207 Granulation Jobs

As a Plant Operator/ Technical Assistant at SEZ PLANT II, your role will involve working with granulation, compression, and Wurster coater processes. Additionally, as an Executive/Sr. Executive, you will be responsible for overseeing granulation, compression, coating, capsule filling, and E-BMR activities. Key Responsibilities: - Operate and maintain granulation, compression, and Wurster coater equipment - Execute processes efficiently to ensure high-quality production - Collaborate with team members to meet production targets - Ensure compliance with safety and quality standards - Troubleshoot any technical issues that may arise during the production process Qualifications Required: - Minimum 3 years of experience in a similar role - Proficiency in operating process equipment such as Fitter & Electrician - Strong understanding of granulation, compression, and coating processes - Knowledge of safety and quality assurance protocols In addition to the specific job roles mentioned, SEZ PLANT II focuses on maintaining high standards of quality and compliance with regulatory requirements.,

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitization and sterilization of the items to be sent into Grade-B area Destruction of the rejected & unwanted materials and recording of the same Release of vaccine from blending to filling area To follow the usage of personnel protective equipment (PPE) during handing of corrosive liquids, WFI and steam Solution preparation Operation of Filter integrity machine Perform aseptic operations in Grade B area Any other tasks assigned by the supervisor.

Role & responsibilities Hiring for OSD Formulation Site, Mohali Punjab Production Technician & Officers ( Granulation/ Compression/ Coating/ Capsule/ Packing) Quality Control Analyst (Officer/Senior Officer) Analyst Role must have exposure-HPLC with empower software, GC & Dissolution in FG/Stability Lab Preferred candidate profile Mandatory USFDA Plant Exposure Production Technician- ITI/Diploma QC Analyst- B.SC/M.SC in Chemistry Note- Sun Pharma does not seek payment of any kind from a prospective candidates for employment with Sun Pharma or authorise any agency or any individual to collect or charge any fees or charges for recruitment. Please be cautious while dealing with any recruitment agency or anyone asking you to pay money representing himself to be representing Sun Pharma

To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications: ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4-6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills: Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

Greetings from Zydus Group! We are hiring for our AHL manufacturing unit, Matoda. We are looking for Operators with relevant experience in Compression , Coating, Granulation. Interested candidates are required to send their CVs on noor.m.judge@zyduslife.com

1. Plan and execute production schedules, 2. Supervise granulation, blending, compression, and coating operations, 3. Strong knowledge of pharmaceutical manufacturing processes (API, DC granules, FDF), regulatory standards (GMP, WHO, USFDA)

Meeshos Creative Intelligence Unit is the powerhouse behind all of this. We're a vibrant mix of video wizards, visionary designers and captivating storytellersWe collaborate closely with our business teams to produce impactful creatives that don't just look good but deliver business results. You'll find our creative magic across diverse areas: Branding: Shaping our brand identity, launching sale, awareness campaigns, and unlocking new market opportunities. Performance Marketing: Driving growth across Meta, Google, and the Play Store. Integrated Channels: Crafting engaging push notifications and WhatsApp campaigns. Homepage & Category Pages: Making our app and web experience irresistible. Strategic Projects: Diving into exciting new video formats and, yes, GenAI ! Your Mission: Lead the AI-Powered Creative Revolution As our Production Head , you wont just be managing; youll be leading the charge in defining how we create and scale content. This isn't your typical production role. We're looking for someone who breathes user-first,innovative thinking and wants to explore AI and its capabilities into every step of the creative process. You'll be instrumental in captivating audiences in Indias Tier 2, 3, and 4 cities by shaping our motion and video content strategy. We need someone who can solve complex communication challenges with deeply contextual, high-performing video formats that resonate culturally and drive engagement at an unprecedented scale. This role is all about blending exceptional creative problem-solving with the ability to build and nurture a world-class team of AI-savvy video specialists. You'll be the bridge between creative, brand, growth, product, and category teams, bringing > What You'll Be Doing (and Loving!) Setting the Vision: Youll lead Meeshos motion and video content strategy across all marketing channels and in-app experiences. Think big, think relatable, think Tier 2, 3 and 4 markets! End-to-End Production: You'll oversee the entire creation pipeline for dynamic video content: from storyboarding to editing, animation, sound design, regional adaptations, and final creative delivery. AI at the Core:Youll use GenAI tools as your primary accelerators for ideation, content creation, visual refinement, and scaling production. This means embedding AI into every single step of the motion workflow. Cultural Storytelling: Develop insight-led and culturally relevant visual narratives that truly speak to the aspirations, humor, and lifestyle of Bharats next billion Motion-First Design: Build a cutting-edge, motion-first design language that seamlessly blends our brand expression with high-performing assets for Meta, Google, YouTube, Reels, and beyond. Operational Excellence: Create and own the execution playbooks and quality standards that ensure speed, consistency, and unparalleled excellence across all our motion and video formats. Creative Experimentation: Champion constant experimentation and content testing. You'll use data and insights to continually optimize storytelling, asset structures, format lengths, and regional targeting. Team Leadership & Growth: Recruit, mentor, and lead a passionate team of motion designers, editors. Empower them to deliver high-velocity content with both consistency and > Cross-Functional Impact: Collaborate closely with marketing, product, and growth teams. Youll co-own key performance indicators (KPIs) and creatively unlock massive impact through your > Stay Ahead of the Curve: Continuously monitor shoot and motion trends, platform behaviors, and regional content culture. Youll be the expert, integrating these learnings directly into our daily workstreams.

