399 Scale Up Jobs - Page 7

Overview Leading seasoning development across multiple snack brands and products for the PepsiCo India region. The role includes flavor ideation, seasoning development or reformulation, ecosystem partnerships with flavor and ingredient houses, seasoning scale up and seasoning qualification. Responsibilities Lead innovations and seasoning reformulation to drive human sustainability, Productivity, Competitive Advantage for brand Kurkure and Premium Support Chef and culinary engagements to build a future pipeline Collaborate/Partner with Internal (PD, Marketing, Consumer insights, Sensory and consumer product insights, Quality etc.) and external stakeholders (Seasoning suppliers) to leverage th...

Key Responsibilities: Handle end to end scale up activities from Lab to Pilot to Commercial Scale . Absorb the process from the PELAB / R & D and study the same and come out with queries considering the plant constraints and ask to modify the same if not feasible in the Plant. To observe the lab demo batches in PE Lab / R & D and identify Critical requirements of the process and provide the same. To select the equipment's for scale up & discuss with R & D and Production and finalize it. To act as a tool between Production, QC, QA with R & D / PELAB to absorb the technology from Lab to Plant. To observe the initial scale up batches critically & debottleneck the problems faced in the Plant. To...

Job Title: Dy Manager Technology Transfer Location : Mumbai Location Industry: Pharma Industry Experience: Minimum 2 years . Division: API Key Role & Responsibilities: Able to scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale Coordination with R&D team for generating negative study data, concluding to optimize process parameters Observe R&D demo batches & preparation of demo batches report Identify & propose ideas/ technology to improve process efficiency, effective utilization for unit process & operations Preparation of BFD, PFD, P&ID, mass balance, energy balance sheets Skills: Technology Transfer, Process, Scale-up, optimization, validation, PFD, P&ID, BFD, troubl...

Hiring for Research Scientist for a leading Pharma mnc at Pune. ADC's Role & responsibilities Job Description He will be involved in setting up the lab at R&D for Antibody Drug Conjugates (ADCs) molecule development. Also he should have experty in know-how for ADC molecule development. The candidate will play key role in designing, synthesizing and characterizing ADCs. He should have knowledge of bioconjugation chemistry,antibody engineering & analytical techniques. He will be involved in the decision of the capex requirements and upgrade in house technology platform to next level in view future demand. He should have through knowledge of optimization of conjugation processes for scalability...

Hiring for Principal Scientist for a leading Pharma MNC at Pune. Role & responsibilities Reporting to : Associate Director Job Summary : To develop synthesis processes of highly potent and/or cytotoxic ADC drug-linkers and transfer processes to internal/external clients and collaborate with manufacturing teams to deliver robust chemical processes that are suitable for commercial-scale manufacturing, while ensuring safety and regulatory compliance. Key Responsibilities: 1. Detailed technical evaluation of project enquiries received from the customers/ BD team. 2. Literature search, scouting the appropriate routes, and Drug-linker process optimization. 3. Execution of Bioconjugation Chemistry ...

Job Overview: The PDL Scientist - Injectable will be responsible for the development, optimization, and scale-up of sterile injectable formulations and manufacturing processes. The role demands expertise in injectable formulation science, process engineering, and compliance with regulatory and quality standards. Role & responsibilities Formulation Development: Design and optimize sterile injectable formulations, including solutions, emulsions, and suspensions. Perform compatibility and stability studies of active pharmaceutical ingredients (APIs) with excipients. Process Optimization: Develop robust, scalable manufacturing processes for injectable formulations. Define and optimize critical p...

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.

Lead end-to-end tech transfer of OSD products from R&D to commercial manufacturing sites, conduct scale-up and process validation activities, and provide technical support during regulatory audits and inspections.

Role & responsibilities 1. Capacity Planning of New / Existing Products 2. Solvent Recovery improvements 3. Process monitoring for yield improvement & failure investigation. 4. Process monitoring, process data collection, trend data preparation and discussion with concern department. 5. New product technology absorption 6. Trouble Shooting of Equipments & Processes 7. Utility calculation for cost reduction & Energy Conservation. 8. Plant Equipment modification as per Process requirement. 9. PFD, P&ID & Plant Layout Preparation 10. Material & Energy balance calculations 11. Equipment specification data sheet preparation, Techno-commercial preparation for procurement. 12. Equipment sizing, sel...

Vibonum Technologies Pvt Ltd (Althera Groups) is hiring Assistant or Deputy Manager - Technology Transfer Executive for its OSD Pharma manufaturing plant at Nanjangud, Mysore. Role & responsibilities Review of Technology data package and preparation of Gap analysis document. Preparation of technology transfer protocol and report. Co-ordination with FD for smooth Tech Transfer. Monitoring of validation batches at production site. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. Review of MPCR and protocol. Planning for Execution of Process design, Process qualification batch. Coordination with Product...

Roles and Responsibilities Team lead for upstream for day to day planning and co ordination Develop processes for recombinant DNA technology, fermentation techniques, and product intermediate processing. Design and execute experiments to optimize process parameters for scale up and commercial production. Collaborate with cross-functional teams to transfer technologies from lab to pilot plant and manufacturing scale. Troubleshoot issues related to process development, optimization, and operation.

