Analyze blend or component failures and recommend corrective actions that lead to continuous improvement within the Plant, Drive effective SPC (statistical process control) program and RCA (root cause analysis) process, Lead the integration of change initiatives to ensure continuous improvement of processes and systems, Engages staff in safety awareness (relative to Global Lab Safety Standard), quality conformance (Global Quality Manual) , and drives Best-In-Class Laboratory practices, policies, procedures, and test methods, Continuously strive to improve plant operations to maximize efficiency and effectiveness to generate a BiC operation, Develop and administer the departmental budgets and achieve annual expense against plan with achieving ongoing continuous improvement initiatives, 5 years of experience in quality control procedures, Technical knowledge of quality systems and concepts, Superior leadership skills and associated behavioural attributes, Ability to drive a Continuous Quality Improvement environment and Best-In-Class laboratory practices, Proficiency with laboratory techniques and modern analytical instrumentation and LIMS software systems, The ability to drive continuous improvement for Best-In-Class performance by optimizing production processes through analyzing current performance, reducing losses /defects and identifying future opportunities, Excellent interpersonal skills and ability to work effectively with staff at all levels both internally and externally, Experience in Chemical and Petro-Chemical Industry, Experience implementing operating in a TQM/ TPM/ Lean Manufacturing principles environment, Must work cooperatively with Analytical Development, Manufacturing, Regulatory and Quality Assurance departments, Individuals experienced with cell culture, RT-qPCR, Immunofluorescence, Flow Cytometry and cell based assays preferred, Oversees overall day-to-day work operations in the QC Analytical lab; in-house and external product testing across product lines, associated support lab functions, and ensures documentation completed in accordance with cGMPs, Partners with analytical development to achieve method readiness to initiate validation, write validation protocol, gather and interprets data generated by analytical development/QC labs and writes/reviews validation reports, Participates in execution of method validations and transfers within and outside of AIRM, Interacting with contract laboratories to support sample testing, data analysis and investigations as required, Oversees QC equipment validation, maintenance and calibration, and QC laboratory scheduling and maintenance, Establish personal and QC analytical group goals to meet deliverables based on issued objectives, Author and approve SOP's, protocols, reports, data summaries and quality systems internally as well as at CROs and CMOs, Monitor and trend QC data; complete routine record review of test data and related documents for in-process testing, drug substance and drug product release and stability testing, Collaborate with regulatory to support IND/NDA/MAA filings/amendments on CMC sections, Support regulatory PAI and GMP inspections in a global environment, Implement GMP systems in QC and ensure compliance with documented policies, Interacts with all levels of management on a routine basis and will oversee the development of the QC Analytical function, Works on complex and diverse problems giving guidance and suggestions, Actions may have implications on operations, budget and credibility, PhD, MS or BS in Molecular Biology, Chemistry, Pharmaceutical Sciences, Life Sciences or equivalent, PhD + minimum 5 years or MS/BS + minimum 10 years of relevant experience in QC or equivalent experience in commercial pharmaceutical industry, Excellent knowledge of cGMP, ICH, USP and global compendial regulations and guidance, Possesses a positive, can-do attitude and creatively solves problems, Responsible for implementation of task order QC Plan. Ensure that they are documented correctly and closed out in a timely manner, Manage the stability testing program, ensuring any issues are promptly communicated, Manage the department purchase of equipment and materials and ensure availability of all materials required for testing, Manage and co-ordinate with Engineering and external instrument calibration/maintenance companies to maintain QC instrument calibration and maintenance to specified schedules, Manage the investigation and documentation of any retesting in the QC laboratory, Manage contract laboratory testing laboratories, ensuring compliance to GLP and agreed testing deadlines and costs, Adhere to all company and legislative EHS requirements. Such meetings may be in person or by telephone at the discretion of the FD and/or CO, Responsible for all compliance issues as they apply to the functional operation of this contract, Develops, implements, and maintains a quality control plan that is tailored to the contract and encompasses all facets of the operation, Inspects work in progress and finished work for discrepancies in accordance with the quality control plan and contract requirements, Responsible for inspecting work accomplished by Chugach and subcontractor personnel, to identify any flaws or defects, Responsible for coordinating with customer personnel on all matters relating to the quality or quantity of contractor work, Responsible for oversight of all vendor subcontractors performing work for or on behalf of Chugach at this project location, Coordinates with Chugach and subcontractor functional managers and supervisors to ensure quality