QC SKILLS, EXPERIENCE, AND JOB REQUIREMENTS

Published: Nov 25, 2025 - The Quality Control (QC) Professional has strong attention to detail, analytical thinking, and a thorough understanding of quality standards and regulatory guidelines. This position requires proficiency in using inspection tools, interpreting technical documents, and conducting accurate tests to evaluate product conformity. The individual also communicates effectively across departments, maintains precise documentation, and adapts to evolving quality systems and technologies.

Essential Hard and Soft Skills for a Standout QC Resume
  • Quality Inspection
  • SPC Analysis
  • Root Cause
  • ISO Standards
  • Six Sigma
  • Calibration Methods
  • Technical Reporting
  • Sampling Methods
  • Control Charts
  • MSA Checks
  • Attention Detail
  • Clear Communication
  • Problem Solving
  • Critical Thinking
  • Time Management
  • Teamwork Skills
  • Adaptability Skills
  • Decision Making
  • Strong Organization
  • Professional Integrity

Summary of QC Knowledge and Qualifications on Resume

1. BA in Environmental Science with 4 years of Experience

  • Relevant work experience, preferably within a biological and/or pharmaceutical industry.
  • Experience in a Quality Control setting.
  • Experience with aseptic processing in an ISO 5 clean room and biosafety cabinets.
  • Knowledge of cGMP regulations and FDA/EU guidance related to the manufacturing of cell-based products.
  • Knowledge of Good Tissue Practices.
  • Detailed knowledge of CAR-T QC test methods and related equipment.
  • Excellent written and oral communication skills.
  • Must be able to accommodate shift schedule.
  • Must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
  • Must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
  • Comfortable with speaking and interacting with inspectors.

2. BS in Chemistry with 3 years of Experience

  • Experience working in a QC lab setting.
  • Impressive, demonstrable track record and skills/experience gained within similar positions.
  • Highly proficient in the use of key analytical equipment (HPLC, IR, UV) and the testing of finished products.
  • Experience of working in a GMP environment.
  • Good IT skills, e.g., Microsoft Office (Word, Excel and Outlook).
  • Able to credibly and communicate (written and verbal) at all levels.
  • Highly customer-focused and passionate about delivering excellent customer service.
  • Ability to achieve and maintain high standards with meticulous attention to detail.
  • Must have first-class planning, organizational and time management skills.
  • Ability to work accurately in a busy and demanding environment, adhering to strict deadlines/timescales.
  • Strong analytical and problem-solving ability.

3. BA in Industrial Technology with 2 years of Experience

  • Relevant hands-on pharmaceutical laboratory experience.
  • Demonstrated computer proficiency, e.g., word processing, spreadsheets, graphing, etc.
  • Good knowledge of cGMPs and laboratory practices.
  • Able to be familiar with basic laboratory instruments.
  • Excellent observation skills and problem-solving abilities.
  • Ability to follow analytical procedures and protocols.
  • Good laboratory techniques.
  • Ability to work in a methodical and organized fashion.
  • Ability to write in a concise, logical fashion.
  • Ability to manage multiple responsibilities with a high degree of self-motivation.
  • Good oral, written, and interpersonal English communication skills.
  • Ability to effectively utilize scientific information resources within the assigned area of responsibility.

4. BS in Chemical Engineering with 4 years of Experience

  • Related industry experience, food or pharmaceuticals industry, preferably in biotechnology or human pharmaceuticals.
  • Laboratory documentation preparation, review and revision experience.
  • Strong interpersonal, oral and written and communication skills, ability to effectively communicate, both orally and in writing, with peers and area management.
  • Understanding of applicable regulatory, GMP, and safety requirements.
  • Ability to learn and comprehend a wide variety of GMP activities, including inspection, sampling, testing and release of materials.
  • Experience working in a GMP environment.
  • Ability to manage multiple tasks, projects simultaneously.
  • Knowledge and ability to implement, track and ensure adherence to all safety training for equipment related to the QC team.
  • Knowledge of testing and associated equipment protocols and requirements and applicable instrumentation and procedures.
  • Ability to develop and fit in with the QC team, ensuring a competent workforce that can effectively accomplish department and company objectives.

