… Hassle-free … For your Quality Engineer resume format, use the reverse chronological type because it gives hiring managers a clear timeline view of the applicant’s work history, key responsibilities, and accomplishments. Compilation ANDA / Dossier and submission of annual updates for ANDA / Dossier. Crafting a Quality Assurance Associate resume that catches the attention of hiring managers is paramount to getting the job, and LiveCareer is here to … Free New Quality assurance Resumes for Pharmaceutical Panies Free Download 425088 from 6050 + Free Collection Template Examples Download , entry level qa analyst resume – newskeyfo Analyst Resume Sample Best Beautiful Resume for Qa Analyst Resume Examples for Quality Analyst Beautiful Gallery Quality Quality assurance Analyst Resume Lovely Quality assurance Analyst 30 Sample Qa … If you're ready to apply for your next role, upload your resume to Indeed Resume to get started.) On call coverage. Pharmaceutical quality assurance resume samples. 15-16 quality assurance cover letter samples | 626reserve.com. Be familiar with delinking closed accounts from existing Signature Card to help review closed account report when needed as backup, Remediate any audit exceptions cited by internal audit functions (i.e: QCM reporting, KYC trigger report, QCT review), Perform duties & responsibilities specific to department functions & activities, and other duties & responsibilities as required or assigned by Management, Familiarize and stay updated on all policy and procedure (P&Ps) updates in the Big Green Book, internal Preferred Banking Procedures (including EaglesNet), BSA/AML KYC policies in Collaborate, and any Regulatory changes to ensure QA review is audited in line with current standards. Chose the Best Quality Assurance Resume Format . Created with Sketch. Overtime is generally worked at the end of the work shift, Demonstrated ability to work well with others, Tremendous attention to detail and commitment to error-free work, Grade Level is dependent upon industry experience, Release for products for local distribution, Complete QA tasks related to local packaging/repackaging processes, Support processing and resolution of technical product complaints, Co-ordinate the handling of rejected product and associated destruction activities, Co-ordinate the handling of product returns and associated QA assessment to determine disposition, Participate in supplier audits and self-inspections as required, Collate data for the Quality Management Review Process where required; and, Raise and investigate deviations and complete associated CAPA actions as required, Experience within a Quality Assurance role in a Pharmaceutical environment, Ability to prioritise workload in a changing environment, work efficiently and autonomously, Demonstrate a winning spirit through creating a can-do attitude and positive energy amongst others, Intermediate level in MS Office Applications, Outlook, Excel and Word, Conducting monthly internal GMP audits as directed by QA Supervisor/Manager, Conducting daily walkthroughs of assigned projects, Releasing “Quarantined” product into good upon the receipt of documentation from the client, Monitoring inventory adjustments by reviewing data gathered by operations personnel, Notifying Operations Manager and QA Supervisor/Manager of any unusual trends, Conducting random checks of inbound receipt put always for accuracy, Verifying that the system is identifying “quarantined” product accurately, Verifying that the system is identifying “released” product accurately, Work closely with Operations to identify and correct any system or human generated discrepancies inclusive of corrective and preventative action, Assist in trending data to look for ways to improve quality processes, Verify that the system is identifying “quarantined” product accurately, Guide warehouse in determining root cause of discrepancies and the development of corrective actions, Make suggestions on quality improvements and facilitate change control process when changes are made, Maintain thorough knowledge and understanding of all Standard Operating Procedures (SOPs) pertaining to the review process, Familiarity with all laboratory techniques and equipment applicable to the tasks performed in the laboratory, Highest commitment to GMPs with regards to the recording of laboratory data for testing of pharmaceuticals and medical devices, Must have a solid grasp of the fundamentals and importance of teamwork in the contemporary business world, Must be capable to work at a desk and computer terminal for up to three hours at a time, and for up to eight hours on a given day, Working knowledge of all produce items in the warehouse, Ability to properly stack pallets, preventing damage to product, Minimum 1 year produce handling experience, Must have strong speaking, reading, writing, and typing skills, Preferred background in computer software including Microsoft Office and Microsoft Windows, Stand for extended periods of time; bend, stoop, reach, push, pull, squat, turn body, and walk, Lift and move cases (selecting product and placing on a pallet) ranging in weight up to 75 lbs continuously to and from heights ranging from floor to