61 Aseptic Jobs

Role & responsibilities Execute daily production operations and ensure the efficient functioning of the department. Supervise and monitor manufacturing processes to ensure compliance with quality standards. Review and maintain production-related QMS elements, including Change Control, Deviation, Event Investigation, and Corrective and Preventive Actions (CAPA). Prepare and review Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and Batch Packing Records (BPRs). Address and resolve production issues promptly to minimize downtime and ensure continuous production. Respond to challenges or bottlenecks and implement mitigation strategies within defined timelines. Ensure that all processes and documentation comply with SOPs and protocols. Maintain and review all production-related records, including batch records, equipment logs, and production output reports. Prepare regular reports on production output, efficiency, and quality metrics for management review. Coordinate with the maintenance department to resolve equipment breakdowns and ensure smooth production activities. Oversee the document control system to ensure the availability and integrity of quality documents. Preferred candidate profile Bachelor's or Masters degree in Pharmacy, Life Sciences, Biotechnology, or a related field. Minimum of 1 year of experience in a production/QMS-related role within the pharmaceutical, biotechnology, or manufacturing industry. Strong understanding of QMS principles, regulatory compliance, and production processes. Ability to analyze and resolve production-related challenges effectively. Proficiency in documentation, report preparation, and adherence to SOPs.

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 13 Sep 2025, Saturday TIME: 09:00 AM to 2:00 PM Fresher's & Experienced (0 6 Years) Production: Drug substance (* Shift applicable) Sterile aseptic operation Autoclave /DHS operation Automated CIP/SIP operation Cell culture Aseptic operation Zonal Centrifuge operation Facility commissioning QMS/ Deviation/ Change control/ CAPA/ Investigation of deviation Qualification requirement: M.Sc/B.Sc (Life Science) , B.Pharm/M.Pharm , Diploma / ITI Benefits PF, ESIC, Transportation/Local Allowance, Canteen Facility, GMC Venue CHIRON BEHRING: Plot No. 3502, GIDC Estate, Ankleshwar, Gujarat 393002

Role & responsibilities Production: Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions, filtration, Lyophilizes. Having Injectable Experience of Shop floor supervising activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions, filtration, Lyophilizes. Operations and Training and QMS. Engineering: Having Injectable Experience of Instrumentation and Process Mechanical (Hands on Experience on Filling Lines, Lyophilizers, Track and Trace System) and HVAC, Utilities.

ROLE OBJECTIVE: A key objective of this role is to oversee the daily operations and ensure that all activities are conducted in alignment with company objectives. This role involves managing staff, optimizing processes, and Quality management systems with high standards. The Assistant Manager is expected to step in and take charge in the absence of the Manager, ensuring the seamless continuation of operations. Role & Responsibilities: Assist in planning and execution of daily production schedules to meet operational goals. Supervise and motivate production staff; resolve conflicts and support professional development. Monitor and maintain production-related QMS elements such as Change Control, Deviations, CAPA, and Event Investigations in track-wise systems. Review and prepare production-related documents, including SOPs, BMRs, and BPRs. Conduct training programs and evaluations on cGMP and SOPs as per schedule or Training Need Identification (TNI). Troubleshoot production issues and ensure timely resolution to avoid operational delays. Ensure that all processes and documentation are carried out in accordance with SOPs, protocols, and regulatory standards. Maintain accurate and up-to-date records, such as batch records, equipment logs, and quality reports. Generate and submit reports on production performance, efficiency, and quality metrics. Coordinate with the Maintenance team to ensure timely resolution of equipment breakdowns. Oversee the document control process to ensure integrity and accessibility of quality records. Liaise with cross-functional departments to facilitate seamless production activities. Desired Candidate Profile: Bachelor's or master's degree in Pharmacy, Life Sciences, Biotechnology, or a related field. Minimum 610 years of relevant experience in sterile/aseptic or injectable manufacturing. Hands-on experience in QMS practices and compliance-driven production environments. Knowledge of cGMP, regulatory audits, and process validations. Proficiency in handling process equipment such as autoclaves, DHS systems, PFS Filling Machine, Mixing Vessel, and Packing Line. Understanding of utilities such as Diesel Generators, HT Panels, Power Transformers, etc. Functional Skills Required: Strong knowledge of QMS tools (Deviation, CAPA, Change Control, etc.). Ability to review and draft GMP documentation. Equipment troubleshooting and maintenance coordination. Good understanding of production equipment and utility systems. Capability to manage and optimize manpower deployment. Competence in generating performance and compliance reports. Behavioral Skills Required: Leadership and team management. Decision-making and problem-solving. Strong communication and interpersonal skills. Time management and ability to handle pressure. Continuous improvement mindset. Proactiveness and accountability. Learn more at: https://www.biotechhealthcare.com Biotech is an Equal Opportunity Organisation promoting diversity while ensuring no discrimination on any ground, including gender, race, religion, age, sexual orientation, disability, etc.

