377 Osd Jobs

Lead HVAC Engineer ( 2 positions) Qualification: BE Mechanical/ B TECH Mechanical Experience: 12 to 16 years into similar profile with HVAC Design or HVAC Engineer Job Description Basic understanding of the equipment and systems of API, Oral Dosage, Injectable and Biotech formulation facility Read and understand isometric, P&ID and as built drawings Understanding of API / Formulation Process equipment Operation HVAC system design & Calculation BMS system design & Calculation Basic understanding of all types of facilities like OSD, Injectables & Oncology Knowledge and understanding of a

Role & responsibilities Review and authorize change controls, assessing their impact on regulatory submissions. * Coordinate and organize meetings with cross-functional teams to discuss IRs, DRLs, and CR letters from agencies; circulate Minutes of Meeting (MoM) and follow up on action items. * Compile and coordinate high-quality CMC regulatory submissions for the US market in compliance with current regulatory guidelines and timelines. * Assess change controls from formulation plants and categorize them based on risk to product quality and compliance. * Plan, review, and submit CBE, CBE-30, and Prior Approval Supplements (PAS). * Draft high-quality responses to regulatory agency letters (IR, DRL, CR) within stipulated timelines. * Evaluate and interpret post-approval changes including: * Alternate excipients * Alternate packing materials * Alternate API source additions * Site and pack additions * Review key regulatory documents such as specifications, process validation reports, hold time reports, stability protocols/data, Nitrosamine risk assessment reports, and technical packages. * Assist in developing standards and SOPs for operations and production procedures. * Stay updated with evolving global and regional regulations affecting submissions. * Provide daily activity updates to the Regulatory Affairs Manager. * Prepare monthly reports and provide timely updates to superiors. * Uphold the highest standards of professional integrity in all RA activities. * Actively participate in continuous improvement initiatives within the department. Preferred candidate profile * Master's degree in Pharmaceutics, Pharmaceutical Analysis, Regulatory Affairs. * Strong knowledge of US FDA regulatory guidelines and CMC documentation. * Excellent communication, coordination, and documentation skills. * Attention to detail and ability to manage multiple priorities effectively.

Walk-in Drive @ Hyderabad on 3rd Aug 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles. Venue: Hotel Ravila Grand, Plot No 9, Mumbai Highway Road, Opposite Pranaam Hospital Lane, Sri Durga Colony, Madeenaguda, Hyderabad, Telangana 500049 Open Positions Department: Production (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production, BMR, Production QMS, Change Control, Deviation, CAPA. Department: Packing (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Bangalore Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-5 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Pondicherry Key Skills: HPLC, GC, UV, IR, KF, FTIR, Dissolution, LIMS, GLP Department: Quality Assurance-IPQA (OSD) Experience: 2-5 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: IPQA, BMR Review, BPR Review, Line Clearance, In process & process validation sampling. Department: Formulation & Development (OSD) Experience: 2-7 years Qualification: M.Pharm Job Location: Bangalore Key Skills: Planning & Execution of Lab scale experiments. DOE, Quality by Design, Product Development, Stability Protocol, Regulatory Market. Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

please share your CV on renu.kumari@adecco.com or watsapp on 8758695449 Role & responsibilities 1. Compression (OSD MFG) Technician / Operator 3 to 8 yrs ITI, Diploma 2. Compression (OSD MFG) Staff / Officer 3 to 7 yrs B.Pharma, M.Pharma Preferred candidate profile

To prepare and review Validation Master Plan QMP, VMP, PVMP, Handling and storage of all quality document like BMR, investigation. CAPA and all other quality management, CAPA Monitoring of PPQ, requalification activities, OSD

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control Experience: (01 12Years) HPLC/ Stability/ GC/ IP/ FP/ RM/ Validation/ Reviewer QUALIFICATION : B.Sc, M.Sc, B. Pharm and M.Pharm with relevant experience DESIGNATIONS: Officer, Jr.Executive, Executive, Sr.Executive & Asst. Manager INTERVIEW VENUE: Hotel: RAUNAK Restaurant Ground Floor, Opp. Axis Bank, Bitna Road, Kalka Shimla National Highway, Pinjore, Haryana 134102 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates Experience in HPLC - Formulation is Mandate Preferred for Male Candidates Share with your friends, collegues and in known groups for better reach CONTACT INFO: E-mail: Harishwar.M@hetero.com & Contact: 8121005416, 9218677050 for further info