5. BS in Microbiology with 3 years of Experience

  • Must have related laboratory experience.
  • Knowledge of Chromatography, HPLC, Concentration determination, pH, Total Organic Carbon, Gel-based protein separation, EF, Plate-Based Assay, and conductivity.
  • Understanding and knowledge of procedures and practices in the assigned area.
  • Must have developed basic technique skills and be capable of working within established procedures.
  • Able to work with a moderate degree of supervision.
  • Able to familiarize with basic statistical tools to analyze data in relation to trend results.
  • Able to familiarize with data management processes such as Trackwise or LIMS, or capability to learn basic use and navigation within the systems.
  • Ability to identify and escalate problems to superiors.
  • Ability to manage one or more tasks in a manner that promotes effective schedule adherence.
  • Ability to manage changing priorities in a productive and positive manner.
  • Ability to communicate effectively with colleagues in the department, building trust and respect.
  • Ability to learn and incorporate Lean Lab and Six Sigma principles into the daily work environment.
  • Able to achieve Yellow Belt Certification within the company's Six Sigma program.
  • Must have technical writing skills (write basic protocols, prepare complex reports without a template).
  • Able to solve problems and perform troubleshooting competencies.

6. BS in Biology with 4 years of Experience

  • Must have technical competencies.
  • Working knowledge of HPLC, UPLC, GC, Dissolution, M, or UV spectrophotometers.
  • Good verbal and written English.
  • Must have a naturally positive, upbeat attitude.
  • Able to be flexible and responsive.
  • Able to maintain confidentiality at all times.
  • Must have a high level of confidence, integrity and motivation.
  • Knowledge in all aspects of 21 CFR 210 and 211.
  • Knowledge of root cause analysis and technical writing.
  • Ability to work effectively in a fast-paced, timeline-driven, extremely high-expectation environment, is flexible to occasionally work overtime on short notice.
  • Able to take initiative and exhibit resourcefulness in problem-solving, experienced in working in a collaborative team environment.
  • Must understand chemical components and safety practices required for handling chemicals used in the laboratory.

7. BA in Industrial Technology with 6 years of Experience

  • Strong initiative and enthusiasm to complete ambitious tasks and learn new technologies related to CAR T products.
  • Experience in GMP quality control or manufacturing.
  • Work experience in GMP quality control or manufacturing.
  • Strong understanding of applicable USP, ICH, and Ph Eur regulations related to intermediate, release, and stability testing.
  • Excellent verbal and written communication skills.
  • Extensive Cell-based Bioassay/ELISA and/or Immunology background.
  • Extensive experience with scheduling, testing, and data review of QC chemistry assays for in-process, release, and stability samples.
  • Experience with QMS systems, including OOT/OOS/invalid investigations and working cross-functionally to support CAPA and proactive initiatives.
  • Experience in training and mentoring laboratory analysts, with a focus on team building.
  • Experience in troubleshooting analytical equipment and methods.
  • Ability and desire to work in a fast-paced environment, manage large projects and implement microbiology programs.
  • Experience interacting with hosting internal and external auditors.

8. BS in Chemical Engineering with 4 years of Experience

  • Must have laboratory experience.
  • QC lab testing experience, sterility testing, endotoxin, chemical properties testing, nuclease detection assays, FTIR, USP water testing, spectroscopy and electrophoresis.
  • Knowledge and control of analytical equipment, including calibration and maintenance.
  • Knowledge of cGMP, cGDP, cGLPs, ISO13485, and 21 CFR regulations.
  • Knowledge of USP and ACS guidelines and criteria.
  • Strong writing and verbal skills to effectively read and write SOPs, reports, and communicate.
  • Proficient in software such as Word, Excel, and Outlook.
  • Strong problem-solving, multitasking, and prioritization skills.
  • Ability to lift and carry at least 30lb and stand for extended periods of time.
  • Knowledge or experience of the monitoring of cleanrooms and production areas.
  • Experience with aseptic technique to perform critical testing.
  • Basic background in microbiology.
  • Must have statistical knowledge and techniques.
  • Experience using laboratory and inventory management systems (Process Pro).