The ideal candidate brings 1-7 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assurance, water/air monitoring, microbial ID/trending, and method validation; establish contamination control strategy and support media fills and aseptic behaviors Manage QC lab workflows: RM/PM/FG testing, HPLC/GC operations, stability studies, instrument calibration/qualification (IQ/OQ/PQ), and review of analytical reports and CoAs Additional info: Education: B.Sc./M.Sc. in Microbiology/Biotech with sterile USFDA experience Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment. Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.

Role & responsibilities Manufacturing of cell line/cell culture based AG for FG Cell culture operations, including inoculation and observatory monolayer work Compilation of all commercial batch data and BMR filling RM/PM issuance, sterilization, and monitoring of all supportive data Maintaining procell-related modules, areas, and utility fixed assets Receiving NPD from R&D and scaling up for commercialization Areas, equipment validation, and maintenance Cell bank passage history maintenance and reconciliation Preferred candidate profile Throughout knowledge of cell line/primary culture Propagation of cell line & maintenance Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Responsibilities include production operations, equipment handling, cleaning, maintenance, QA/validation support, & GMP compliance. Must follow SOPs, ensure timely activities, & reports. Male candidates only. Understand the role before applying.

Area of Responsibilities Success Indicators: - Oversee dairy processing from Milk reception, milk processing and further processing of Mozzarella Cheese, SMP, butter, ghee and aseptic flavored milk. - Controls the process of maintaining, reviewing and updating procedural documentation within the department. - Manage processing team and drive trainings, improvements and shift planning. - Ensures regulatory, quality and hygiene standards are maintained and that necessary documentation standards are in place. - Manages health & Safety compliance and assists with implementation of corrective actions. - Maintain all processing related data and report writing. - Ensure timely booking of all Production on daily basis. - Conduct reconciliations run to run to track yield. - Conduct regular team meetings to review performance of line. - Maintain proper GMP and hygiene standard within the department. - Take active participation in audit such as FSSAI, FSSC 22000, YUM Audit and ensure all compliance in place. - Product compliance - Product grading/sensory results - Product physico-chemical & microbiological test results - Health and Safety results of the department - Yield and loss results - Hygiene and quality audit compliance - External and internal audit - First time release product Activities- - Manage plant manning levels to meet production schedules and optimize resources. - Conduct daily meetings with Team Managers to communicate results, plans and issues. - Coordination of all processing activities, ensuring all HACCP & GMP techniques are applied - Daily reporting to site management team of attainment to KPI’s - Ensure timely CIPs and cleaning of all machineries and areas. - Ensure that all daily production plans optimize plant utilization and minimize wastage. - Monitor departmental training plans and needs. - Timely booking of all Production on daily basis in SAP. - Manage the recording of hazards and the progressing of corrective actions. - Coordinate health & safety and risk assessment audits. - Ensure regular Health & Safety meetings occur within the department. - Monitor daily losses and report exceptions. - Review monthly overhead budget to ensure targets are met. - Work along with quality chemist to ensure that all quality and regulatory standards are maintained. - Work with the continuous improvement team to improve areas of concern. - Work with Engineering Manager to plan & coordinate plant maintenance as per schedule. EXPERIENCE: Essential Responsibilities - Experience with atleast 5 years’ supervisory experience in Mozzarella Cheese, SMP, Butter, Ghee and aseptic flavored milk processing and packing. - Working knowledge of FSSAI, FSSC 22000, YUM FSA Audit quality standards. - Thorough knowledge and understanding of pasteurization, evaporation, drying, blending and packing. - Knowledge of international industry code & practice - Experience in operating fully automated dairy plants - SAP R3P working knowledge QUALIFICATION: Essential - Graduate in dairy technology (Bsc / MSc / B.Tech / M.Tech - Dairy Technology ) - Knowledge in Fast Moving Consumer Goods industry - Computer literacy (MS Office applications) COMPETENCIES: - Computer literate to the level of being able to develop own reporting packages and spread sheets. - Ability to lead and manage multinational work force. - Clear communication ability. - Must be dynamic self-motivated person. - Proven delivery ability. - Ability to deal with complex issues. - Ability to direct. - Ability to get things done.