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

Execute day-to-day production activities as per production plan. Operate and monitor production equipment (Granulation, Compression, Coating, Packing, etc. based on plant). Ensure adherence to cGMP, SOPs, and regulatory guidelines during all production activities. Maintain batch manufacturing records (BMRs), logbooks, and online documentation. Coordinate with QA, QC, Maintenance, and Warehouse for smooth operations. Implement safety, quality, and housekeeping standards within the production area. Support investigations (deviations, OOS, incidents) and assist in CAPA implementation. Train new operators / apprentices on processes and equipment. Participate in qualification/validation activities of equipment and area.

Exposure in Blending Activities Exposure in Documentation Exposure in Vaccine

Candidate having minimum 3 to 5 year experience in Granulation, Compression & Coating section in pharmaceutical industry. Interested candidate can call on this mobile no-+91-78310 31890, 9816336040 Food allowance Health insurance Annual bonus Provident fund

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Permanent Basis on 21-09, Sunday Exp: 1 to 8 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Dahej No Interview & Joining Charges Required Candidate profile Interview Venue: SDP HR Solution, 611, Golden Square, Beside DMart, Near ABC Circle, Bholav, Bharuch No of Openings Officer - 30 Senior Officer - 16 Executive - 4 Assistant Manager - 4 Manager - 2

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Permanent Basis on 21-09, Sunday Exp: 1 to 8 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Dahej No Interview & Joining Charges Required Candidate profile Interview Venue: SDP HR Solution, 611, Golden Square, Beside DMart, Near ABC Circle, Bholav, Bharuch No of Openings Officer - 30 Senior Officer - 16 Executive - 4 Assistant Manager - 4 Manager - 2

Zydus Lifesciences Limited , formerly known as Cadila Healthcare Limited, is an Indian multinational pharmaceutical company headquartered in Ahmedabad, which is primarily engaged in the manufacture of generic drugs Company : Zydus Lifesciences Limited Location : Ahmedabad Experience : 2 to 8 Years Qualification : Diploma in Mechanical / Pharmacy / Chemical or relevant field JOB DESCRIPTION : 1. Granulation & Compression Operator Responsibilities : Operate granulation equipment (RMG, FBD) and compression machines (tablet press, capsule filling). Follow batch manufacturing records (BMR) and ensure compliance with cGMP and SOPs. Conduct in-process checks (weight, hardness, thickness, friability). Perform equipment cleaning, setup, and changeover. Maintain production documentation and coordinate with QA/QC for line clearance. Troubleshoot equipment issues and escalate to maintenance when needed. Handle raw materials, granules, and finished products with care and accuracy. Participate in audits, training, and continuous improvement initiatives. 2. Wurster Coating Operator Responsibilities : Operate and monitor Wurster Coating machines for tablet/capsule coating processes. Ensure uniform coating thickness and quality as per product specifications. Prepare coating solutions and manage parameters like spray rate, inlet temperature, and airflow. Perform cleaning and changeover of coating equipment as per SOP. Maintain accurate records of coating batches and process parameters. Conduct in-process checks for coating integrity, weight gain, and visual inspection. Coordinate with QA/QC for sampling and documentation. Ensure compliance with GMP, safety, and hygiene standards. General Requirements: Prior experience in OSD formulation in reputed pharma companies like Zydus, Intas, Torrent, Cadila, etc. Willingness to work in shifts . Strong understanding of GMP documentation , equipment handling, and production protocols. Good communication and teamwork skills.

