13 Qc Documentation Jobs

As a Quality Engineer at our manufacturing facility in Vasai Sativali, you will be responsible for various tasks related to ensuring the quality standards of our products. Your duty hours will be from 10:00 am to 6:30 pm, focusing on maintaining high-quality standards in the manufacturing industry. A minimum of 1 year of experience in Mechanical Engineering is required for this role. Your primary responsibilities will include following up on Material Test Certificates with sub-vendors and suppliers, conducting technical reviews of TC as per ASTM specifications, reviewing Purchase Orders and Technical Specifications, preparing and sending Order Acknowledgements to customers, communicating stage-wise progress to customers, and managing final documentation and control. To excel in this role, you must have a strong engineering background in manufacturing and fabrication technology. You should be adept at reading and interpreting test certificates with respect to various technical characteristics. Experience in Quality Control documentation, audits, and handling third-party inspections in fabrication will be beneficial. As a male candidate aged between 20 to 35 years, you should possess computer skills in Windows and AutoCAD. The company offers benefits such as Provident Fund, bonuses, and ESIC leave salary. The joining period for this position is a maximum of 30 days. This is a full-time and permanent position that requires expertise in metal fabrication for at least 1 year. The work location for this role is in Mumbai, Maharashtra, and you will be expected to work in person. Join us in maintaining high-quality standards and ensuring customer satisfaction through your attention to detail and technical expertise.,

As a Senior QC Manager in Noida Phase-2, you will be responsible for overseeing quality control activities in the laboratory and production environment. With 7 to 10 years of experience, you will utilize your expertise in material analysis, lab testing, and product quality management to ensure compliance with regulatory standards and meet customer requirements. Your key responsibilities will include performing material testing and inspection to ensure quality compliance, identifying defects in materials and collaborating with procurement for corrective actions, maintaining accurate records for quality control processes, preparing Certificates of Analysis (COA) for products, and overseeing the calibration and maintenance of lab equipment. Additionally, you will be responsible for approving products for dispatch based on quality assessments, ensuring adherence to Good Laboratory Practices (GLP), conducting various analytical tests, addressing customer quality claims, participating in sensory evaluations, managing the sampling department, and ensuring regulatory compliance. To be successful in this role, you should hold a Bachelor's degree in Chemistry, Biology, or a related field (Master's degree preferred), have 7 to 10 years of QC experience in industries such as pharmaceuticals, cosmetics, or essential oils, possess expertise in lab testing methods like GC, GCMS, and refractive index, and have knowledge of regulatory standards such as KOSHER, HALAL, and MSDS. Strong communication and organizational skills will also be essential for effectively carrying out your responsibilities.,

Excellent job opportunity for QA - AQA Specialist in Unison Pharmaceuticals Pvt Ltd, Moraiya, Ahmedabad About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. You are invited to join one of India's fastest growing pharma companies in India!! Experience: 4-9 Years Location: Moraiya Designation: Officer/Sr. Officer / Executive Section : Analytical QA (Lab QA) Must have: Candidate should have working exposure of OSD facility Job profile (Not limited to): To review analytical documents i.e. worksheet, specification, method of analysis, stability protocol & summary report and logbook etc. of Quality Control department. To participate in investigation and reporting of lab incident, OOS/OOT and any other quality related issues. To co-ordinate with other departments for QC related activities and review of data entry. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career!!! Regards Team HR Unison Pharmaceuticals Pvt. Ltd.

URGENT HIRING !!! For more information call or WhatsApp +91 9289584545 Mail us at: [HIDDEN TEXT] location's : Canada , Australia , New Zealand , UK, Germany , Singapore ( Not In India ) Benefits : Medical Insurances , Travel allowances , Flight Tickets , Meals , etc. Key Responsibilities: Developing and Implementing Quality Standards: Establishing and enforcing quality standards, procedures, and documentation for the entire organization. Monitoring and Auditing: Overseeing the planning and execution of audits, inspections, and testing to evaluate product quality.This includes analyzing key quality metrics and conducting root cause analysis of quality issues. Team Leadership: Leading and managing the QA/QC team, providing training, and fostering a culture of quality. Collaboration and Communication: Working closely with other departments like product development, engineering, and operations to ensure quality is integrated throughout the product lifecycle. Continuous Improvement: Identifying areas for improvement in the production process and implementing corrective actions to prevent future issues. Ensuring Compliance: Ensuring that all products, processes, and documentation comply with relevant legal and regulatory standards. Documentation: Maintaining accurate records of quality checks, audits, and other quality-related activities.

