You will be responsible for strictly following cGMP, Safety, and Environmental Practices in the manufacturing facility. Your duties will include filling Batch Manufacturing records and equipment cleaning records, as well as following Good Manufacturing practices during operations. It will be important to ensure Good Housekeeping in the plant area and equipment, and to use proper personal protective equipment as required. You will be in charge of planning and ensuring the availability of raw materials for daily production according to the production plan. Additionally, you will need to maintain documents such as Issue and dispensing register, and carry out processes as per Batch Manufacturing Record without any deviation. It will be crucial to adhere to data integrity in online documentation and handle hazardous operations safely. Part of your role will involve effectively utilizing resources such as utilities, personnel, and machinery to support efficient production processes.,
As the Project Manager within Piramal Pharma Solutions" Engineering & Projects department based in Digwal, Hyderabad, you will have the overarching responsibility of managing projects from start to finish. This includes tasks such as design, budgeting, vendor coordination, and ensuring timely completion within optimal costs. Your role will involve ensuring compliance with various regulatory standards such as GMP, ISO 14001, and OHSAS 18001. Additionally, you will lead the commissioning, validation, and operational readiness of facilities and equipment, while proactively managing safety and environmental risks by implementing robust SHE practices. Continual improvement will be a key focus, achieved through risk assessments, CAPA implementation, and providing comprehensive training to both internal teams and contractors. Reporting directly to the Site Head, you will oversee a team of 6-8 individuals. To excel in this role, you are expected to bring at least 15 years of experience in Manufacturing, GMP, Safety, and resolving technical customer queries. Strong communication skills are essential for effective collaboration with various stakeholders. Key competencies required for this position include QMS handling, understanding changing regulatory requirements, confidence in facing audits, team management, conducting quality investigations, possessing analytical knowledge, collaborating with cross-functional teams (CFTs), and serving as the Single Point of Contact (SPOC) for CDMO projects. Your main responsibilities will revolve around the identification, evaluation, and implementation of projects within set timelines and budgets. This will involve designing facilities, selecting vendors and contractors, inspecting equipment and materials, issuing specifications and drawings, evaluating project progress, preparing budgets and schedules, overseeing project commissioning, validating facilities, and ensuring compliance with ISO14001:2004 and OHSAS 18001:1999 requirements. You will also be responsible for identifying risks and hazards, developing objectives and targets under EMS & OHSMS, implementing operational controls, conducting root cause analysis for non-conformities, and driving continual improvement in OHS & EMS Management Systems. Additionally, identifying SHE training needs, ensuring SHE requirements with contracted services and providers, and maintaining a focus on safety and environmental practices will be crucial aspects of your role.,
As an IT Manager at Piramal Pharma Solutions API Services in Digwal (V), Telangana, India, your primary responsibility will be to ensure the efficient operation of the IT department in alignment with Piramal's IT objectives while meeting acceptable service levels for the user community. You will report to the Head of Department-IT and work closely with key stakeholders, both internal (SLT) and external (Clients and Customers). To excel in this role, you should have at least 10 years of industry experience, with 3-7 years of experience leading significant IT services and delivery in medium or large global pharma organizations. Your technical skills should include expertise in Industrial Automation Systems (PLCs, SCADA, DCS, MES), OT-IT Convergence, Industry 4.0 concepts, Database Management (SQL, NoSQL), and Automation Platforms (Python, Ladder Logic, C#). Proficiency in project management methodologies like Agile, Scrum, or Waterfall will be advantageous. Your managerial skills will be crucial in overseeing end-to-end implementation of manufacturing IT solutions, managing relationships with automation vendors and IT service providers, and ensuring compliance with industry standards such as ISO 27001, ISA 95/99, and GxP. Industry-specific expertise in compliance awareness (GAMP 5, 21 CFR Part 11) and quality systems (LIMS, EBR) will be highly beneficial. As part of your roles and responsibilities, you will be involved in implementing commercial applications like Process Historian and LIMS, analyzing system performance, developing engineering solutions, integrating new equipment, and resolving technical issues. You will also be responsible for training internal employees, supporting clients in application improvements, and providing exceptional customer service. Your success in this role will depend on your excellent written and oral communication skills, self-motivation, attention to detail, and time management abilities. A customer service orientation, willingness to work off-shift times if necessary, and the ability to work effectively in a team-oriented environment will be key attributes for thriving in this position.,
As a member of our team, your primary responsibilities will include the development and validation of methods for Assay, Dissolution, and related substances. You will also be responsible for the calibration of analytical instruments to ensure accurate and reliable results. Conducting routine and stability samples analysis of OSD formulations will be a key part of your role. To excel in this position, you must possess a good quality mindset and have a thorough understanding of GLP requirements. Your ability to write technical reports and prepare power point presentations will be essential for effectively communicating your findings and recommendations. Join us in this dynamic role where you will play a crucial part in ensuring the quality and accuracy of our analytical processes.,