Interview for SVP Formulation Plant in Bharuch on Permanent Payroll on 21-09 Experience: 2 to 6 Yrs Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch Venue: SDP HR SOLUTION 611 Golden Square Bs Dmart Bholav Bharuch Required Candidate profile Autoclave Operator Granulation Operator Manufacturing Operator Grinding Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling & Sealing Operator Lyo Operator Labelling Operator

Interview for SVP Formulation Plant in Bharuch on Permanent Payroll on 21-09 Experience: 2 to 6 Yrs Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch Venue: SDP HR SOLUTION 611 Golden Square Bs Dmart Bholav Bharuch Required Candidate profile Autoclave Operator Granulation Operator Manufacturing Operator Grinding Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling & Sealing Operator Lyo Operator Labelling Operator

Key Responsibilities: 1. Sales Strategy Development & Execution : Develop and implement regional sales strategies to achieve revenue and growth targets for pharma machinery. Identify new business opportunities and client segments to maximize market penetration. Regularly assess the competitive landscape to adjust strategies for greater success. 2. Client Relationship Management: Build and maintain strong relationships with key stakeholders, including decision-makers in pharmaceutical companies and other relevant organizations. Understand customer needs and provide solutions that align with their business goals. Resolve customer complaints and issues quickly to maintain long-term relationships. 3. Business Development & Lead Generation: Generate new leads through market research, networking, and cold calling. Organize product demonstrations and presentations for potential customers. Participate in relevant trade shows, industry conferences, and events to showcase products and services. 4. Sales Forecasting & Reporting: Prepare monthly, quarterly, and annual sales forecasts, and report regularly to senior management. Track sales metrics and KPIs to ensure targets are met. Analyze sales data to optimize sales approaches and improve performance. 5 . Cross-Functional Coordination: Coordinate with the technical team to ensure customer requirements are accurately understood and met. Collaborate with the marketing team to create sales collateral, promotional material, and campaigns that support sales activities. 6. Team Management (if applicable): Lead, guide, and motivate a small team of sales professionals (in case of Regional Manager role). Set clear performance goals, monitor progress, and provide constructive feedback. 7. Market & Product Knowledge: Keep abreast of industry trends, new product developments, and emerging technologies in pharma machinery. Maintain in-depth knowledge of the companys product portfolio and value proposition. Qualifications & Skills: Education : Bachelor’s/Master’s degree in Engineering, Business Administration, or related fields (preferably in a technical discipline). Experience: Manager Sales: Minimum 5-6 years of experience in sales in the pharma machinery or related industry. Industry Knowledge : Strong understanding of the pharmaceutical manufacturing sector, machinery, and equipment. Skills: Proven track record in sales, with a focus on B2B sales, especially in the industrial or pharma sector. Strong negotiation, communication, and interpersonal skills. Ability to understand technical products and communicate them effectively to non-technical stakeholders. Proficiency in CRM software and MS Office suite. Leadership : Experience managing sales teams and driving performance. Travel: Willingness to travel frequently within the region for client visits and business development. Compensation & Benefits:

