About the Role : Assistant Manager – Process Engineering Location : R&D Jigani (Requires travel among our cross functional units) Responsibilities : Perform and lead risk assessment exercises in support of API process scale up & validation activities. Collaborate with R&D to ensure successful API product development and technical transfer to Manufacturing. Coordinate Scale up & validation activities including, but not limited to, protocol training, execution by validation and other departments, data collection, deviation resolution, and CAPA initiation, in support of assigned validation projects. Maintain knowledge and comprehensive understanding of peptide regulations and current interpretations affecting equipment, product, and process. Scale up & Validation representative on site project team and resource to other departments for API product and process knowledge. Develop specialized technology/unit operations knowledge and provide training to operations as content expert for manufacturing standard operating procedures (SOPs). Perform troubleshooting and investigation on unexpected issues. Own equipment-related deviations, CAPAs, and changes. Lead or participate in investigations, problem-solving activities such as root cause analysis, FMEA, problem analysis, and in development/implementation of countermeasure for quality, safety, environmental events. Provide process technical expertise for requirements, design, selection, installation, qualification, operation, maintenance, and reliability of process equipment and facilities. Perform and summarize improvement opportunities in technical reports, investigations, plant/lab trials, data analysis, and process modeling. Active participation and engagement in the meetings and activities of the assigned process team and safety/environmental sub-teams. Ensure process complies with current industry regulatory expectations, new regulations, and corporate policies and programs for Quality, Health and Safety & Environmental, Process Safety. Qualifications : B.Tech – Chemical Engineering Minimum 4-6 years of relevant experience in API products. Experiences in API Process Development & Scale up/ Process validation Required Skills : Strong written and oral communication skills Strong leadership and organizational skills Knowledge in managing multiple project objectives or assignments Technical Writing. Show more Show less
We are looking for experienced managerial candidates with a minimum of 8 to 12 years of hands-on experience in API Production . The ideal candidate should have a proven track record in independent handling of production plant. Requirement is for our manufacturing unit VPL Chemicals located in Dabaspet, Nelamangala. Key responsibilities include; Production planning & resource allocation. Ensuring the production as per plan. Receiving technology and executing trial & validation. Maintaining/creating the cGMP system along with QA. Controlling cost in production by achieving yield, improving productivity and optimizing resources. Maintaining the facility and QMS as per audit compliance. Other skills - SAP/ERP
We are #hiring Maintenance Executive with 1- 3 years experience in API Pharma for our manufacturing unit VPL Chemicals located in Dabaspet, Nelamangala. Education Qualification - Diploma/B.Tech Mechanical Engineering. 1. SOPs and Validation Reviews: Review SOPs, validation protocols (DQ, IQ, OQ, PQ), apex documents, and reports to ensure regulatory compliance. 2. Preventive Maintenance: Plan and monitor preventive maintenance schedules to minimize machinery downtime and maintain operational efficiency. 3. Utility and Equipment Maintenance: Oversee the maintenance of utility equipment such as compressors, chillers, cooling towers, boilers, RO/DM plants, reactors, and vacuum pumps. 4. Mechanical and Electrical Maintenance: Perform mechanical (gearboxes, hydraulics, pneumatics) and electrical maintenance tasks, including support for boiler systems. 5. Regulatory Compliance and Miscellaneous: Maintain the plant as per GMP standards, manage waste disposal as per norms, and execute additional tasks assigned by management.
We are #hiring Quality Control - Executive for our manufacturing units VPL Chemicals and Symbio Unit 2 located in Dabaspet and Tumkur respectively. Job Description 1. Testing of raw materials, in-process samples, finished products as per SOP/STP. 2. Calibration of QC Lab instruments. 3. Identifying the chemicals testing requirements for testing of samples on regular basis plan for procurement of chemicals, standards and glassware. 4. Preparation qualification of in-house working standards and review of validity of reference standards and impurities as per Pharmacopoeia. 5. Upkeep of calibration records, working standards records and timely completion of log books in line with audit requirements. 6. Testing of excipients, Enzyme samples, Process development samples. 7. Preparation of Spec/STP/SOP revisions as per TT documents and product monograph requirements. 8. Hands on experience on testing of APIs, formulations and Dissolution apparatus etc. 9. Preparation of MV protocols / reports, execution summary as per guidelines.
