123 Unit Operations Jobs - Page 2

Job Title Production Operator City, Country - Dahej, India Hybrid/Remote/On Site/ - On Site At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities Accurate Raw Materials Charging according to SOP/Batch sheet & instruction from Shift in-charges. Maintain & Control Operating parameter of Process as per SOP/Batch sheets. Unloading of intermediates / Fractions / products from equipment (Reactor/Batch still, Tank etc.). Loading of RM, Materials & Blending Operations Utilizes computer technology for data entry/retrieval and calculations & also for generating reports. Ensure Clean & dry Container (TOTE, IBC, Drum) before use. Labelling on each container/storage & piping Sampling as per SOP/Batch sheets. Material shifting & Lifting between Storage area & Equipment as per requirement in SOP/Batch sheets. Record Downtime for equipment. Preparation of Equipment for Maintenance. (Depressurize, Empty, Isolation, Tagging) for Spot permits, Class I & Class II permits as required. Check Equipment for safe operation after completion of maintenance work. Follow HS&E guidelines & ensure a safe workplace. Report unsafe conditions & act to avoid near misses. Fire Watch for any Class I permit as & when required. Basic knowledge of Chemical plant Unit Operations and fundamentals Ensure daily/day-to-day batch & continuous operations, data entry in batch-sheets per plant requirements. Coordinate with a few functions like Engineering & Maintenance for plant related works, Participate in Idea Generation sessions, various safety initiatives & small group activities. We bring. Empowerment to make meaningful contributions while upholding ethical standards. Recognition and celebration of your efforts and accomplishments. Opportunities for growth and advancement for those who embrace innovation and take initiatives. Opportunity to build a career making a significant impact on billions of lives, with the freedom to shape your own path. Responsibility and accountability in living company values and driving sustainable solutions. Supportive environment where individuals are empowered to progress and contribute to meaningful change. You bring. Diploma Chemical engineering or B. Sc (Organic Chemistry -preferred) 6 10 years of Production experience Should be able to work as a member of the team/Excellent team player Good shop-floor execution skills, open-minded & demonstrating safe & quality work following guidelines during shift operations Equal opportunities commitment dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate if there s a place for everyone at dsm-firmenich. As a committed equal opportunity employer, we ensure our recruitment practices are inclusive and fair. We encourage the recruitment of a diverse workforce, representative of the communities in which we work, by using inclusive language, diverse interview panels, and diversified sourcing strategies. Selection is based on qualifications, competency, experience, performance history and fit with the team to advance fair and equitable opportunity. Employment decisions are based upon job-related reasons regardless of an applicants race, color, ethnicity, national origin, religion, gender, gender identity or expression, sexual orientation, age, disability, backgrounds, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world s growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet. dsm-firmenich is a Swiss Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Position Summary : This is a client facing leadership position within the Process Team, responsible for supporting multiple mid to large sized projects. The Lead Process Engineer will mentor less experienced Engineers; Piping Designers; and CAD Designers in the generation of design documents per the ARCADIS Design Deliverables Matrix. Typical design elements include Front End Engineering Design studies (Feasibility through the Basis of Design), P&IDs, equipment specification, design coordination through all project phases, process modeling, and reports on specific technical topics required by the project team. The Lead Process Engineer is expected to demonstrate expertise in a variety of process engineering unit operations and biological manufacturing methods and semi- conductor processes, supported by a wealth of design and/or operation experiences. Additional work activities include supporting other ARCADIS offices and Central Operations (i.e. Business Development) in ARCADIS Strategic Initiatives and presenting at relevant industry conferences and publications. The Lead Process Engineer will be mentored by the Discipline Manager and other Senior SME Design Staff within the greater ARCADIS Team. Essential Duties and Responsibilities : Engage with all levels of ARCADIS and client organizations on technical discussions related to the fields of Chemical and Biological Process Engineering. Manage large project team and support the Discipline Manager in completion of performance reviews for these team members. Advise as SME in the development of engineering documents, leveraging experience, good engineering judgment, and external resources. Accountable for overall execution of the Process Design including technical quality, budget, and schedule. Coordinate construction activities for large projects; manage TBA, Submittals, RFI, and vendor activities, field evaluations, and commissioning support. Applies good engineering judgement to daily work, able to support design decisions with sound reasoning and published data when appropriate. Advanced understanding of unit operations encountered in the field of Chemical Engineering with a special emphasis on those present in the Life Sciences, semi-conductor, and other highly technical fields. field. Able to explain theory surrounding these elements and teach the concepts to others. Provide mentorship and on the job training to less experienced engineers across the ARCADIS organization. Attend training seminars/events and conduct industry research to further expertise in key processing technologies. Publish and present technical work in support of professional development and ARCADIS strategic initiatives. Support other Arcadis Offices, Marketing, and Business Development as a Technical Resource and in the development of proposals and marketing material. Competencies: To perform the job successfully, an individual should demonstrate the following. Continuous Learning Assesses own strengths and weaknesses. Pursues training and development opportunities. Seeks feedback to improve performance. Shares expertise with others. Strives to continuously build knowledge and skills. Culture - Supports a culture of excellence. Contributes to a collaborative environment that rewards teamwork, mentorship, best-in-practice development, and pride in workmanship. Customer Services Displays courtesy and sensitivity. Manages difficult or emotional customer situations. Meets commitments. Responds promptly to customer needs. Solicits customer feedback to improve service. Planning and Organizing Prioritizes and Plans work activities. Uses time efficiently. Plans for additional resources. Integrates changes smoothly, Sets goals and objectives. Works in an organized manner. Teamwork Balances team and individual responsibilities. Contributes to building a positive team spirit. Exhibits objectivity and openness to others views. Gives and welcomes feedback. Puts success of team above own interests. Use of Technology Demonstrates required skills. Adapts to new technologies. Keeps technical skills up to date. Troubleshoots technological problems. Uses technology to increase productivity. Qualifications : Education/Experience: Graduate/masters degree or equivalent in (Chemical Engineering); and 15 to 20 years related experience from design and engineering background and Pharmaceuticals/Bio Pharmaceuticals domain. Language Ability: Read, analyze and interpret complex documents. Respond effectively to sensitive inquiries. Write speeches and articles using innovative techniques. Make persuasive presentations on complex topics to management, public groups and/or boards of directors. Mathematical Ability: Apply advanced concepts such as exponents, logarithms, quadratic equations and permutations. Apply operations to such tasks as frequency distribution, test reliability/validity, variance analysis, correlation technique, sampling theory and factor analysis. Reasoning Ability: Apply logical thinking to a wide range of intellectual and practical problems. Deal with nonverbal symbolism (e.g., formulas and equations) in difficult phases. Deal with a variety of abstract and concrete variables. Software Skills: Proficiency in MS Office Suite, intermediate knowledge of VISIO, Bluebeam Revu, Hydraulic Flow Software (titles may vary), Process Modeling Software (i.e. SuperPro), Navisworks Supervisory Responsibilities (Added Advantage) : May have up to 8 direct reports. Manage large project teams and support Process Discipline Manager with performance review feedback for team members.

Role & responsibilities Chemical Industry exp Distillation - Simple, column distillation Material handling Drying Filtration experience Unit Operations

Role & responsibilities Hospital Operations Management: - Lead the day-to-day operations across all five hospitals to drive consistent, high-quality patient care and service delivery. - Drive operations excellence through process improvement, benchmarking, and performance optimization. - - Implement hospital-wide policies, clinical protocols, and operational SOPs in alignment with corporate standards. P&L and Financial Management: - Full accountability for Profit & Loss of the regional hospital cluster. - Monitor and manage financial performance, ensuring revenue growth and cost control. - Oversee budgeting, forecasting, and financial reporting in collaboration with Finance. - Identify areas for operational savings without compromising quality of care. Consultants & Clinical Partner Management: - Build and manage strong relationships with doctors, consultants, and medical specialists. - Ensure consultant engagement, satisfaction, and retention. - Oversee consultant contracts, scheduling, performance, and grievance redressal. - Facilitate collaboration between consultants and hospital teams to optimize clinical outcomes. Operations Excellence: - Continuous improvement in patient care, process efficiency, and service innovation. - Conduct regular audits, reviews, and feedback sessions to elevate hospital performance. - Ensure uniformity in service delivery and patient experience across all facilities. Leadership & Team Management: - Lead Hospital Administrators and department heads across the region. - Conduct performance reviews, training, and capacity building for leadership teams. - Foster a culture of accountability, innovation, and collaboration. Strategic Planning & Growth: - Develop and implement growth strategies aligned with business objectives. - Analyze market trends and competitive landscape to identify new opportunities. - Expand services, specialties, and infrastructure as per regional needs. Regulatory & Quality Compliance: - Ensure adherence to NABH, JCI, and other applicable standards. - Manage risk, patient safety, and medico-legal issues with a proactive approach. - Maintain zero-tolerance for regulatory breaches and patient safety lapses. Preferred candidate profile Masters degree in Hospital Administration / MBA in Healthcare / MHA or equivalent. - Proven multi-unit hospital management experience with P&L ownership. Strong leadership, financial acumen, and crisis management capabilities. - Excellent communication and stakeholder management skills. - Knowledge of hospital accreditation standards, compliance, and clinical workflows. - Proficiency in English and Telugu preferred.

You are a highly motivated and skilled Process Engineer with a background in mineral processing or metallurgical engineering. You will be responsible for optimizing mineral beneficiation processes, improving operational efficiency, and ensuring product quality and environmental compliance across mineral processing plants or pilot-scale units. Your exposure to base metal processing will be highly appreciated. Your responsibilities will include designing, implementing, and optimizing mineral processing flowsheets such as crushing, screening, grinding, flotation, magnetic separation, HMS/DMS, etc. You will analyze ore characteristics and interpret mineral data to support process design and performance tuning. Working closely with operations teams, you will identify bottlenecks and improve recovery rates, throughput, and energy efficiency. Monitoring daily plant performance metrics and troubleshooting process-related issues will also be part of your role. Additionally, you will assist in commissioning, testing, and scale-up of new processing equipment and technologies. It is essential to prepare and maintain mass balances, process control documents, and technical reports. Collaboration with geologists, metallurgists, mining engineers, and R&D teams on process development initiatives is crucial. Ensuring compliance with safety, quality, and environmental regulations is a key aspect of your job. Staying updated on new technologies, process innovations, and industry trends is also expected. To be successful in this role, you should have a strong understanding of unit operations used in mineral beneficiation and refining. Familiarity with mineralogy and ore behavior in processing contexts is essential. Experience using process simulation software (e.g., METSIM, HSC Chemistry, JKSimMet) is considered an asset. Knowledge of safety standards and environmental compliance in mineral processing plants is required. Excellent analytical, problem-solving, and communication skills are necessary. You should be able to work in cross-functional teams and adapt to field or plant environments. Ideally, you should hold a Bachelor's or Master's degree in Mineral Processing, Metallurgical Engineering, Geology, or Chemical Engineering. A minimum of 3-6 years of hands-on experience in a mineral processing or extractive metallurgy environment is preferred. Preferred skills for this role include experience in process commissioning, debottlenecking, or optimization projects, working knowledge of data acquisition and control systems (PLC, SCADA), understanding of geometallurgy and its application in process design, and exposure to pilot plant trials or laboratory-scale mineral testing. This is a full-time position that requires in-person work at the designated location.,

As a Chemical Engineering fresher at our Vapi location, you will have the opportunity to apply your theoretical knowledge to practical challenges in pharmaceutical API and intermediate manufacturing. If you have a B. Tech or M. Tech in Chemical Engineering and a passion for developing skills in process design, troubleshooting, and operations within a regulated and innovative pharmaceutical environment, this role is perfect for you. Your key responsibilities will include assisting in developing and optimizing chemical processes for API and intermediate production, designing and conducting lab and pilot-scale experiments to enhance process efficiency, supporting process control initiatives to ensure product quality and consistency, monitoring process parameters and production data for performance enhancements, troubleshooting process and equipment issues under supervision, participating in safety assessments and implementing EHS measures, supporting compliance with cGMP, environmental, and regulatory standards, and collaborating with cross-functional teams such as production, QA/QC, and maintenance. Additionally, you will be expected to stay updated on industry best practices, safety norms, and new technologies. Desired qualifications for this role include a B. Tech / M. Tech in Chemical Engineering (Freshers are welcome; industrial internship is an added advantage), strong foundational knowledge of core chemical engineering concepts, familiarity with chemical process simulation tools (e.g., Aspen Plus, ChemCAD), strong analytical and problem-solving abilities, good verbal and written communication skills, a proactive attitude, awareness of safety, environmental, and regulatory compliance relevant to chemical plants, and the ability to work both independently and as part of a team. If you are ready to embark on a journey of learning and growth in a dynamic production environment, this role is tailored for you.,

About The Position Technical Service Engineers perform a variety of technical support work for the Hydrocracking, Hydrotreating, Lube Hydroprocessing, and Residuum Hydrotreating technologies as well as other refining technologies This work includes catalyst and licensing proposals, technical service, process designs, and startup support, Key Responsibilities Provide technical service to customers of joint ventures including Chevron Manufacturing for hydroprocessing technology Lead technical service activities e-g starting up and monitoring new and existing hydroprocessing units in facilities worldwide Advise and mentor colleagues on complex technical problems to build organizational capability in the organization Work closely with technical and commercial teams to solve customer problems and win business Improve technical tools and standardize engineering methods Travel 40% of the time Interpret operating data to monitor catalyst performance, recommend operating guidelines, and estimate remaining catalyst life Plan and lead in-plant shutdown and startup assistance, including catalyst loading, regeneration, and sulfiding consultation Administer plant performance test runs as required Answer clients operating questions to stay close to the customer and win future catalyst business Level of support is dependent on the marketing strategy for each customer Includes process equipment troubleshooting May include site visits and/or periodic operating data reports Participate in conceptual design studies in support of licensed unit re-vamps or debottlenecks Required Qualifications A bachelors degree in chemical engineering with more than 10 years relevant work experience Hydroprocessing Experience Experience in hydroprocessing design, operations, kinetics, and data analysis Experience working in a refinery as a process engineer responsible for monitoring and performing field activities for hydroprocessing units Process Design Experience Must have basic knowledge of process design tools such as HYSIS or Pro/II (or similar process simulator), heat exchanger design tools, etc Field Experience Basic understanding of how equipment functions in the field and overall plant operation are required Interpersonal Skills Must work constructively with others (inside and outside Chevron) to achieve positive results via the Chevron Way Must act with integrity and honesty, accept constructive feedback well, and use recognition Teamwork skills a must Communication Skills Ability to communicate with clients to effectively sell our technology and represent Chevron in a positive light to outside companies Ability to communicate well with teammates and managers during project and tech service work required Organizational/Leadership Skills Demonstrated ability to plan, schedule, and manage multiple work activities to meet customer needs and expectations required Must possess ability to manage a team and delegate work out to team Must be able to interact with a variety of experience levels and position types Ability to design a variety of unit operations such as heat exchangers, vessels, distillation columns, etc is a plus Chevron ENGINE supports global operations, supporting business requirements across the world Accordingly, the work hours for employees will be aligned to support business requirements The standard work week will be Monday to Friday Working hours are 8:00am to 5:00pm or 1 30pm to 10 30pm, Chevron participates in E-Verify in certain locations as required by law, Show

Job Opening Process Engineer for a leading Chemical Industry for Vapi, Gujarat Location. Qualification: B.Sc. or M.Sc. Transportation - Free Canteen - Subsidized Interview Mode: Face to Face (Compulsory) Requirement: Good knowledge of pipe line calculation, heat of reaction, project work handling, discerning of equipment.

Role & responsibilities: Responsible for Process plant unit operations. Supervise, Monitor & Control of process parameters. Ensure Safe operation of plant. Daily report on production activities. Follow all SOP. Follow all Safety procedures. Preferred Candidate: Candidates with Highest Qualification must be only in: B.Sc. - Chemistry Diploma - Chemical Diploma - Petrochemical

Experience in Plant Scale up, Technology Transfer Strong understanding of key chemical engineering subjects (Heat transfer, mass transfer and Chemical reaction engineering) Exposure on process optimization, debottlenecking, process intensification, scaleup studies ","vacancyKeyroles":" Technology transfer of process for scaleup from Lab scale to commercial scale. Preparation of BFD, PFD, Mass balance , energy balance, MOC compatibility and design basis Involves Process optimization, scaleup and scale down of unit operations (reaction, filtration, drying, crystallization, distillation etc.) Process modification and improvement for optimized capex and opex (achieving target norms) Process Intensification using next generation techniques of flow chemistry and working on reaction kinetics Close collaboration with process safety team to study process for thermal safety (DSC, ARC, RC1E) etc. Close collaboration with R&D scientist for optimizing and conceptualizing process flow at plant scale. Anticipating problems of commercial scale and resolve during process development stage Close collaboration with Engg. Lab team for process scale-up, scale down and engineering optimization, engineering data generation (VLE data, crystallization PSD, filtration rate, drying curve, extraction studies etc.) Close collaboration with pilot team for piloting activities, BEP preparation, P&ID preparation, participating in hazop, and successful piloting activity. Close collaboration with MPP and Dedicated design team for transfer of finalized process (tech transfer package) Working on established plants and processes for troubleshooting and eliminating process challenges Optimizing process with minimum effluents and maximum productivity

About Astound Commerce Astound Commerce is a global digital commerce company that provides end-to-end services from creating a data-driven strategy and delivering UX services to building an eCommerce solution for a variety of clients such as Cartier, Neutrogena, Puma, Diageo, Adidas, and L Or al. With 20+ years of experience, 1,400+ eCommerce specialists, more than 3,000 projects completed, and dozens of industry accolades, we excel at maximizing the brand and business value of every digital commerce touchpoint. Astound Commerce currently operates in 14 countries with 20 offices worldwide. In this role, you will get to Provide advice and support company-wide, worldwide on a variety of legal issues on a daily basis in a timely and effective manner; Function as a subject matter expert for corporate governance and securities matters across the global portfolio of companies, including working closely with the principals and senior management; Review, Drafting, and Negotiating of Commercial Contracts with Technology Partners, Vendors, and Customers (emphasis on professional services and software development engagements); Work closely with other business units to achieve and maintain legal compliance; In-House legal operations, including management of outside counsel, global insurance coverage, intercompany relationships, and high-level business unit operations globally; Legal process creation for local and global legal/operational units; Intellectual property, including management of global trademark docket; Your skills and qualifications The ideal candidate would be a recent Law School graduate (3-5 years out of school), who possesses: Excellent legal project management and organizational skills; Excellent independent problem-solving and troubleshooting skills; Strong ability to balance legal risk against business drivers; Excellent research and writing skills; Strong ability to independently multitask and prioritize projects; Natural ability to thrive in a fast-paced environment; Desire to be a teacher, leader, and student, as is expected from all team members; Highly Preferred Experience with international matters; Excellent communication skills; Proficiency in MS Office, Google Apps (G Suite), and cloud-based applications generally; Previous experience with CRM based task management tools (i.e. JIRA / Confluence) is preferred; 2+ Years of relevant work experience; What we offer in return Off-the-Charts Career Growth: lear career path and a performance review system, career coaching, training and certifications, mentoring and knowledge sharing Well-being Is Top Priority: Parental leave, paid time off, comprehensive health and medical plans Real Work-Life Balance: Remote, in-office, or hybrid working modes; flexible hours; work-life balance support on every stage and level Culture of Success: Culture of collaboration that encourages innovation every step of the way; 20 offices spanning four continents bring diverse perspectives that drive tangible results for our clients worldwide.

Lead plant operations at a specialty chemical manufacturing unit with end-to-end responsibility for production, quality, HSE, and stores. Drive operational efficiency, safety compliance, and process improvement. Required Candidate profile BE Chemical with 15–20 years of experience in plant operations within the chemical industry. Must have strong leadership in production, HSE compliance, and inventory management using SAP.

Role & responsibilities : P&L Management, Operational efficiency based on Process Excellence, Service Experience Management, Clinician Engagement & Clinical Excellence, Revenue Enhancement through internal optimization of leads conversion, Statutory compliances. Key Responsibilities P & L Management: Based on the Annual Budget, develop detailed Quarterly Plans with milestones, collaborate with cross functional teams to deliver and achieve targets. Identify key levers that contribute to top line achievement & EBIDTA track efficacy. Revenue generation : through Lead Management and Conversions; every product to be monitored; OP to IP conversions; ensure prescribed Pharmacy/ Investigations fulfilled internally; leakages minimized. Ensure Package and Pricing is profitable. Analysis and growth of different specialties, budget vs actual achievement, timely rectification of lags. Dashboard, KPI Monitoring & Ad Hoc Support - Monitor all revenue streams to ensure on track, proactively identify scope for higher margins, leakages. Proactively monitor patient billing transactions to minimize any intentional or unintentional leakages and take steps to prevent repetition. Ensure Credit billing is error free, enabling payments are received without deductions. Monitor receivables to ensure collections within 45 days. Track Average Revenue per occupied bed; Average Revenue per Patient, ALOS, admissions and discharges TAT, payor mix. Cost Management :Track material consumption, gross contribution margins, monitor pay out to revenue achievement, analysis of discount percentage. Conduct productivity analysis on doctor pay-outs and identified inefficiencies to optimize doctor cost. Create pre-defined surgery packages in the Hospital Information System to track and control consumption. Manage Unit operating costs manpower, infrastructure maintenance, electricity, consumables Cost and stock optimization of Pharmacy and non Pharmacy items. Bench marking against other unit scores. Wastage and loss tracked and minimized. Collaborate with SCM to ensure product selection and costs are leveraged optimally. Service Experience Management: Commit to the implementation of the service differentials in the Service Experience Plan; ensure frontline employees are trained and empowered to fulfill the Service Promise. Monitor real-time interactions with customers, regularly seek firsthand feedback from a cross section of customers and energize the team with the passion to delight every single customer. Seek frontline staff and customer suggestions to continuously raise the bar through service innovations, value-adds, experience enhancements. Institutionalize sharing with frontline employees specific service wins, success stories, encourage them to implement. Create a platform and mechanism to analyse constructive feedback periodically, arriving at a structured Improvement Plan and an implementation Path to ensure sustained improvement. Operational efficiency: Ensure facility is managed as per defined standards of maintenance; infrastructure is well maintained. Ensure clinical protocols are adhered to and clinical verticals are well equipped to manage their function efficiently. Interact with Clinicians and ensure operational requirements are up to expectations. Service delivery standards are adhered to. Support services function as per standard; non medical services are process compliant. TATs are monitored and outliers are proactively addressed. Close coordination and liaison with heads of departments/ in-charges to ensure operations are efficiently managed, costs are controlled without impacting service standards. Work closely with IT to optimise technology to improve customer experience and employee work flow. Ensure HIS improves operations & functionality. Ensure IT supported process controls and alarms are in place to detect and prevent fraud in billing. Manage Inventory efficiently ensuring optimization and effective control. Ensure facility is audit compliant and all departments adhere to defined protocols. Ensure all statutory and licenses, renewal of agreements are up to date. Clinician Engagement: Interact with Consultant teams to improve patient care outcomes, service experience deliverables and overall customer satisfaction. Build rapport with Visiting Consultants, facilitate their experience with the Unit, integrate them into the Motherhood Hospitals culture and processes, ensure their patients are handled well. Build new specialties to improve footfalls and conversions. Ensure facility handle Doctor Referral cases smoothly. Quality and Clinical governance: Coordinate and support NABH certification, surveillance audits & post audit closure. Ensure Unit preparedness for compliance. Effectively monitor Clinical quality indicators, ensuring compliance. Active participation in Committee meetings Mortality, Morbidity Infection control, Grievance, Safety. Monitor clinical outcomes viz IVF Outcomes success rates, Normal vs LSCS, Open and close audits for MRD, monthly reports ( PNDT, communicable diseases, deaths and births) Collaborate with Medical Services to organize Medical Education seminars, conferences to up-skill Clinician and Nursing teams. People Management & Stakeholder Alignment: Lead & manage the Unit team - ensure employees are trained, motivated and empowered to achieve Goals. Celebrate successes, recognize outstanding performance. Build skills and talent, encourage cross function learning and multi tasking. Build synergy so that clinical and operations teams function seamlessly. Business Development: Facilitate community outreach activities; showcase the service focus of the brand to build potential customer bases. Organize with Sales and Marketing, promotional campaigns / technical presentations to facilitate new product development with major focus on brand establishment, market penetration. Gather market intelligence, tracking competitor activities and providing valuable inputs for fine tuning marketing strategies Qualification: MHA/MBA Experience: 8-14 Years Interested applicants can share the CVs @ tejaswita.s@motherhoodindia.com

Job Title: Process Engineer Level: FLO Location: Kharach, Kosamba Business: Pulp & Fibre Function: Job Responsibility/Specific Skill Set: Knowledge of unit operations, unit process, safety standards Routine & non-routine job planning and execution Manpower handling and problem-solving skills Good communication skills & ability to act quickly Company Overview: Birla Cellulosic, Kharach is a leading company in the Pulp & Fibre industry, providing high-quality products and solutions to its customers. With a strong focus on innovation and sustainability, Birla Cellulosic is committed to delivering excellence in all aspects of its operations. Role Overview: The Process Engineer will be responsible for overseeing unit operations and processes, ensuring adherence to safety standards, planning and executing routine and non-routine jobs efficiently, handling manpower effectively, and demonstrating strong problem-solving skills. The role requires excellent communication skills and the ability to act quickly to address operational challenges.

Job Purpose Sr. No. KRA Supporting Action 1 Contract Workforce Management Coordinate and support in managing of contract workforce under contractual agreements for smooth running of unit operations Gate pass system/ compliances, Grievances handling. Monitor quarterly limit of overtime for CL and assist to SH-ER to take suitable action in this regard 2 Statutory Compliances of Contract labour management Adherence to laws, regulations, and statutory requirements set forth by government authorities or regulatory bodies for compliance management To assist SH-ER in 100% compliance : Ensure to zero variance between Monthly Attendance of CL , Wages Register & OT - Payment, Bank Statement and finally PF, ESI contribution. Regular follow up with contractors and respective area incharges to ensure the same. Monitoring of all statutory compliance i. e. contractor s license, W. C. policy etc. Checking of Statutory registers, PF/ESI contributions on time, Bonus etc. 3 Administration Contractor manpower bill checking and timely processing PF/ESI bill checking and timely processing Checking of wage registers and ensuring zero discrepancies. 4 MIS & Reports Prepare the MIS reports Compile and maintain record of monthly highlight and lowlights 5 Safety To ensure implementation of ABG safety system & procedures and follow it.

Lead plant operations at a specialty chemical manufacturing unit with end-to-end responsibility for production, quality, HSE, and stores. Drive operational efficiency, safety compliance, and process improvement. Required Candidate profile BE Chemical with 15–20 years of experience in plant operations within the chemical industry. Must have strong leadership in production, HSE compliance, and inventory management using SAP.

Key Result Areas Role-specific: Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM. Attend the training session of EHS, cGMP and HRD. Ensure process equipments/instruments are in Qualified in state. Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution. Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks. Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records. Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve. Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. TECHNICAL /FUNCTIONAL SKILL: Expertise in Upstream unit operations (CHO based mammalian expression systems). Strong Hands on experience with SUB (Up to 2000 L scale) Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area. Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects Experience on risk assessment tools and change management. Experience on the Equipment Qualification and commission aspects

Key Result Areas Role-specific: Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM. Attend the training session of EHS, cGMP and HRD. Ensure process equipments/instruments are in Qualified in state. Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution. Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks. Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records. Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve. Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. TECHNICAL /FUNCTIONAL SKILL: Expertise in Upstream unit operations (CHO based mammalian expression systems). Strong Hands on experience with SUB (Up to 2000 L scale) Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area. Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects Experience on risk assessment tools and change management. Experience on the Equipment Qualification and commission aspects

Division Department Sub Department 1 Job Purpose Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target Utilise shift resources optimally to get desired production output Regulate usage of consumables in the production process at optimum level to save cost Key Accountabilities (2/6) Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement Review and monitor critical in-process parameters like NFD, camera challenge, RH temperature etc. Review and perform all operations as per GMP and safety norms by reviewing all processes and documents for compliance Maintain system integrity by updating online documentation Perform qualification and calibration of equipment as per schedule and update output of all activities in the system Key Accountabilities (3/6) Prepare manufacturing records and update online documentation to meet production and cGMP requirement Maintain online documentation and timely entries in BPR and supporting documents by operating SAP and CipDox Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (4/6) Monitor adherence to safety guidelines in the block during a shift for packing activities to create safe working environment Monitor safety systems and ensure procedures are followed in shift and near-miss cases are reported to HSE timely Ensure availability and usage of PPEs in the shift by coordinating with HSE department Ensure compliances to safety training targets by monthly reconciling attendance records Key Accountabilities (5/6) Provide training to staff & workmen for packing activity by regular interactions with them to get quality product Provide training to staff and daily workers for packing activities and safety procedures Conduct training related to equipment handling, cGMP, documentation and unit operations Key Accountabilities (6/6) Provide new ideas and simplify processes to reduce process cycle time and achieve new targets Provide new ideas during idea sessions for better productivity with minimum cost Identify the complexities and suggest process simplification areas to achieve new target with optimum utilization of resources Reduce and simplify documentation for better accuracy and to meet ALCOA (Attributable Legible Contemporaneous Original Accurate) Major Challenges Meeting shift target due to unavailability of adequate resources. Overcome by efficient work load distribution Maintaining cGMP requirements during system downtime. Overcome by coordinating with engineering and technical support team Key Interactions (1/2) Quality assurance and control for batches release as per packing plan (Daily) Engineering for preventive maintenance and help in modification (as per need) Safety for awareness training and near miss issue (Daily) Store for daily dispensing plan and availability of packing materials (Daily basis) Key Interactions (2/2) Maintenance contractor for any machine repairs (Need Based) Dimensions (1/2) Direct Reports : 3 Achieve average volume of 200 mn (FY2015-16) Average number of BPR s handled : 200 Average number of batches in packing : 200 Average number of sales order dispatched : 80 Achieve internal OTIF more than 90% Achieve Zero reportable accidents/ incidences during packing activities Achieve 0% errors in online documentation Meet 100% compliance to SOP and Safety regulation Dimensions (2/2) Key Decisions (1/2) Resources allocation and work distribution for each shift Key Decisions (2/2) Up-gradation in facility and documents to Section Head - Packing Modification in equipment to Section Head - Packing Deviation and implementation of CAPAs Section Head - Packing Education Qualification B. Pharm. / B. Sc. (Chemistry) Relevant Work Experience 1-5 years of experience in packing with knowledge of handling of QMS activity, qualification and other related documents

1 Production Manager 10 to 15 years in API -Production & Qualification - MSc.(Organic Chemistry)/ MTech Chemical (Technology)/ BSc.(Chemistry): job Role Knowledge about utility Operations and Control Knowledge about Shop Floor operation and managing of manpower on shop floor. Batch planning, Execution with timeline operation. Experience for troubleshooting during operation. Quality product Production as per Guidelines. Knowledge of ICH-Q7A/WHO GMP and USFDA Experience for Documentation as per SOP and GMP guidelines. Experience for unit operations like- reactors- GLR- SSR/Hastelloy autoclave (hydrogenation), Clean room Operations, Jet mill operations, AHU, and Related utility Brief Knowledge of steroidal molecules/ Anticancer molecules, Handling, and operations. Customer, national and international audits Handling. Regulatory audit like USFDA, TGA/WHO Geneva experience. Training experience to the subordinate in production department. experience in BOQ preparation and coordination with store Finished goods handling and operation as per customer requirements . 1 Tumkur, Karnataka

Responsible for all activities like production, technology transfer, plant modification as per product Prepare monthly production plan base on marketing monthly projection Review batch sheet & logbook Review of All improvement & targets at unit level

The Quality Engineer is part of the Materials, Equipment, and Quality team within Chevron s ENGINE Center and provides support to Capital Projects and Business Unit Operations. This role will ensure Nondestructive Evaluation (NDE) systems, tools, methodologies, governance, and assurance are operationalized to remain competitive, improve predictability, mitigate risk, and to help generate leading performance outcomes. This role provides subject matter expert level consulting services to project and business leaders and peers, to enable successful application of NDE tools and processes across the enterprise. Key responsibilities: Interface with downstream, upstream and projects worldwide in multiple time zones to provide guidance on advanced NDE methods in Ultrasonics, Electromagnetics and Radiography Perform on-site advanced NDE inspections for critical Fitness-for-Service evaluations and cost optimization at BUs and Projects globally Champion Non-Intrusive Inspections (NII) for manufacturing facilities and projects by providing guidance and performing advanced inspections for better turn around performance Facilitate within Business Units and Projects using a risk-based approach Chevrons Performance Demonstration Qualification (PDQ) for contractor NDE personnel. Provide detailed NDE procedure reviews and witness qualifications to applicable codes and standards Deliver NDE training to BUs and Projects and Project partners such as EPCs in NDE methods and provide certification support. Perform research and development on new and emerging NDE technologies that have a direct impact on process safety Participate and be a core member of Chevrons Community of Practice (CoP) and participate in regional JIP and Consortiums in NDE area. Develop and maintain risked based NDE management systems, plans, and tools with customers, and internal and external partners, and provide overall oversight and assurance to project and facility operations and turn around activities. Oversee and participate in NDE Assurance activities and participate on cross functional teams and on industry committees. International travel and working outside of normal business hours shall be required to support customers. Required Qualifications: BS Engineering in one of the core disciplines - Chemical, Mechanical, Electrical from a recognized (AICTE) university Advanced Ultrasonic and Electromagnetic certifications in Phased Array, Time of Flight Diffraction, Eddy Current/Remote field Minimum of 3 ASNT or ISO Level III certifications Successful passing of Chevron Performance Demonstration (PDQ) Qualifications or equivalent ASNT - ISQ examination. Extensive knowledge of all applicable codes such as ASME, ISO, AWS, API, and DNV Experience performing advanced ultrasonic procedure qualifications (PAUT) to ASME and API codes Preferred Qualifications: 10+ years experience in Non-destructive testing, Asset Integrity and inspection area. Previous representation and participation in industry committees such as API, ASME, and ASNT Demonstrated working knowledge of corrosion damage mechanisms and how they affect fixed equipment. Experience inspecting sub-sea pipeline welds utilizing automated ultrasonics and qualifying to industry standards Hands on expertise on critical issues leveraging all advanced inspection techniques including Ultrasonics, Electromagnetics, Radiography.

Simreka (Devtaar GmbH) is looking for Chemical Engineer to join our dynamic team and embark on a rewarding career journey Develop and implement chemical processes to produce chemicals and related products Design and optimize equipment configurations for chemical processes Conduct research to identify, develop, and improve chemical processes Ensure compliance with safety and environmental regulations Monitor and troubleshoot production processes to identify and resolve problems Collaborate with cross-functional teams to ensure efficient and effective process development and implementation Develop and maintain accurate records of process data, procedures, and specifications Design and conduct experiments to support process development and optimization Knowledge of safety and environmental regulations Strong communication and analytical skills Bridge science and softwareapply formulation and chemistry knowledge in a digital R&D environment.

Eastern Naphtha-Chem Pvt Ltd is India's leading manufacturer of Beta Naphthol, Naphthalene, Sodium Sulfite, and other naphthalene series industrial chemicals Role & responsibilities Primary responsibility for all all aspects of production, yield and quality targets for beta naphthol plant. Production planning, targets fulfilment and production activities as per SOPs. Oversight and guidance of supervisors / shift in charge and operating personnel. Overall responsibility for production including capacity/ utilization/ OEE/ etc, raw material consumption ratios improvement, energy and electricity usage optimization, breakdown maintenance and resolution, regular maintenance plan development and implementation, etc. Collaboration with R&D Team for plant improvement initiatives Identification of recurrent equipment breakdowns, and preventive maintenance and coordinating with maintenance personnel to complete the jobs safely & effectively. Optimization of manpower planning Training of personnel Development of systematic protocol for each chemical unit process within plant including preparation of SOPs, BMSs, Protocols, reports, etc. Preparation, maintenance, and refinement of daily and monthly reporting systems and MIS. Key responsibility includes accurate estimation of plant raw material input ratios. Responsibility for quality control within plant Preferred candidate profile Education: BSc/ MSc in Chemistry or BTech/ MTech in Chemical Engineering Experience: >20 years in Chemicals/ Process Industry Functional Area: Production, Plant Operations and Maintenance, Operations Improvement Experience in production in dye/ organic intermediates (preferably unit processes like sulfonations, distillations, alkali fusions, carboxylations, solvent recovery and handling, etc.)

Pilot Plant Responsibilities: Managing manpower based on shift activities in Pilot Plant. Demo batch monitoring for new NPDs or development of existing products in R&D. Equipment mapping for the new projects to be performed in Pilot Plant. Identifying requirements and involving in facility modifications as per process CCPs and HACCPs with the maintenance team. Facilitating the requirements of raw materials (RMs), chemicals, solvents, and packing materials (PMs) for pilot batches. Preparation and review of master BMR. Involving and monitoring CCPs with the R&D team during batch execution. Compilation and preparation of scale-up reports. Following project stage cycle after scale-up until commercial production. Preparing capacity calculations and costing for scale-up completed projects by coordinating with Production and Finance teams. Reviewing physical monthly stock in Pilot Plant as per SAP. Coordinating with cross-functional teams in reviewing and approving TTD. Involving in preparation of validation documents for commercial batches. Monitoring validation batches at commercial scale. Ensuring online documentation of Pilot Plant as per SOP. Involving in trial batches performed at 3P sites. Involving in new equipment trials and compiling reports. Ensuring adherence to environmental health and safety rules and procedures. Preferred candidate profile Diploma in chemical Engineering/ B.Tech In Chemical Engineering Kilo Lab/Pilot Plant - Extraction process experience would be added advantage Male candidates preferred Should be willing to travel SAP Knowledge Reach out to saheed.s@omniactives.com to share cv or refer the suitable candidates.