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 02.08.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D Candidates also eligible Position : Executive / Senior Executive Qualification : M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 02.08.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

Manager 1 Engineering Educational Qualification BE Mechanical Experience 15-17 years in OSD Project/Maintenance Job Summary: Handling of overall site facility maintenance, Scrap yard, online documents and QMS documentations. Responsibilities: Planning and execution: Utility section: Preparation of the material BOQ for the structural steel, pipe and pipe fittings as per company standard practices. Supervision of the fabrication work as per approved drawings for the structural and pipe and fittings for the utility services. Supervision of the insulation work, Painting works as per color coding and related activities. Measurement sheet checking and certification of work completion as per company requirement. Installation of the Utility lines and any other equipment which is part of the utility services. Unloading and shifting of the equipment as per company requirement with safety. Issuance of the work permits for above work and execution of the work with safety. Quality Improvement in mechanical works such as Machine Installation and structural fabrication work, piping and insulation works. Supporting role in installation of the process equipment used in OSD and Non OSD. Co-ordination with the external contractors and consultants for the execution of the work and modification in drawings as per site requirement if required. Reconciliation of the structural and piping material. Weekly report preparation for the status of the project work and up gradation of the same to planning department. Qualification of the equipment as per company guidelines and procedures and report closures. Plant Maintenance Brownfield projects in the OSD block and changes required in same as per company requirements. Planning, procurement and installations of the process equipment. Break down Maintenance & Preventive maintenance coordination. Material requisition slip Preparation and issuance and approval of the same. GMP Documents preparation and signing. Maintenance management (B/D and PM) of utility equipment. PR / Indenting for all Process equipment and Spares. Compliance of audit and internal observation points. Workout the energy conservation, Execution, Monitoring. Solvent storage and distribution and related activities.

Titlle : Manager 1 Engineering Educational Qualification : B Tech/BE Electrical/ Electronics & Instrumentation Engineering Experience: 14 years & above Requirement : 1. To ensure prompt attention and resolve issues of all operational and breakdown maintenance activities related to Utilities, HVAC System, and Water System. 2. To ensure timely execution of Preventive Maintenance of Utilities, HVAC System, Water System & Process Machineries performed as per the SAP schedule and maintain accurate record of the same. 3. To provide Technical assistance & Support for efficient operation of ETP. 4. Review and approve QMS related activities in EDMS & Trackwise systems to ensure compliance and documentation Integrity. 5. Responsible for Compliance of Internal & External Audits. 6. Tracking WBS code for all, CAPEX, Projects & Aspire Projects 7. Conduct Monthly review of MTTR, MTBF & KPIs 8. Following up with OEM, third Party service s & AMC to ensure timely service delivery and issue resolution. 9. Maintaining and ensuring Safety and discipline for all engineering related work and personnel of Engineering. 10. To provide Training to Subordinates to enhance their operational efficiency. 11. To performed any other duties assigned by HOD.

Hi Jobseeker, Greetings from Laurus Labs Ltd...! Please find the below Opening for OSD Production at Laurus Labs Ltd - Visakhapatnam. Acthutapuram. Department : OSD Production Designation : General Manager Exp : 24+ years Interested candidates can send their resume to Sarvani.gontu@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period : Regards, HR Team Laurus Labs Ltd

We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 27th May 2025 (Sunday) Interview Location: Ahmedabad Timings: 9:00 am 5:00 pm Interview Venue: PTC-Sigma Block No. 2, 3, 4, 5, Sigma Commerce Zone,Nr Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad – 380015 ? Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ /B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG – Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

Key responsibilities include literature reviews, pre-formulation, pellet formulation, stability studies, process validation, technology transfer, troubleshooting, and maintaining documentation like QAQN, MFR, FPS, and logbooks. Perks and benefits Accommodation, Transportation and Mediclaim.

