281 Who Jobs - Page 6

Candidate should technically sound for assigned profile- Candiadte should have regulatory exposure in previous organisation

Exp 4–6years in healthcare/pharma BPO ,U.S. Healthcare Technical Knowledge Proficiency in LOINC, ICD-10, CPT, NDC, RxNorm, SNOMED CT. Tools & terminology tools (Symedical, Clinical Architecture), EHR/EMR system Geetha : 9902419093

Department: Production Location: Plant ( Bavla) Shift: Rotational Shifts (Day/Night/General) To ensure smooth execution of capsule filling operations within the Oral Solid Dosage (OSD) manufacturing section, ensuring compliance with cGMP standards, safety protocols, and production targets. Key Responsibilities: Operate, monitor, and manage capsule filling machines (e.g., Bosch, ACG Pam, Fette, etc.) within the OSD manufacturing unit. Supervise and guide operators and contract workforce during production shifts. Ensure accuracy and completeness of Batch Manufacturing Records (BMRs) and adherence to Standard Operating Procedures (SOPs) . Perform line clearance , conduct in-process quality chec...

Oversee the formulation, blending, and packaging processes in compliance with GMP and industry regulations Ensure adherence to quality control standards, safety norms, and environmental regulations Optimize resource utilization Required Candidate profile Coordinate with R&D, QA/QC, and supply chain teams for smooth product flow. Liaise with management on production planning, reporting, and audits. Maintain documentation as per regulatory guidelines.

We are looking for an experienced Quality Assurance Manager to lead and oversee QA activities at our API manufacturing facility.

Recorders and Medicare Systems Pvt Ltd is looking for RA Executive to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available ...

Oversee the formulation, blending, and packaging processes in compliance with GMP and industry regulations Ensure adherence to quality control standards, safety norms, and environmental regulations Optimize resource utilization Required Candidate profile Coordinate with R&D, QA/QC, and supply chain teams for smooth product flow. Liaise with management on production planning, reporting, and audits. Maintain documentation as per regulatory guidelines.

Number of requirements 1 / Level 3 rd Experience: 6 to 7 Years Job Overview: As a SAP CRM Consultant specializing in Application Support Management, the primary responsibility will be to provide ongoing application support, maintenance, and request fulfillment enhancements for SAP CRM systems. The consultant would have to work closely with business users to understand their needs and ensure that the CRM application remains reliable, secure, and aligned with GB ( Business Unit) goals. Qualifications: Bachelor's degree in a relevant field, such as Computer Science, Information Technology, or Business. Proven experience in SAP CRM On Premise application support and management. ( 6-7 years) Stro...

Job Title: Assistant Manager - Quality Compliance (Supplier Quality Assurance) Department: Quality Compliance Reports to: Quality Compliance Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 68 years of experience in Quality Assurance / Quality Compliance within the pharmaceutical industry, with at least 2 years in a Supplier Quality Assurance role. Preferred: Exposure to regulatory inspections (e.g., USFDA, MHRA, TGA), and experience in working with global suppliers. Job Purpose To lead and manage Supplier Quality Assurance (SQA) activities ensuring all th...

Qualification - BSC- Nursing, Pbsc Nursing Infection Prevention Policies: Develop, implement and update infection prevention policies and procedures in compliance with relevant guidelines and regulations. Education and Training: Provide education and training to hospital staff, including nurses, physicians and support staff, regarding infection control principles, practices and prevention strategies. Surveillance: Monitor and analyze infection rates within the hospital, conducting surveillance of healthcare-associated infections to identify trends and areas of concern. Isolation Protocols: Establish and enforce isolation protocols for patients with contagious diseases, ensuring proper precau...

Note to Hiring Manager: In support of BNP Paribas APAC's Diversity Commitment, Hiring Managers are to consider at least 1 Asia Pacific national, 1 male and 1 female candidate for the position to be filled. Position Purpose Facilitating transaction processing of instructions received from Client to ensure all settlement of trades in Global markets. Providing round the clock service to cover client queries across ASIA, EMEA and US regions. Reconciling client positions to match with the market positions. Being a team player and a manager to achieve team co-ordination, adhere to BNP policies and follow the agreed timelines to avoid any breach in SLA. Responsibilities Job summary Roles & Responsi...