knee, waist, shoulder, and overhead, Use hands and fingers to peel and stick labels on cases, Must have the ability to talk and hear; must be able to hear warning horns on moving machinery and equipment, Specific vision abilities required to perform this job include close and distance vision, depth perception, color vision, peripheral vision, and the ability to adjust focus, Must be able to climb on and off the box of the truck, The ability to interact with department heads regarding corporate compliance, Must be highly motivated and able influence and motivate others, Ability to manage multiple tasks effectively & efficiently, 1-3 years experience in a Validation role within the pharmaceutical industry, 1-2 years experience in creating and maintaining SOPs preferred, Demonstrated above average written communication skills in the English language, Sales Force (preferred, but not required), Minimum of 2 years of experience in data operatons, quality control, support or client service, At least 2 years of working in EMEA work shift and working with colleagues abroad, Bachelor's college degree in Information Management, International Business, or similar concentration, Demonstrated analytical skills; ownership over his/her work and/or assigned subject, Strong organizational and problem-solving skills, attention to detail, background in process-oriented tasks, Excellent English comprehension (written and verbal), Ability to work in a global team, especially in a collaborative team environment, Ability to work under tight deadlines and multiple tasks, Familiarity with data science and database management is a plus, Establish and maintain rapport with vendors through positive and consistent communication, 2-3 years minimum working in a production or QA/QC, production or Warehouse environment, Proficiency in Microsoft Word & Excel, Email, 5+ years of relevant pharmaceutical/scientific experience, Demonstrated ability to interpret and organize scientific data, High degree of problem solving ability (e.g. Here are some examples of a well-written work experience section. Best Quality Assurance Resume Example | LiveCareer. Must operate as a team member, Provide support for product complaint management including complaint registration, investigation, trending and follow-up with customers, Audit reports and raw data for compliance with protocols, SOPs and regulations, Communicate compliance requirements at all levels, Bachelor’s degree or equivalent in a scientific discipline with a minimum of 3 years’ experience in the pharmaceutical or medical device industry or Master’s Degree with a minimum of 2 years’ experience, Minimum 1 year of experience in regulated operations, Understanding of the FDA QSR regulations, Medical Device Directive, ICH Q7, and the ISO 13485 standard, Experience with product complaint handling, including investigation and documentation, Perform quality/process monitoring functions allowing Biologics to maintain a proactive quality program and to exceed customer expectations, as well as industry and regulatory quality standards, Identify quality assurance opportunities by leading/participating in internal and/or external audits; including completion of all documentation requirements (audit checklists, reports and written/verbal communication), Develop, implement and revise quality audit plans for existing and new clients according to contract requirements, Support the development and review of Standard Operating Procedures (SOP); ensure content is aligned with SOP requirements and applicable regulations, Efficiently and effectively partner cross-functionally with Pharmacy Operations, Patient Support Services, Quality Control, Program Management, and others as required to ensure compliance, Use critical thinking skills to support the development and closure of Corrective Action Preventive Action (CAPAs) and risk assessments, Analyze quality trending reports and present key observations/recommendations to stakeholders, Lead or assist with identifying non-conformances with requirements, provide suitable recommendations and facilitate ongoing quality improvements, Works with co-workers as a team to ensure customer satisfaction and a pleasant work environment, Adheres to company policies and individual store guidelines, Re-creating defects within the software and determining the cause of the issue, Ability to follow a test case or test set to achieve specific results, Ability to receive a customer’s database and restore it, Understand the capabilities of the Configuration Manager, including backup, restore, etc, Familiarity with SQL Server Management Studio, Keep the QA server cleaned up by deleting old databases when detects are verified, Maintain documentation for quality assurance procedures, programs, and initiatives, Maintaining a professional attitude at all times, Experience as a tester or in light accounting, Conduct training verifications for the USCO Service department and work directly with managers and supervisors to ensure timely turnaround for sign off on the verifications, Maintain his/her own training requirements and follow overall company policies and expectations, Cross train with Manager and peer for any other assignments as