If you interested, please share you CV on below details. Email : renu.kumari@adecco.com WhatsApp : 6364920532 Operator / Technician Role - Aseptic Area Manufacturing Skill - operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI Category Operator Staff / Officer Aseptic Area Manufacturing Skill operation and supervising of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification B. Pharm/M. Pharm Category Staff

Role & responsibilities Setup and Operation of Equipment : Operating aseptic filling equipment such as filling machines, capping machines, and sterilization units autoclaving in accordance with standard operating procedures (SOPs) and regulatory guidelines. Sterilization and Sanitization : Ensuring all equipment and materials used in the filling process are properly sterilized and sanitized to maintain aseptic conditions and prevent contamination. Quality Assurance : Conducting in-process checks and inspections to verify product integrity, including visual inspections, measurement checks, and sampling for microbiological testing. Documentation and Record Keeping : Maintaining accurate records of production activities, including batch records, equipment logs, and deviation reports, to ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements. Cleaning and Maintenance : Performing routine cleaning, maintenance, and calibration of equipment to ensure optimal performance and minimize downtime. Safety and Compliance : Adhering to safety protocols, including wearing appropriate personal protective equipment (PPE), and following all SOPs and regulatory guidelines to maintain a safe working environment and product integrity. Problem Solving and Troubleshooting : Identifying and resolving equipment malfunctions, process deviations, or quality issues promptly to prevent product loss and ensure consistent product quality. Team Collaboration : Collaborating with other operators, supervisors, quality control personnel, and maintenance technicians to coordinate production activities, address issues, and support continuous improvement initiatives. Training and Development : Participating in training programs to stay updated on new equipment, processes, and regulatory requirements, and continuously improving skills and knowledge related to aseptic filling operations. Continuous Improvement : Contributing to process improvement initiatives by suggesting and implementing efficiency enhancements, quality improvements, and cost-saving measures to enhance overall production effectiveness. Preferred candidate profile Candidates required with minimum Experience - 2 to 6 years Candidates required with minimum educational background - (Bsc /Diploma/ITI/B.Pharm) Perks and benefits

Hi, Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Operators 2) Technician 3) Aseptic Operator 4) Aseptic Officer Education: ITI/Diploma/Bsc/Msc/B Pharma / M Pharma Experience: 3 to 10 Years. Interested candidates please connect on below contact details. Mayuri Shah Senior Consultant (Life Sciences & Pharmaceutical) Mail id : mayuri.shah@adecco.com M-(whatsapp) 7984968546/ 9714846221 Adecco Group India

