294 Mhra Jobs - Page 5

Your Responsibilities: Overall Site Operations & Control: Take responsibility for the operations and control of the entire site to meet targeted production, quality levels, and cost at each production stage, while maintaining optimal operational efficiency. Quality & Regulatory Compliance: Ensure adherence to Minimum Quality Standards/HPR as per Reckitt Global Quality Standards and guarantee compliance with regulatory standards such as MHRA/SAPHRA/FDA/TGA. Industrial Relations: Maintain healthy industrial relations with unions and external associates. Project Support: Provide technical backup to the team for ongoing projects. Procedure Review & Approval: Review and approve procedures and ins...

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.

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.

Roles and Responsibility Develop high-quality regulatory documents, including clinical trial applications, marketing authorizations, and periodic safety update reports. Collaborate with cross-functional teams, including regulatory, clinical, and product development, to ensure compliance with regulatory requirements. Conduct thorough reviews of regulatory documents to ensure accuracy, completeness, and adherence to company standards. Stay up-to-date with changing regulatory requirements and industry trends to improve document quality and compliance. Provide training and guidance to junior writers on regulatory affairs and medical writing best practices. Participate in the development of new r...

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...

Position Summary The Safety Specialist I is an integral part of the safety team at Precision and performs all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR) for clinical trials and/or post-marketing safety programs. Essential functions of the job include but are not limited to: Process ICSRs according to Standard Operating Procedures (SOPs) and project/program- specific safety plans Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability Enters data into Argus Safety Database Code events, medical history, concomitant medications and tests. Draft case narratives Assesses information to be queried and follows ...

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...

Role Overview: You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of the team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. Key Responsibilities: - Conduct HPLC analysis of Solid Orals and Nasal pro...

Scope of the role Scope - This role is responsible for Responsibilities Supervision Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable Contributor Good Products knowledge Creative As...

About The Role : Job Title Bond Analytics Analyst LocationMumbai, India Role Description OverviewBusiness Division Deutsche Banks Corporate Bank (CB) a market leader incash management, trade finance & lending, securities services and Trust & Agency Services. Focusing on the treasurers and finance departments ofcorporate and commercial clients and financial institutionsacross the globe, our universal expertise and global network allows us to offer truly integrated and effective solutions. OverviewBusinessTrust and Securities Service (TSS): With offices in New York, California, London, Frankfurt, Milan, Lisbon, Dublin, Hong Kong, Singapore and Tokyo, the Trust and Securities Services team at D...

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a Trusted Emerging Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top managem...

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Work Location: Kothur (Formulation Division) Interview Date: Saturday, 20th September 2025 Time: 9:00 AM to 2:00 PM Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad 500034 (Opp. A.P. Productivity Council) Open Positions: Analyst - Quality Control (OSD & Sterile) Experience: 3 to 5 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc (Organic/Analytical/General) Chemistry Key Responsibilities: Adherence to GLP, GDP, cGMP, and ALCOA+ standards. Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus. Demonstration of QC testing...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Responsible for auditing Apotex Enterprise sites, Apotex and Apotex Pharmachem...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Responsible for auditing Apotex Enterprise sites, Apotex and Apotex Pharmachem ...

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...

As a Safety Specialist I at Precision, your role will involve performing all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR) for clinical trials and/or post-marketing safety programs. Key Responsibilities: - Process ICSRs following Standard Operating Procedures (SOPs) and project/program-specific safety plans - Triage ICSRs, evaluate data for completeness, accuracy, and regulatory report ability - Enter data into Argus Safety Database - Code events, medical history, concomitant medications, and tests - Draft case narratives - Assess information to be queried and follow up until queries are satisfactorily resolved - Generate timely, consistent, a...

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.

- Key Responsibilities Plan, organize, and monitor manufacturing operations to ensure timely and efficient production and dispatch of pharmaceutical formulations with accurate yield and reconciliation. Ensure compliance with cGMP norms and regulatory standards including WHO, EU GMP, PICS, TGA, MHRA, and USFDA on the shop floor. Lead process validation activities to ensure manufacturing processes meet quality and regulatory requirements. Collaborate with QA and QC departments on handling product complaints and recall analysis. Manage production schedules, coordinate with supply chain, and optimize resource utilization to meet business goals. Oversee production team performance, training, and ...

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...

Regulatory Affairs Management- Understands the regulatory framework, including regional trends, for various types of applications and procedures for biological therapeutic products (Biologics, Biosimilar, Novel Biologics and Vaccines) in India and ROW markets. Provides regulatory input on procedural and documentation requirements as defined by Health Authorities such as Indian regulatory authority, Emerging markets and ROW countries. Review of documents (e.g. RCGM-PCS, CTA, MAA, PAC, response documents, study protocols, regulatory maintenance documents, PSURs, etc.). Analysis of regulatory procedures and special designations used during development, authorizations and extension of the produc...

Scope of the role Scope - This role is responsible for Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Reporting to (Business) Regional Sales Manager / Sr. Regional Sales Manager Reporting to (Matrix) NA No of Reportees Direct NA Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, institutional administrators Key Internal Stakeholder(s) RSM, ZSM, BDM, NSM / SM, PMT, HR & Sales Admin Competencie...

Scope of the role Scope - This role is responsible for Responsibilities Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable Contributor Good Products knowledge Creativ...

Scope of the role Scope - This role is responsible for Responsibilities Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Reporting to (Business) Zonal Sales Manager Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable...