The ideal candidate should have at least 3 years of experience of working in Pharmaceutical Production floor where the person is responsible for shift operations. The incumbent would typically be responsible for: Ensuring the targets are met keeping in mind safety and quality guidelines. Management and upkeep of facility, materials and manpower. Troubleshooting in operations, validations and equipment qualification Coordination with other functions like QC, QA, Warehouse among others. Knowledge and Adherence to SOPs , regulatory requirement Preparing Batch Manufacturing Records, Protocols, Reports, Investigation Reports, and Qualification Reports. Work on Continuous improvement Plans (like Capacity and Manpower Utilization, Product Cost Effectiveness, Effluent Control and Safety Improvement, etc.)
Role & responsibilities POSITION SUMMARY The primary function of the Environmental Health and Safety Manager will be to create a strategic partnership with department leaders to assist in identifying workplace safety and health risks and implementing control measures that align with site and corporate initiatives. The EHS Supervisor is responsible for knowing, interpreting, and appropriately applying all applicable federal, state, and local laws, statutes and regulations. MAJOR DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned Lead site audits, risk assessment activities and implement corrective action promptly to ensure company and regulatory compliance. In partnership with operational leadership, set up and maintain safety training programs in all applicable safety competency areas. Assure training is appropriately documented, reviewed constantly to assure compliance and timeliness and maintain appropriate written records/documentation of such training being conducted and reinforced. Perform facility safety audits to ensure company and regulatory compliance. Exhibit safety awareness and safe work practices. Preparation and presentation of safety training programs and orientation information. Test and inspect safety equipment such as eyewashes, showers, fire extinguishers, etc. Guide and promote safe work performance by enforcing safety policies, implementing safety campaigns, and training managers and employees in safe practices and first aid. Supervision of physical security. Ensure that the security for the building is functioning well at all times. Assist with the maintenance of the card entry system. Recommend and implement methods to increase the quality of products and/or services. Comply with federal, state and local safety regulation by interpreting standards, enforcing adherence to regulations, completion of regulatory documents and advising management on needed actions. Maintain all necessary records for the same. Disseminate Occupational Safety and Health Administration (OSHA) rules and regulations. Eliminate or minimize hazardous situations by developing and recommending safety policies and procedures to senior management. Watch for and report irregularities such as fire hazards, unlocked doors, etc. Notify emergency services in case of fire or if in the presence of unauthorized persons. Inspect and ensure that the ETP / STP / WTP are functioning well and all relevant standards are being met. Ensure that all waste material is stored / removed in a safe and timely manner. Notify higher management of any discrepancies that might arise. Assist with the maintenance of Personal Protective Equipment. Assis with the maintenance of MSDS library. Responding to and investigating incidents. Participate in self-development activities. Train and communicate the importance of safety to all the existing and new employees and be able to strongly recommend and influence safe work practices. Maintain inventory and oversee distribution of controlled drug substances as pertains to on-site use for scientific purposes. Ensuring all safety norms are adhered to when consignments are shipped out. Complete and file all federal and state documentation as required. Work closely with all scientific staff and all other departments of the organization. Fleet management pertaining to movement of man and material. Assist in the development of the annual budget and track performance against the plan. Willing to put in long hours, if required depending on exigencies. Writing reports and making presentations on safety and security to higher management. Perform other duties as may be reasonably assigned in the course of business Preferred candidate profile B.Tech Chemical Engineering/ M.Sc Chemistry with Min 10 to 12years of EHS experience in Pharma Industry. Experience of EHS in R&D/Manufacturing pharma would be added advantage. Fluency in English is mandatory.
Role & responsibilities The Inventory Accounting Assistant Manager is responsible for performing the following tasks related to period close: Executing period close jobs/procedures in ERP such as standard cost rollup, period close, subledger accounting (SLA), purchasing, etc. Perform accounting edit checks & diagnostics to identify, analyze, and clear any errors that are preventing period close Reconcile inventory subledger and the walk to the ending value in the general ledger at the item-lot level Prepare and record capitalization & amortization adjustments for purchasing and manufacturing variances Perform monthly reserve analysis and adjustments Cost analysis, inventory control, product unit cost reporting Participating in projects and COE initiatives that improve the accounting practices and procedures and Provide support for special projects on an as needed basis Analysis of materials wise cost absorption and performing variances analysis Standard cost Updation - annual Preparation of Product Costing/ MIS / Estimated plant performance statement Reconcile and record surplus/deficit related to the annual physical inventory counts Prepare and summarize detailed rollforward/rollback of physical inventory count to year-end. Support internal/external audit requests Support efforts to improve or modify system accounting logic/mapping Monitor and test inventory processes and methodologies to ensure compliance with company accounting policies Calculate monthly ASC 606 inventory derecognition adjustments Perform periodic inventory forecasts Passing monthly closing entries in the books. Support the annual standards update Maintain and improve existing reporting and the development of new reporting. Support the general accounting element of strategic business initiatives and transactions, including mergers and acquisitions and the related due diligence and integration activities, as needed. Preferred candidate profile Accounting Graduate/Masters, / CMA-Inter / CA-Inter or any other Graduate degree in Accounting or equivalent experience; 11-13 years of accounting experience inventory accounting / cost accounting highly preferred Enterprise software experience required, Oracle experience required Management of diverse data population good organizational skills Ability to interact with various levels of employees, customers and vendors Strong analytical skills Good communication skills Good time management skills Ability to manage multiple priorities Shared services experience is preferred. This role is based out our global shared services center located at Hyderabad.