workmanship and timely completion of all tasks, Reports to the CPM on all issues, problems, accomplishments, and results of surveys, inspections, meetings, and observations relating to performance of Chugach and subcontractor personnel, Maintains inspection records and submits monthly reports to the customer on all quality control inspections conducted, Ensures that inspections performed on airframe, engines and components are in accordance with Leidos Policies and procedures, maintenance manuals and approved technical data, Monitors workmanship and materials to verify that the Company and FAA rules, regulations, and standards are complied with, Performs buyback inspection on non-routine items and provides inspection sign offs as required, Ensures that aircraft modifications or component changes are in compliance with maintenance manual procedures or approved technical data procedures, Ensures all required inspection items (RII) are completed and documented properly, Ensures that receiving inspections of incoming parts, components, equipment supplies and materials is completed in accordance with the Leidos General Maintenance Manual (GMM), Ensure assistance in the classification of repairs and alterations in relation to Major or Minor Repairs, Ensure appropriate forms are completed to document any major repair or alteration, Monitors/audits aircraft inspection reports, log pages and records for accuracy and completeness of entries prior to being sent to the Aircraft Records Department, Conducts daily audits of aircraft work packages including checks/inspections forms, log pages, routines and non-routines, modification orders, etc. Review and approve ono-chromatographic and chromatographic data, Co-ordinate and manage any laboratory investigations and approve any retesting required. - Choose from 15 Leading Templates. investigating special cause variation, changes in failure or repeat rates, other unusual behavior of reagents, consumables, or data), including assessment of impact, root cause identification, and appropriate corrective and preventive action, Ensure consistent compliance with applicable federal, state, and local regulations and quality-related best practices in development, validation, use, and documentation of analytical and functional test methods for reagent lot qualification, stability studies, and related activities, Bachelor of Science in Molecular Biology or related field with 8+ years of industrial experience, Working knowledge of local, state, and federal laboratory regulations, Knowledge of analytical methods for enzyme activity assays, oligonucleotide purity and composition using HPLC and spectroscopic techniques, and qPCR-based functional testing. 439 and University of the Pacific Physical Plant as it relates to construction activity and deliverables, Assist the CCPM, design team, Facilities with inspections for the final punch list, Monitor Quality Control measures on multiple job sites simultaneously with proper coordination and documentation, At least three (3) years in a supervisory capacity, Cross Connection Control Specialist certified, Bachelor’s Degree in Project Management, Construction Management, Engineering, Architecture, Facilities Planning and Management, or related field, Knowledge of Federal Occupational Health and Safety Standards (OSHA). ... Quality Control Inspector resume 3. 21+ Experienced Resume Format Templates – PDF, DOC Did you know that resumes also keeps up with the trend? responsible for management, Assist with the development, documentation, implementation, assessment, auditing, and training of a quality system (QS) in support of company quality initiatives and to ensure compliance with quality standards, contract specific documents, certification requirements, and legal/regulatory requirements, Provide technical and engineering support for proposals, plants/materials, construction, sales, and estimating teams during pre-bid, construction, and post-construction phases of a project to ensure quality opportunities are optimized and all aspects of QS are met, Conduct specification reviews, develop project Quality Control (QC)/Quality Assurance (QA) plans, generate material submittals, develop and review mix designs and may stamp if needed, review quality data and inspections, and manage QC/QA subcontractors to assure timely project success, Provide customer service with internal and external technical training on materials production and/or construction processes to ensure customer satisfaction is achieved, Establish, maintain, and leverage relationships with local public agency technical staff, customers, and local inspection/testing companies, Support evaluation and implementation of new material technologies throughout the company as applicable, Support operations during preparation of budgets, forecasts, project quality estimates, and during management of all quality management finances to achieve positive financial performance, 10 years of any combination of experience in quality systems, technical,managerial and/or construction, Excellent technical knowledge of materials and construction concepts, Strong Microsoft Office Suite and database skills, Ability to properly manage and prioritize resources, people and projects, Sound decision making ability with the experience to balance consensus against authority as appropriate, Team player, with strong leadership skills, who can operate effectively within a matrix management environment, Excellent consultative and communication skills (written and oral) and ability to interface effectively with all levels of management, Conducts