16 Quality System Jobs

The personnel handling this profile will be responsible for performing reactions as per the project requirements. You will document observations in relevant notebooks, follow instructions from the supervisor, and work in a group or individually to accomplish tasks efficiently. Your responsibilities will include performing synthetic chemistry reactions, conducting reaction workups, purifying compounds using column chromatography, crystallization, and re-crystallization techniques. You will operate lab equipment and ensure samples are given for analysis, recording results and updating the supervisor/group leader on synthesis progress. It is vital to record experiment/reaction observations, results, resource utilization, and other related activities in the laboratory or e-notebook promptly and confidentially. You should maintain instruments/equipment by ensuring calibration, preventive maintenance, cleanliness, and reporting breakdowns to maintenance promptly. You must be knowledgeable about the MSDS of handled chemicals, emergency response procedures for spillage, leakage, or fire, and adhere to waste segregation guidelines as per EHS norms. Following EHS and quality system requirements is crucial for individual and lab safety. Attending mandatory trainings, updating training records upon completion, and ensuring confidentiality are also part of your role.,

As a skilled Production Operator at our organization, you will be responsible for ensuring adherence to all required SAFETY norms throughout the production process. Your primary duties will include operating production machines following Standard Operating Procedures (SOP), maintaining discipline in line with organizational rules, and producing high-quality products as per the quality plan. It will be crucial for you to achieve the set Production Targets while also performing basic maintenance and lubrication tasks. In addition to your operational responsibilities, you will be required to fill up production reports with relevant information, update the traveler, and send materials for the next operation. You must accurately record production and stoppage entries in the PPC system and conduct in-process inspections as per ISO-9001 work instructions. It is essential to maintain Quality and Cleanliness standards for incoming, in-process, and outgoing materials. Your role will also involve following OHSAS and EHS statutory work instructions to ensure health, safety, and environmental compliance. This includes safe material handling, machine operation, use of personal protective equipment (PPE), and environmental protection practices. Effective communication with your shift engineer regarding production, quality, maintenance, safety, and environmental concerns is key to success in this position. You will be expected to drive Continuous Improvements both personally and operationally while adhering to Total Productive Maintenance (TPM) requirements and maintaining a high level of 5S in your work area. Material handling procedures must be followed diligently, and Lean practices in line with SMT BS 2.0 requirements should be maintained. As part of the Production team, you may need to work at different stations within the organization as required. It is imperative to understand and follow instructions from your superiors at all times. The ideal candidate for this role will possess competencies in ALLEIMA core values, quality system, and manufacturing safety. Operating skills in Pilger, Degreasing, heat treatment, nondestructive testing (ECT/UT), and straightening machines are essential. Creativity, flexibility, teamwork, fire safety, and First Aid training are additional competencies that will be beneficial in this role. A minimum experience of 2 to 5 years in a similar position along with a Diploma in Mechanical Engineering are the educational qualifications required for this position. If you meet the above criteria and are interested in this opportunity, please send your resume to priyank.patel@alleima.com and Haresh.gajjar@alleima.com. We look forward to welcoming a dedicated and competent Production Operator to our team.,

Strong interpersonal and people management skills Knowledge of ISO 9001:2008 and ISO 13485:2003 standards (preferred) Proficiency in interpreting engineering drawings For further information, please call 8050011328

Were currently seeking a highly skilled and experienced Quality Engineer to join our team. In this role, you will be responsible for ensuring the safety and quality of our products and procedures through rigorous inspections, implementation of quality control measures, and identification of areas for improvement. You will collaborate with cross-functional teams to address quality issues, drive continuous improvement, and contribute to building high-quality products that exceed customer expectations. The ideal candidate will possess a strong background in engineering or quality assurance, exceptional attention to detail, and a proactive mindset. If you are passionate about quality and delivering excellence, we encourage you to apply and become a valued member of our team.

* Project Coordination. * Product & Process Development. * Technical Documentation & Planning. * Vendor & Customer Coordination. * Quality & Compliance. * Cost & Resource Management.