Role & responsibilities Handle Administrative works at the site, Preferred candidate profile -Any graduate who is active and has good communication skills. -Immediate joining -Preferable male candidates. - 0 to 2 years experience. - Should be working onsite at our Shameerpet, Genome Valley office. Position is on contract rolls.
Role & responsibilities The Senior Oracle Database Administrator (DBA) will serve as a key member of Curias Enterprise Applications and Infrastructure team, responsible for the design, implementation, maintenance, and optimization of Oracle database platformsincluding Oracle E-Business Suite R12.2, Oracle RAC, and Oracle Data Guard environments that support Curias global operations. This individual will play a critical role in ensuring database availability, scalability, performance, and compliance, while collaborating closely with application owners, infrastructure teams, and vendors to sustain and enhance enterprise systems across manufacturing, quality, finance, and scientific domains. This is a senior hands-on technical role, ideal for an experienced professional who can balance strategic oversight with deep technical execution. This role is not intended for entry-level or early-career candidates. Key Responsibilities **Core Database Administration** Lead the installation, configuration, administration, and upgrade of Oracle E-Business Suite R12.2, Oracle RAC, and Data Guard environments in line with Curias IT and GMP standards. Oversee cloning, patching, and refresh cycles of production and non-production environments, ensuring consistency, documentation, and minimal downtime. Manage Oracle Clusterware, ASM, and RAC environments to support high availability and disaster recovery. Implement, monitor, and fine-tune backup/recovery strategies using RMAN and Oracle Enterprise Manager. Maintain Data Guard configurations for physical and logical standby databases across multiple global sites. Conduct capacity planning, performance tuning, and proactive monitoring of system resources. **Systems Integration and Application Support** Partner with the Enterprise Applications team to support Oracle EBS integrations with surrounding systems (e.g., Salesforce, TrackWise Digital, LIMS, SAP Concur, ADP, etc.). Support application-tier and database-tier troubleshooting in collaboration with development and infrastructure teams. Participate in system validation and change control processes to ensure alignment with GxP and IT governance requirements. Coordinate with managed service providers (MSPs) and cloud hosting partners to maintain system uptime and patch compliance. **Security, Compliance, and Governance** Ensure adherence to data security, access control, and compliance with Curia’s policies and regulatory standards (e.g., SOX, FDA 21 CFR Part 11). Maintain proper audit and traceability controls in database and application environments. Support disaster recovery testing and documentation for critical systems. **Process Optimization and Continuous Improvement** Identify and drive opportunities for automation, standardization, and performance optimization. Provide technical mentorship and guidance to junior DBAs and other IT team members. Prepare and maintain system documentation, SOPs, and runbooks for all database operations. Collaborate with IT Business Analysts and Enterprise Architects to evaluate and implement emerging Oracle technologies or enhancements that add business value. **Operational Readiness and Support** Provide 24x7 on-call support on a rotational basis for production incidents, upgrades, and cutovers. Participate in major IT projects including ERP upgrades, carve-outs, migrations, and global transformation initiatives. Support quarterly Oracle EBS and database patching cycles, ensuring validation and minimal disruption to operations. Qualification and Experience: 10+ years of progressive experience as an Oracle DBA, including 3+ years in a senior or lead DBA role supporting mission-critical enterprise systems. Hands-on experience with: Oracle E-Business Suite R12.2.x (Financials, Projects, SCM, HRMS, etc.) Oracle Database 12c/19c, Oracle RAC, Data Guard, ASM, and Oracle Enterprise Manager (OEM) Performance tuning, capacity planning, and disaster recovery design Demonstrated ability to manage multiple projects, work collaboratively across global cross-functional teams, and meet aggressive timelines. Experience working in validated environments (GMP/GxP) preferred. Familiarity with SQL Server or APEX administration is a plus.
The Senior Quality Management Systems (QMS) Analyst will play a key role in managing and supporting Curias TrackWise Digital platform, which serves as the enterprise Quality Management System (QMS) and Document Management System (DMS). TrackWise Digital is a managed application on the SalesForce Cloud. This role requires a strong understanding of quality system processes - including Change Control, Deviations, CAPA, Complaints, Audits, and Document Control - combined with technical expertise in TrackWise Digital configuration, workflow management, integrations, and validation. The ideal candidate will bridge business needs and technical capabilities, ensuring that Curia’s global quality operations are efficiently supported, compliant with GMP regulations, and aligned with enterprise system governance standards. This is a role for an experienced professional with demonstrated initiative and ownership. Candidates who may not meet all requirements should demonstrate the ability to learn quickly, proactively seek knowledge, and deliver measurable value through innovation and continuous improvement. Key Responsibilities **System Administration & Support** Serve as the primary system administrator for Track Wise Digital (QMS and DMS), overseeing configuration, user access, roles, and security. Provide production support for day-to-day operations, including issue resolution, workflow troubleshooting, and coordination with vendor support. Support release patches, regression testing, upgrades, and environment validation. **Process & Configuration Management** Configure and enhance modules such as Change Control, CAPA, Deviations, Complaints, and Document Management in Track Wise Digital. Partner with business stakeholders to gather and analyze requirements, define solutions, and validate system changes. Implement approved configuration changes, test scripts, and validation documentation per GXP and CSV (Computer System Validation) standards. **Enhancement & Project Work** Work on minor enhancements (under 80 hours) directly; for larger enhancements, coordinate scoping and written estimates with IT management before execution. Support integrations between Track Wise Digital and other enterprise applications such as Oracle ERP, SAP, and LIMS. Collaborate with QA and IT validation teams to ensure compliant and timely deployment of enhancements. **Compliance & Documentation** Ensure ongoing compliance with GMP, FDA, and ISO 9001/13485 quality system requirements. Maintain up-to-date validation documentation, user access reviews, and change control records. Participate in audits and regulatory inspections, providing system information and documentation as needed. **Collaboration & Governance** Partner closely with Corporate Quality, IT Compliance, and Enterprise Applications teams to ensure alignment with Curia’s governance and data integrity principles. Contribute to the development and enforcement of global standards for TrackWise Digital configuration, usage, and documentation. Qualifications Education Bachelor’s degree in computer science, Life Sciences, Quality Management, or related field. Experience 5+ years of experience supporting a QMS/DMS application like TrackWise Digital (preferred) in a GMP or regulated environment. Strong understanding of quality management processes (Change Control, CAPA, Deviations, Complaints, Audits, Document Control). Hands-on experience with system configuration, testing, and validation documentation. Familiarity with integration concepts between QMS/DMS and ERP, LIMS, or CRM systems. Knowledge of CSV, 21 CFR Part 11, and GxP requirements. Technical Skills TrackWise Digital configuration and administration Workflow design and form configuration Data extraction/reporting (e.g., TWD Analytics, SQL basics) Validation and documentation management Soft Skills Strong analytical, communication, and problem-solving skills Ability to work independently and manage multiple priorities Proven initiative, ownership mindset, and commitment to quality and compliance Additional Notes This position is part of the Enterprise Applications team. It will collaborate with other analysts supporting Oracle ERP, SAP, Salesforce, and other enterprise systems to ensure end-to-end process continuity. Candidates must be detail-oriented, quality-driven, and able to thrive in a dynamic, global, cross-functional environment.
Role & responsibilities The Research Scientist Trainee is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Principal responsibility is the synthesis, purification, and identification of chemical intermediates and target compounds. A major component in the scientist's performance rating will be based on productivity. Preferred candidate profile M.sc Organic Chemistry (Only) freshers who can join as trainees on contract roll for 1 year. -Good chemistry knowledge -Onsite work
Role & responsibilities The Accounts Payable Intern is responsible for processing and maintaining the accounts payable records and performing accounts payable reconciliation. MAJOR DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. 1. Process accounts payable transactions in accordance with CURIA Global Accounting Policies # 7, Payables, Accruals and Other Liabilities. Processing includes voucher keying, working with scanning software for input (AP Express or other form of automation) 2. Process and communicate with vendors and CURIA employees on payment status, statement reconciliation and issues in a timely and consistent professional manner. 3. Provide assistance to all departments for vendor and invoice inquiries. 4. Perform other duties as may be assigned during business. Other Skills Excellent communication skills, written and verbal, with the ability to clearly communicate. Moderate knowledge of Microsoft Excel and Outlook QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Education and/or Experience B.com / M.com / MBA (Finance) Fresher passed out in 2025 and 2024. Language/Communication Skills Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. Mathematical Skills Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. Reasoning Ability Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Role & responsibilities Check daily hygiene of Plant and P.P. Area as well as its surroundings. Follow up the daily routine maintenance to the concerned department by issuing job orders. Coordinate daily with Warehouse personnel to issuance of all raw materials as per batch planning. Doing daily dispatch by coordination with the Warehouse, Quality Control, and Quality Assurance Department. Coordinating with various departments. Coordinate and execute related activities for Change control, Deviation handling, Corrective & Preventive action (CAPA), Out of Specification, Out of Trend, Incidents are investigated & resolved through electronic software Like; Stratas, Velocity EHS & Oracle, etc. Responsible for the preparation of the operation-related SOP's, to meet the cGMP & regulatory requirements. Handle all production-related transactions (like Pick Slip generation, raw Material reservation, Material Transfer, Material Transaction in Batch, etc.)