Role & responsibilities Perform granulation process operations as per SOP and batch requirements. Handle RMG (Rapid Mixer Granulator) machine for mixing and wet granulation. Operate and monitor FBD (Fluidized Bed Dryer) machine for drying granules. Ensure cleaning and maintenance of equipment (RMG, FBD, and associated accessories) as per cGMP and safety guidelines. Record operational parameters, cleaning logs, and maintain proper documentation. Follow SOPs, GMP, and safety protocols during operations. Coordinate with production and quality teams for smooth batch execution. Preferred candidate profile Experience: 14 years in Pharma Production (Granulation). Hands-on experience in RMG & FBD operations . Knowledge of cGMP guidelines, equipment cleaning, and documentation . Ability to work in shifts and follow strict compliance requirements.

Roles and Responsibilities Operate and maintain OSD (Oral Solid Dose) manufacturing equipment, including compression machines, granulation lines, dispensing systems, and packaging machinery. Ensure compliance with cGMP guidelines during production operations to ensure product quality and regulatory compliance. Collaborate with cross-functional teams to resolve issues related to equipment maintenance, process optimization, and productivity improvement. Conduct routine inspections of equipment and facilities to identify potential problems before they become major issues. Participate in training programs to enhance knowledge of new technologies and procedures.

Job Title: HVAC Executive (MNC) Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: Minimum 5 Years Salary: Up to 7 LPA 9796871050 Job Description: We are looking for an experienced HVAC Executive to join our team in the pharmaceutical industry. The ideal candidate should have hands-on experience in HVAC system validation, operation, and maintenance along with a strong understanding of Quality Management Systems (QMS). Key Responsibilities: Ensure smooth operation, preventive maintenance, and breakdown maintenance of HVAC systems. Execute and monitor validation activities for HVAC systems as per regulatory guidelines. Maintain proper documentation in compliance with cGMP, regulatory, and company requirements. Prepare and review SOPs related to HVAC operations and maintenance. Coordinate with cross-functional teams to ensure uninterrupted facility operations. Support quality audits and inspections by providing HVAC-related documents and compliance reports. Monitor and control environmental conditions (temperature, humidity, differential pressure, etc.). Implement energy efficiency and cost optimization measures in HVAC operations. Ensure adherence to QMS standards including deviation handling, CAPA, and change control. Desired Candidate Profile: B.Tech in Mechanical related engineering discipline. Minimum 5 years of experience in HVAC operations and maintenance in a pharmaceutical manufacturing environment. Strong knowledge of HVAC validation, QMS practices, and regulatory compliance. Ability to troubleshoot HVAC equipment and systems. Excellent documentation, analytical, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Facility Management & Administration Executive / Sr. Executive Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (in Pharma Industry) Salary: Up to 7 LPA (Negotiable) 9796871050 Job Description: We are looking for an experienced Facility Management & Administration Executive/Sr. Executive with strong exposure to pharmaceutical industry facility operations. The candidate will be responsible for managing housekeeping, pest control, laundry, security, canteen services, contract labour management, and ensuring compliance with QMS and cGMP requirements. Key Responsibilities: Oversee facility management services including housekeeping, pest control, laundry, security, and canteen operations. Manage and monitor contract labour workforce ensuring compliance with labour laws and company policies. Implement and monitor QMS practices in facility operations with adherence to pharma industry standards. Coordinate with internal departments to ensure seamless support for production and administrative functions. Ensure compliance with cGMP, safety standards, and regulatory requirements in all facility-related operations. Prepare and maintain records, SOPs, and documentation related to facility management. Handle vendor management, service contracts, and negotiations. Support audits and inspections by providing facility and administration compliance documents. Drive continuous improvement initiatives in facility management and cost optimization. Desired Candidate Profile: Graduate / Diploma / MBA preferred with relevant specialization. 5+ years of experience in facility management & administration in a pharmaceutical industry. Strong knowledge of QMS, cGMP, and pharma compliance requirements. Experience in managing contract labour and third-party vendors. Excellent organizational, leadership, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: QMS Production Executive Industry: Pharmaceutical (OSD Plant) Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (OSD Pharma Plant) Salary: Around 6 LPA 9796871050 Job Description: We are seeking an experienced QMS Production Executive to join our Oral Solid Dosage (OSD) pharmaceutical manufacturing plant. The ideal candidate should have in-depth knowledge of Quality Management Systems (QMS) and hands-on experience in managing production activities in compliance with cGMP and regulatory requirements. Key Responsibilities: Ensure compliance with QMS requirements in production operations. Manage and maintain production documentation including BMR, SOPs, deviations, and change controls. Monitor and review CAPA, deviations, OOS, and audit observations related to production. Coordinate with QA, QC, and regulatory teams to ensure smooth operations. Support qualification and validation activities for equipment and processes. Implement best practices to ensure adherence to GMP, safety, and regulatory guidelines. Train production staff on QMS and compliance requirements. Support internal and external audits and regulatory inspections. Desired Candidate Profile: B.Pharm / M.Pharm or equivalent qualification. 