As a Quality Executive/ Assistant Manager at Varun Beverages Limited, you will play a crucial role in ensuring the quality of our products from raw material to the finished product. Your responsibilities will include maintaining product quality at the highest standards by following best practices in quality assurance. You will be responsible for monitoring the water quality testing schedule as per PepsiCo guidelines and ensuring that water quality specifications are maintained accordingly. It will be essential for you to maintain the quality system during your shift and review documents daily in compliance with PepsiCo standards. Preparing the syrup as per schedule within the specified time frame and following the syrup testing schedule to maintain specifications are key tasks in your role. Monitoring and maintaining the sugar delta as per the target in each batch will be critical to ensuring product quality. Maintaining sanitary and hygienic conditions in the processing area to achieve the desired micro results is paramount. You will also need to adhere to the process requirements as per AIB (Food Safety), LRQA, FSSAI, and QAS standards. The ideal candidate for this position should have a B.Tech in Food Technology or M Sc., B Sc. in Chemistry or Food Technology, along with 3 to 8 years of experience in CSD & Water Line in the Beverage Industry. If you are passionate about maintaining quality standards and have the necessary qualifications and experience, we invite you to apply for this position. Join us at Varun Beverages Limited and be a part of a dynamic team dedicated to delivering a refreshing beverage experience to our consumers. Apply now by sending your resume to poulamee.saha@rjcorp.in.,

The Quality Compliance Senior Manager plays a crucial role in the Clinical & Research Quality (CRQ) team for the R&D Quality Organization at Amgen. The CRQ team ensures that research and development activities are conducted ethically and responsibly, meeting the highest standards of quality and compliance to keep patients safe and protect their welfare. This position involves providing leadership to maintain excellence in R&D Quality Processes, mentoring Amgen staff in India, managing day-to-day activities, and ensuring compliance with regulations globally. Additionally, the Quality Compliance Senior Manager will support the digital quality management system (DQMS) and provide end-to-end quality support for managing Quality Incidents/Quality Events, including approving investigations and CAPA plans. Roles & Responsibilities: - Overseeing deviations, audits, and inspections across R&D Quality - Managing the Amgen India R&D Quality team - Facilitating deviation investigations and ensuring documentation within the electronic quality management system - Supporting Global Patient Safety and Global Development teams in inspection management activities - Leading continuous improvement initiatives for CAPA management practices - Collaborating with cross-functional partners to ensure effective processes aligned with industry best practices - Monitoring quality metrics, key performance indicators, and performing root cause trending - Maintaining knowledge of current regulatory and quality practices/issues - Managing archival and retention of audit documentation Basic Qualifications and Experience: - Masters degree with 10-12 years of Pharma and Biotech R&D or commercial manufacturing Quality experience - Continuous Improvement/Change Management experience preferred Additional Competencies/Skills: - Exceptional attention to detail and accuracy - Ability to work independently and proactively in a fast-paced environment - Proficiency in Smartsheet, Microsoft Office Suite, and virtual collaboration tools - Good team building skills and ability to develop employees over time - Familiarity with project management tools and methodologies - Knowledge of GCP, GLP, and/or GPvP - Experience working in a multinational environment - Excellent verbal and written communication skills - Strong problem-solving abilities and adaptability - Collaborative attitude and ability to build positive relationships across diverse teams Amgen ensures equal opportunities for individuals with disabilities throughout the job application process and employment. The company supports professional and personal growth through competitive benefits, a collaborative culture, and comprehensive Total Rewards Plans aligned with industry standards. Join Amgen to make a lasting impact on patient care and your career growth. Apply now at careers.amgen.com.,

Overall responsibility for Program integrity & Quality activities across the KN business Ensuring overall compliance around SGS code of conduct, SGS code of integrity , conflict of interest, impartiality are being effectively implemented across all SBU of KN business. Conduct checks at random on quality of packs review/File audits for the different SBU s Certification and RBS of Knowledge and work around on the required improvements with the relevant SBU s Conduct the shadow audits at random for the various types of audit standards and in different locations ( announced/unannounced) for the different SBU s Certification and RBS of Knowledge and discuss on the improvements with the relevant SBU Report on performance of quality system/overall integrity compliance to the management of SGS for review and as a basis for improvement of overall systems as appropriate. Have regular meetings with the different knowledge SBU and discuss on their performance of quality/program integrity system, Their performance on relevant KPI pertaining to the SBU. Participate in Internal audits and Management reviews of the different SBU of Knowledge. Keep a close observation on our performance of the IFIA(TIC) . Observe regarding Impartiality and conflict of interest issues if evident in any SBU. Ensure full compliance with the Company s Code of Integrity & Professional Conduct and Impartiality policy and encourage others to do so. Collaborates with teams across business on total quality of the products and services provided by the knowledge . Work collaboratively, negotiate and engage with key stakeholders to facilitate delivery and compliance with the quality strategy Ensure strong communication between teams under leadership to facilitate exchange of information and in order to implement change and improvements.

