Quality Control Job Vacancies in Roorkee

Conducting visual inspections of products or materials to identify defects or inconsistencies. Assisting with the execution of quality control tests and procedures. Using quality control equipment and software to analyze and improve standards. Documentation and Record Keeping:Accurately documenting inspection results and test data. Maintaining records of quality control activities and findings. Adhering to Quality Standards:Ensuring that products and processes meet established quality standards and specifications. Identifying and reporting any deviations or non-conformances.

Skill Set for QA Manager (Pharmaceutical Company)1. Technical Knowledge: Good Manufacturing Practices (GMP): Comprehensive understanding of GMP regulations and guidelines. Regulatory Compliance: Knowledge of regulatory requirements and standards (e.g., FDA, EMA). Quality Control (QC) Processes: Proficiency in developing and implementing QC tests and procedures. Validation and Qualification: Expertise in validation processes (e.g., equipment, process, cleaning validation). Documentation: Ability to maintain accurate and thorough QA documentation, including SOPs and batch records.2. Analytical and Problem-Solving Skills: Root Cause Analysis: Ability to conduct thorough investigations to identify the root cause of quality issues. Risk Management: Proficiency in risk assessment and management techniques. Data Analysis: Strong skills in analyzing QC test results and other data to make informed decisions.3. Leadership and Management: Team Leadership: Ability to lead, mentor, and develop a QA team effectively. Project Management: Skills in managing projects, timelines, and resources efficiently. Decision-Making: Capable of making sound decisions under pressure and in a timely manner.4. Communication and Interpersonal Skills: Written Communication: Strong skills in writing reports, SOPs, and other QA documentation. Verbal Communication: Effective communication skills for presentations and interactions with regulatory bodies, management, and cross-functional teams. Interpersonal Skills: Ability to build and maintain positive relationships with colleagues, regulatory authorities, and other stakeholders.5. Attention to Detail: Accuracy: Ensuring all QA activities and documentation are accurate and precise. Thoroughness: A meticulous approach to quality checks, audits, and compliance activities.6. Continuous Improvement: Innovation: Ability to identify areas for improvement and implement innovative solutions. Best Practices: Keeping

Drug Regulatory Documentation & Sop Preparation.compliance & Documentation as per Iso 13485 & Medical Device Regulations.internal-external Audit Compliance.

Systematic planning and preparation of product labels, handling and distribution of product BOMs SOP and specification sheets.Process control to eliminate deviation in FGs.Knowledge of QMS principles / GMP requirements in a food industryKnowledge of shop floor activities and man managementShould have robust knowledge of FSSC 22000 & FSSAI regulationsKnowledge of analytical techniques and operation of basic instruments used in quality function of a food process industryPersonal Attributes:Able to communicate and motivate coherently (both written & verbally)Using problem solving skills and root cause analysis to resolve and/or mitigate operational issuesGood supervisory, planning & training skillsHigh level of integrity and characterReady to work in rotational shiftSelf-starter and able to anticipate work requirementsFlexible to change schedule and hours of work to meet the needs of the plantAbility to undertake and perform duties to a satisfactory level in a busy work environment

1. Testing of raw materials, packing materials, Intermediate & finished products asper laid STP and preparing test reports & COA.2. Performing stability testing to assess & ensure product stability complies as perclaim.3. Monitoring & maintaining good housekeeping conditions in Q. C lab .4. Preparing analysis reports for the tested samples, and recording .5. Calibration of all laboratory instruments and devices used in the testing.6. Retaining reference samples from each batch of products released to the market.7. Reviewing & updating SOP & STP of raw , finished & packaging material .