training, performance reviews, and establishes development plans for QC Technicians, Leads and manages the Customer Complaint Process. Responsible for investigating “product quality” complaints, Responsible for leading and driving Quality engagement and the journey to a Quality culture, Acquire basic technical knowledge of product line with the goal of partnering with the technical team for issue resolution, Coordinates scheduling and manages overtime, Responsible for Quality Management System as AS9100 Management Representative. Responsible for the Quality Control Department at a Phase 1/2 contract manufacturing organization. Capital requests, equipment qualification, etc.). Supervises the processes all non-accrual and charge-off entries in core for commercial lending as well as all OREO transfers. Represent the team in non conforming material disposition meetings, Hold regular meetings with the team to provide performance appraisals, drive accountability and feedback. Manage issues with non-conforming product to assure proper control, minimize loses, and provide analysis to drive the elimination of future occurrences, Provide training in the area of food science, regulatory requirements, and quality measurement systems to appropriate personnel. resume; you can edit and target this resume toward a specific employer any time you get ready to apply for a new position. Acting as a working manager, serves to coordinate all technical activities in an efficient manner to insure that the project requirements and deadlines are met, Act as liaison with other professionals and field personnel to accomplish the efficient and smooth implementation of project directives, 10 years of Construction including 5 years of US DoD Fuels Construction, 5-7 years Quality Control on US DoD Fuels Construction (Current CQM Certificate), Certifications (Not Mandatory) API 653, Aboveground Storage Tank Inspector; API 570, Process Piping Inspector; Steel Tank Institute SP 001 Tank Inspector; NACE CIP Level II or higher; and NACE CP Level I or higher, 30 Hour OSHA, CPR, 40 Hour HAZWOPER, Knowledge of Outlook, Work, Excel and PowerPoint preferred, Ability to work on US military bases is required, Flexibility to work outside normal business hours as required, BS degree with progressive experience in Quality including at least 5 years in a manufacturing environment, Experience in complex assembly involving assembly of mechanical, electrical and electronic components, Will work with Mil-Spec and close tolerance quality standards, Interface with Production Coordinator on Quality issues, Maintain flow of work through Quality and assist in the preparation of the production schedule as it involves work going through the quality department, Manage a team responsible for the delivery of a strong Quality Control system as it relates to the refurbishment activities of a nuclear power plant. Quality Assurance Resumes: So, selecting a suitable resume template is also a duty of candidate. Distributes appropriate information to plant and sales/marketing personnel, Maintains up to date knowledge of normatives and standards, Ensure compliance requirements are met through organizational and procedural measures including implementation of Group guidelines, performing trainings, monitoring compliance etc, Proactively manage health & safety of employees to continuously improve the company's health & safety performance, Develops and improves products to increase customer satisfaction, 4 year degree in Chemistry or similar technical degree, Minimum of five years of experience in cement industry required; quality control supervision desired, Thorough understanding of cement chemistry, X-ray and advanced chemical, physical and microscopic analytical and testing procedures, Knowledgeable in the following analytical methods: XRF, Spectrophotometry, wet chemical methods, physical testing, and clinker/cement microscopy, In depth knowledge of relevant ASTM specifications and procedures, Excellent interpersonal, oral and written communications skills, Proficient computer skills and familiarity with Windows Microsoft Office and SAP preferred, Ability to work as a member of a team in a Total Quality environment, Manages the Quality Operations Stability Program and Capital Budget, Prepares appropriate documents for regulatory submission, Manages the Quality Control/PDS Reference Standards Program, Retention Program, Instrument IQ/OQ/Audits Program, LAS system, Controlled Substances system and SOPs, Participates in technical and special project teams, Interacts with USP and other compendial organizations on monograph and reference standard issues, Support QA operations by approving data generated by all laboratories. Develops new standards and upgrades calibrations as required, Maintains a close working relationship with Sales & Marketing and customers. This handout contains resume examples that will help you get started. Ensure validation documentation (related to manufacturing, packaging & testing) is current for all products, Manage the Product Transportation and Cold Chain qualification program including shipping packaging configurations in accordance with Health Canada GUI-0069, Assist with the labeling artwork developments & changes to printed packaging components. Lead variety of tests and analysis which involve wet chemical and/or instrumental methodology. 