Responsible for analytical testing, documentation, instrument handling, compliance, method validation, troubleshooting, audits, and driving process improvements in the lab.

Urgent opening for Head QA with rich experience in MHRA site. Job location Chandigarh

Required skill : IBM filenet P8Added advantage AWS, FileNet BAW, Dev Ops Responsibility: Experience in IBM FileNet BAW Administration and application maintenance. Experience in installation of FileNet P8 , ICN Experience in installation and configuration of WebSphere 8.5/9.0 Hands on FileNet upgrades Experience of P8 migration from on-premises to cloud environment Experience in troubleshooting day to day user service requests /incidents on call. Experience in change request creation andimplementation. Experience in working with other support/middleware teams for issues resolution. good communication & inter-personal skills. Experience in working with agile process Deliver and Maintain high-quality application software solutions that meet Business Users requirements. Effectively communicating through excellent written and verbal communication skills. Contributing to the development of a solution design and/or strategic deployment roadmap. Contributing to project documentation, including, but not limited to requirements documents, technical design, test plans, and knowledge transfer documentation. -Participating in multiple projects simultaneously. -Demonstrating strong customer-facing skills by building and maintaining positivecustomer relationships. -Preparing, maintaining, and submitting weekly activity/progress reports and time recording 100% PART 3 Duties and Responsibilities List in order of importance and state approximate weightage accorded to each. Deliver working software that meets the functional/non-functional requirements of business users. Deliver high quality software consistent with the principals of continuous integration. Develop and manage effective relationships peers, customers and managers. Adhere to SDLC and Allianz Technology Group Standards 60 % Work with the technical team in resolving complex issues and troubleshooting Conduct code reviews of other peers and ensure code quality is not compromised Estimate delivery costs and timeframes to meet the needs of project managers aligned with business priorities. Challenge business requirements and OSD requirements that do not deliver customer value or do not make appropriate use of technology. 30 % Co-operate with and actively contribute to the health and safety of themselves and others within the workplace. 10 % PART 4 Qualification, Experience, Technical and Functional Skills Must-Have: -B.E, B Tech, MCA or equivalent qualification. -The candidate should have 8 to 14 years of professional experience in FileNet P8 Admin -BAW, AWS experience would be added advantage -Knowledge and understanding of on-premises and cloud enterprise software deployments. -Strong analytical, technical and problem-solving skills. -Strong communication skills. -Adhere to Allianz internal standards and best practices for consistent, high quality project delivery. Good to Have: Working knowledge of any Linux, DB tools Experience in DevOps tools like Jenkins / docker / etc.

Department: Formulation Development. Job Title: Research Associate / Sr. Research Associate - Formulation Development Experience: 2 - 4 Years Reporting to: Manager Formulation Development Location: Hosur, Tamil Nadu. Qualification M. Pharm in Pharmaceutics Candidate should be from English medium. Job Description: Preparation of product initiation from (PIF). Literature search/ Patent search/ Formulation strategy for formulation. Interpretation of stability study reports. Leading team in effective manner. Market sample / innovator sample procurement in coordination with the marketing team, providing training to team members. Reference/comparator product procurement and evaluation. Test license application. Preparation of costing formula. Execution of Bio batches. Procurement of Raw materials, Packing materials & Lab equipment. Preformulation studies / Drug excipient compatibility study review and further plans. Monitoring formula development activity for lab scale batches / pilot batches. Providing costs for new product development. Preparation of documents viz product development report, stability protocols, product specifications, formulation certificate, master formula record. Resource organization and coordination with relevant departments viz. purchase, R&D, Analytical, Quality Control, Quality Assurance, production and Engineering etc. Organizing seminars by internal staff and external vendors. Providing justification and response to queries received from regulatory authority. Formulation development and scale up. Stability Studies. Analytical data and stability data compilation. Maintenance of Lab Notebooks and Project files.