As the Strategy Manager for PPL's three businesses - PPS, PCC, and CPD, your primary responsibility will be to drive the development of the strategy roadmap and strategic initiatives for the organization. You will work closely with internal stakeholders such as Business Heads, CXOs, Legal, Compliance, Investor Relations, and select Board members, as well as external consultants and investment bankers. Reporting directly to the Vice President of Strategy, you will lead a team of three members. The ideal candidate should hold a full-time MBA in Marketing, Operations, Finance, or Strategy from a Premier B School and possess 5-7 years of experience in strategy roles within the Pharma industry. Consulting experience is desirable but not mandatory. Critical qualities for this role include the ability to work strategically and collaboratively across businesses, proficiency in quantitative and qualitative analysis, scenario planning, and a strong understanding of strategy, pharma operations, M&A, and finance. Effective communication and interpersonal skills are crucial, along with the ability to influence key stakeholders without direct authority. Your key roles and responsibilities will involve driving strategic business initiatives, leading large programs and projects, identifying market trends, developing strategic roadmaps, and long-range plans. You will also be responsible for providing governance practices, creating collaterals for key review meetings, and developing external content for conferences and media interactions. Overall, you will serve as a key liaison between the Executive Committee members and other senior leaders within the organization, ensuring alignment and communication on various business aspects. This role requires a proactive and strategic mindset, strong analytical skills, and the ability to drive execution while fostering collaboration across multiple geographies and functions.,
As a Shift Operation Engineer, your responsibilities will include handling the shift operation and completing related documentation as required by SOP. You will be responsible for achieving targeted production, ensuring smooth, efficient, uninterrupted, and trouble-free operation and maintenance of the water plant, HVAC, and other utility equipment as per SOPs. Implementing best practices to comply with quality, safety, and regulatory requirements will be crucial in this role. Your tasks will also involve preparing, ensuring, and monitoring compliance of SOPs and related documentation of the engineering department. Initiating Change controls and Deviations, CAPA in the electronic system as per the need is essential. Monitoring operation, filter cleaning, filter replacement, and preventive maintenance activity of the HVAC system as per SOP, as well as checking and reviewing utility, water system, and HVAC Log books are part of your duties. It will be important to keep awareness of operational standards such as ISO 9001, ISO 14001, ISO 45001, and 13485, as well as following the regulations of various agencies like USFDA, EU, TGA, MHRA, ANVISA, WHO, Schedule M, etc. You will participate in qualification & requalification of machine/equipment and provide functional support for qualification, validation, and calibration activity. Active participation in DMS, OE, and EHS activities, as well as engagement in the process, will be required. Executing preventive maintenance plans of the respective area and ensuring good documentation and record-keeping are key tasks. Ensuring compliance of service floor activity and smooth operation and maintenance of utilities to provide uninterrupted services are also part of your responsibilities. Allocating jobs to workmen, supervising work for quality, and timely completion, as well as identifying repeated breakdowns and planning corrective actions to avoid recurrence with the engineering manager, will be important. Providing guidance and support to executives and workmen and imparting induction activity to all new joiners are also expected duties. Overall, your role will involve ensuring the proper working of HVAC systems & air conditioning units to maintain operational efficiency.,
As a Quality Control Analyst at Piramal Pharma Limited in Pithampur, your primary responsibility will be to perform testing on in-process samples, raw materials, finished drug products, and stabilities to support production and regulatory filings. You will be reporting to the QC Lab Supervisor. To excel in this role, you should have 0-1 years of experience in a cGMP laboratory setting. It is essential that you are familiar with cGMP and FDA requirements to ensure the quality and compliance of the testing processes. Your attention to detail, analytical skills, and understanding of regulatory standards will be crucial in contributing to the quality control operations of the company. Join our team at Piramal Pharma Limited and be a part of our commitment to delivering high-quality pharmaceutical products that meet regulatory standards.,
You will be responsible for performing testing on in-process material, bulk drug substance, finished drug product, and stability samples in a cGMP laboratory setting. Your role will involve ensuring compliance with cGMP and FDA requirements. The position reports to the QC lab Supervisor. The ideal candidate should have 2 to 6 years of experience in a cGMP laboratory environment and be familiar with cGMP and FDA requirements.,
The role involves planning and resource allocation for routine operations within the analytical development function. You will be responsible for ensuring timely analysis of finished products and raw materials for various projects. Your duties will include reviewing analytical data, raw data, daily usage logbooks, and lab notebooks to support operations. You will also be involved in preparing and reviewing critical documents such as Analytical Method validation protocols, reports, method transfer protocols, and Standard Operating Procedures (SOPs). Additionally, you will conduct literature searches and provide guidance on new method development. Another key aspect of the role is to review data for stability studies and ensure timely analysis of samples. You will need to identify resource needs and initiate procurement to prevent delays in project deliverables. Supporting product technology transfers and ensuring compliance with safety measures will also be part of your responsibilities. In terms of quality management, you will be required to raise change controls, ensure data integrity, and adhere to Good Manufacturing Practices (GMP). You will also handle documentation related to Quality Management Systems (QMS), Environmental Management Systems (EMS), and Occupational Health & Safety Assessment standards. As part of your job authority, you will review analytical data, plan and allocate resources, prepare and review SOPs, and technology transfer documents. You will also review calibration data, logbooks, and lab notebooks, as well as identify and report any near misses, hazards, or unsafe conditions. Other responsibilities include implementing QEHS policies and objectives, ensuring the use of personal protective equipment (PPE) during operations, and managing incidents and non-conformities effectively. You will also oversee work permit systems during maintenance activities and ensure proper waste disposal procedures are followed.,