Roles and Responsibilities -Conduct material sampling and lab testing (concrete, aggregates, steel) as per IS standards. -Assist in routine site inspections, internal audits, and quality checks. -Prepare and maintain QA documentation, including test records, logs, and reports. -Support curing, compaction, and on-site quality monitoring activities. -Coordinate with lab technicians, vendors, and site engineers for quality compliance. -Report any quality issues or non-conformance to the senior QA/QC team. -Ensure construction quality is maintained as per client requirements and technical specifications.

Role & responsibilities Inward/Outward Register QC Documentation like Inprocess/Finished Reports Stock Register maintaining Batch sheet maintain Courier Local and Export both Make COA for local parties Helping Vijaybhai to make any kind of documents like CAPA Making PO or any kind of documents if related department person is absent Making documents for ISO Audit Halal Documents Making supportive documents for party audit Maintaining Lab equipment calibration reports

Responsible for maintaining GDP and GLP in lab. Responsible for maintaining all laboratory testing documents according to GLP requirements and sustain all records in an accurate and legible manner Responsible for preparation of COA.

We are seeking a meticulous and experienced Manager Quality Control to lead and enhance our quality control operations at Synnat Pharma Private Limited. In this pivotal role, you will be instrumental in overseeing all aspects of quality control, ensuring adherence to Good Laboratory Practices (GLP), and maintaining a robust Quality Management System (QMS). Your expertise will be crucial in driving Analytical Method Development, managing CAPA and Change Control processes, and upholding Data Integrity standards. You will lead a team of QC analysts, providing training and mentorship to foster a culture of excellence. The ideal candidate will possess a strong understanding of ICH Guidelines and Regulatory Compliance, with hands-on experience in GC and HPLC. This role demands a proactive approach to QC process improvement, meticulous QC documentation, and the ability to conduct thorough analytical data reviews. Job Details: Industry: Active Pharmaceutical Ingredient (API) Department: Quality Control Role: Manager - Quality Control Location: Visakhapatnam Compensation: 12 -15 LPA Experience Required: 10 - 15 years Employment Type: Full-time Required Qualification: Bachelor's degree in Chemistry, Pharmacy, or a related field Responsibilities: Analytical Method Development and Validation Lead the development, validation, and transfer of analytical methods for API testing in compliance with ICH and regulatory requirements. Review validation protocols and reports, ensuring accuracy and completeness. Troubleshoot analytical challenges and provide technical guidance. Collaborate with AR&D to optimize methods for both new and existing products. Ensure complete documentation of method development and validation activities. Quality Management System (QMS) and Compliance Maintain and improve the QMS to comply with regulatory standards (US FDA, EU GMP). Oversee CAPA and Change Control processes to address quality deviations. Conduct internal audits to ensure procedural compliance and identify improvement areas. Ensure adherence to Data Integrity principles across QC operations. Serve as the key QC contact during regulatory inspections and audits. Laboratory Operations and Equipment Management Supervise daily QC laboratory operations and ensure efficient sample testing. Oversee calibration and maintenance of laboratory instruments (GC, HPLC). Monitor lab environmental conditions and implement corrective actions where needed. Ensure sufficient availability of reagents, standards, and consumables. Implement lab safety procedures and optimize workflows to improve turnaround time. Team Leadership and Performance Management Lead and mentor QC analysts, fostering a collaborative and improvement-driven culture. Conduct performance evaluations and provide development-focused feedback. Design and deliver technical training programs to enhance team capability. Assign responsibilities to ensure a balanced workload and accountability. Address employee concerns and promote a positive, inclusive work environment. Data Analysis and Reporting Oversee review and interpretation of analytical data for compliance and reliability. Approve QC reports including Certificates of Analysis (CoAs). Identify trends and take proactive measures to address quality concerns. Present QC metrics and insights to management and cross-functional stakeholders. Maintain accurate records and use statistical tools to evaluate data. General Expectations and Past Experiences: Strong understanding of pharmaceutical QC principles and global regulatory standards (US FDA, EU GMP). Demonstrated expertise in analytical method development and validation with hands-on experience in GC and HPLC. Proven track record of maintaining QMS aligned with ICH guidelines. Experience managing CAPA, Change Control, and Deviation processes. Deep commitment to Data Integrity and documentation compliance. Strong leadership skills with a track record of mentoring high-performance teams. Excellent interpersonal, communication, and analytical problem-solving abilities.