Responsible for R&D functions, Process development, scale up, Technology Transfer, Trouble shooting, Lab experiments, Documentation,Products Literature search, Preparation of samples, Compliance of EHS/ISO standards etc. in Speciality Chemical plant Required Candidate profile M.Sc. with 10 to12 yrs relevant exp in speciality chemical mfg industry. Sound exp of handling lab instruments like HPLC, GC, KF, IR, UV, Spectrometer, Analyser, Auto Titrator,, Viscometer etc is must Perks and benefits Negotiable

Role & responsibilities To observe lab experiments during lab demonstration at optimization stage and suggest Negative experiment based on plant equipment and feasibility. Preparation of process summary, volume calculation, Mass balance, utility load, effluent load and costing. To identify and propose new ideas & technology to improve process efficiency, smooth unit operation/unit processes and effective utilization of resources To identify recovery and reuse of solvents. Ensure right equipment selection as per process requirement. Suggest required modification in equipment as per process requirement. Support the external job work activity to achieve desired yield & quality. Coordinate with ...

JD for External Manufacturing - Process Engineering Role & responsibilities: Identify 3rd parties for execution of Scaleup and manufacturing projects Identify 3rd parties with different capabilities Facility visit and Preliminary facility assessment report covering all the capabilities To co- ordinate with safety and quality team for audit and approval To co -ordinate between 3rd party and internal legal team to finalize CDA SWOT analysis of 3rd party Statutory and Legal compliance of 3rd party - confirmation from SCM to be co ordinated Collection of last 3 years audited finance report and to share with finance team to understand the financial stability of the organization To Co-ordinate wit...

Roles and Responsibilities Lead process development activities for API manufacturing processes, focusing on scale up and technology transfer. Develop and implement new technologies to enhance capacity and improve efficiency in existing processes. Collaborate with cross-functional teams to identify areas for improvement and optimize processing conditions. Ensure compliance with regulatory requirements during all stages of product development. Provide technical support to production teams to resolve issues related to process operations. Desired Candidate Profile 3-8 years of experience in pharmaceutical industry, preferably in hormonal manufacturing or similar field. B.Tech/B.E. degree in Chem...

Executive for Micro R&D 1 Post based in Amritsar. The ideal candidate brings 6 - 8 yrs exp. 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...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 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 improv...

The ideal candidate brings 10- 15 yrs exp 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 ...

Role & responsibilities To observe lab experiments during lab demonstration at optimization stage and suggest Negative experiment based on plant equipment and feasibility. Preparation of process summary, volume calculation, Mass balance, utility load, effluent load and costing. To identify and propose new ideas & technology to improve process efficiency, smooth unit operation/unit processes and effective utilization of resources To identify recovery and reuse of solvents. Ensure right equipment selection as per process requirement. Suggest required modification in equipment as per process requirement. Support the external job work activity to achieve desired yield & quality. Coordinate with ...

1. API synthetic process tech transfer to plant and scale-up at plant. 2. BMR and scale-up documents preparation. 3. Process Validation 4. Plant batch trouble shooting 5. Production of API at plant. Required Candidate profile 1. Knowledge of process development and tech transfer 2. API plant working experience 3. Working experience in pharma company with good production knowledge. 4. Knowledge of GMP

Job Summary We are seeking a dynamic Formulation Scientist in BRaIN for designing and development of formulation, process, and ensure seamless end to end product development. Roles & Responsibilities You will be responsible for the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible to co-ordinate closely with analytical team to devise effectiveProof of Concept (POC). You will be responsible to support in scale-up to pilot/plant scales for OSD Products. You will be responsible for performing pre-formulation studies for material char...

This role involves managing flying activities related to pilot pulling operations, ensuring adherence to QHSE standards during both charged and uncharged conditions The primary responsibilities include executing flying tasks for pilot pulling work, operating the TX system and ground equipment, and maintaining effective communication with stakeholders The job requires ensuring compliance with safety standards, including PPE and safe work practices at the worksite, and documenting site-related procedures during various work condition .Applicants should hold a DGCA RPAS Licence, have experience with medium-sized RPAS flying, possess strong communication and multitasking skills, and be adaptable...

Role & responsibilities Plan and execute pilot plant operations . Handle pilot-scale equipment. Support process optimization to improve yield, purity, cycle time, and cost. Execute and monitor technology transfer from R&D to pilot plant and production. Identify and troubleshoot process deviations and suggest corrective actions. Maintain BMRs, logbooks, and process documentation in line with GMP and regulatory requirements. Ensure equipment readiness, cleaning validation, and calibration compliance. Coordinate with cross-functional teams (R&D, QA, QC, Production, EHS) for smooth project execution. Ensure adherence to safety, health, and environmental practices at all times. Preferred candidat...

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. (OSD/Oral Solution -Exp) We have opening for Formulation R&D Department. Position : Executive / Sr.Executive Experience: 4 - 8 Yrs. Job Location: Pashamylaram - Patancheruv (Telangana State) Salary : As Per Company Norms Qualification: M .Pharm Job Description: 1) Candidate must have experience in handling oral dosage forms for US and EU markets 2) Candidate must have knowledge in developing oral solid dosage forms and liquid oral dosage forms/Oral Solution Exp. 3) Must have hands-on experience in Scale-up Batches, Exhibit Batches and DOE Experiments. 4) Must have experience in Development related documentation and PDR ...

Hello Applicants Hiring for Process Engineer for the leading chemical company at Gujarat location Designation: Process Engineer Experience: 3+ Years in process engineering within EPC, oil & gas, chemical, or related industries Education: BE chemical Location: Ahmedabad Role & responsibilities : Process Engineering & Design Carry out basic engineering: process flow diagrams (PFDs), heat & material balances, equipment sizing. Perform detailed engineering: equipment datasheets, specifications, operating philosophies, and line sizing. Thermal Design & Equipment Sizing Conduct thermal design, rating, and optimization of heat exchangers using HTRI software. Project Execution Codes, Standards, and ...