5+ years of experience in OSD pharma production with strong QMS exposure. Strong understanding of cGMP, QMS, and regulatory compliance. Good documentation, analytical, and problem-solving skills. Ability to work independently and lead a team effectively. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Production Supervisor Industry: Pharma (MNC) Location: Bari Brahmana, Jammu Qualification: M.Sc. Chemistry / B.Pharm Experience: 3 to 6 years Salary: Up to 5 LPA Contact: 9796871050 Job Responsibilities Supervise day-to-day production activities in OSD, Capsule, and Tablet manufacturing plant . Ensure adherence to cGMP, SOPs, and regulatory guidelines during production. Monitor production processes to meet daily, weekly, and monthly targets. Maintain accurate documentation and batch records as per pharma compliance. Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations. Implement continuous improvement practices to enhance productivity and reduce wastage. Ensure proper training and guidance to operators and shop floor staff. Maintain strict compliance with EHS (Environment, Health & Safety) standards. Key Skills & Competencies Strong knowledge of pharma production processes (OSD, Tablets, Capsules). Familiarity with regulatory audits (USFDA, MHRA, WHO, etc.) . Excellent leadership, team handling, and communication skills. Ability to handle deviations, change control, and CAPA. Good problem-solving and decision-making abilities. Desired Candidate Profile 36 years of relevant experience in a reputed Pharmaceutical OSD plant . Hands-on experience in tablet/capsule manufacturing processes. Strong understanding of GMP compliance and documentation practices . Candidates with exposure to multinational pharma setups will be preferred. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: OSD Packaging Supervisor Industry: Pharmaceutical Qualification: B. Pharma Location: Bari Brahmana (Jammu) Experience Required: 2 to 5 Years Salary: Up to 5 LPA (Negotiable) 9796871050 Job Description: We are seeking a skilled and detail-oriented OSD Packaging Supervisor to join our pharmaceutical team. The candidate should have experience in Oral Solid Dosage (OSD) packaging operations, ensuring compliance with GMP standards and regulatory requirements. Key Responsibilities: Supervise daily packaging activities of OSD products as per production schedules. Ensure compliance with cGMP, SOPs, and regulatory guidelines during all packaging operations. Monitor line clearance, in-process checks, and reconciliation of packaging material. Handle and train packaging staff to maintain efficiency and quality standards. Maintain documentation including batch packaging records, deviation reports, and logbooks. Coordinate with quality assurance and production teams for smooth operations. Implement safety measures and maintain housekeeping standards in packaging areas. Support regulatory audits and inspections with packaging-related documentation. Desired Candidate Profile: B. Pharma degree is mandatory. 2 to 5 years of experience in OSD packaging operations in a pharma manufacturing setup. Knowledge of blister, strip, and bottle packaging lines. Familiarity with cGMP, QMS, and documentation practices. Strong leadership, communication, and team management skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Granulation Operator Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Qualification: ITI / Diploma Experience Required: 3 to 6 Years Salary: Up to 4 LPA 9796871050 Job Description: We are looking for an experienced Granulation Operator to join our pharmaceutical manufacturing unit. The candidate will be responsible for operating and monitoring granulation equipment and processes while ensuring compliance with cGMP and safety standards. Key Responsibilities: Operate and monitor granulation machines (RMG, FBD, multi-mill, sifter, etc.). Perform granulation activities as per SOPs, BMR, and regulatory requirements. Ensure proper cleaning, calibration, and maintenance of equipment. Monitor critical process parameters (temperature, pressure, RPM, etc.). Maintain accurate documentation of production processes and equipment logs. Support in process validation and qualification activities. Adhere to safety protocols, GMP standards, and quality guidelines. Coordinate with production, maintenance, and QA teams for smooth operations. Desired Candidate Profile: ITI / Diploma in relevant discipline. 3 to 6 years of experience as a Granulation Operator in the pharmaceutical industry. Hands-on experience in handling RMG, FBD, sifter, multi-mill, and related granulation equipment. Knowledge of cGMP, documentation, and safety compliance. Team player with good communication and problem-solving skills. https://www.linkedin.com/in/satnam-singh-37b9b518/

