General Job Description Interact with cross functional teams (BD / CROM / Supply Planning / Material Planning Team) to provide and process information in response to inquiries, concerns and requests about pharmaceutical products and related services. Main Job Role and Responsibilities deal directly with CFT either by telephone, electronically or face to face respond promptly to inquiries, concerns & requests and communicate / coordinate with internal departments obtain and evaluate all relevant information to handle product and supply related inquiries Facilitate order acceptance direct requests and unresolved issues to the designated resource record details of inquiries, comments and complaints record details of actions taken Education and Experience PG in Pharmaceuticals or equivalent. MBAs would be preferred basic pharmaceuticals knowledge knowledge of relevant computer applications knowledge of administrative procedures numeric, oral and written language applications Expected work experience: 1-2 years in pharmaceutical or similar field(s) Key Competencies PG in Pharmaceuticals or equivalent. MBAs would be preferred basic pharmaceuticals knowledge knowledge of relevant computer applications knowledge of administrative procedures numeric, oral and written language applications Expected work experience: 1-2 years in pharmaceutical or similar field(s) interpersonal skills communication skills - verbal and written listening skills problem analysis and problem-solving attention to detail and accuracy data collection and management adaptability ability to take initiatives stress tolerance Show more Show less
Position: Manager - Production Derma (Ointment, Cream, Lotion, Gel) Key Responsibilities: Responsible for all the activities starting from RM dispensing till the products reaches the packing stage. To approve the instructions relating to production operations (SOPs & Batch manufacturing) and ensure their strict implementation. To ensure that the production operations are carried out as per cGMP regulations, required initial and continuing training of the department personnel. To ensure that requisite documentation like monthly stock statements, production reports are made. To ensure that calibrations and preventive maintenance are done at regular intervals. To coordinate with PPIC regarding production schedule To coordinate with QA, QC and stores for implementation of planned production schedule. To ensure that plant hygiene including cleaning and sanitation is performed and maintained. To ensure the implementation of Safety, Health and Environment policy requirements in the plant. Responsible for carrying out Environmental Management System related activities. Coordination with Vendor for smooth functioning of manufacturing process. To review and approval of risk assessments. Candidate Profile: Education: B. Pharmacy or M. Pharmacy Experience: 15-20 years in Pharmaceutical Production with proven experience in Derma (Ointment, Cream, Lotion, Gel) Regulatory Manufacturing facility. Strong Leadership, People Management, Experience in Regulated markets (USFDA) is essential. Show more Show less
Company Description Aurobindo Pharma Limited is an integrated global pharmaceutical company headquartered in Hyderabad, India. The company develops, manufactures, and commercializes a wide range of generic pharmaceuticals, branded specialty pharmaceuticals, and active pharmaceutical ingredients in over 150 countries. With 25 manufacturing and packaging facilities approved by leading regulatory agencies like USFDA, UK MHRA, and WHO, Aurobindo Pharma has a robust product portfolio across 7 major therapeutic areas including CNS, Antiretroviral, and Antibiotics. The company is supported by a strong R&D set-up to innovate and deliver high-quality products. Role Description This is a full-time on-site role for a Transdermal Operator located in Hyderabad. The Transdermal Operator will be responsible for the day-to-day operation of transdermal manufacturing equipment, ensuring adherence to SOPs and safety standards. Tasks will include the preparation of batches, machine maintenance, quality control activities, and documentation of production records. The Transdermal Operator will work closely with the quality and R&D teams to ensure the highest standards of product quality. Qualifications Experience in operating pharmaceutical manufacturing equipment Knowledge of SOPs, GMP, and safety protocols Quality control and documentation skills Mechanical aptitude and problem-solving skills Excellent attention to detail and ability to work in a team Experience with transdermal systems is a plus High school diploma or equivalent; additional technical certification is preferred
As a pharmaceutical customer service representative, you will be responsible for interacting with cross-functional teams including Business Development, Customer Relationship Management, Supply Planning, and Material Planning Team. Your main role will involve dealing directly with the cross-functional team members via various communication channels to address inquiries, concerns, and requests related to pharmaceutical products and services. You will need to respond promptly to these communications, coordinate with internal departments, and ensure the smooth processing of information. Your responsibilities will also include obtaining and evaluating all relevant information necessary to address product and supply-related inquiries, facilitating order acceptance, and directing unresolved issues to the appropriate resources. It will be essential for you to maintain detailed records of inquiries, comments, complaints, and the actions