406 Scale Up Jobs - Page 3

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...

Summary The primary responsibility of this position is to advance fundamental understanding and execution of the scale-up and alignment processes in support of Axalta growth and lean initiatives. This position also has responsibility to develop or improve coatings process technologies and formulations. The focus will be on paint, coatings and finished product scale-up, manufacturing support, and overall process improvement. This includes the use of various measurement techniques to quantify paint properties and understanding the relationship between key product attributes and critical process factors from laboratory to commercial scale. Job Responsibilities Design and perform experiments to ...

Role & responsibilities Prepare and implement MPRs / SOPs for shop floor operations. Process optimization and capacity debottlenecking using mass/energy balances. Lead continuous improvement in yield, safety, quality, and waste reduction. Commission new products / projects: prepare BFD/PFD/P&ID/MPR/SOPs and DCS updates. Act as a process expert and trainer for production staff. Analyze utility and raw material variances; prepare management reports. Coordinate with Engineering for preventive maintenance. Investigate incidents and support operations troubleshooting. Perform additional duties assigned by the HOD. Preferred candidate profile Bachelor's / Masters in Chemical Engineering. In-depth ...

Role & responsibilities Develop PFDs, P&IDs, mass & energy balances. Optimize process parameters and reduce cycle time. Select and size process equipment (Reactors, Heat Exchangers, Filters, etc.) Support commissioning, risk assessments, and DCS changes. Prepare SOPs/MPRs and support troubleshooting. Drive process improvements while ensuring HSE & quality compliance. Perform additional duties assigned by the HOD. Preferred candidate profile Bachelor's / Masters in Chemical Engineering. In-depth understanding of chemical/non-chemical hazards, BEP, and basic engineering. Strong HSE & Quality systems knowledge. Skilled in DCS, automation, multistage synthesis, and large-scale chemical productio...

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. (OSD / Injectable - 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/Injectable Exp. 3) Must have hands-on experience in Scale-up Batches, Exhibit Batches and DOE Experiments. 4) Must have experience in Development related documentati...

Job Overview: The Product Development Leader (PDL) for Oral Solid Dosage (OSD) will play a pivotal role in leading the development of oral solid dosage forms such as tablets and capsules from early formulation stages through to commercialization. This position requires strong leadership skills in overseeing product development strategies, managing cross-functional teams, ensuring timely project execution, and maintaining compliance with regulatory standards. The PDL will work closely with formulation development, analytical services, regulatory affairs, and manufacturing departments to deliver high-quality pharmaceutical products. Roles & Responsibilities: Formulation Development and Optimiz...

Authorize to prepare and review the following documents: a. Trial Batch /Development Batch Manufacturing Record. b. Trial Batch / Scale up batch protocol & report. c. All other documents (If any) from R&D and other locations 2. Responsible for monitoring of Trial / Development / Scale up / Exhibit batches to be executed in manufacturing area. 3. Responsible to coordinate with CFT members for preparation of production plan related to Trial/Development/Scale-Up/Exhibit batches. 4. Responsible to maintain the area with GMP compliance. 5. Responsible for handling of new products from R&D and other locations 6. Responsible for handling of technical issues/OOS/Deviation investigation related to on...

New Chemical Entity- Design & Development (Research & Development) 1. Design & Discover NCE molecules a. Literature search and design route of synthesis b. To help in designing patentable structures of pharmacophore (prodrug design) c. IPR clearance d. Design routes of synthesis e. Synthesis of NCE’s molecules to generate library 2. Synthesis process development and validation a. Development of non-infringing rout of synthesis for lead compound b. Feasibility study c. To finalize the route of synthesis. d. Experiment design according to final route of synthesis e. Development and optimization of synthesis process f. Process Validation 3. Interpretation of analytical data (HPLC, GC, SOR, etc)...

Title: Deputy Mgr / Mgr / Sr Mgr - Technology Transfer (Process Engg) Level : Deputy Manager / Manager / Sr Manager Qualification: BE / B.Tech in Chemical Engg (Mandatory) In Pharma / API Industry / Crop Sciences / Speciality Chemicals This opening is for those working presently at R&D Centres only. Those associated with Mfg Plants doing Technology Absorption are not eligible. Experience: Minimum 10 years to 20 years. Team : 3 - 4 Those working without a team below are in-eligible. Working : Alternate Saturday off. We need Chemical Engineers working at R&D Centres in Process Engg / Technology Transfer function and taking care of Technology Transfer. Industry: You should be working in Process...

Evaluating routes within the laboratory with guidance synthetic methods with guidance Improving understanding of the chemical reactions that occur during the processes carried out within the lab. Required Candidate profile Process Development/Process Chemistry experience is essential, Having an in depth understanding of reaction mechanisms and basic chemical reaction principles.

Role & responsibilities Cell Culture & Production Support: Perform aseptic handling and maintenance of cell cultures (e.g., Vero, BHK or other cell lines) in adherent and/or suspension formats. Prepare and sterilize culture media, buffers, and reagents as per batch requirements and SOPs. Monitor and record cell growth parameters, viability, and morphology. Scale-up cell cultures for downstream processing or viral seed production. Facility & Environmental Monitoring: Conduct routine facility checks including temperature, humidity, pressure differentials, and cleanroom conditions. Coordinate and ensure compliance with environmental monitoring schedules (viable/non-viable particles, surface, an...

