246 Osd Jobs - Page 3

Imagine your career taking you to the depths of innovation and the heights of impact. Our people enable continuous progress. Their commitment, collective expertise, and unique capabilities are the engine room behind SBM Offshore s True. Blue. Transition. - shaping the future of energy, and beyond. About Us: SBM Offshore is the world s deepwater ocean-infrastructure expert. Our work is already resulting in cleaner, more efficient energy production. True. Blue. Transition. is our promise to enable that into the future while at the same time using our expertise to support new and existing markets in the blue economy. It starts with Advancing our Core: continuing to advance the decarbonization of traditional energy production. While Pioneering More: helping to enable the energy transition and using our unique capabilities in ocean infrastructure to support more industries to grow sustainably. Sharing our experience for a better blue tomorrow. As a Senior Project Engineer , you play a pivotal role in the successful delivery of complex projects. With a minimum of 10 years of experience, you are responsible for overseeing and coordinating all technical and administrative project activities, ensuring the project objectives are met efficiently and within budget and time constraints. This senior role requires strong leadership and in-depth expertise across multiple project disciplines. Key Responsibilities : You lead the development and management of project plans, schedules, and budgets, ensuring alignment with project objectives and stakeholder expectations. You oversee coordination between engineering, procurement, and construction teams, ensuring all project requirements are thoroughly met. You conduct and oversee advanced technical evaluations, risk assessments, and feasibility studies to guide project decision-making. You monitor and drive project progress, proactively identifying risks and implementing corrective actions to ensure milestones are met. You lead the review of technical documentation, ensuring adherence to industry standards, safety regulations, and company policies. You act as key liaison with clients, contractors, and regulatory bodies, ensuring clear communication and collaboration across all project phases. You provide guidance and mentorship to the project engineering team, fostering a culture of continuous improvement and technical excellence. You mentor more junior project engineers and support their development Project Role: Package Manager Ref.: Project plans and GEMS. The Package Manager (PKM) is the front-line of the supply chain within the project and he/she is responsible to deliver the package to meet project requirements in terms of safety, budget, schedule and quality. The Package Manager (PKM) assumes the role of the Purchaser Representative in the Purchase Order (PO). The main responsibilities are: Serve as the Project Manager for the assigned packages, and act as the primary point of contact with the Supplier. Deliver the package in accordance with all project requirements, ensuring safety, quality compliance, adherence to schedule, and budget constraints. Manage all aspects related to the delivery of the package, including setting up, planning, and managing Package Health Checks. Ensure all project requirements are followed and executed in accordance with the contract, project management plans, and technical specifications. Ensure all relevant technical requirements are known and addressed by maintaining a close relationship with the PKE and the supporting team. Understand the technical requirements of the package by liaising with the Package Engineer (PKE). Developing and maintaining a close relationship with the engineering team to anticipate potential delays or changes. Manage the package interface with the Supplier and ensuring that the activities align with project priorities. Monitor package execution and proactively raising alerts to implement corrective action plans. Report package progress to the Project Management Team throughout the projects life. Control and closing all TQ, TD, NCR, VOR (in liaison with Engineering and Quality when required by PMT) of the assigned package(s). Ensure inspection is properly managed and close out all OWL, SOB, OSD, and Punch list items raised against the package. Prepare for package handover to the Completion/Construction Team, and organize handover sessions timely when applicable. Provide support and participating (if needed) in construction, integration, pre-commissioning, and commissioning activities. Ensure continuous improvement by sharing package best practices and lessons learned. Complete timely package close out of the PO. Qualifications : Bachelor s degree in Engineering. Minimum 10 years of experience in project engineering within the oil and gas sector, with demonstrated expertise in large-scale projects. Strong leadership, problem-solving, and decision-making skills. Proficiency in project management tools and methodologies. GENERAL INFORMATION SBM Offshore N.V. is a listed holding company that is headquartered in Amsterdam. It holds direct and indirect interests in other companies that collectively with SBM Offshore N.V. form the SBM Offshore Group ( the Company ). For further information, please visit our website at www.sbmoffshore.com. The companies in which SBM Offshore N.V., directly and indirectly, owns investments are separate entities. SBM Offshore is proud to be an Equal Employment Opportunity and Affirmative Action employer. SBM Offshore does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

Job description Coordinating for getting necessary Export NOC permission for Amneal OSD Performing key activities of Supply Chain function for Raks Preparing Manufacturing Plan for API division (Experience of Manufacturing Planning & Materials planning is must) Coordinating for RM delivery with SSSM (Purchase) team Coordinating for RM release with QC team Day to day coordination with cross function team

Project Role : Infra Tech Support Practitioner Project Role Description : Provide ongoing technical support and maintenance of production and development systems and software products (both remote and onsite) and for configured services running on various platforms (operating within a defined operating model and processes). Provide hardware/software support and implement technology at the operating system-level across all server and network areas, and for particular software solutions/vendors/brands. Work includes L1 and L2/ basic and intermediate level troubleshooting. Must have skills : Microsoft Intune Good to have skills : NAMinimum 2 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Infra Tech Support Practitioner, you will engage in the ongoing technical support and maintenance of production and development systems and software products. Your typical day will involve addressing technical issues, providing solutions, and ensuring the smooth operation of various platforms. You will work both remotely and onsite, collaborating with team members to implement technology at the operating system level across server and network areas. Your role will also include troubleshooting hardware and software issues, ensuring that all configured services operate effectively within defined processes. Roles & Responsibilities:- Expected to perform independently and become an SME.- Required active participation/contribution in team discussions.- Contribute in providing solutions to work related problems.- Assist in the documentation of technical processes and procedures to enhance team knowledge.- Provide training and support to junior team members to foster a collaborative environment. Professional & Technical Skills: - Must To Have Skills: Proficiency in Microsoft Intune.- Good To Have Skills: Experience with endpoint management solutions.- Strong understanding of operating system-level support and troubleshooting.- Familiarity with network protocols and configurations.- Experience in managing software deployment and updates. Additional Information:- The candidate should have minimum 2 years of experience in Microsoft Intune.- This position is based at our Gurugram office.- A 15 years full time education is required. Qualification 15 years full time education

Hiring Compression, Granulation & Coating Operators on Permanent Payroll for Formulation Pharma Company in Ankleshwar Any ITI / DPharm / Diploma with 2 to 6 Years Experience CTC Up to 4 LPA Send CV on sdpbharuch@gmail.com & Call on 7600033423 Required Candidate profile No Placement Charges Share with your Friends & Colleagues!!! Join Our Group: https://chat.whatsapp.com/G6OMAxOdIPw3UhPmdA9Cah Follow Our Channel: https://whatsapp.com/channel/0029VaDwTZoHgZWddec9BL0y Perks and benefits Transportation & Canteen Available Medical Bonus

Hiring Compression, Granulation & Coating Operators on Permanent Payroll for Formulation Pharma Company in Ankleshwar Any ITI / DPharm / Diploma with 2 to 6 Years Experience CTC Up to 4 LPA Send CV on sdpbharuch@gmail.com & Call on 7600033423 Required Candidate profile No Placement Charges Share with your Friends & Colleagues!!! Join Our Group: https://chat.whatsapp.com/G6OMAxOdIPw3UhPmdA9Cah Follow Our Channel: https://whatsapp.com/channel/0029VaDwTZoHgZWddec9BL0y Perks and benefits Transportation & Canteen Available Medical Bonus

We are seeking an experienced SCCM Engineer to join our IT Infrastructure team. The ideal candidate will have deep expertise in SCCM , infrastructure management, Windows workstation patching , and software distribution. You will play a critical role in managing, maintaining, and optimizing endpoint management solutions, ensuring secure and efficient deployment across the enterprise. Key Responsibilities: Manage and maintain SCCM infrastructure for patch management, software distribution, and operating system deployment. Execute Windows workstation patching and maintain compliance with security policies. Develop and manage OSD (Operating System Deployment) images for Windows 10/11 . Support migration and upgrade processes to Windows 11 . Perform software packaging and distribution using SCCM and Intune . Implement and manage Intune Autopilot , Conditional Access policies , and compliance settings . Conduct server patching , SQL patching , and maintain patch compliance across the environment. Develop SQL reports and dashboards for monitoring patch status and deployment metrics. Write and maintain PowerShell scripts for automation and administration tasks. Ensure timely remediation of vulnerabilities via patching and endpoint configurations. Required Skills and Qualifications: Proven hands-on experience with SCCM/MECM in an enterprise environment. Strong understanding of Windows infrastructure and endpoint lifecycle management. Experience with software distribution and Windows patch management . Solid experience with Intune for endpoint management, including Autopilot and Conditional Access policies . Experience with OSD , Windows 11 upgrades , and imaging tools. Familiarity with server and SQL patching procedures. Proficiency in PowerShell scripting for automation and reporting. Experience creating and maintaining SQL-based reports . Preferred Qualifications: Microsoft certifications (e.g., MCSA , MCSE , MD-102 ). Experience in hybrid environments involving both SCCM and Intune . Familiarity with compliance and security best practices. Mandate Skills SCCM, Infra, Software distribution, Windows workstation patching Other skills : Imaging, Windows 11, OSD migration, Intune Auto pilot, Intune Conditional policy, Server patching , SQL patching , SQL reporting, PowerShell, Patching with Intune, Software distribution with Intune.

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation Development Quality Assurance Department (Formulation) Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDRs, PDR’s, MFR’s and MPR’) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audits for Cross functional Departments in Formulation Division and External Division. Conducting and Coordinating Employee Trainings. Responsible for Review and Approval of Vendor Qualification Should have experience in IPQA and Analytical QA (OSD/Injectable) Ref to Friends or colleagues. Please Share me update resume: careers@biophore.com Total Exp: Current CTC: Exp CTC : Notice Period: Designation:

Leading the Quality Control Teamaccording to the norms of GMP (Good Manufacturing Practices) to ensure international quality standards and adherence to various regulatory requirements. Developing and reviewing cGMP compliance related documents like global procedures, methods, standards, specification, validation protocols, summary reports. Implementation of management system for Change control, CAPA, OOS, Risk analysis, deviation management system, incidents (Lab ware LIMS, eQMS,Track wise) and complaint management system. Actively participated in QTA between CMO and receiving/transferring site. Review and approval of APQR. Root cause analysis/ Failure investigation and corrective and preventive action planning Change control management system, CAPA, OOS, deviation management system, incidents Corrective and preventive action planning (CAPA) against the regulatory requirement. Implementation of CAPA effectiveness checks against the regulatory and existing quality system requirements. Deep knowledge in LIMS (Caliber/ LabWare management system and Thermo LIMS). GAP assessment of the quality system for process optimization and to assess the regulatory requirements against the gaps observed. Development and review of cGMP compliance related documents like global procedures, methods, standards, specification and validation protocols, summary reports. Immediate Joiners will be prefered. Kindly share resume on dipika.parmar@milanlabs.com

Responsible for handling all activities pertaining to Tablets & Capsules & Pellets Mfg. Responsible to handle the team to achieve the set targets & maintain qualitative & quantitative as well as cGMP aspects. Perks and benefits Accommodation & Transportation And Mediclaim

Job description Handle BMR and batch repacking records, Verify daily balance checks and calibration activities, Maintain production records, Perform and verify line clearance at manufacturing and packing stages, Issue and retrieve production documents Required Candidate profile (M.Sc. / B. Pharm. / M. Pharm.) with 1 to 5 years Experiences in OSD manufacturing Graduate candidates and knowledge about cGMP Practice, QMS tools knowledge, Production and Manufacturing documentation process. We are looking for local candidates ONLY. Role: Production & Manufacturing - Other Industry Type: Pharmaceutical & Life Sciences Department: Production, Manufacturing Employment Type: Full Time, Permanent Role Category: Production & Manufacturing - Other Candidate worked in production compliances / remediation / and having experiences of managing quality system document (CCN / CAPA / investigation etc.) Note : We also invite CV for various position in Production, QA, QC, F&D & Maintenance kindly forward the same to E Mail : hr@expertpharmaceuticals.com

* Batch Manufacturing * BMR / BPR - Documentation * Co-Ordination with QA * Manufacturing Parameters Review *SOP & Documentation * Man Power Allocation * Quality Management System Required Candidate profile Candidate should have experience of Production of Formulation Plant. If interested, please call at: 7742408300/ 7742408200 & mail your resume at: lksaddiassociate@yahoo.co.in Perks and benefits Salary will not be constraint for right candidate.

Dear All, We are conducting Walk-in Interview at Ahmedabad for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 22nd June 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.E/B.Tech 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. Sr. Executive/ Assistant Manager: B.E/ B.Tech with 5-10 Years Process Equipment( Electrical / 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 and Utility. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration . QMS documentation exposure is required. Warehouse: Officer to Senior Executive B.Sc./M.Sc. / B. Pharma graduate with 5 to 10 years of experience in handling of warehousing activities. Exposure of handling Raw Material, Packing Material receipt Dispatch and issuance activities. Having good knowledge of QMS area and equipment qualification related activities. Well versed with SAP MM module with WMS. Handling of expired, rejected, non-moving and obsolete inventory. Having exposure of USFDA/MHRA and other regulatory audits. 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.

JOB DESCRIPTION Job Title: QC Microbiology Analyst Job Location: Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Education : M.Sc. Microbiology Equal Opportunity Employer . Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team Good speaking-listening-writing skills, attention to details, proactive self-starter Ability to work successfully in a dynamic, ambiguous environment Ability to meet tight deadlines and prioritize workloads Ability to develop new ideas and creative solutions Should be able to work in team and flexible for working in shifts Should be a focused employee Good documentation capability Experience : 1 -3 YEARS Skills and Capabilities Microbial analysis of water, OSD products, Injectable products, Environmental monitoring Education : Demonstrated Capability : Specific requirements for this role Experience : Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Role Accountabilities Responsible for Sample receipt of raw materials, in process, finished product and stability samples. Responsible for Microbiological analysis, Bacterial Endotoxin Test and Chemical analysis of different grades of water (PW/WFI/POW) as per the respective specification. Responsible for sample management and coordination with team for smooth operation of samples release activity. Responsible to perform the Bioburden and Microbial Limit Test. Responsible to perform the Method verification activity for BET, MLT and Bioburden test. Responsible for environmental monitoring of clean rooms in Microbiology laboratory. Responsible for all microbiological related activities like Media receipt, Media stock maintenance, Preparation of media, Sterilization, Growth Promotion for media, Culture maintenance and Media Disposal. Monitoring and review of Temperature monitoring data record of equipment and clean room. Monitoring of differential pressure in QC Microbiology Laboratory. Responsible for disinfectant preparation, cleaning, and fumigation of microbiology laboratory. Follow the required EHSS policies and Good hygiene practice. Undertake other responsibilities related to Microbiology as per requirement. Core Purpose of the Role : Microbiology analysis (Bioburden, MLT, Test for specified organisms, BET analysis) Chemical analysis for water samples Environmental Monitoring Utility Monitoring Water sampling Microbiology lab maintenance

HIRING FOR FORMULATION UNIT - INJECTABLE/ OSD JOB DESCRIPTION AND EXPERIENCE: WORK LOCATION: Hetero Labs Limited, UNIT V & VI, Polleypally, Jadcherla, Mahabubnagar OSD- PRODUCTION Experience: (02-07Years) Compression, Granulation, Coating, Capsule filling, Inspection INJECTABLE-PRODUCTION Experience: (02-06Years) Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer, Visual Inspection INJECTABLE/OSD - PACKING Experience: (01-05Years) Blister Packing, Bottle Packing. QC & QC- Micro Experience: (01-07Years) HPLC, GC, RM,PM, Stability, IP/FP, Microbiology QUALIFICATION : I.T.I, Diploma, B.Com, B.Sc, B.Tech, B. Pharm, M.Sc with relevant experience DESIGNATIONS: Operator, Sr.Operator, Jr.Officer, Officer, Jr.Executive, Executive & Sr. Executive INTERVIEW VENUE: PHARMA JOBS: Talent Acquisition center, Bhagyaradhi Degree College, 1st Floor, IDPL X Road, Jeedimetla Road, Hyderabad DATE &TIME: 22nd June'2025 (Sunday); 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! CONTACT INFO: E-mail: Harishwar.m@hetero.com & Cont: 8121036004 for further info

Role & responsibilities : a. Plan, manage, and oversee the work activities of QC and Microbiology laboratories to ensure lab testing provides the highest quality analytical support for manufacturing in a timely and compliant manner, adhering to protocols, cGLP, and safety regulations. b. Manage analytical method validation of products, method transfer, stability studies, and related activities to ensure compliance with regulatory and quality standards c. Provide leadership, management, performance evaluation, and training to all laboratory employees to maintain a competent and motivated team. d. Execute and approve all laboratory operations, including reviewing and investigating any laboratory data that is outside of established trends. e. Ensure all vendors are qualified and comply with vendor qualification standards, aiming for optimal utilization of reduced testing procedures. f. Establish and implement a KPI system to ensure an optimal balance between test quality and cost efficiency. g. Collaborate closely with other departments to ensure the plant's compliance with the Quality Management System (QMS). Preferred candidate profile Candidates having experiences in Pharma formulation(OSD) of EU/USFDA plant are preferred

Walk-in Interview for Zydus Lifesciences Ltd. Moraiya - Ahmedabad at Moraiya| 22nd June 2025 | We are recruiting for our Ahmedabad Units at Moraiya, Ahmedabad. Walk-in Interview Details Date : 22nd June 2025 Interview Location: Moraiya, Ahmedabad Timings: 9:00 am 3:00 pm Interview Venue: Zydus Lifesciences Limited, Moraiya Opp. Akshar industrial Park, Survey No.417,419&420, Sarkhej- Bavla N.H. No.8A, Village: Moraiya, Tal: Sanand, Dist: Ahmedabad- 382210, Gujarat, India Job Location: Ahmedabad Education Qualification: M.Sc. / M. Pharm / B. Pharm / B.sc /Diploma/ ITI Experience: 3 13 Years Production- OSD: Officer / Assistant manager : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Plant Operator/ Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Packing: Plant operator/Technical Assistant: Blister Line(BQS), CVC Bottle Line, Sachet Packing (Wraptech) Warehouse: Officer / Sr. Executive: RM, PM, FG, Dispensing, Dispatch , Documentation Plant operator/Technical Assistant: RM, PM, Dispensing and dispatch Engineering Technician: Instrument Technician - Fitter/Electrical/Process equipments/ HVAC Operation/HVAC Validation/ Instrumentation/ Water system Quality Assurance (IPQA) Officer / Assistant Manager: IPQA in process (Mfg. and Pkg.) / QMS

Receive and Log Complaints : Record and evaluate complaint submissions from customers regarding manufacturing defects or issues. Ensure all complaints are logged accurately in the complaint management system. Investigate Complaints : Conduct thorough investigations to determine the root cause of the complaint. Coordinate with internal departments (Quality Assurance, Regulatory Affairs, Production) to gather necessary information. Communicate with Stakeholders : Communicate with customers to understand their concerns and provide updates on the investigation. Liaise with healthcare providers, if applicable, to acquire relevant complaint information. Regulatory Compliance : Ensure timely processing of complaints in accordance with regulatory requirements. Generate and submit reports to appropriate authorities and government agencies as required. Corrective Actions : Recommend and implement corrective and preventive actions (CAPA) to address and prevent recurrence of issues. Monitor the effectiveness of implemented actions. Documentation and Reporting : Maintain detailed records of all complaint investigations and resolutions. Prepare trend reports and metrics to capture and analyze complaint data. Audit Preparation : Participate in activities to prepare for audits and inspections. Ensure all documentation is compliant with GMP (Good Manufacturing Practices) standards.

Job Summary : Pharmaceutical experience is mandatory. Engineer designs, installs, and maintains systems like security, fire alarms, communication, and audio-visual systems, focusing on the technical aspects of these low-voltage electrical systems. Areas of Responsibility : Design and Planning: Develops and designs ELV systems for various projects, including commercial, residential, and institutional buildings Installation and Maintenance: Performs ongoing preventive maintenance and repair work on facility electrical and ELV systems. Project Management: Monitors work progress and site safety in compliance with contractual and statutory requirements. Technical Skills: Expertise in various ELV systems, including fire alarms, public address, security systems, and audio-visual systems. Knowledge of relevant codes, standards, and regulations. Ability to prepare drawings, documents, and statutory submissions. Familiarity with cable fault detection, insulation resistance tests, and preventive maintenance Assists project managers in overall project operations, coordination, and handover. Supervises junior technical staff and subcontractors to ensure smooth project execution. Knowledge of relevant codes, standards, and regulations Ability to prepare drawings, documents, and statutory submissions. Compliance and Regulations: Ensuring compliance with all relevant regulations and industry standards. Experience of Projects of Injectable / OSD block for Pharmaceuticals industries Job Location : Central India / South India (For Greenfield Project)

Walk In Drive For Production OSD In Formulation Division @ Bachupally Department:- Production OSD Qualification :-ITI | BA | Diploma | B Com | BSC | B Pharmacy Experience :- 1 To 3 Years Skills :- Operators:- Coating | Compression | Granulation | Capsule Filling | Blister CAM Packing Operators:- Primary And Secondary Division :- Formulation Interview Date:- 21-06-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-I, Bollaram Venue Location:- H. No-1-77/1,3rd floor, Mahi's Vista, Bachupally X Road's, Medchal(Dist),Hyderabad,500090 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Coating , Granulation , Compression, Capsule Filling , Blister Packing , Cam Cartontor, Hi Cartonator, Primary Packing , Secondary Packing, Documentation. About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Interpret medical images such as X-rays, MRIs, CT scans, and ultrasounds to diagnose and monitor various conditions Collaborate with referring physicians to provide accurate, timely diagnostic reports and recommendations for further evaluation or treatment Ensure the appropriate imaging protocols are followed and maintain compliance with safety and radiation regulations Supervise and guide radiologic technologists, review image quality, and ensure accurate patient identification and documentation Stay updated with advancements in radiologic technology and integrate new techniques to improve diagnostic precision and patient car

Job Description Version. no.: The Job Responsibilities of the position holder are : Responsible for performing the analytical activities as per Analytical competency matrix (Format No.BDI-QCSG004F23) and On job training and Practical Demonstration for Chemical and Instrumentation (Format No.BDI-QCSG004F19). Analysis of In process, SFG, Finished Goods, Raw material & stability sample, Analytical method validation/Verification, of OSD and LVP as per defined Protocol or procedure and related documentation as per GLP and GMP in time. Responsible for receiving sample and their documentation. Responsible Data entry in SAP. Responsible for sending the sample to outside laboratory and ensure their analysis as per requirement from Outside Commercial Lab as and when required. Calibration of instruments, as and when required. Preparation of volumetric solution, reagent, and test solution, as and when required. Ensuring the timely updation in the documents as per the Pharmacopeial amendments. Responsible for maintaining the resource in the quality control department. To ensure the compliance of the requirement of cGDP/cGDP and Data integrity while performing all activities in the laboratory. Ensuring the Compliance to EPD Global Guidelines. Facing internal and external audits and ensuring compliance. Implementation of GLP / GMP requirements. Coordinating and aligning the practices and procedures in line with the COBC requirements. SOP training in Isotrain of self-train within stipulated time. Any other task assigned by reporting manager. In absence of the position holder, the sub-ordinate Executive / Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working. Signatures _____________ Position holder ______________________ Authorized by JOB FAMILY: Operations Quality t

