Pharmaceutical Quality Assurance Jobs

About Company- We are a WHO-GMP Certified company , having 29+ yrs of experience in Pharma sector. Consern's portfolio comprises of over 400+ products and a nexus of prescribing Doctors from Neuro, Gynea, Cardio, Diabetics, Derma, Gastro, Ortho & General health care.Job role- - Review QC doc (Online or Offline)- Review audit trail- Knowledge of QC instruments - Documents for OOS/OOT incident

As a Medical Officer, your main responsibilities will include providing medical care to patients, performing routine check-ups, diagnosing illnesses, prescribing medication, and coordinating with other healthcare professionals to ensure the well-being of patients. You will also be responsible for maintaining accurate medical records, participating in medical research, and staying up-to-date with the latest medical advancements and technologies.To excel in this role, you must possess a strong understanding of Medical Microbiology, as well as a Doctorate in Medicine or equivalent qualification.

Job Openings for 3 Pharmaceutical Quality Assurance Executive Jobs with minimum 2 Years Experience in Siltara, Raipur, having Educational qualification of : B.Pharma, M.Pharma with Good knowledge in Quality Check, Hplc, Uv-visible Spectrophotometer, LAB Testing, Pharmaceutical Quality Control, Quality Analysis, Testing etc.

Job Opening: Quality Assurance (QA) Officer with IPQA ResponsibilitiesLocation: On-site Nalagarh, Himachal PradeshExperience: 3+ years mandatory experienceQualification: B. Pharm / M. PharmLanguage & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) MandatoryAbout the Role:We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.Key Responsibilities: Core QA Functions:Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.Conduct internal quality audits and assist in external audits by clients or regulatory agencies.Maintain and update SOPs, manuals, and master documents in accordance with current regulations.Oversee document control systems and archival processes.Train employees on cGMP practices and quality systems.In-Process QA (IPQA) Responsibilities:Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.Line clearance before batch start-up and between changeovers.Sampling of in-process materials and verification of critical process parameters.Real-time review and recording of BMR/BPR entries during production.Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.Immediate reporting and documentation of any deviation or non-conformance observed.Desired Profile:B. Pharm / M. Pharm with a strong academic and technical background.Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.Hands-on experience with IPQA activities and on-floor quality monitoring.Excellent written and spoken English communication skills MandatoryProficiency in Microsoft Office (Word, Excel, PowerPoint) MandatoryGood understanding of WHO-GMP, Schedule M, and other applicable quality regulations.Strong coordination skills, attention to detail, and documentation accuracy.Join a team committed to delivering excellence through quality-first manufacturing.If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!#QualityAssurance #IPQA #PharmaJobs #QAOfficer #BPharmJobs #MPharmJobs #PharmaCareers #GMPCompliance #NalagarhJobs #QualityFirst #IndianPharma #HimachalPharmaJobs #AuditReady

Q.A AND Q.C DEPARTMENT.AND PRODUCTION DEPARTMENT AND STORE

We have vacant of 2 Quality Control Officer Jobs in Lote, Ratnagiri, Experience Required : 2 Years Educational Qualification : Professional Degree, Other Bachelor Degree Skill Quality Check, Pharmaceutical Quality Control, QA-quality Assurance, Inspections, Quality Analysis, Quality Control etc.

We have immediate requirements for the post of QA/QC profile with well knowledge of freshers as well as experienced candidates.

We have an urgent opening for Quality Assurance Executive for a leading Chemicals Mfg CompanyJob Profile: Quality Assurance ExecutiveLocation: AnkleshwarSalary Range Approx- 4-5LPA Experience - 4 or 5 years only pharma line (API experience )REPORTING TO : Head QARESPONSIBILITIES:1. To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.2. Assistance in preparation of SOP of various departments/ preparation of draft SOPs. 3. During plant round QA Executive to verify documents as per cGMP and GLP norms.4. Line Clearance activities for manufacturing and packaging before process starts.5. To issue the deviation form, Change control form, Out of Specification form, Customer complaint form, OOT form, investigation for etc. as per request from respective dept.6. Review and verification of Analytical and Batch Manufacturing Record and filing BMR. QA verification and release of finish product.7. To prepared documents & records and monitoring of activities as per SOPs8. Distribution, retrieval and control of SOPs, documents/records of all dept.9. To participate the internal audits, customer audit, regulatory inspection.10. To Attend QR meeting as per schedule.11. To ensure data integrity as per procedure.12. To review manufacturing, store, QC activity.13. To prepare approved vendor list and maintain vendor qualification.14. Conduct traceability Activity.15. Preparation and maintain CAPA log.16. To ensure that deviations, product recall, return goods and customer Complaints, OOS, OOT by CAPA and Root Cause analysis are investigated, fill up of report and log the same.17. To collect data and prepare the annual product review.18. To witness and verify process validation, cleaning validation and equipment qualification and to prepare protocol and report. 19. Returned Material: Investigate and make