Hiring for Manufacturing (OSD) at Amneal Pharma for SEZ Matoda, Ahmedabad plant (Oral Solid - OSD Requirement) 1.Manufacturing & Packing (Tablet/Capsule) Requirement For Officers & Executives Designation: Officer/ Sr. Officer /Executive Qualification: B. Pharm, ITI,Diploma Total Experience: 02 to 06 years Area: Coating, Granulation, Compression, Packing (Bottle Packing only) Machine Exposure along with 21 CFR compliance: RMG, FBE, Fette compression, Auto coaters, bottle packing line with Track & Trace system. Desired Profile: Candidates should have hands on experience along with knowledge of 21 CFR compliance in equipment's like RMG, FBE, V-Blender, Fette compression machine, Auto coater, CVC Line and packaging line equipment with Track and Trace system. Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing/Packaging area of OSD. Able to understand & have relevant knowledge of SCADA operation & 21 CFR requirements. Able to understand & operate fluid Bed equipment To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches. To maintain the areas and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To impart training of operation and cleaning related SOP to all subordinates and operators Co-ordination for IQ / OQ for any new equipment / system To perform PQ for any new equipment / system To follow all concern departmental SOP's for day to day operation and cleaning To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record To perform online documentation with respect to departmental procedures as per good documentation Maintaining the change parts for all equipment at manufacturing. Interested candidate can share cv on chandanid@amneal.com with caption "CV for Production"

Piramal Pharma Limited is hiring for Production Role . Interview Date : 27th July Sunday Interview time : 9:00 - 2:00 pm Address : Plot No. 67-70, Sector-2, Pithampur. Job Description T echnical staff : Granulation/Compression Required Experience: 01-2 years Qualifications: B. Pharma/M. Pharma/BSC/M.Sc. (Chemistry) Job Profile : Candidate should have very good knowledge of production Department with the experience of granulation , Coating , Compression, Packing (Bottle Packing) etc. Candidate should have very good knowledge of production Department with the experience of CVC Packing (Bottle Packing) etc. Contact Peron : Anuj

Role & responsibilities Granulation Supervisor Responsibilities: Supervise the granulation process, ensuring compliance with Batch Manufacturing Records (BMR) and adherence to Good Manufacturing Practices (GMP) . Ensure effective process adherence, timely production, and achievement of department goals. Focus on yield improvement , identifying and implementing strategies to optimize production efficiency and minimize waste. Monitor and maintain granulation equipment, ensuring smooth operation and troubleshooting as needed. Collaborate with cross-functional teams to address any production or quality-related issues. Provide training and mentorship to junior staff, ensuring operational efficiency and safety. Analyze production data and report on key performance indicators (KPIs) to senior management for continuous improvement. Granulation Pharmacist Responsibilities: Responsible for operating and overseeing more than two granulation machines during production, ensuring quality and quantity targets are met. Perform regular quality checks at various stages of production to maintain high-quality standards. Ensure proper machine performance, identify potential issues, and support troubleshooting and preventive maintenance activities. Ensure compliance with GMP and regulatory standards throughout the production process. Collaborate with Quality Control and Maintenance teams to resolve operational challenges and maintain machine performance. Maintain accurate production records, monitoring machine performance and production metrics. Pellets Supervisor Responsibilities: experience in pellets manufacturing in a regulated OSD pharmaceutical environment. Strong understanding of GMP, GDP, regulatory (USFDA/EU/WHO) guidelines. Good documentation, team management, and communication skills.

Role & responsibilities 1. Drive product robustness for all products in area of responsibility and lead the third party operation team. 2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities. 3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs. 4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to transfers of Drug Product Manufacture and Packaging. 5. Be familiar with statistical tools to analyze data. 6. Provide third party and techno-commercial leadership in the areas of production and packaging process and process optimization using pharmaceutical processes. 7. Knowledge of all pertinent technical information related to an assigned product. Detailed knowledge of the operation, maintenance, and utility of all manufacturing and/or packaging equipment for assigned projects. Thorough familiarity with cGMPs, SOP's, relevant government regulations, and current industry standards. 8. Responsible for Techno-commercial activities for all dosage form. 9. Responsible for Sourcing / coordinate with LL/TP manufacturers for product related documents. 10. Supplier Identification: • Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for markets. 11. Supplier Qualification and Onboarding: • Developing and implementing a robust supplier qualification process to ensure that selected suppliers meet the necessary standards and regulations in coordination with quality team. Preferred candidate profile PHARMA THANKS YOU REGARDS MILAP RATHOD (7486829377) call or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips Increment letter Previous company relieving letters Education Documents and ID Proofs Help Us Spread the Word (Refer): Circulate it in your Social Networking sites and groups for better reach and Refer your friends and colleagues, it could be a great opportunity for someone in need! WORK LOCATION: Hetero Labs Limited, UNIT V Polleypally, Jadcherla, Mahabubnagar CONTACT INFO: E-mail: Ashok.ch@hetero.com & Contact:8555912639 for further info.