9. BS in Food Science with 3 years of Experience

  • Aviation/maintenance experience or related aviation training.
  • Previous Technical Record processing and Quality Control or auditing experience.
  • Able to familiarize with Aircraft Maintenance Programs (AMPs) and tracking software.
  • Able to familiarize with Transport Canada Aviation regulations and standards.
  • Able to familiarize with Transport Canada and/or aviation-related technical manuals and documents.
  • Proven proficiency in the MS Office suite, working knowledge of RAAS.
  • Strong verbal and written communication skills.
  • Must have exceptional attention to detail.
  • Ability to manage high volumes of documentation and paperwork on a daily basis.
  • Strong data entry skills with exceptional attention to detail.

10. BS in Chemistry with 2 years of Experience

  • Experience quality or process-related functions.
  • Ability to develop an understanding of QMS fundamentals.
  • Proven skills in the areas of staff communication and engagement.
  • Strong verbal and written communication with investigative interview experience.
  • Strong familiarity with MS Excel, Word, Adobe PDF, and PowerPoint.
  • Strong commitment to enhancing quality culture among local leadership and staff.
  • Able to embrace the HDR brand promise and values.
  • Able to represent HDR's commitment to fulfill project responsibilities and obligations to the client and internal management stakeholders.
  • Must provide professional and ethical direction for the company and staff.

11. BS in Microbiology with 3 years of Experience

  • Prior experience with UNet-DonorNet and UNOS compliance reporting.
  • Experience with tissue banking and AATB compliance.
  • Experience in a clinical or medical office setting.
  • Must have strong interpersonal skills, including written and verbal communication, with a continuous focus on customer service.
  • Basic medical terminology.
  • Proficient in Microsoft Word and data entry.
  • Must have a strong attention to detail and work with a high degree of accuracy.
  • Must be highly organized with the ability to manage time appropriately, prioritize and multitask.
  • Knowledge of data management.
  • Must have patience and maintain focus through interruptions.
  • Must be able to remain professional while dealing with confidential information.
  • Experience working in a collaborative team environment.

12. BS in Manufacturing Engineering with 6 years of Experience

  • Experience within the cosmetic or pharma industry.
  • Knowledge of GMP and GLP.
  • Capable of performing routine laboratory activities.
  • Good command of English for effective oral/written communication.
  • Demonstrated experience in investigations, change control, validation, batch record review, analytical data review and/or audits.
  • Strong leadership/interpersonal skills for influencing and teamwork in a team matrix environment.
  • Strong decision-making/problem-solving skills.
  • Ability to prioritize and meet deadlines while handling multiple projects under time pressure.
  • Practical project management software and spreadsheet skills, proficient computer operation skills.
  • Good organizational skills, detail-oriented and accurate, analytical skills.

13. BA in Biochemistry with 5 years of Experience

  • Good at English skills.
  • Experience in the E-commerce domain.
  • Testing experience in multiple platforms/devices/browsers.
  • Understanding of Web development.
  • Experience with relational database concepts and SQL queries.
  • Experience in the Magento platform.
  • Ability to develop/execute automation tests.
  • Ability to verify the accuracy of sales data.
  • Understanding of software development processes.
  • Good problem-solving, analytical, and critical thinking skills.
  • Good communicator, teamwork, or independence.
  • Ability to provide test estimates for projects.
  • Strong time and task management skills.

14. BS in Biology with 4 years of Experience

  • Proven experience in direct utilization of problem-solving tools (for example, RCA tools including 5-Whys, TapRooT, Fishbone/6M, Kepner-Tregoe, Comparative Analysis, etc.) with shown success.
  • Demonstrated experience working in a regulated environment, preferably in biologics/pharmaceuticals.
  • Prior experience in a Quality Control and/or Quality Assurance role.
  • Exposure/Experience in Root Cause Analysis and/or LEAN/six sigma experience or Operation Excellence tools.
  • Solid technical writing skills.
  • Proven communication and interpersonal skills.
  • Ability to drive functional, technical, and operational excellence.
  • Ability to evaluate data and make recommendations based on data.
  • Ability to make recommendations based on trends and trend analysis.
  • Ability to work in a fast-paced environment with the ability to prioritize effectively to meet timelines.
  • Strong facilitation skills for groups, including staff-level employees.