Single window to customers for all QA related activities Customer complaints Target Zero/As per agreement with cust. Repeat complaint from cust-Target Zero Complaint closure–As per agreed timeline System compliance audit from Existing and New cust. Required Candidate profile Overall coordination for New development parts/ECNs Manufacturing feasibility of new RFQs/ECN received from new/existing customers Development (APQP) timeline preparation & agreement with customer

Std room operations and experience of -CMM , Contour , Profile projector , Surface roughness measurement , Calibration of instruments GD&T Quality system IATF 16949 requirements .Exposure to various customer audits TPM QM Pillar activities. Required Candidate profile 8 -12 YEARS working experience, DME, Std room operations and Hands on experience of -CMM, Quality System,IATF 16949 documents etc

Interested may share their resume on sv12@svmanagement.com Role- Achieving Plant's objectives through People Management. It focusses on employee's career growth, talent management and implementing best HR practices, thereby leading plants towards GPTW culture. This role is also responsible for deploying efficient administration practices and ensuring legal compliance. Responsibility- Awareness & Adherence of IATF, DOS, MSES-A and AHQ Quality Systems. Planning and formulating Manpower Budget to meet current and future business requirements Recruiting Staff and OEs as per budget and ensuring company policies are adhered to during the process Analyzing and strengthening HR KPIs to improve Direct Manpower productivity and White-collar efficiency Implementing "HR Best Practices" and establishing a holistic culture at plants to boost employee morale. Achieving Statutory compliance pertaining to Labor Laws and HR audits. Driving and achieving high performance among employees by Talent Management and Career Resolving employee concerns by advocating grievance redressals Development initiatives like timely goal setting (LSIP), KRA review, Facilitating employee development through effective need-based training, designing training calendar based on requirements and executing the same Liasioning with various stakeholders and handling administrative functions. Execution and Adherence to EHS Management Systems in Area of Control Candidate- MBA HR with 15 Plus years of expr in Manufacturing, Auto sector. Special Skills: Talent Acquisition, L&D, PMS, HRIS/HRMS, Labor Laws.

Position - Deputy Manager- Mechanical Employment Type- Fixed Term Employment on ERDA Rolls for 03 Years, it will be regularised, based on performance. Location- Makarpura, Vadodara Qualification- Essential: ME / M.Tech (Mechanical Engineering) Desirable: Ph.D. in Mechanical Engineering Experience Description- (Minimum 14 years to Maximum 18 years) Work experience in a testing laboratory or quality control department of industries in field of Mechanical testing Key Responsibilities 1. To plan and monitor the day-to-day activities of mechanical section (including HTLS lab and Seismic lab) 2. To achieve the revenue targets of section 3. To prepare capital & recurring expenditure budget for the section and take suitable actions/measures accordingly . 4. Purchase activities of lab. Including RFQ preparation, indent processing, technical evaluation 5. Planning and implementation of quality system in the lab for all requirements of ISO/IEC : 17025-2017 6. To achieve annual revenue and capital budget decided by Management. 7. Prepare and monitor capital & revenue expenditure. 8. Improvement of productivity Skills required to perform above job effectively Technical: 1. Knowledge of Mechanical engineering and materials used in electrical systems 2. Expertise related to mechanical testing of items used in electrical applications 3. Knowledge of quality system requirement as per ISO -17025 Behavioural: 1. Ability to take initiative, prioritize work, organize resources to achieve results and meet the deadlines set. 2. To interact positively with superiors, subordinates & team. 3. Ability of lead the team. IT: 1. Basic knowledge of computers & MS office 2. Knowledge of ERP software