Role & responsibilities Perform process design and development in association with scientist for drug product formulation and manufacturing Identify the manufacturing gaps to suite developed process and solution harmonization and implementation of QbD concept during the development and scale up stage Planning and execution of scale up batches at R&D as well as manufacturing sites, execute controlled experiments to optimize processes, address yield and quality issues and drive implementation of solutions Selecting and designing of the equipments/ instruments which can cater the requirement at R&D as well as manufacturing sites. Preferred candidate profile Candidates with the relevant experien...

Role & responsibilities Plan and execute lab-scale experiments for process development and optimization of hormonal APIs. Perform literature search (using SciFinder, Reaxys, etc.) and develop synthetic routes for hormonal molecules. Support scale-up from lab to pilot and commercial scale; address challenges during tech transfer. Characterize intermediates and final APIs using analytical tools (HPLC, GC, NMR, etc.). Document all experiments in ELN or lab notebooks as per cGMP & GLP standards. Assist in drafting process development reports, risk assessments, and technology transfer documents. Ensure EHS (Environment, Health & Safety) compliance during lab and pilot activities. Collaborate with...

Dear Candidate, We are looking for formulation scientists for our Ophthalmic in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 6-12years Role & Responsibilities: Formulation & Process Development Independently develop formulations for ophthalmic, injectables and nasal sprays Design and interpret DoE studies for optimization and robustness Technology & Excipient Evaluation ...

Greetings from MSN Labs...! Walk in Drive @11th Oct 2025 Department - Engineering- API Qualification: B. Tech/ Diploma Experience: 03- 08 Yrs Designation: Executive/ Sr. Executive Roles- Fitter/ Electrician/ Mechanical/ HVAC Required Key Skills: Must have experience in API Manufacturing. Department - TSD- API Qualification: B. Tech Experience: 3 -8 YEARS Designation: Executive / Sr. Executive/ Jr. Manager JOB DESCRIPTION: Must have exposure on Scale up Validations/ improving the solvent recovery/ Standalone capacity Enhancement/ Implementation of new technology etc. Walk In details Venue- MSN Laboratories Pvt Ltd. (Oncology Unit), Kardanur (V), Patancheru(M), Hyderabad Date- 11-Oct-2025 @9.0...

Responsibilities: Experience in handling chemicals and solvents at laboratory scale. He should be conversant for preparing mass balance, SOP writing. Good in multi step synthesis. Good knowledge of chemistry and prepare to work independently. Helping in Trail batch preparation, to co ordinate in R&D Scale up trails. Required Skills: Knowledge of scale up. Good chemistry knowledge for product development. Having knowledge of reaction chemistry, Hydrogenation, nitration, halogenation,. Having knowledge of R & D batch process, equipment and Product reactions, know about distillation, filtration, chlorination, condensations etc. Required Qualification : B.Sc/M.Sc - Chemistry

Role & responsibilities a) Observing the lab experiments and generating the necessary data for scale-up additionally generating Process Engineering calculations by using Simulation tools during the lab experiments. b)Suggesting for the process Safety, optimization study based on the need of the process wrt Safety Risks as well Quality. c)Analyzing and planning the modifications of equipments required for the execution of the scale-up batches . d)Should possess Knowledge on new technology usage for the Critical Operations for NCE’s. e)Should Possess Knowledge on Quality Management Systems (cGMP requirements). f)Extensive knowledge on MS office and effective communication Skills .

Role & responsibilities Implement norms for safety culture and 5S in laboratory. Improve existing products Conduct Laboratory findings and derive inference | conclusions Adhere to departmental policies and SOPs Comply with statutory and regulatory requirements Develop new products Provide technical support to cross-functional teams and customers Monitor protection for intellectual property Keep abreast with latest trends in research, technology and competition Eligibility Individuals who have cleared 10th and 12th in first attempt (50% and above) MSc | BSc (50% and above), with no academic gap. Interested candidates can share their CV to honey_panchal@atul.co.in.

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 ...

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...

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...

Description: Work as part of a dynamic and high-performing team and perform cutting-edge, high-quality Process Research Development (route selection, development of new and novel chemistry, reaction optimisation, process and isolation development, process understanding). Apply your skills (or learn new ones) working from mgs to kg’s with state-of-the-art equipment as part of a highly customer facing team. Key Responsibilities: 1. Delivery high quality laboratory work to support programs from early phase development through to commercialisation. 2. Propose new routes, process improvements, and make observations that will support the phase appropriate development of processes. 3. Document your...

Responsible for routine R&D tasks by using standard techniques,procedures & equipment, Adapt & optimize or develop new methods/procedures, PD, Technology Transfer, Scale Up, Troubleshooting, Lab experiment,Documentation,Lab assignment, EHS Compliance Required Candidate profile M.Sc.(Chem) with 3 to 6 yrs relevant exp in R&D/ PD lab of reputed Chemical/API industry. Sound exp of handling lab instruments like HPLC, GC, KF, IR, UV, Spectrometer, Analyser, Auto Titrator etc

Process Profile -API