As a Senior Project Engineer , you play a pivotal role in the successful delivery of complex projects. With a minimum of 10 years of experience, you are responsible for overseeing and coordinating all technical and administrative project activities, ensuring the project objectives are met efficiently and within budget and time constraints. This senior role requires strong leadership and in-depth expertise across multiple project disciplines. Key Responsibilities : You lead the development and management of project plans, schedules, and budgets, ensuring alignment with project objectives and stakeholder expectations. You oversee coordination between engineering, procurement, and construction teams, ensuring all project requirements are thoroughly met. You conduct and oversee advanced technical evaluations, risk assessments, and feasibility studies to guide project decision-making. You monitor and drive project progress, proactively identifying risks and implementing corrective actions to ensure milestones are met. You lead the review of technical documentation, ensuring adherence to industry standards, safety regulations, and company policies. You act as key liaison with clients, contractors, and regulatory bodies, ensuring clear communication and collaboration across all project phases. You provide guidance and mentorship to the project engineering team, fostering a culture of continuous improvement and technical excellence. You mentor more junior project engineers and support their development Project Role: Package Manager Ref.: Project plans and GEMS. The Package Manager (PKM) is the front-line of the supply chain within the project and he/she is responsible to deliver the package to meet project requirements in terms of safety, budget, schedule and quality. The Package Manager (PKM) assumes the role of the Purchaser Representative in the Purchase Order (PO). The main responsibilities are: Serve as the Project Manager for the assigned packages, and act as the primary point of contact with the Supplier. Deliver the package in accordance with all project requirements, ensuring safety, quality compliance, adherence to schedule, and budget constraints. Manage all aspects related to the delivery of the package, including setting up, planning, and managing Package Health Checks. Ensure all project requirements are followed and executed in accordance with the contract, project management plans, and technical specifications. Ensure all relevant technical requirements are known and addressed by maintaining a close relationship with the PKE and the supporting team. Understand the technical requirements of the package by liaising with the Package Engineer (PKE). Developing and maintaining a close relationship with the engineering team to anticipate potential delays or changes. Manage the package interface with the Supplier and ensuring that the activities align with project priorities. Monitor package execution and proactively raising alerts to implement corrective action plans. Report package progress to the Project Management Team throughout the projects life. Control and closing all TQ, TD, NCR, VOR (in liaison with Engineering and Quality when required by PMT) of the assigned package(s). Ensure inspection is properly managed and close out all OWL, SOB, OSD, and Punch list items raised against the package. Prepare for package handover to the Completion/Construction Team, and organize handover sessions timely when applicable. Provide support and participating (if needed) in construction, integration, pre-commissioning, and commissioning activities. Ensure continuous improvement by sharing package best practices and lessons learned. Complete timely package close out of the PO. Qualifications Bachelor s degree in Engineering. Minimum 10 years of experience in project engineering within the oil and gas sector, with demonstrated expertise in large-scale projects. Strong leadership, problem-solving, and decision-making skills. Proficiency in project management tools and methodologies. SBM Offshore N.V. is a listed holding company that is headquartered in