Role & responsibilities For operator Role - Aseptic Area Manufacturing Skill - operation of filling machine (vial or sealing machine) , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Job Title: Senior Nurse - Operations Theatre Company Name: Manipal Hospitals Job Description: The Senior Nurse in the Operations Theatre at Manipal Hospitals is responsible for providing high-quality nursing care to patients undergoing surgical procedures. This role involves coordinating and managing nursing activities in the operating room, ensuring a safe and efficient environment for both patients and the surgical team. The Senior Nurse will assist in the preparation and maintenance of the operating theatre, manage surgical instruments and supplies, and support the surgical team before, during, and after procedures. Key Responsibilities: - Monitor and assess patients' condition before, during, and after surgery. - Prepare patients for surgical procedures, including explaining the procedure and obtaining informed consent. - Ensure that the operating room is properly set up and stocked with necessary supplies and instruments. - Assist the surgical team during procedures by passing instruments, suctioning, and maintaining sterility. - Maintain accurate and detailed patient records related to surgeries and post-operative care. - Collaborate with other medical staff to develop and implement patient care plans. - Provide guidance and mentorship to junior nursing staff and students. - Stay updated with current trends and best practices in surgical nursing care. - Participate in quality improvement initiatives to enhance patient safety and care. Skills and Tools Required: - Advanced clinical nursing skills, particularly in perioperative care. - Strong knowledge of surgical procedures, aseptic techniques, and infection control protocols. - Excellent communication and interpersonal skills to interact with patients, families, and the healthcare team. - Critical thinking and problem-solving abilities to manage unexpected situations. - Ability to work effectively in a fast-paced and high-pressure environment. - Familiarity with electronic health records (EHR) and relevant healthcare software. - Leadership and organizational skills for managing nursing staff and operational tasks. - Current nursing registration and relevant certifications in perioperative nursing or surgical specialties. This position offers an opportunity to make a significant impact on patient care within a dynamic healthcare environment. Candidates should possess a high level of professionalism and a commitment to delivering excellence in nursing care. Roles and Responsibilities About the Role As a Senior Nurse in the Operations Theatre at Manipal Hospitals, you will play a vital role in delivering high-quality perioperative care. You will be responsible for assisting in surgical procedures, ensuring patient safety, and maintaining sterile environments. Your expertise will contribute to the overall efficiency of the operating room and the well-being of patients. About the Team You will work as part of a dedicated team of healthcare professionals, including surgeons, anesthetists, and nursing staff. The team emphasizes collaboration and communication to provide optimal patient care. You will have the opportunity to work alongside experienced colleagues and participate in continuous professional development to enhance your skills. You are Responsible for - Assisting surgeons and anesthetists during surgical procedures by preparing instruments and equipment. - Monitoring patient vital signs and ensuring their comfort throughout the surgical process. - Maintaining a sterile environment and adhering to infection control protocols. - Educating patients and their families about pre-operative and post-operative care. To succeed in this role – you should have the following - A Bachelor’s degree in Nursing and a valid nursing license. - Significant experience in the perioperative setting, preferably as a surgical nurse. - Strong knowledge of surgical procedures and aseptic techniques. - Excellent communication and teamwork skills, with the ability to remain calm under pressure.

Position Title: Shift officer- Aseptic PET Line Function: Dairy Qualifications: B.Tech in Dairy/Food Technology Experience: Minimum 2 - 7 years experience in multiple products manufacturing like UHT milk, flavored milk Juice, juice with milk blend in PET in reputed /large organization. Must have exposure in UHT plant operation & to lead a sizable team Core Competencies: In-depth knowledge of Dairy/Beverage products manufacturing plants, process technology and product development. Knowledge of food safety, regulatory requirements for food safety and hygienic engineering (OSH&R). Analytical skills in problem solving. Communication and networking. General understanding of financial analysis and relevant business drivers. The marginal contribution of the various products. An understanding of the competitor's products, how the product is distributed and the consumer's preferences.

JD- 1.Experience in the beverage/packaging industry Specialization in auto-mechanic or aseptic is a plus 2.Experience in field activities 2-3 Years & Fluent in English 3.Travel up to 90 % (Including International Locations). Required Candidate profile 4. Knowledge about (B&R, siemens, Elau & AB) Electrical or Aseptic. 5. Report to the Installation Site Manager for team site activities 6.Report after sales opportunities detected on Customer site

Title: Block Head (Parenteral Production) Job Grade: G8 Deputy General Manager Educational Qualification: B.Pharm / M.Pharm Location: Baska, Gujarat Experience: Knowledge of parenteral manufacturing operations Understanding regulatory guidelines Leadership & Team Management Skills Problem Solving & Decision-Making Proficiency in handling production documentation & compliance Min. 15 years of experience working in sterile manufacturing plant or Block In-charge experience Position Summary Responsible for plant operations from material procurement to product dispatch along with operational activities, manufacturing actions, lean management, training, regulatory compliance, cross functional coordination, new product projects, new CAPEX projects, safety and administrations. Monitoring and control of the manufacturing environment, plant hygiene, compliance to requirement of current Good Manufacturing Practice, EHS, local and international regulatory norms. To coordinate for external/regulatory GMP audits at plant and to ensure timely compliance of audit observations. Optimum utilization of man, material and machinery of pharmaceutical products and assuring adequate resource arability with focus of safety and quality first. Ensuring lean management, operation excellence, GEMBA, yield improvement and waste reduction etc. with action plan and its implementation. Responsible to review and approve the qualification related documents as URS, DE, FAT, SAT, IQ, OQ, PQ etc. To coordinate with FDD/PDD (R&D)/ MSTG for execution of trial/ exhibit/ process validation batches and trouble shooting. Implementation of effective control on budgetary provisions and cost reduction measures. Supervision of proper production planning, plan execution as per schedule and ensure that products are produced and stored according to appropriate safety, cGMP requirement. Ensuring protection of the product from contamination and maintain quality as required. Participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement.