4 0 obj Knowledge of BIM 360 not mandatory, but would need to be willing to learn the program and assist others, Broad understanding of construction industry/scopes of work, Good time management skills and organizational skills, At least five (5) years experience in the capacity of full time Quality Assurance/ Control Management, Advanced degree or QA/QC training preferred, Aviation experience not mandatory, but preferred, Bachelor’s degree in related discipline or 7 years related job experience equivalent to the same, 5 years of experience in Quality Management Systems, Experience in office operations, preparing reports and performing inspections in a quality environment, Extensive knowledge of business and management principles involved in strategic planning, resource allocation, human resources, leadership, service delivery methods, and coordination of people and resources, TQM (Total Quality Management), training or certifications (ISO, CQM, Six Sigma), Ability to use personal computers and standard desktop software to compose reports, correspondence, and memorandums; review drafts and finished documents for appropriate grammatical usage; answer questions relating to office operations and established policies and procedures, Must have the ability to understand and formulate statements of work, develop policies and procedures. Verify incoming raw materials, Conduct analytical testing as directed by technical. If you’re not sure how to start, attend a resume writing workshop for assistance or view resume 1 0 obj Although it alone will not get you a job or internship, a good resume is an important element toward obtain-ing an interview. Support and implements EHS programmes and initiatives, Minimum of a Scientific Bachelor’s degree (preferably Chemistry) with 5+ years’ experience of sterile products in a pharmaceutical company, Must possess process and manufacturing knowledge of injectable processes (Aseptic and TS), Capability to manage team, set clear goals, communicate clearly and ensure progression to completion, Review all data obtained during all quality assurance activities to ensure consistency with company policies and procedures, Maintain a working knowledge of government and industry quality assurance codes and standards, Lead investigations into customer complaints regarding quality, ensure systems are in place to address customer quality issues, returns, complaints, Continuously develop and improve the adequacy of existing Quality Assurance procedures and processes, Lead, mentor, & coach your QA/QC team by promoting a culture of quality awareness, Work collaborative with Corporate Quality to develop, implement and sustain a quality-based program that meets or exceeds the company and customer requirements, Serve as a quality liaison with Corporate Quality and ensure consistent practices and deliverable meet quality standards, Prepare, maintain, enforce, and update the Quality Plan to drive performance using ISO standards across all aspects of the Program. Frequent standing and walking around the facility primarily on the factory floor, Supervisor Responsibilities-3 to 5 indirects, Type of Supervision Position works under: (close, moderate, minimal) Works under minimal supervision, Errors-Mistakes made in this position can have significant financial impacts on the business (>$500,000), Relationship Responsibilities-A cross functional role interfacing with all functions of the business, Engineering, Accounting, IT, Manufacturing, Service Parts, Sales, Tactical and Sourcing, Business Planning, HR, all Suppliers, and all Customers. Looking at the importance of such jobs we have collected a few quality assurance resume templates for you. Pro Tip: The PDF resume format is almost always the best, unless the job description specifically asks for a Word doc to be sent in. Perceptive, self-motivated, collaborative and capable of working with a geographically diverse footprint through remote management skills, Proven ability to communicate professionally in a corporate environment, work in cross-functional collaborative teams and implement organizational change management, Good communication skills, and experienced in remote management, Ability to participate and contribute to the senior leadership team’s seamless delivery to client, Direct supervision of employees and activities in the quality control department in the performance of plant lab testing and analysis, Develop and drive a high-level quality strategy for the manufacturing site to facilitate compliance to ISO, Baker Hughes QMS and customer requirements, BS in (other related science field) or chemical engineering, 5 years of experience in Chemical Manufacturing support and Quality Management, 4 years of experience in Quality Control or Analytical Lab, Ensure safe operation of the Quality Control Lab, Provide direction and leadership to effectively lead a technical team, Give scientific input in developing and improving analytical methods, Ensure laboratory compliance with cGMP requirements, Ensure both high level and detailed customer relationship for analytical projects and tech transfer, Improve accuracy, efficiency and throughput of analytical testing methods, Give final approval of analytical results, Co-manage specifications and methods for raw materials, in-process and finished products, Leads and continuously develops the skill set of a staff of professionals who analyze products, raw materials and in-process mixtures in support of multiple chemical manufacturing processes as well as special projects such as new material evaluation, and R&D front runs, Develops, implements, maintains and performs both internal and external quality control activities including analysis, instrument qualification/preventive maintenance, method validation, and training, Schedules and