15. BS in Chemistry with 2 years of Experience

  • Experience in Quality Control in the medical device industry.
  • Experience working in an ISO 13485 or FDA-regulated environment.
  • Experience use of gauges, instruments and other measuring devices preferred, able to read blueprints.
  • Experience working in a cGMP, ISO and/or pharmaceutical/medical device regulated environment.
  • Excellent communication skills, both written and verbal.
  • Comfortable working in a fast-paced environment.
  • Effective time management, multitasking and organizational skills.
  • Strong attention to detail and cross-functional team experience.
  • Must have computer skills in systems such as Microsoft Word and web-based software programs.

16. BS in Microbiology with 3 years of Experience

  • Must have related QC experience.
  • Experience with sampling techniques and inspection standards.
  • Must have basic math skills and the ability to utilize Excel for basic calculations and graphing.
  • Must be able to speak, read, and write English fluently, as well as write technically and summarize information into data reports using Microsoft Word.
  • Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations.
  • Excellent observation skills with a bias for “corrective action” and improving work environment processes and procedures.
  • Demonstrated ability to make critical decisions regarding product quality or quality system compliance.
  • Ability to assess and articulate risk when evaluating a situation.
  • Knowledge of basic validation, equipment calibration, and change requirements.
  • Demonstrated understanding of the use of calibrated equipment.
  • Proven capability to prioritize responsibilities and complete tasks on schedule.
  • Must be able to work independently in a fast-paced manufacturing environment.
  • Basic knowledge of SAP.
  • Experience working in an FDA-regulated environment.

17. BS in Pharmaceutical Sciences with 2 years of Experience

  • Able to work thoroughly and observant with an eye for detail.
  • Understanding of the requirements for the products.
  • Excellent communication and collaboration skills, with the ability to uphold integrity.
  • Able to work efficiently, organized, detail-oriented, and able to complete tasks in time time-sensitive manner.
  • Demonstrated ability to manage multiple projects simultaneously.
  • Able to curious thinker who looks for new solutions.
  • Production experience in a wide variety of roles.
  • Lab and/or Quality Control experience.
  • Ability to prolonged periods at a desk and on a computer.
  • Ability to move product testing samples, materials, or documents up to 25 pounds.
  • Ability to walk or navigate laboratory and production facilities.
  • Must be able to lift or move up to 25 pounds at a time.
  • Must wear proper personal protective equipment (PPE).

18. BS in Chemical Engineering with 4 years of Experience

  • Experience in manufacturing Quality Control testing environment.
  • Must be technically adept in wet chemistry, analytical methods, and sophisticated technologies.
  • Proven problem-solving and troubleshooting skills in laboratory testing and equipment.
  • Proficient with GC, HPLC, AA, FTIR, and Titrators.
  • Strong work ethic, self-motivated and able to follow through on responsibilities and complete tasks with minimal supervision.
  • Able to work with others in a respectful manner and as a member of the team to achieve all goals set forth in the department.
  • Excellent communication and organizational skills.
  • Proficient in Microsoft Office, Lotus Notes, SAP, and various databases.
  • Understanding of ISO, IATF, and ITAR regulations.
  • Demonstrated excellent attendance and reliability.
  • Able to flexibility to work overtime, extended shifts and/or other shifts on occasion.
  • Strong commitment to safety systems and OSHA-required standards.

19. BS in Microbiology with 2 years of Experience

  • Ability to apply basic statistics and compare data trends.
  • Effective verbal/written communication, interpersonal, and team-building skills.
  • Excellent organizational, problem-solving, prioritizing and follow-up skills.
  • Ability to handle multiple tasks/projects simultaneously.
  • Working knowledge of cGMPs in the laboratory environment.
  • Excellent communication skills, written and verbal.
  • Problem-solving skills, including root cause analysis.
  • Knowledge of basic statistics.
  • Must be able to read, write, and understand English.
  • Must be able to follow verbal and written instructions.
  • Ability to verify numbers, words and alphanumeric combinations across multiple media.
  • Must be open to occasional off-shift and weekend hours.
  • Ability to apply basic statistics and compare data trends.
  • Effective verbal/written communication, interpersonal, and team-building skills.
  • Excellent organizational, problem-solving, prioritizing and follow-up skills.
  • Ability to handle multiple tasks/projects simultaneously.