Role & responsibilities Lead and manage the Quality Control team to ensure timely and accurate analysis of finished products (OSD & Injectables). Review and approve analytical reports, ensure compliance with GLP and cGMP standards. Oversee operations involving HPLC, GC, UV, IR , and other sophisticated instruments. Ensure proper implementation of MPCL and maintain all microbiological standards in compliance with regulatory guidelines. Handle all regulatory audits (USFDA, MHRA, WHO, etc.) and prepare necessary documentation. Manage OOS/OOT investigations and ensure CAPA implementation. Coordinate with cross-functional teams (QA, production, regulatory affairs) to ensure product quality. Train and mentor junior staff; ensure continuous skill development within the QC team. Manage documentation including SOPs, specifications, STPs, and logbooks. Preferred candidate profile B.Pharm / M.Pharm / M.Sc in Chemistry or equivalent. 12 15 years of relevant experience exclusively in the pharmaceutical industry (OSD & Injectables) . Strong knowledge of GLP, MPCL, and finished product QC . Proven team leadership and people management skills. Experience in handling regulatory inspections and audits. Good communication and documentation skills.

Good knowledge of QMS, Change control , Deviation. Having knowledge of Validation, APQR and other qulaity complience..Responsibilities: Perform analytical testing using various techniques, including HPLC, GC, UV-Vis, FTIR, and other relevant methods. Prepare and standardize solutions and reagents. Analyze and interpret test results, ensuring accuracy and compliance with specifications. Document all testing activities and results in accordance with GMP/GLP guidelines. Maintain and calibrate laboratory equipment. Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA). Prepare and review QC documentation, including SOPs, test methods, and reports. Participate in internal and external audits. (Senior Analyst) Provide technical guidance and training to junior analysts. (Senior Analyst) Assist in method development and validation.

To get GA drawing approval from client in consultation with V TOP& Marketing Execute DQ. Documentation of project,tracking &reporting of project status report Update Brahma& reports, collect all reports like kick off Updating Drawing approval report Required Candidate profile Co-coordinating with factory & marketing team Co-ordination of activities between design, planning, material production and vendor management Keeping track of short supplies Updating PLC FDS

Role & responsibilities Develop, implement, and maintain Quality Management Systems (QMS) including AS9100 & ISO 9001 standards. Ensure inspection & testing of raw materials, subcontracted, in-process, and finished parts. Conduct and manage internal & external audits , ensuring compliance with industry standards. Investigate quality issues, perform root cause analysis , and implement corrective & preventive actions. Oversee calibration and maintenance of gauges, instruments, and test equipment . Manage supplier approvals/disapprovals and drive supplier quality improvement. Ensure compliance with ISO 14001:2015 EMS requirements. Guide, mentor, and train team members to maintain a customer-focused quality culture . Ensure compliance with OEM requirements including PWC and Collins Aerospace . Preferred candidate profile 1215+ years of relevant experience in aerospace quality management . Strong knowledge of AS9100, ISO 9001, ISO 14001, QMS . Hands-on experience with PWC & Collins Aerospace requirements . Strong leadership, problem-solving, and analytical skills. Excellent communication & interpersonal skills. Ability to drive continuous improvement and manage cross-functional teams.

Develop QC formats for Inward Inspection, In-Process Inspection, Job-Work Inspection, and Finished Goods Inspection. Design and implement Operational Control Procedures (OCPs) for all key production stages. Monitor and verify QC reports generate