Real Staffing’s Post

Navigating the complexities of Quality Control (QC) in the pharmaceutical industry requires not just a keen eye for detail, but also a partner who truly understands the intricacies of the field. As a Technical Resourcer at LSC, my focus is on connecting QC professionals with opportunities that not only match their skill set but also propel their careers forward. For QC professionals looking to advance their careers, consider these five must-haves: 1. Regulatory Knowledge: Stay updated with FDA, EMA, and other regulatory bodies' guidelines. This knowledge is crucial for ensuring compliance and maintaining the highest quality standards. 2. Analytical Skills: A robust understanding of analytical techniques and the ability to interpret data accurately are essential for making informed decisions that impact product quality. 3. Attention to Detail: Precision is key in QC. A meticulous approach to your work can prevent costly errors and ensure product integrity. 4. Communication Skills: Clear and effective communication is vital when collaborating with cross-functional teams and when documenting processes and outcomes. 5. Continuous Improvement Mindset: The pharmaceutical industry is ever-evolving. Embrace ongoing learning and adaptability to stay ahead in your field. If you are a QC professional, looking for a new opportunity, connect with me to discover what opportunities await you!

Opportunity

urgent contract roles

#hiring Quality Assurance Specialist, Austin, United States, fulltime #jobs #jobseekers #careers #Austinjobs #Texasjobs #ScienceTechnology Apply: https://lnkd.in/gam6ezuj Job Description Quality Assurance Specialist Job Description Maintain a safe, fast-paced, and positive laboratory environment. Interact directly with clients on an as-needed basis. Assist in training of other personnel as requested. Ensure safety and compliance with governmental regulations. Interact with FDA and clients as needed in the event of an inspection/audit. Follow all applicable Good Clinical Practice Regulations. Generally monitor studies to assure Management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with Good Clinical Practice Standards. For any given study, be entirely separate from and independent of the personnel engaged in the direction and conduct of that study. Conduct inspections and maintain records or inspecting studies at adequate intervals and maintain written and properly signed records of each analytical/in-phase or periodic inspection. Report any problems which are likely to affect study integrity to the Principal Investigator and Management immediately. Maintain a copy of a master schedule of all studies, include all pertinent information. Maintain copies of all protocols pertaining to all studies for which the unit is responsible. Determine that no deviations from approved protocols or standard operating procedures were made without proper authorization and documentation. Review all Adverse Events and Serious Adverse Events reported. These are reviewed for accuracy, completion, and ensured to be communicated to the Study Sponsor and IRB

#hiring Quality Assurance Specialist, Austin, United States, fulltime #jobs #jobseekers #careers #Austinjobs #Texasjobs #ScienceTechnology Apply: https://lnkd.in/dEG3giqd Job Description Quality Assurance Specialist Job Description Maintain a safe, fast-paced, and positive laboratory environment. Interact directly with clients on an as-needed basis. Assist in training of other personnel as requested. Ensure safety and compliance with governmental regulations. Interact with FDA and clients as needed in the event of an inspection/audit. Follow all applicable Good Clinical Practice Regulations. Generally monitor studies to assure Management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with Good Clinical Practice Standards. For any given study, be entirely separate from and independent of the personnel engaged in the direction and conduct of that study. Conduct inspections and maintain records or inspecting studies at adequate intervals and maintain written and properly signed records of each analytical/in-phase or periodic inspection. Report any problems which are likely to affect study integrity to the Principal Investigator and Management immediately. Maintain a copy of a master schedule of all studies, include all pertinent information. Maintain copies of all protocols pertaining to all studies for which the unit is responsible. Determine that no deviations from approved protocols or standard operating procedures were made without proper authorization and documentation. Review all Adverse Events and Serious Adverse Events reported. These are reviewed for accuracy, completion, and ensured to be communicated to the Study Sponsor and IRB

Opportunity

🔶Protocol For Continued Process Verification Expectations to New and Existing (Legacy) Products 📊📒📈💊 ▶️Process Validation:- The collection and evaluation of data, throughout the product life-cycle, which provides documented scientific evidence that a processis capable of consistently delivering quality products. (WHO) ▶️Process Validation is defined as the collection and evaluation of data, from the process design stage through commercial production, which establishes scientific evidence that a process is capable of consistently delivering quality product. (USFDA) ▶️Stages of Process Validation 🟣Stage 1 – Process Design 🟠Stage 2 – Process Qualification ⚪Stage 3 – Continued Process Verification #pharmaceuticalindustry #qualitymanagementsystem #regulatoryaffairs #regulatorycompliance #researchanddevelopment #processimprovement

#hiring Quality Assurance Specialist, Austin, United States, fulltime #jobs #jobseekers #careers #Austinjobs #Texasjobs #ScienceTechnology Apply: https://lnkd.in/dEG3giqd Job Description Quality Assurance Specialist Job Description Maintain a safe, fast-paced, and positive laboratory environment. Interact directly with clients on an as-needed basis. Assist in training of other personnel as requested. Ensure safety and compliance with governmental regulations. Interact with FDA and clients as needed in the event of an inspection/audit. Follow all applicable Good Clinical Practice Regulations. Generally monitor studies to assure Management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with Good Clinical Practice Standards. For any given study, be entirely separate from and independent of the personnel engaged in the direction and conduct of that study. Conduct inspections and maintain records or inspecting studies at adequate intervals and maintain written and properly signed records of each analytical/in-phase or periodic inspection. Report any problems which are likely to affect study integrity to the Principal Investigator and Management immediately. Maintain a copy of a master schedule of all studies, include all pertinent information. Maintain copies of all protocols pertaining to all studies for which the unit is responsible. Determine that no deviations from approved protocols or standard operating procedures were made without proper authorization and documentation. Review all Adverse Events and Serious Adverse Events reported. These are reviewed for accuracy, completion, and ensured to be communicated to the Study Sponsor and IRB

#hiring Quality Assurance Specialist, Austin, United States, fulltime #jobs #jobseekers #careers #Austinjobs #Texasjobs #ScienceTechnology Apply: https://lnkd.in/gm8v8JxT Job Description Quality Assurance Specialist Job Description Maintain a safe, fast-paced, and positive laboratory environment. Interact directly with clients on an as-needed basis. Assist in training of other personnel as requested. Ensure safety and compliance with governmental regulations. Interact with FDA and clients as needed in the event of an inspection/audit. Follow all applicable Good Clinical Practice Regulations. Generally monitor studies to assure Management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with Good Clinical Practice Standards. For any given study, be entirely separate from and independent of the personnel engaged in the direction and conduct of that study. Conduct inspections and maintain records or inspecting studies at adequate intervals and maintain written and properly signed records of each analytical/in-phase or periodic inspection. Report any problems which are likely to affect study integrity to the Principal Investigator and Management immediately. Maintain a copy of a master schedule of all studies, include all pertinent information. Maintain copies of all protocols pertaining to all studies for which the unit is responsible. Determine that no deviations from approved protocols or standard operating procedures were made without proper authorization and documentation. Review all Adverse Events and Serious Adverse Events reported. These are reviewed for accuracy, completion, and ensured to be communicated to the Study Sponsor and IRB