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63 Granulation Jobs - Page 3

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2 - 6 years

2 - 6 Lacs

Srikakulam, Vizianagaram

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Role & responsibilities * Candidate should have minimum 3 years of experience in Production - OSD Formulation handling Granulation / Blending / Compression / Coating / Packing etc. * Should have machines operating experience & trouble shooting experience. * Should have BMR / BPR Preparation and online documentation experience. * Should be from USFDA approved plant only. Perks and benefits Best in the industry.

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8 - 12 years

10 - 15 Lacs

Ahmedabad, Mumbai (All Areas)

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International Sales & Marketing /pharma process Granulation machines & Capital equipment's technical knowledge & experience is must require, The job involves to consistently meet sales and booking targets as per budget for all Kevin products. Required Candidate profile Experience of Granulation process, Pharma Machinery, Ability to build relation with clients Good communication skill Note : Please do not apply who has No experience of International Sales markets. Perks and benefits Best in the Industry, Well defined Travel policy.

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6 - 10 years

4 - 9 Lacs

Bengaluru

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Job Title: Production Supervisor 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 companys 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 Core Purpose of the Role: Should have expertise in granulation, compression, and coating area is mandatory. The candidate should have 5 to 9 years of experience in any pharmaceutical organization and the qualification should be Bachelor or post-graduate in pharmacy. The handling of machine setup, troubleshooting, operation, change over, and cleaning of manufacturing equipments like FBP, RMG, Roller Compacter, Fluid bed Wurster granulator/coater, tablet compression and tablet coating machine are the key requirements. Should handle the IQQC instruments like Halogen moisture analyser, Tap density apparatus, sieve shaker, Hardness tester etc. Should have good knowledge of data integrity concept (ALCOA+), GDP and cGMP norms. Should have good communication skills. He should have experience of audit handling. Should have a good knowledge of housekeeping, area maintaining as per client visit, internal and external audits. Role Accountabilities: The person will be accountable for monitoring of Production activity, the primary role and responsibility will be closely involvement in all manufacturing activities, area maintaining as per audit requirement. Also, will be involved in internal and external client visits and audits. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: 5 to 9 years Skills and Capabilities: Should expertise in granulation, compression, and coating area is mandatory The handling of machine setup, troubleshooting, operation, change over, and cleaning of manufacturing equipment’s like FBP, RMG, Roller Compacter, Fluid bed Wurster granulator/coater, tablet compression and tablet coating machine are the key requirements. Should handle the IQQC instruments like Halogen moisture analyser, Tap density apparatus, sieve shaker, Hardness tester etc. Education: Qualification should be Bachelor or post-graduate in pharmacy Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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12 - 17 years

14 - 19 Lacs

Pune

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Project Role : Operations Engineer Project Role Description : Support the operations and/or manage delivery for production systems and services based on operational requirements and service agreement. Must have skills : Rockwell Automation FactoryTalk PharmaSuite Good to have skills : NA Minimum 12 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 10+ years of experience in MES recipe design and deployment in pharmaceutical manufacturing.-This position is based in Hyderabad, Pune, Chennai, Bangalore.-A full-time 15 years of education is required. Qualifications 15 years full time education

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2 - 7 years

2 - 7 Lacs

Ahmedabad

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Unison Pharmaceuticals is urgently seeking talented Production Supervisors for our OSD Production team. Apply now to become a part of our team!! Experience: 2-6 years Job Role : 1) Compression Supervisor 2) Granulation Supervisor Designation: Officer / Sr. Officer / Executive Qualification: B.Pharma/M.sc Location: Moraiya, Ahmedabad. No. of Openings : 3 Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career. Regards HR department

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1 - 6 years

3 - 7 Lacs

North District

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Roles and Responsibilities Operate production equipment such as autoclaves, blister packers, bottling machines, capsule fillers, granulators, lyo (lyophilization) machines, ointment makers, osd machines (osd-general & osd-beta), vial washers & tunnel dryers. Ensure quality control measures are in place to maintain high-quality products. Collaborate with team members to achieve production targets efficiently. Maintain accurate records of production processes and results. Participate in continuous improvement initiatives to enhance productivity.

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9 - 14 years

8 - 14 Lacs

Dahej

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Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have in depth knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 8 to 15 Years

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3 - 8 years

2 - 7 Lacs

Dahej

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Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

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2 - 6 years

3 - 5 Lacs

Bengaluru

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*Should have knowledge on SSR, BLR types of reactors, traydryers *Should have exposure in cGMP, Data integrity, Documentation, Safety aspects. *Should have knowledge of Chemical reactions, Pharma area, milling operations *Should have Knowledge of Deviation, Change Control, CAPA *Should have knowledge of reviewing of SOP, BMR, ECR, GMP documents/records *Experience in handling steam/continuous/batch distillation *Should have hands on experience in filters, reactors

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1 - 3 years

2 - 4 Lacs

Ahmedabad

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Res 4 operating machinery to produce pharmaceutical granules & ensure the entire process adheres to strict Qlty Stds. & GMP guidelines, while maintaining accurate documentation throughout production runs. Required Candidate profile Diploma with 1-3 Yrs of Exp. & with prior knowledge of granulation & packaging processes. Familiarity with GMP guidelines. Ability to operate and troubleshoot production equipment.

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2 - 5 years

2 - 4 Lacs

Bengaluru

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A Production Granulation, Compression, and Coating Machine Operator job involves operating and maintaining equipment used in pharmaceutical manufacturing, ensuring product quality and adherence to GMP standards, and performing tasks like granulation, compression, and coating of tablets .

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7 - 12 years

6 - 7 Lacs

Pune

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Role & responsibilities Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, filling, and packing for oral dosage products. 5. SOPs and Documentation Prepare, update, and maintain Standard Operating Procedures (SOPs), BMR, and BPR documents. 6. Document Maintenance Ensure proper maintenance of documents, including BMR, BPR, cleaning records, calibration logs, environmental records, and equipment usage logbooks. 7. Manpower Allocation Allocate and manage manpower for the effective utilization of resources. 8. Production and Packing Oversight Oversee and manage the overall manufacturing and packing activities in the oral department. 9. Compliance with cGMP & GDP Monitor and implement Current Good Manufacturing Practices (cGMP) and Good Distribution Practices (GDP) within the department. 10. Quality Management System: Handle the Quality Management System (QMS), including initiating, investigating, and completing change control, deviations, and incidents. 11. Equipment & Area Qualification: Monitor and review equipment and area qualification activities and ensure timely reporting. 12. Validation Activities Coordinate with QA and QC departments for product process validation and cleaning validation activities. 13. Production Target Achievement Ensure daily and monthly production output targets are achieved. 14. Cross-Department Coordination Facilitate coordination between Quality Assurance, Quality Control, Warehouse, and Engineering departments. 15. Material Availability Check Ensure availability of required raw materials (RM) and packaging materials (PM) as per the production plan and schedule. 16. Training & Development Conduct training programs on SOPs, GMP, technical procedures, and identify training needs for department personnel. 17. BMR/BPR Handover to QA Ensure completed BMR and BPR are handed over to the QA department before dispatch activities. Required Candidate profile: 1. 07-10 years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet functions, ERP

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3 - 7 years

3 - 5 Lacs

Jammu

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Responsible for handling production packing lines Responsible for cGMP during production activity Responsible for In-Process analysis in Shifts (as per the instruction mentioned in BMR & BPR) Ensure training, master batch records, SOPs and other documents are current and compliant under cGMP Handing Manpower Responsible for daily Production activities as per production planning

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