applicable Conduct direct upload of training records from two repositories onto the training database on a monthly basis, Review, edit documents for punctuality and accuracy and ensure approvals are obtained accordingly, Provide training records and evidence of training during scheduled internal and external audits of USCO, 2-3 years administrative experience , detailed oriented, proactive, attention to accuracy , excellent customer service both internally and externally, Preferred background: Administrative and training , working with databases and multitasking, Top 5 characteristics to be successful in this role: Organized, Detailed Oriented, accurate, focused, business professional How is performance measured: When we get no training observations during internal and external audits of the USCO organization, High School Diploma/GED required, Bachelor Degree preferred, 3+ years experience in an industrial plant environment required, Must be able to work the shift outlined in the position, Manages work groups representing multiple processes and/ or regions, Bachelors or Master Degree or University Degree or equivalent plus 5+ years of relevant experience as a first level and/or second level manager, Must have 5+ years of relevant experience in commercial pharmaceutical manufacturing settings overseeing Quality Assurance, Demonstrated strong management and leadership skills in implementing program/organization strategies, Provides leadership and guidance to Quality, Manufacturing, Development, Research and Sourcing departments. Proficiency with access databases preferred, Self-motivated, driven, and works well with others, Desire to pursue a career in Contact Center Quality Assurance field, Performs quality inspection and documentation for incoming biopsies, Reviews and approves records and associated data in support of cGMP operation activities, Creates batch records, product labels and performs label verification processes, Performs quality reviews and approvals of batch records. Responsible for specific project work such as process improvement/remediation and maintain ownership and responsibility for specific QA processes. Quality Professional with over 10 years of experience. I always ensured top-level performance from my colleagues as well. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. This includes awareness and understanding of the QMS as it applies to the LOC, Ensure that local operations are in full compliance with the GSK QMS, GxP and regulatory requirements, by performing the following, Undertake assigned activities and support the development of internal procedures and systems, compliant to the GSK QMS, as well as local regulatory requirements, as assigned by the Commercial Quality Manager, including the following, Successful completion of relevant tertiary qualifications – science degree, Minimum of 3- 5 years experience within the Pharmaceutical / Consumer Healthcare industries, preferably with Commercial exposure, Strong understanding of and experience in quality assurance systems particularly in the areas of batch release, product incidents, artwork control and in the conduct of audits, Strong knowledge of regulatory requirements pertaining to GMP/GDP, Good knowledge on effective quality documentation systems, Proactive, self starter and highly motivated, Ability to work autonomously and as part of a team, Professional written and verbal communication skills, Influencing and stakeholder management skills, Analytical mind and good problem solving skills, Good time management skills, with ability to multi-task and work under pressure, Concise and persuasive in the description of the different QA situations, Ensures raw materials, in-process and finished products meet company and/or ISO standards, Minimize down time by reducing production rework and recalls, Perform tests and experiments for process analysts or engineers, May perform set-up of processing equipment, Monitor, audit and provide guidance to line operators, Process test runs and prepare records, charts, and graphs of results for presentation to process analyst or engineering to identify problems, inefficiencies or test new products, Provide clerical and administrative support related to documentation requirements, May audit good manufacturing practices document files relating to the maintenance, repair and calibration of manufacturing equipment in order to ensure compliance with external and internal quality assurance requirements, Resolves routine questions and problems, and refer more complex issues to higher levels, Works under direct supervision and follows standard procedures and written instructions to accomplish assigned tasks, High School Diploma/GED or equivalent combination of experience, education and/or training, Minimum of 0-2 years of related / relevant experience to position or specialization, Ability to apply basic skills and possesses the ability to develop advanced skills using tools and equipment appropriate for the position or specialization, Ability to perform standardized duties and tasks, Review cGMP Controlled Documents such as master batch production records, test methods, and specifications. 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