20. BS in Food Science with 4 years of Experience

  • Experience as a core tester.
  • Must have experience in testing web services, API using tools like Postman, SOAPUI.
  • Sound understanding and experience in Agile Scrum frameworks and practices.
  • Experience with keyword-driven testing, test data-driven framework, or BDD.
  • Experience in building the automation test framework using Selenium WebDriver.
  • Proficient in using automation tests by scripting with any object-oriented programming language, such as Python, Java, and C#.
  • Solid test plan and test case writing skills.
  • Excellent understanding of SDLC and quality process.
  • Solid knowledge of testing design techniques and testing strategies.
  • Good English communication.
  • Able to commit to quality, attention to detail.
  • Strong analytical skills.

21. BA in Industrial Technology with 6 years of Experience

  • Quality assurance experience or quality control experience, and a management position.
  • Knowledge in HACCP, FSSC 22000, and ISO system.
  • Strong understanding of different software for quality assurance processes.
  • Must have experience in managing and working with interdepartmental team members.
  • Knowledge of the internet and e-business processes, disciplines and standards.
  • Strong analytical skills and experience with the implementation and administration of Quality Assurance metrics, such as defect profiles and performance to entry/exit criteria.
  • Excellent problem-solving, interpersonal communication and project management skills.
  • Strong leadership skills that inspire team confidence and respect while motivating team members in a creative and effective manner.
  • Must have a desire for achieving excellence in customer satisfaction, process and product quality and reliability.
  • Strong English skills for working communication.

22. BS in Pharmaceutical Sciences with 11 years of Experience

  • Experience in a major infrastructure project.
  • Related work experience in the field of quality management.
  • Experience in a management capacity.
  • Must have Lead Auditor certification (ISO 9001 or equal), ASQ certification (CMQ/CQE), or other related certifications.
  • Able to maintain active membership in a nationally recognized Quality organization.
  • Must have management ability and extensive knowledge of Quality Management practices, processes and current technology.
  • Experience in directing and implementing quality management systems and standards specified by ISO 9000, ASME, ANSI, ASTM and similar organizations.
  • Ability to communicate clearly, conduct presentations to management and interface effectively with a diverse group of professionals.
  • Proficient in analyzing situations in business terms, i.e., ROI, cost per unit, etc.
  • Strong interpersonal skills to work with other departments in a tactful and effective manner.
  • Strong leadership and management skills, excellent written and verbal communication, strong analytical, problem-solving, and risk assessment skills.
  • Ability to make public presentations.
  • Strong attention to detail.
  • Strong working knowledge of ISO Quality Management Systems Standards.
  • Ability to direct and manage team members with day-to-day activities as well as special projects to assure timely completion.

23. BA in Quality Management with 5 years of Experience

  • Working experience in the pharmaceutical or biotech field.
  • Excellent analytical mindset and skills, including hands-on experience with analytical methods such as HPLC, UPLC, GC, Mass Spectrometry and USP compendial testing, etc.
  • Strong working experience in managing CMOs, timelines and deliverables.
  • Strong method troubleshooting skills and scientific understanding of chemistry or analytical chemistry.
  • Able to familiarize with regulatory guidance documents (ICH, USP, CFR, general guidance).
  • Prior working experience in a regulated environment (GMP, GLP, etc.)
  • Strong time management skills with attention to detail and a desire to achieve team and individual goals.
  • Comfortable working in a team environment and interacting with other team members within the group and various departments of the company.
  • Excellent verbal and written communication skills (SOPs, professional reports, emails).

24. BS in Biology with 4 years of Experience

  • Previous experience that provides the knowledge, skills, and abilities to perform the job.
  • GMP QC testing experience.
  • Raw material testing experience.
  • Hands-on experience with FTIR, Flow Cytometry, BacT/Alert, EndoSafe, and Mycoplasma Q-PCR.
  • Experience with investigations, including OOS, Environmental monitoring, as well as safety testing experience (sterility, endotoxin, mycoplasma).
  • Demonstrated knowledge of multiple applicable techniques such as FTIR, Flow Cytometry, ELISA, BacT/Alert, EndoSafe, and Mycoplasma qPCR.
  • Knowledge of applicable regulatory authority, compendia and ICH guidelines.
  • Ability to understand and independently apply GMPs and/or GLPs to everyday work with regard to documentation and instrument use.
  • Proficient in Microsoft Excel and Word.
  • Proven ability to interpret data by performing trend analysis.
  • Proven ability in technical writing skills.
  • Ability to independently optimize analytical methods.
  • Proven problem-solving and troubleshooting abilities.
  • Good written and oral communication skills.
  • Must have time management and project management skills.
  • Ability to work in a collaborative work environment with a team.

25. BS in Manufacturing Engineering with 6 years of Experience

  • Quality Control experience in the biotech and/or pharmaceutical industry.
  • Extensive experience performing laboratory investigations.
  • Able to be well-versed in Molecular Biology techniques, qPCR, cell-based assays, ELISA, Western blot, SDS PAGE, Cell and Tissue Culture operations and principles and has a good understanding of Contract testing and procedures.
  • Working knowledge of quality systems and regulatory requirements and working with cross-functional teams.
  • Strong knowledge of GMP, SOPs and quality control processes.
  • Strong acumen for analyzing and interpreting data and statistics.
  • Extensive experience performing laboratory investigations.
  • Must demonstrate a high level of commitment to delivering timelines and milestones to achieve business objectives.
  • Ability to communicate and work independently with scientific/technical personnel.
  • Comfortable in a dynamic environment with minimal direction and able to adjust workload based upon changing priorities.
  • Ability to apply GMP regulations and international guidelines to all aspects of the position.
  • Strong organizational skills, ability to prioritize and manage through complex processes/projects.

26. BS in Microbiology with 7 years of Experience

  • Must have certification in Six Sigma or related methodology.
  • Highly experienced in developing, implementing and validating methods for HPLC and GC-MS.
  • Quality Control and Product Safety experience in a commercial or manufacturing environment.
  • Operations background or experience.
  • Able to analyze involves the interpretation of statistical process control charts and flow charts on all in-process, finished products and laboratory STD plus instruments.
  • Knowledgeable about the test methodology in use in the QC Laboratory.
  • Ability to benchmark test method protocols within and across the industry.
  • Knowledge and experience in Method Development and Improvement.
  • Able to conduct process capability analysis, correlation and regression analysis to assess variables causing process variation.

27. BA in Biochemistry with 5 years of Experience

  • Relevant Quality Control Lab experience.
  • Experience training for Quality Control and other team members.
  • Experience with internal and customer audits.
  • Demonstrated leadership skills.
  • Knowledge of Quality standards such as ISO 13485, FDA, ICH (International Council for Harmonization), with a good understanding of CAPA, Risk Assessments, Deviation investigation and Change Control and Document Review processes.
  • Working knowledge of HPLCs, UV, FTIR and other analytical equipment.
  • Understanding of how to set up and maintain product stability programs and sample/raw material retention programs.
  • Able to familiarize with SAP, Trackwise, Agile, E1, and LIMS systems.
  • Able to be versed in continual process improvement practices.
  • Excellent interpersonal, communication and organizational skills with good attention to detail.
  • Ability to produce and present original quality communication materials for internal and external audiences.
  • Must be able to commute between Bedford and Chelmsford facilities.

28. BA in Industrial Technology with 6 years of Experience

  • Quality control experience in the pharmaceutical industry, supporting cGMP areas.
  • Leadership experience, preferably managing direct reports.
  • Demonstrated subject matter expert in several microbiological disciplines.
  • Must possess strong organizational skills and a demonstrated ability to be self-directed while managing multiple projects.
  • Demonstrated Leadership traits that build and foster trust, respect, cooperation, and collaboration across the organization.
  • Must have excellent collaboration skills with colleagues both within and outside of the department.
  • Must possess effective communication skills that effectively facilitate project or workflow efficiency and/or distribute information.
  • Able to coordinate activities and tasks in a high-throughput and high-quality RFT environment.
  • Effective listening and coaching skills.
  • Strong attention to detail.
  • Expertise with Labware LIMS and/or Softmax Pro.