Roles and Responsibilities Perform calibration, electrical maintenance, formulation, HVAC operations, process engineering, and process maintenance tasks to ensure smooth plant operations. Conduct quality control checks on equipment and processes to identify areas for improvement. Collaborate with cross-functional teams to resolve issues related to OSD (Oral Solid Dose) production. Ensure compliance with safety protocols and regulations in the pharmaceutical industry. Maintain accurate records of work performed and report any defects or anomalies.

As the Head of Quality Control at a leading Pharma MNC located in the Chandigarh Vicinity, you will be responsible for overseeing the quality control operations of highly regulated plants, specifically focusing on tablet/capsule/pallets/OSD products with a preference for injections. With over 20 years of experience in the industry, you will demonstrate a track record of excellence in maintaining MHRA and EUGMP profiles, along with multiple successful audit exposures. In the realm of Quality Assurance, you will showcase a deep understanding of the latest updates outlined in the ICH Q9 guidelines. For Quality Control, you will exhibit proficiency in the Updates related to ICH Q2R2 Analytical method validation. Moreover, your leadership skills will be put to the test as you manage a large team, drawing upon your prior experience in handling sizable teams effectively. A key requirement for this role is a proven track record of stability, demonstrating your ability to navigate challenges in the pharmaceutical quality control landscape with resilience and expertise.,

The position of Head of Quality Assurance at a Leading Pharma MNC in Chandigarh Vicinity offers a competitive salary of up to 60 LPA. As a qualified candidate, you must possess over 20 years of experience in managing highly regulated plants, with a strong focus on Tablet/capsule/pallets/OSD products, and preferably injections as well. Your expertise should include an excellent MHRA and EUGMP Profile, along with a track record of multiple successful audit exposures. In the realm of Quality Assurance (QA), you are expected to be well-versed with the latest updates in ICH Q9 guidelines. Additionally, in Quality Control (QC), familiarity with Updates in ICH Q2R2 Analytical method validation is crucial. Your experience should also demonstrate proficiency in handling large team sizes and showcasing proven stability in your previous roles. If you meet these mandatory requirements and are ready to take on a leadership role in ensuring the quality standards of pharmaceutical products, we encourage you to apply for this challenging yet rewarding position.,

Project Role : Technology Architect Project Role Description : Design and deliver technology architecture for a platform, product, or engagement. Define solutions to meet performance, capability, and scalability needs. Must have skills : Microsoft Intune Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time educationRoles and ResponsibilitiesDesign and implement Intune-based device management strategies for Windows, iOS, Android, and macOS.Configure and manage compliance policies, configuration profiles, and app deployments.Integrate Intune with Azure AD Conditional Access, Defender for Endpoint, and Autopilot.Monitor and troubleshoot device enrollment, policy deployment, and application delivery.Collaborate with security and infrastructure teams to ensure endpoint security and compliance.Provide technical support and training to end-users and IT staff on Intune-related services. Technical Experience & Professional AttributesExpertise in:Microsoft Intune (Endpoint Manager)Azure AD, Conditional AccessWindows Autopilot, Co-management with SCCMPowerShell scripting for automationStrong understanding of MDM/MAM concepts and Zero Trust security.Professional traits:Analytical, proactive, collaborative, and customer focused. Additional InformationCertifications:Microsoft Certified:Endpoint Administrator AssociateMicrosoft 365 Certified:Modern Desktop Administrator AssociateTools:Microsoft Endpoint Manager, Azure Portal, Power BI (for reporting), M365* A 15 years full time education is required Qualification 15 years full time education