We are #hiring Quality Control - Executive for our manufacturing units VPL Chemicals and Symbio Unit 2 located in Dabaspet and Tumkur respectively. Job Description 1. Testing of raw materials, in-process samples, finished products as per SOP/STP. 2. Calibration of QC Lab instruments. 3. Identifying the chemicals testing requirements for testing of samples on regular basis plan for procurement of chemicals, standards and glassware. 4. Preparation qualification of in-house working standards and review of validity of reference standards and impurities as per Pharmacopoeia. 5. Upkeep of calibration records, working standards records and timely completion of log books in line with audit requirements. 6. Testing of excipients, Enzyme samples, Process development samples. 7. Preparation of Spec/STP/SOP revisions as per TT documents and product monograph requirements. 8. Hands on experience on testing of APIs, formulations and Dissolution apparatus etc. 9. Preparation of MV protocols / reports, execution summary as per guidelines. Show more Show less
Looking for Executive with 3-5 years experience in API - Pharma Production Department. Job Description 1. Managing day-to-day production operations while ensuring optimal utilization of materials, equipment, and personnel. 2. Ensuring full compliance with Good Manufacturing Practices (GMP), ICH guidelines, and applicable regulatory requirements including those set by the FDA and EMA. 3. Maintaining accurate and complete documentation of all production activities, including batch records, deviations, and related reports. 4. Driving continuous improvement initiatives by applying Lean Manufacturing and Six Sigma methodologies. 5. Actively participating in new product introductions and technology transfer activities to support seamless integration into production processes. Other skills - Knowledge of SAP an additional advantage.
Looking for Executive with 3-5 years experience in API - Pharma Production Department. Job Description 1. Managing day-to-day production operations while ensuring optimal utilization of materials, equipment, and personnel. 2. Ensuring full compliance with Good Manufacturing Practices (GMP), ICH guidelines, and applicable regulatory requirements including those set by the FDA and EMA. 3. Maintaining accurate and complete documentation of all production activities, including batch records, deviations, and related reports. 4. Driving continuous improvement initiatives by applying Lean Manufacturing and Six Sigma methodologies. 5. Actively participating in new product introductions and technology transfer activities to support seamless integration into production processes. Other skills - Knowledge of SAP an additional advantage. Show more Show less
We are #hiring Executive - Analytical R&D with 1-3 years experience for our R&D located in Jigani. Job Responsibilities Independently able to handle HPLC / GC Analysis by UV, IR, potentiometer, KF titrator etc. Calibration of instruments Good understanding on GLP documentation Literature search for Analytical methods Educational Qualification: MSc (Analytical chemistry/organic chemistry), M. Pharm (Chemistry/Analysis) Area of expertise: HPLC, GC, Testing Other skills: Adaptability & Communication
You are an Executive with 3-5 years of experience in API - Pharma Production Department. Your role involves managing day-to-day production operations to ensure optimal utilization of materials, equipment, and personnel. It is crucial to uphold full compliance with Good Manufacturing Practices (GMP), ICH guidelines, and regulatory requirements from FDA and EMA. Your responsibilities include maintaining accurate documentation of all production activities, such as batch records, deviations, and related reports. You are expected to drive continuous improvement through Lean Manufacturing and Six Sigma methodologies. Additionally, you will actively participate in new product introductions and technology transfer activities to facilitate smooth integration into production processes. Having knowledge of SAP is considered an additional advantage for this role.,
We are hiring Executive - AR&D with 1- 3 years experience for our R&D facility in Jigani, Bangalore. Qualification - M.Sc (Analytical Chemistry/Organic Chemistry), M. Pharm (Chemistry/Analysis) Job Description Independently able to handle HPLC / GC. Analysis by UV, IR, potentiometer, KF titrator etc. Calibration of instruments. Good understanding on GLP documentation. Literature search for Analytical methods. Area of expertise - HPLC, GC, Testing Other skills - Adaptability & Communication
You are required to have experience in the API Pharma industry to join as an Executive/Sr. Executive - Quality Assurance at VPL Chemicals in Dabaspet, Nelamangala. Your responsibilities will include reviewing and approving change controls, investigation reports (such as OOS, OOT, Market Complaints, Return Goods, Recalls), handling regulatory and customer audits, conducting self-inspection audits, preparing and reviewing SMF, VMP, and SOPs, managing customer queries, vendor qualification program, and training program. Your area of expertise should be in analytical data review. Additionally, you should have knowledge of cGMP systems and regulatory guidelines to excel in this role.,