water purified water system operator is responsible for operating and maintaining a water treatment facility, ensuring that the water meets quality standards and is delivered safely to the community. This role involves monitoring equipment, performing maintenance, conducting tests, and adhering to regulatory requirements. Key Responsibilities: Operating Equipment: Operate pumps, valves, and other equipment to control the water treatment process. Monitoring Water Quality: Conduct regular tests and inspections to ensure water meets quality standards. Maintenance and Repairs: Assist in maintaining and repairing plant equipment. Data Logging: Maintain accurate records of water output, chemical analysis, and equipment usage. Safety: Adhere to safety guidelines and procedures to ensure a safe working environment. Troubleshooting: Help troubleshoot equipment issues and implement corrective actions. Compliance: Ensure compliance with regulatory requirements for water treatment and safety. Skills and Qualifications : Knowledge of water treatment processes and equipment. Effective communication and problem-solving skills. Ability to work in a team environment. Knowledge of safety regulations and procedures.
As a Senior Executive/Executive in the Stability Section at Kimia Biosciences, you will be responsible for maintaining stability schedules, handling inward and withdrawal of stability and hold time samples, preparing stability reports, extrapolating stability data, determining shelf life, and being well-versed in OOS and lab incidences as well as data integrity issues. Kimia Biosciences is renowned for its people-centric approach, emphasizing a friendly work culture where ideas are valued, and employees are given space and freedom to make and implement decisions. The company's management style integrates excellence with best Human Resource practices to foster a competitive edge in the Pharmaceutical market by attracting top talent and fostering a corporate culture of equality and growth. The organization boasts a committed, high-performing team of professionals who have significantly contributed to its growth and success. The working environment at Kimia Biosciences is characterized by simplicity, informality, and flexibility, with a strong emphasis on values, fostering an intellectually stimulating atmosphere for employees. Prospective applicants are attracted to our culture, which prioritizes its people and is known for its diverse and knowledgeable talent pool. The review procedure is based on performance, meritocracy, and equity, ensuring a fair and transparent evaluation process. If you are someone with experience in stability schedules, handling samples, preparing reports, and familiar with OOS and data integrity issues, and seeking a challenging role in a reputable API manufacturing company in Gurgaon, then this opportunity at Kimia Biosciences might be the perfect fit for you.,
Role Overview: At Kimia Biosciences, we value our people and prioritize a people-first approach. As a dynamic API manufacturing company based in India, we pride ourselves on being world-class in innovative technology. Our growth from 2012 to 2020 is attributed to the commitment, ability, and relentless efforts of our employees. We have a team of committed, high-performing, passionate, and excellent professionals who have contributed significantly to our development and growth. Our management style combines wisdom with excellent Human Resource practices to compete in the pharmaceutical market by attracting top talent and fostering a corporate culture of equality and growth. Key Responsibilities: - Must have experience in various analytical method transfers from ADL to QC - Preparation of Analytical method validation protocols and reports - Experience in analytical method validation and reviewing of Analytical method validation reports - Familiarity with published guidelines on analytical method validation and transfer - Awareness of data integrity issues Qualifications Required: - Relevant experience in analytical method transfer and validation - Knowledge of published guidelines on analytical method validation - Understanding of data integrity issues (Note: No additional details of the company were provided in the job description),
As a Senior Executive/Executive in the Stability Section at Kimia Biosciences, you will play a crucial role in maintaining stability schedules, handling inward and withdrawal of stability and hold time samples, preparing stability reports, extrapolating stability data, determining shelf life, and being aware of OOS, lab incidences, as well as data integrity issues. Key Responsibilities: - Maintain stability schedules - Handle inward and withdrawal of stability and hold time samples - Prepare stability reports - Extrapolate stability data and determine shelf life - Be aware of OOS, lab incidences, and data integrity issues Qualifications Required: - Must have experience in maintaining stability schedules - Familiarity with inward and withdrawal of stability and hold time samples - Proficiency in preparing stability reports - Knowledge of extrapolating stability data and determining shelf life - Awareness of OOS, lab incidences, and data integrity issues At Kimia Biosciences, you will be part of a dynamic API manufacturing company in India that values its people and follows a people-first approach. The company prides itself on being innovative and attributes its growth to the commitment and relentless efforts of its employees. The management style combines excellence with best Human Resource practices to create a competitive edge in the Pharmaceutical market. The working environment is simple, informal, and flexible, with a strong emphasis on values. You can expect a people-friendly work culture, where ideas are valued, and you have space and freedom to make and execute decisions in an intellectually stimulating environment. Performance reviews are based on meritocracy and equity.,
Job Responsibilities 1. Engineering Operations & Maintenance Lead and manage preventive, predictive, and breakdown maintenance for equipment, utilities, HVAC, water systems, and infrastructure. Ensure optimal performance and uptime of manufacturing equipment and utilities (Reactors, centrifuge, dryers, pumps, AHUs, chillers, boilers, pws systems, HVAC, Air compressors, etc.). Manage calibration of instruments as per schedule. Drive continuous improvement in equipment reliability and energy efficiency. 2. Project Management Plan and execute CAPEX projects (facility upgrades, new installations, expansions). Coordinate with cross-functional teams, vendors, and contractors to ensure timely and cost-effective project completion. Ensure qualification and validation of new equipment as per cGMP. 3. Compliance & Regulatory Adherence Ensure engineering compliance with regulatory requirements: GMP, WHO etc. Maintain documentation for engineering audits (SOPs, equipment logs, preventive, calibration records, validation & requalification etc.). Support audits and inspections; address observations related to engineering and facilities. 4. Utility & Facility Management Oversee operation and maintenance of utilities: HVAC, purified water, Chillers, Air compressors, Boiler, power supply etc. Ensure HVAC and environmental systems support required cleanroom classifications and environmental controls. 5. Team Leadership & Development Lead and mentor the engineering and utility team. Develop skill matrix and training plans for team members. Foster a culture of safety, ownership, and continuous improvement. 6. Budgeting and Cost Control Prepare and manage engineering budgets (OPEX and CAPEX). Monitor and control expenses, ensuring cost-effective operations.
