditing: Conduct regular internal audits to assess the effectiveness and compliance of the IMS processes and procedures. Identify risks and areas for improvement, work with stakeholders to implement corrective actions and preventive measures. Training & Awareness: Develo...

Job Purpose We are looking for a qualified IT QA professional to support the implementation, validation, and compliance of electronic systems in accordance with global regulatory standards. The role ensures the effective functioning of key systems like TrackWise, AmpleLogic, LIMS, SAP, and eLMS while driving data integrity, compliance, and quality excellence across business operations. Roles & Key Responsibilities Ensure implementation and compliance of electronic systems (TrackWise, AmpleLogic, LIMS, SAP, eLMS, MES) as per global regulatory guidelines (USFDA, EU, WHO, PMDA, CDSCO, etc.). Review and support validation/qualification of software (DQ, IQ, OQ, PQ), ensuring timely closure of pro...

Job Summary The Policy Servicing Specialist will be responsible for managing and maintaining life and annuities insurance policies. This role requires a keen eye for detail and proficiency in MS Office to ensure accurate policy servicing. The candidate will work in a hybrid model primarily during day shifts with no travel required. The role is crucial in supporting the companys mission to provide exceptional insurance services. Responsibilities Manage and maintain life and annuities insurance policies to ensure accuracy and compliance with company standards. Utilize MS Office tools to efficiently process and update policy information. Collaborate with internal teams to resolve policy-related...

About The Role Skill required: Marketing Operations - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designAct of overseeing all activities and tasks needed to maintain a desired level o...

Responsible for supplier audit planning, scheduling, and conduct supplier audits. Responsible for vendor/ supplier quality and management issues. Responsible for implementation of ISO 13485 requirements Responsible for formulating, document, and maintain quality standards and ongoing quality objectives. -Analysis of raw material, In-process samples, and finished product. -Auditing OEM and verify the process control and quality, suggest changes if required to improve quality. -Responsible to escalate technical issues to the design team and Providing product feedback and customer suggestions to the R&D and Product Management team, also tracking the continuous improvement of the products. -Resp...

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Operations Designation: LifeScience Regulatory Svs Sr Analyst Qualifications: Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes b...

Set up bolus compression machines acc. to production specifications, Adjust machine settings, Identify & report mechanical issue, Load raw materials (powder/granules) into the machine hoppers, Maintain accurate production logs.

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Job Purpose We are looking for a qualified IT QA professional to support the implementation, validation, and compliance of electronic systems in accordance with global regulatory standards. The role ensures the effective functioning of key systems like TrackWise, AmpleLogic, LIMS, SAP, and eLMS while driving data integrity, compliance, and quality excellence across business operations. Roles & Key Responsibilities Ensure implementation and compliance of electronic systems (TrackWise, AmpleLogic, LIMS, SAP, eLMS, MES) as per global regulatory guidelines (USFDA, EU, WHO, PMDA, CDSCO, etc.). Review and support validation/qualification of software (DQ, IQ, OQ, PQ), ensuring timely closure of pro...

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 ARCHER 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 onshore and offshore teams to ensure quality compliances and processing accuracy for daily operations. Independently audit population/sample proportion of the ...

POSITION SUMMARY: Team Leader Managing your team effectively to achieve desired and optimum utilization of resources. Ensuring team member productivity. training and managerial tasks to deliver as per deadline and up to client satisfaction. Ensuring team member productivity, work accuracy and effectiveness. Develop and mentor team members through leadership and training while completing other managerial tasks required to deliver as per deadline and up to customer satisfaction. JOB RESPONSIBILITIES: 1. Daily workflow management to ensure maximum capacity to the project pool 2. Ensure schedule adherence for self & team 3. Effective operations management by overcoming daily hurdles of absenteei...

Handling Quality management system and regulatory support & reviewer. Change control, CAPA,OOS,APQR. Compliance verification at Site. Dispatch compliance. BMR and Work sheet compliance before release. Document and Data control and training.

Role & responsibilities Lead, mentor, and manage the Pharmacovigilance QA team to ensure effective execution of QA activities. Develop, implement, and maintain QA processes, procedures, and tools aligned with regulatory guidelines (e.g., ICH, FDA, EMA). Monitor and ensure compliance of pharmacovigilance activities with applicable regulations and internal SOPs. Conduct risk assessments and develop mitigation plans to ensure PV compliance . Oversee the management and closure of CAPAs (Corrective and Preventive Actions) following audits or inspections. Plan, coordinate, and conduct internal and external audits of PV processes, systems, and vendors audits ( Risk Based Audit approach ). Lead audi...

Quality Management System (QMS): Implement and maintain QMS in line with cGMP and regulatory requirements. Review and control SOPs, specifications, master documents, and records. Ensure timely execution and closure of change controls, deviations, CAPA, and risk assessments. Support continuous improvement initiatives in QMS processes. Audit & Compliance: Prepare and participate in internal, external, customer, and regulatory audits (e.g., USFDA, MHRA, WHO, EU). Ensure audit observations are tracked, addressed, and closed within timelines. Conduct periodic self-inspections to ensure plant-wide compliance. Document Control: Manage issuance, retrieval, archival, and control of GMP documents. Ens...

As a Quality Control (QC) Officer in the pharmaceutical (Formulation) industry located at Waghodia GIDC, Vadodara, your main responsibilities will include: - Performing quality checks on raw materials, in-process materials, and finished products. - Carrying out lab testing using instruments like HPLC, GC, UV, FTIR, etc. - Ensuring all work complies with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other regulatory requirements. - Identifying and reporting any issues like defects, deviations, or non-conformities. - Maintaining accurate records, including test reports and documentation. - Working closely with production and QA teams to address and resolve quality-re...

About The Role Skill required: Marketing Operations - Quality Management Designation: Quality Auditing Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designAct of overseeing all activities and tasks needed to maintain a desired ...

We are seeking a detail-oriented and experienced Quality Engineer to join our team in the LED TV manufacturing division. The ideal candidate will be responsible for monitoring and improving the quality of our manufacturing processes,

To ensure the GMP and GLP compliances. To participate in OOS, OOT, Deviation and complaint investigation, root cause analysis and to review investigation report. To carry out closure activities. To compile data provided by manufacturing, warehouse, QC for preparation of complaint investigation report. To prepare and review trends of OOS, OOT, Deviation, complaints, customer audit/inspection. To initiate change controls pertaining to QA and to review change controls of other departments w.r.t impacted activities. To review change control trend. To compile data for and prepare, review risk assessment reports w.r.t. Deviation, OOS, OOT, Nitrosamine impurities, elemental impurities, etc. To appr...

Level: L2+L3 L2 (Experience 3-5 Years, Incase not explicitly mentioned) Log and manage Problem Management (PM) tickets with end-to-end ownership in SNOW. Coordinate initial problem records with relevant SMEs and CUSTOMER SPOCs. Automate PM workflows and dashboards in SNOW. Lead weekly and monthly governance meetings to analyze trends and recurring issues. Identify potential problems through trend analysis, incident patterns, and RCA. Drive RCA and CAPA submissions within defined timelines. Coordinate change management for deploying permanent fixes. Continuously improve PM processes based on lessons learned. Publish monthly PM reports and dashboards, and weekly reports to resolver groups. Mai...