Post - API Pharma Production Engineer Location - SUPA Ahmed Nagar Experience - 02-04 yrs Email - punemechanical@gmail.com Contact - 9356395439 Skills - API , Pharma Production , PPC Education - BSC / MSC Chemistry / Bio technology

The role involves preparing and reviewing regulatory documents, ensuring compliance with national and international guidelines, and supporting product registration processes. Required Candidate profile Looking for a Regulatory Affairs Officer with 2-3 years of experience in the Pharma/API sector. Candidates should have strong MS Office skills and good communication abilities.

IND/NDA/ANDAs/Amendments and Biologics to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws The Manager, Regulatory Affairs CMC is responsible for developing and implementing regulatory strategies related to Chemistry, Manufacturing, and Controls (CMC) for pharmaceutical or biologic products Having prior experience of handling pre-approval and post-approval regulatory activities for multiple dosage form including Sterile, Sterile (Injectables/Ophthalmic/Otic/IV Bags) dosage forms in US market either for Aseptic sterilization or Terminal sterilization or both

Responsible for formulation development for OSD, external preparations, oral liquids, and injectables. Responsible for pre-formulation studies, prototype development, and scale-up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (A, C, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation.

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. uality Management Systems (MS): Implementat...

Job Title: Sr. Executive Location: Bavla - Plant Department: QA Reporting To: Head of QA Employment Type: Full-Time Key Responsibilities: Prepare and review Cleaning Validation Protocols and Reports , including product matrix and MACO (Maximum Allowable Carry Over) calculations. Develop and execute protocols and reports for Clean Equipment Hold Time and Dirty Equipment Hold Time . Prepare, review, and finalize Process Validation Protocols and summary reports, utilizing analytical results and batch documentation data. Prepare and review Product Hold Time Protocols and Reports to ensure product quality throughout storage. Conduct thorough review of manufacturing documentation, including Master...

Job Title: Site Manager / Assistant Site Manager No. of Positions: Site Manager - 1 | Assistant Site Manager - 1 Company Name: The South Indian Manufacturing Company Company Website: www.saibol.com Location: Madurai (Local candidates preferred or must be willing to relocate) About the Company The South Indian Manufacturing Company is a reputed pharmaceutical manufacturer committed to excellence in quality, compliance, and operations under strict GMP/ISO standards. Qualifications Graduate / Postgraduate (Science, Engineering, or Management preferred) Experience 7 - 10 years in factory/site operations management Preference for candidates with WHO GMP pharma management experience Candidates fro...

Johnson Controls is looking for Sr. Analyst - RTR EMEA to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Operate and maintain WTP RO UV and softener systems Ensure purified and process water as per pharma standards Perform routine maintenance of pumps valves filters membranes Monitor pH TDS conductivity hardness and microbial load Required Candidate profile Diploma BE in Mechanical Electrical Chemical 2 to 5 yrs exp in WTP RO Softener Pharma Utilities Knowledge of cGMP WHO norms Maintain logs and support GMP WHO

M.Pharma/Phd - Phytochemistry, pharmacognosy, Nataral Products Chemistry 5 - 7 Years 8 - 10 LPA Location - Thane West Phytochemical Expertise product Development Extraction System Design Quality Control prepare Regulatory Documents

Key Responsibilities Lead and manage the Quality Assurance department, ensuring compliance with GMP norms and regulatory requirements of WHO, EU GMP, PICS, TGA, MHRA, USFDA, and other global agencies . Develop, implement, and monitor Quality Management Systems (QMS) across all QA functions. Ensure strict adherence to SOPs and continuous improvement practices in line with regulatory expectations. Oversee handling of rejected materials, market complaints, product recalls, deviations, change controls, CAPA, and CCF . Manage end-to-end Validation and Qualification activities (process validation, cleaning validation, equipment qualification, analytical method validation, etc.). Ensure audit readi...

Job Description Responsible for submissions of Response to Deficiencies to Health Agencies of Europe, Australia, New Zealand and Canada market and Customers. Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required. To provide Regulatory inputs during product development, manufacturing and testing and to evaluate all types of change proposals during product life cycle Work Experiance Should have worked in Regulatory Affairs Dept for regulated markets like EU/UK, Australia, Canada, US etc (minimum 1-2 years). Submission of new submissions, deficienc...

Equipment & Utility Maintenance Troubleshooting & Repairs Compliance & Documentation Continuous Improvement Safety & Housekeeping To carry out installation, operation, maintenance, and troubleshooting of electrical systems, equipment, and utilities. Required Candidate profile Knowledge of electrical circuits, PLCs, VFDs, control systems, and instrumentation. Understanding of GMP, WHO, USFDA, MHRA requirements. Hands-on experience in troubleshooting electrical automation .