Role & responsibilities Production Planning Inventory Management Supply Chain Coordination Demand Forecasting Process Improvement Reporting & Analysis Team Leadership & Development Compliance & Documentation Cross-Functional Collaboration Preferred candidate profile Education: Bachelors degree in Supply Chain Management, Production Management, Industrial Engineering, or a related field. A Masters degree or relevant certification (e.g., APICS, Six Sigma) is preferred. Experience: Minimum of 6-10 years of experience in production planning, inventory control, or supply chain management within the pharmaceutical or API manufacturing industry. Proven track record of managing production schedules, optimizing inventory levels, and coordinating supply chain activities. Experience with SAP systems and inventory management software.
Position Summary. Formulation Operator is responsible for carrying out manufacturing activities related to oral solid dosage (OSD) forms, including granulation, compression, and coating operations. The role ensures all processes are executed in compliance with GMP, SOPs, and safety guidelines while achieving required production targets and product quality standards. Key Responsibilities. 1. Granulation Operate and monitor granulation equipment (RMG, FBD, Blenders, Sifters). Perform material charging, mixing, wet granulation, drying, and sizing activities. Ensure granulation parameters are followed as per BMR/BPR. Conduct in-process checks such as LOD, bulk density, particle size, and granule uniformity. Maintain cleanliness of granulation area and equipment. 2. Compression Set up, operate, and troubleshoot tablet compression machines. Perform machine changeover, tooling installation, and parameter adjustments. Carry out in-process quality checks (weight variation, thickness, hardness, friability). Monitor tablet defects and take corrective actions. Ensure die and punch handling as per SOP to prevent damage or contamination. 3. Coating Operate coating machines (auto coater/equipment). Prepare coating solutions/suspensions as per approved instructions. Monitor critical coating parameters (spray rate, inlet/outlet temp, pan speed). Conduct IPC tests for coating uniformity, weight gain, and appearance. Handle cleaning and line clearance. Documentation & Compliance Complete BMR/BPR and logbook entries accurately and on time. Follow cGMP, GDP, and safety protocols strictly. Participate in line clearance, deviation reporting, and CAPA implementation. Ensure adherence to SOPs, safety guidelines, and production schedules. Equipment Handling & Maintenance Perform basic machine troubleshooting and coordinate with maintenance for repairs. Ensure calibration and proper functioning of weighing balances and critical instruments. Maintain 5S and hygiene standards in the work area.
Role Overview: Kimia Biosciences values its people and follows a people-first approach. As a dynamic API manufacturing company in India, we pride ourselves on being world-class in innovative technology. Our growth from 2012 to 2020 is attributed to the commitment, ability, and relentless efforts of our employees. At Kimia, we have a team of committed, high-performing, passionate professionals who have grown with us. Our management style combines wisdom with excellent Human Resource practices. To stay competitive in the Pharmaceutical market, we focus on attracting top talent and providing a corporate culture that fosters equality of growth. Key Responsibilities: - Must have experience in various analytical method transfer from ADL to QC - Preparation of Analytical method validation protocols and reports - Experience in analytical method validation - Reviewing of Analytical method validation report - Must be knowledgeable of published guidelines on analytical method validation and transfer - Awareness of data integrity issues Qualifications Required: - Experience in various analytical method transfers - Proficiency in preparing Analytical method validation protocols and reports - Familiarity with published guidelines on analytical method validation and transfer - Knowledge of data integrity issues (Note: Additional details of the company were not mentioned in the provided job description),
You will be working as a Senior Executive/Executive in the Stability Section at Kimia Biosciences in Gurgaon. Your role will involve the following responsibilities: - Maintaining stability schedules - Handling inward and withdrawal of stability and hold time samples - Preparing Stability reports - Extrapolating stability data and determining shelf life - Handling OOS and lab incidences - Dealing with OOS and data integrity issues You must have experience in these areas to apply for this position. Kimia Biosciences is known for valuing its employees and maintaining a people-first approach. The company emphasizes on providing a people-friendly work culture where ideas are valued, and employees have the space and freedom to make and implement decisions. The working environment is simple, informal, and flexible with a strong emphasis on values. Additionally, the company follows a review procedure based on performance, meritocracy, and equity.,