Strong knowledge of FDA QSR, ISO 13485, EUMDR & regulatory norms. Manage QMS docs, DHFs, CAPAs, audits, suppliers, training & calibration. Support audits, product dev, quality improvements & regulatory compliance. Excellent doc & comm skills needed.QMS Management: Take ownership of QMS documentation, ensuring it's current, accurate, and accessible. Regulatory Compliance: Apply strong knowledge of FDA Quality System Regulation (QSR), ISO 13485, and EU Medical Device Regulation (EUMDR) to all quality processes. Design History Files (DHFs): Manage and maintain Design History Files, ensuring completeness and compliance throughout the product development lifecycle. CAPA Management: Lead and support Corrective and Preventive Actions (CAPAs), from initiation and investigation to implementation and verification of effectiveness. Audits: Facilitate and support internal and external audits (e.g., regulatory inspections, notified body audits), ensuring readiness and effective follow-up on findings. Supplier Quality: Oversee supplier qualification, monitoring, and quality agreements to ensure high standards across our supply chain. Training & Calibration: Manage and track quality-related training programs and ensure timely calibration of essential equipment. Cross-functional Collaboration: Partner with teams like Product Development to integrate quality requirements early in the design process and support overall quality improvements. Regulatory Submissions: Provide critical support for regulatory submissions, ensuring all necessary quality documentation is complete and accurate.

LOB Financial Services PREFERRED SECTOR/INDUSTRY Legal & Compliance DESIGNATION B2 Sr. Analyst QUALIFICATION CS. (Must) LL. B (preferred but not mandatory) JOB RESPONSIBILITIES The role of Sr. Analyst in Legal & Compliance shall encompass various tasks including, but not limited to, the following: Preparation of management committee meetings, board meetings and the GPs of Client funds Drafting of management committee and board meetings minutes and review of GP minutes including maintaining policies/minutes trackers/action logs in this respect Manage corporate and legal & compliance process Ensure quality assurance and checking for all the deliverables Ensure creation of training plans and manuals, quality manuals, SOPs, query log, escalation matrix, guidelines, checklist, etc. Manage team and accountable for QAs/QCs/Analyst work Oversee Implementation of the Quality system in the project Quickly and effectively train resources on process and client tools. Creating SOPs, guidelines, checklist, quality manuals, training manuals etc. Reports to Team lead DESIRED SKILLS & COMPETENCIE Candidate should have at least 3.5 6 yearsexperience in the legal/corporate department of a fiduciary or have worked in a law firm. Candidate should be willing and looking to consolidate and grow the skills and talents in the long term with a company that works in a dedicated team and results-based environment. Technical Skills Knowledge of regulatory and corporate environment for Irish/Luxembourg funds Understand key challenges General Counsels face in running corporate legal departments and functioning of law firms Engage with Clients, support decision making, delivery/governance related discussions Skills in planning, evaluation, research, analysis, training, problem solving and reporting Ability to facilitate and contribute to client sessions to define, illustrate and gain buy in to substantial departmental transformation via legal services Ability to perform email outreach to client Expert in analyzing legal and compliance issues Functional Skills Excellent written and oral communication in English Proficiency in using MS office Suite Experience in managing multiple/large teams Experience in Delivery and related governance Handling Client Escalations, Resourcing, People Management, Project Deliverables Implementing the Quality system in the project Ensuring appropriate use of methods, tools, and techniques in project Co-ordinating customer-related activities including acceptance of the deliverables Engage with Clients, support decision making, delivery/governance related discussions

Open Positions: Officer / Executive / Sr Executive Quality Assurance & Quality Control : Analytical Skill on HPLC, Electrophoresis, Microbiology, Document Review, IPQA, Quality Systems, GMP Compliance, QA-QMS Biosimilars Manufacturing: Downstream (Operation of Chromatography systems) & Upstream (Handling of Single use and Stainless-steel bioreactors) Experience: 2 to 10 years of relevant experience in Biopharmaceutical Qualification: B Sc / B. Pharm/B Tech / M Sc in Microbiology / Biotechnology / Chemistry/M. Pharm Date : 01st June 2025, Sunday Time : 08:30 AM to 06:00 PM (Registration will be closed by 12:00 PM) Venue : Hotel Pride , 5, University Rd, Narveer Tanaji Wadi, Shivajinagar, Pune, Maharashtra 411005, India Note: All positions are based out at Pune, Gotawade.

Should have proper knowledge in Personal Care Products, Should be able to do out of box thinking Lead a team of scientists to develop products in Personal care category Should have proper knowledge of NPD process. Required Candidate profile M.TEC in Cosmetic from leading Cosmetology College or M.Tec from ICT Mumbai Experience Should have 7-8 Years of experience in leading Indian MNC or MNC or 3rd Party Manufcturing, In Personal care