coordinates the routine and non-routine analysis of raw materials, in-process, and finished products according to standard operating procedures, Interprets analytical data and provides understanding of information collected, Provides analytical and technical support to Quality Control Analysts, R&D Chemists, Manufacturing, Quality Assurance, Warehouse, and Sales, Applies knowledge of FDA requirements to ensure cGMP compliance of the lab. The resume format for experienced software engineer can serve as an inspiration for the professionals in this particular field. This means that this professional will spend the majority of work time at the assigned project location for the duration of the project requiring long-term temporary living close to the project site, Certification in discipline (e.g. They do it by testing, controlling, and auditing the production process as well as training staff on quality procedures. Document and report back any key learnings, Participate in development and implementation of QAQC checklists, Mentor and coach trade partners in QAQC processes, procedures and expectations, Assist in coordinating Jurisdictional Authority inspections, Attend meetings in support of field staff, quality development plans per scope, Quality & Commissioning weekly meetings among others, Work with the Owner regarding quality issues, recognition program, quality program improvements and project status, Report directly to Quality & Commissioning Manger, Become crossed trained in Commissioning processes and procedures after you are up to speed with the quality program, Participate in creating the commissioning plan for individual scopes, Coordinate vendors for startup activities, Validate QAQC process through PreConstruction Complete Checklists, P&ID Field Walks, review of documentation submitted by vendors, trade partners and 3rd party inspectors and drive completion of the Commissioning Plan prior to Construction Complete declaration, Periodically participate in design reviews, Be a field presence during Cx activities and complete required checklists, Assist in coordination of Field OAT, vendor startup, FAT activities, EHS walk, DVC request and completion, utility startup requests, Drive any outstanding issues preventing Construction Complete signoff with vendors, trade partners, Skanska team members, Owner, 3rd party inspectors and design team, To ensure Quality specifications of all products including raw materials and packaging meet Syngenta quality standards, To implement Syngenta global/Regional quality guidelines across the country supply chain, Act as site NPI coordinator between site and all other functions like Operations, Commercial, and Finance etc, To implement and maintain Contamination Prevention Plan (Residual Impurity Risk Assessment and Residual Impurity Management) at Karachi site, To monitor & control QC department’s budget, Supervise product and packaging stability / compatibility testing studies when required, Provide QC related technical assistance to production and other departments, Develop & implement standard operating procedures for QC, Ensure supply of quality products to customers by training/audits of our vendors/suppliers, To work in close coordination with Sales & Marketing and Operations for introduction of new products when required, Implement Syngenta quality standards including RIRA management at toller’s end as per guide line, To ensure capability enhancement and development of team members through internal and external interventions, To foster of culture of innovation in QC and processes, 7 to 10 years of experience of working in a Quality Control Laboratory with at least 2 years in managing the department independently in a multi-nation pharmaceutical /chemical/pesticides company or a similar setup, Must have Masters in Chemistry from a reputable University, Excellent Auditing skills like ISO 9000 and RIRA (Residual Impurity Risk Assessment), Knowledge of modern QC and QA tools and techniques, Well versed with SAP environment (APO, SRO, FAO, CIPAC, Pesticide Manual), Responsible for leading a Quality Management Network System globally of key Quality Managers, Maintain, update and oversee quality management system globally including all procedures, guidelines, schedules and IMS documentation, Accountable for global success related to the execution of certification body audits as well as customer and supplier audits including improvement actions and follow-up, Responsible for all documentation and database related to Quality and ISO programs / audits (e.g. Report control issues to the Stress Test Coordinator and Capital Management Manager, Evaluate stress test processes for effectiveness of controls to provide reasonable assurance of accuracy and completeness. <>/ExtGState<>/XObject<>/ProcSet[/PDF/Text/ImageB/ImageC/ImageI] >>/Annots[ 30 0 R] /MediaBox[ 0 0 595.32 841.92] /Contents 4 0 R/Group<>/Tabs/S/StructParents 0>> of Science or Engineering from four-year college or university and seven to ten years related experience and/or training; or equivalent combination of education and experience, Must have prior experience in Beverage or Flavor industry, Familiar with complex instruments (GC, GCMS, HPLC, FTIR), Minimum 5 years of relevant experience in program management, Demonstrated previous success with definition, development, implementation, and ongoing management of processes and best practice implementation, Advanced knowledge of Microsoft Office required, Confidence and proficiency in delivering verbal and written communications. 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