Overall responsibility of QA & Qc activities in the plant Managing Validation, Hygiene, Micro biologist teams in plant Responsible for Implementing & Reviewing the quality mgt system Waste water quality standards Handled Global audits GMP & GHP s Required Candidate profile Having worked in Pharma, FMCG and Aseptic is an advantage Process Statistical knowledge, EOSH and TCCQS systems knowledge Assertive and Ensure plant Compliances ONLY FROM BEVERAGES BACKGROUND

Role & responsibilities 1. Follow the instruction & procedure given in Entry- Exit SOP (Standard Operating Procedure) of Grade C, decartoning area and Grade B’ area. 2. Responsible a procedure for proper functioning or behaviour in aseptic area. 3. Follow the personnel hygiene practices in factory premises. 4. Follow the GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) as per given in SOP. 5. Responsible for monitoring of temperature, relative humidity and differential pressure. 6. Responsible for monitoring of differential pressure of laminar air flow units and pass boxes. 7. Responsible for handling of material movement in production area. 8. Responsible for maintain the document as per GDP and area as per cGMP. 9. Responsible for to maintain day to day records. 10. Responsible for training to new joining chemist, workers and operators for their respective job. 11. Carrying out the line clearance before starting the operation. 12. Responsible for planning of manufacturing as per availability of RM and PM. 13. Responsible for supervision of preparation and filtration of cleaning/ disinfectant solutions and fogging solutions. 14. Responsible for supervision of equipments/ machines and utility readyness before batch manufacturing. 15.Responsible for supervision of operation and cleaning of steam sterilizer, compounding vessel and holding vessel, vial washing machine, sterilization and depyrogenation tunnel, washing and drying and wrapping of garments and pass box and laminar air flow. 16. Responsible for supervision of handling of filters, filter integrity testing apparatus, silicon tubing, decartoning area and hose pipes and cleaning and wrapping of glassware, auxiliary items and machine parts. 17. Responsible for supervision of operation of pH meter and stirrer. 18. Responsible for supervision of aseptic process stimulation, post media fill cleaning and sanitization of machine and area as per procedure. 19. Responsible for destruction of media filled vials. 20. Responsible for supervision for general area cleaning and sanitization of grade ‘C’ and ‘D’ area and fogging activity of respective area. 21. Responsible for verification of load cell. 22. Responsible for verifying the handling of waste generated in production area. 23. Responsible for non viable particle count (online and offline) monitoring. 24. Recording the operation and cleaning details in batch manufacturing record and equipment uses log book. 25. Responsible for handling of equipment like homogenizer, rota evaporator, magnetic stirrer, ultrsonicator, pH meter and fogger. 26. Follow the procedure for dispensing room and responsible for RM and PPM dispensing and additional materials issuance. 27. Responsible for all data entry for batch manufacturing process in pharmacloud system. 28. Responsible for audit preparation and execution. 29.To undergo periodic medical checkup arranged by the company. 30.Performing the task assigned by the supervisor. 31. Reporting regarding unsafe act/ unsafe condition/ accident/ incident to supervisors. Preferred candidate profile Candidate Should have Exposure of Pharma Injectable Plant. Candidate Should well familiar with Pharma Guidelines. Candidate should have good Verbal and Written Communication Willing to Relocate in Navsari, Gujarat, Willing to Work in a Shift.