We are looking for a meticulous and experienced Technology Transfer Manager to spearhead the efficient transfer of technology for solid dosage forms at Evertogen Life Sciences . This pivotal role involves overseeing the seamless transition of OSD products from R&D or third-party development to our manufacturing plant, ensuring successful scale-up, unwavering regulatory compliance, and adherence to the highest quality standards. The ideal candidate will champion the preparation and review of critical technical documents, including technology transfer protocols, BMR/BPR, and process validation reports, while actively coordinating with cross-functional teams such as QA, QC, RA, and Production. This role demands a proactive individual adept at troubleshooting technical challenges, participating in scale-up batches, and driving continuous improvement initiatives. If you are passionate about optimizing pharmaceutical manufacturing processes, possess a strong understanding of QbD principles, and thrive in a collaborative environment, we encourage you to bring your expertise to Evertogen and contribute to our mission of delivering high-quality, affordable medications to the global market. Your contributions will directly impact our ability to meet client needs and maintain a diverse product portfolio. Job Details: Industry : OSD Formulation (Pharmaceuticals) Department : Technical Transfer Role : Assistant Manager Tech Transfer Location : Jadcherla Compensation : Up to 15 LPA Experience : 8+ years Employment Type : Full-time Qualification : M.Pharm / B.Pharm / M.Sc. in Pharma or related field Responsibilities: Technology Transfer Execution & Documentation: Lead technology transfer projects for solid dosage forms, ensuring adherence to timelines and quality standards. Develop technology transfer protocols covering critical process parameters and quality attributes. Oversee preparation and review of essential documentation (Technology Transfer Plans, Gap Analysis Reports, Process Flow Diagrams, BMR, BPR, Process Validation Reports). Coordinate cross-functional activities (R&D, Manufacturing, QA, RA) for seamless transfer and scale-up. Monitor process performance, addressing deviations or challenges. Maintain detailed records of technology transfer activities, ensuring compliance and data integrity. Ensure documentation adheres to cGMP, regulatory requirements (US FDA, EU EMA), and internal standards. Manage document archival and retrieval. Process Validation & Scale-Up: Participate in process validation activities for robust manufacturing processes of OSD Formulations. Analyze process data to identify CPPs and CQAs for process control strategies. Troubleshoot technical issues during scale-up and validation, implementing corrective actions. Evaluate the impact of process changes on product quality. Collaborate with engineering and production to optimize manufacturing processes. Ensure compliance with validation lifecycle management. Quality & Regulatory Compliance: Ensure compliance with cGMP, regulatory requirements (US FDA, EU EMA), and internal standards. Conduct risk assessments and implement mitigation strategies. Participate in audits, addressing findings and implementing corrective actions. Maintain understanding of regulatory requirements and best practices in OSD Formulation. Oversee CAPA implementation. Promote a culture of quality and compliance. Technical Troubleshooting & Continuous Improvement: Lead troubleshooting during initial commercial batches, identifying root causes and solutions. Apply problem-solving methodologies to address technical challenges in OSD Formulation. Identify process improvement opportunities. Utilize SPC tools to monitor process performance. Implement Lean Six Sigma principles. Champion continuous improvement. Cross-Functional Collaboration & Stakeholder Management: Coordinate with QA, QC, RA, and Production teams. Facilitate communication and collaboration among teams. Manage stakeholder expectations. Build relationships with internal and external partners. Generate progress reports, highlighting milestones, challenges, and risks. Present technical data to teams and management. Lead meetings to discuss project status and make decisions. Act as a liaison between R&D, Manufacturing, and stakeholders. General Expectations and Past Experiences: Possess 8+ years of hands-on experience in technology transfer within OSD manufacturing, demonstrating a strong understanding of the entire process lifecycle. Demonstrate proficiency in preparing and reviewing critical technical documents such as technology transfer protocols, BMR/BPR, and process validation reports. Exhibit a thorough understanding of Quality by Design (QbD) principles and their application in pharmaceutical manufacturing. Showcase strong technical troubleshooting skills with the ability to identify and resolve issues during scale-up and commercial manufacturing. Proven ability to coordinate and collaborate effectively with cross-functional teams, including QA, QC, RA, and Production. Demonstrate a solid understanding of regulatory guidelines (US FDA, EU EMA) and CGMP compliance requirements for pharmaceutical manufacturing. Experience risk assessment methodologies and CAPA management systems in a pharmaceutical setting.

Formulation Development, OSD ,

Qualification: Bsc Chemistry/Bpharma Experience : 0 to 5 Years CTC: Up to 4.5 LPA Work Location : Ankleshwar Experince in OSD, Tables, API send cv on sdpbharuch@gmail.com with Sub : Production Ankleshwar Call on 9712914207 Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar No Charges Share with Friends & Colleagues