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Manufacturing Engineering MES Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 5 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-A full-time 15 years of education is required.-This position is based out of multiple locations. Qualification 15 years full time education

About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : Manufacturing Engineering MES Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 7.5 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-A full-time 15 years of education is required.-This position is based out of multiple locations. Qualification 15 years full time education

About The Role Project Role : Custom Software Engineer Project Role Description : Develop custom software solutions to design, code, and enhance components across systems or applications. Use modern frameworks and agile practices to deliver scalable, high-performing solutions tailored to specific business needs. Must have skills : Manufacturing Engineering MES, communication skills verbal and written, microsoft excel Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 3 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-A full-time 15 years of education is required.-This position is based out of multiple locations. Qualification 15 years full time education

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Manufacturing Engineering MES, communication skills verbal and written, microsoft excel Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficient recipe authoring and seamless integration with automation and enterprise systems while adhering to regulatory and industry standards. Roles & Responsibilities:-Develop MES recipes using Rockwell FTPS, ensuring compliance with industry best practices.-Design and implement building blocks for reusable recipe structures.-Work closely with process engineers and manufacturing teams to map end-to-end pharmaceutical processes, with a focus on biologics.-Ensure compliance with pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Participate in the full MES lifecycle, from design and validation to deployment and support.-Perform recipe testing, troubleshooting, and validation in alignment with SDLC (Software Development Life Cycle) methodologies.-Collaborate with DCS teams to ensure seamless MES-DCS integration for automated manufacturing.-Support and maintain MES systems in a validated state, ensuring high availability and performance.-Provide technical expertise in MES implementation and contribute to continuous improvements in manufacturing processes.Must-Have Skills: -MES experience in life sciences manufacturing, specifically with Rockwell FTPS.-Hands-on experience in MES-DCS integration for process automation.-Knowledge of ERP and Data Historian integration with MES.-Hands-on experience in recipe authoring, building block development, and validation.-Strong understanding of pharmaceutical manufacturing, especially biologics. Professional & Technical Skills: -Knowledge of SDLC and pharmaceutical regulations (GMP, GxP, 21 CFR Part 11).-Experience in executing at least one full MES lifecycle project with demonstrated results.-Good communication skills to collaborate with cross-functional teams. Additional Information:-Minimum 5 years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-A full-time 15 years of education is required.-This position is based out of multiple locations. Qualification 15 years full time education

Job Description Department: Production Designation: Jr. Officer - Production (E0) Working Section: Granulation / Compression / Coating Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR. Handling and movement of raw material, bulk, semi-finished and finished goods. Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP. Up-keeping area and machines as per GMP requirements. To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head. Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas. Doing operations as per the SOPs and BMR with online recording in respective documents as applicable. To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department. Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable. To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes. Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield. Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP. Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards. To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP. Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens. To ensure the audit compliance. Trouble-shooting: To attend the problems of machine and process as and when necessary. Any other assignment allocated by production Head. To attend required cGMP/ On Job /Functional training activities as per planner. Work Experience Minimum 3 years, maximum 5 years Education Diploma Vocational Competencies Customer Centricity Developing Talent Collaboration Strategic Agility Process Excellence Stakeholder Management Innovation & Creativity Result Orientation