01Managing the entire QA activities in the plant & Overall implementation of Quality Systems in all units.02Design, Develop and approve all Quality systems in all units. Monitoring, Documentation, and implementation of process development.03Responsible to handle regulatory audits USFDA ISO 9001-14001, EU,WHO, and their compliance in all units without any Major Non Compliance.Making sure that there is stability data to support retest or expiry dates and storage conditions on APIs and/or intermediates where appropriate; and Performing product quality reviews04Handling of statutory audits like Quality, EHS, KSPCB, -CDSCO, weight & scale inspector, Director of Factories & Boilers, Social audits etc and their compliance (Evaluated by No show cause notice and no complaints)05Making sure that critical deviations are investigated and resolved;06Approving all specifications and master production instructions, Test methods, Qualifications07Approving all procedures impacting the quality of intermediates or APIs08Making sure that quality related complaints are investigated and resolved09Adhering to QA budget.10To qualify company for various certifications.11Assuring QMS in all Units.

Accounts Executive / ManagerJob Summary:We are looking for a detail-oriented and experienced Accountant to join our team. The idealcandidate will be responsible for preparing financial reports, conducting financial analysis,recording transactions, and ensuring compliance with accounting standards and regulations.The ideal candidate will possess strong technical skills, excellent communication abilities,and a proactive approach to problem-solving.Key Responsibilities: Prepare Financial Reports:o Compile accurate and timely financial reports, including Balance Sheets, Profitand Loss Statements, and other relevant documents.o Analyze trends, costs, revenues, and financial commitments to predict futureoutcomes and provide actionable insights. Financial Analysis and Advice:o Examine financial data to identify patterns and trends, providing insights andrecommendations for resource utilization, tax strategies, and budgetassumptions. Record Transactions:o Compile, analyze, and enter asset, liability, and capital account entries into theaccounting system.o Document all financial transactions accurately to maintain a clear andtransparent record of the organization's financial activities. Policy and Procedure Maintenance:o Recommend modifications to accounting systems and adhere to generallyaccepted accounting practices.o Strengthen internal controls by developing and documenting business processesto ensure compliance and accuracy in financial reporting. Technical Skills:o Apply familiarity with standard accounting concepts, practices, and proceduresto effectively execute job responsibilities.o Rely on experience and judgment to achieve goals and resolve complexaccounting issues. Collaboration and Communication:o Coordinate activities with Company Chartered Accountants, Clients, andManagement as required to discharge job duties effectively. Audits and Compliance:o Assist with internal and external audits to ensure compliance,

Tablets, capsules, ointments, oral liquids, dry powder injections and cosmetics. Manufacturing Exp.

Business CanSat Consulting is an experienced and affordable quality, regulatory, and licensing consulting firm. We cater to the needs of Psychedelics, Food, Medical Devices, Natural Health Products, and other related industries.Nature & Scope of Position Reporting to the Principal Consultant, the primary responsibility of the Compliance and Quality Associate is to prepare licensing applications, research Acts and Regulations, review batch records, write non-conformance and CAPA reports, and coordinate with clients and others. The candidate must have strong communication and interpersonal skills and must hold to the highest level of integrity and confidentiality. The successful candidate depending on their skills, experience, and performance would also have the opportunity to take part in profit sharing.General Duties & Responsibilities Coordinating with clients and ensuring their operation is compliant with applicable acts and regulations. Assist with the preparation of licensing applications associated with Cannabis, Food, and pharmaceutical industries in Canada and the USA. Ensure that all SOPs and specifications for each procedure are appropriate and followed by the concerned personnel. Review the batch records and release products in accordance with all applicable SOPs and regulations. Conduct internal inspections and gap assessments. Ensure that appropriate manufacturing in-process controls are implemented. Review all documents that describe work instructions and set requirements such as procedures, protocols, test methods, specifications, etc. Ensure all non-conformances, customer complaints, and out-of-specifications are investigated, and root causes are found. Perform employee training for GMP, SOPs, and new positions as required by the client.