Novo Nordisk Global Business Services (GBS) India Department GCM DP RoW Job Location Hyderabad Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global healthNovo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you''ll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). ! The Position As a Manufacturing Specialist (SME), you''ll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top-tier quality with our Contract Manufacturing Organizations (CMO) partners. Your key responsibilities will include: Lead cross-functional teams, ensuring seamless collaboration between Novo Nordisk as the sending Unit and Contract Manufacturing Organizations (CMOs) partners as the receiving Unit. Act as a mentor and support Contract Manufacturing Organizations (CMOs) to ensure Novo Nordisk products are manufactured to the highest quality standards. Provide training, share best practices, and review and approve validation documents to safeguard compliance. Offer oversight and support during the planning and execution of validation and qualification activities. Define, manage, and deliver on complex projects in collaboration with CMOs, Quality Assurance, and project managers. Drive problem-solving initiatives and provide scientific and technical solutions within tight project timelines. Qualifications Bachelor’s /Master’s degree in engineering. Possess 10+Years experience and relevant 5 years of manufacturing experience, especially in an international, multicultural environment. Expertise in aseptic manufacturing processes is non-negotiable. Capable of communicating naturally and effectively with stakeholders at all levels with adept at finding solutions and motivating stakeholders to achieve ambitious goals. Possessing a strong mindset, a focus on continuous improvement, and keen attention to detail. Demonstrates the ability to work independently with minimal supervision, a strong willingness to learn new skills, and the motivation and flexibility to thrive in a fast-paced, dynamic environment. About the Department GCM DP RoW Projects is dedicated to delivering life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department plays a pivotal role in improving the quality of life for patients living with diabetes and obesity. With a focus on Market Access initiatives, the team tailors projects to meet the unique requirements of each country, offering exciting growth opportunities. The department thrives on innovation and problem-solving, overcoming challenges and navigating complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Based in Hyderabad, India, you’ll join a diverse and dynamic team committed to making a difference.

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always upholding Novo Nordisk''s stringent quality standards and adhering to cGMP and regulatory requirements. Lead and manage aseptic manufacturing projects, specifically leveraging your expertise in areas like Formulation/Compounding, Filling, Washing & Sterilisation, Environmental Monitoring, or Clean Utilities. Developing and managing detailed project plans and timelines and communicating effectively with steering groups and key stakeholders. Monitoring progress and proactively securing necessary resources. Developing project risk grids and identifying mitigation strategies with both Novo Nordisk and our Contract Manufacturing Organisation (CMOs). Qualifications Bachelor’s or Master’s degree in engineering. Possess experience of 5-12Years of project management experience with a proven track record of successful project delivery in a highly regulated environment, especially internationally. Aseptic manufacturing experience is a must, and experience with Technology Transfer of biologics is a significant advantage. Professional experience balancing individual drive with effective stakeholder involvement. Proficiency in project management software (e.g., MS Project, Smartsheet, Jira, or equivalent). Demonstrated fluency in written and spoken English is essential. About the Department GCM DP RoW Projects is a dedicated team committed to providing life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department strives to make a meaningful impact on the quality of life for patients living with diabetes and obesity. Our projects are tailored to meet the unique requirements of each country, offering exciting growth opportunities. With a steadfast commitment to innovation and problem-solving, we work to overcome challenges and navigate complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Join us in making a difference.

Responsible for cleaning, sterilizing, inspecting, & packing surgical instruments; maintaining records; ensuring infection control; coordinating with OT/ICU. Requires knowledge of sterilization,attention to detail, & physical stamina.NABH guildeline.

Role & responsibilities Jr. Operator / Operator / Sr. Operator Vial washing, Depyrogenation, HPHV Steam Sterilizer, Production related activities Experience: 0 - 6 years Qualification ITI/Diploma/B.Sc/Equivalent Officer / Executive Production plan, filling activities, cGMP, SOP, Preventive maintenance, Lyophilizer, Aseptic Media fills, HPHV, Handling Filter integrities, DQ, IQ, PQ, OQ. Experience: 0 - 6 years Qualification B. Pharmacy / M. Pharmacy Asst. Manager / Manager QMS, SOPs, cGMP, DQ,IQ ,PQ, OQ Preventive Maintenance, filling activities, Training plan schedules. Experience 9-15 Years Qualification B. Pharmacy / M Pharmacy Preferred candidate profile Preferrable Injectable / Biological Production Experience

Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Vial Washing Operator 2) Filling Machine Operator 3) Aseptic Operator 4) Autoclave Education: ITI/Diploma Experience: 3 to 10 Years. Interested candidates please connect on below contact details.

Role & responsibilities For operator / Technician Role - Aseptic Area Manufacturing Skill - Operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI Category Operator Thanks & Regards Renu Kumari Senior Consultant (Life Sciences & Pharmaceutical) Email : renu.kumari@adecco.com M-(whatsapp) : 6364920532 Adecco Group India