taken to resolve them. To qualify for this position, you should hold a Post Graduate degree in Pharmaceuticals or an equivalent qualification, with preference given to candidates with an MBA. You are expected to have basic knowledge of pharmaceuticals, relevant computer applications, administrative procedures, and possess strong numeric, oral, and written communication skills. Ideally, you should have 1-2 years of work experience in the pharmaceutical or a related field. Key competencies for success in this role include interpersonal skills, effective communication (both verbal and written), active listening, problem analysis, attention to detail, data management, adaptability, taking initiatives, and maintaining stress tolerance in a fast-paced environment. Overall, your role as a pharmaceutical customer service representative will require you to effectively communicate with internal teams, handle inquiries and issues efficiently, and contribute to the smooth functioning of operations within the pharmaceutical sector.,
Company Description Aurobindo Pharma Limited, headquartered in Hyderabad, India, is an integrated global pharmaceutical company that develops, manufactures, and markets a wide range of generic pharmaceuticals, branded specialty drugs, and active pharmaceutical ingredients (APIs) across more than 150 countries. Ranked among the top 10 generic companies in eight European nations, it is the largest generic pharmaceutical company in the United States. With over 30 state-of-the-art facilities approved by leading global regulatory authorities, Aurobindo Pharma ensures the highest standards of quality in its products. The company's robust portfolio spans eight major therapeutic areas and is supported by a strong R&D infrastructure that drives innovation, affordability, and accessibility. Role Description This is a full-time, on-site role for a Purchase Executive located in Hyderabad. The Purchase Executive will be responsible for managing purchase orders and requisitions, handling procurement processes, and ensuring timely and accurate processing of purchasing documents. Additional responsibilities include coordinating with suppliers, maintaining purchasing records, and assisting in the development and implementation of purchasing strategies. Qualifications Experience with Purchase Orders, Purchase Requisitions, and Purchase Management Strong Communication and Procurement skills Excellent organizational and time management skills Ability to work independently and collaboratively in a fast-paced environment Bachelor’s degree in Supply Chain Management, Business Administration, or related field Experience in the pharmaceutical industry is a plus
As a Manager - Production Derma (Ointment, Cream, Lotion, Gel), your role will involve overseeing various activities related to production operations in a Pharmaceutical Manufacturing facility. Your responsibilities will include: - Overseeing all activities from Raw Material dispensing to the final packing of products. - Approving and ensuring strict implementation of production operation instructions including SOPs and batch manufacturing processes. - Ensuring production operations comply with cGMP regulations and conducting initial and ongoing training for department personnel. - Managing documentation such as monthly stock statements and production reports. - Scheduling and overseeing calibrations and preventive maintenance activities. - Coordinating with PPIC for production schedules and with QA, QC, and stores for planned production implementation. - Ensuring plant hygiene, cleaning, and sanitation practices are maintained. - Implementing Safety, Health, and Environment policy requirements within the plant. - Carrying out activities related to Environmental Management System and coordinating with vendors for smooth manufacturing processes. - Reviewing and approving risk assessments. Qualifications required for this role: - Education: B. Pharmacy or M. Pharmacy - Experience: 15-20 years in Pharmaceutical Production with a track record in Derma (Ointment, Cream, Lotion, Gel) Regulatory Manufacturing facility. - Strong leadership and people management skills are essential, along with experience in regulated markets such as USFDA.,
As a Customer Service Representative in the pharmaceutical industry, your role involves interacting with cross functional teams such as BD, CROM, Supply Planning, and Material Planning Team. You will be responsible for providing and processing information in response to inquiries, concerns, and requests about pharmaceutical products and related services. Your main job responsibilities include: - Dealing directly with the cross functional team either by telephone, electronically, or face to face - Responding promptly to inquiries, concerns, and requests and communicating/coordinating with internal departments - Obtaining and evaluating all relevant information to handle product and supply-related inquiries - Facilitating order acceptance - Directing requests and unresolved issues to the designated resource - Recording details of inquiries, comments, and complaints - Recording details of actions taken For this role, you are required to have: - PG in Pharmaceuticals or equivalent. MBAs would be preferred - Basic pharmaceutical knowledge - Knowledge of relevant computer applications - Knowledge of administrative procedures - Numeric, oral, and written language applications - Expected work experience: 1-2 years in pharmaceutical or similar field(s) Key competencies for this position include: - Interpersonal skills - Communication skills - verbal and written - Listening skills - Problem analysis and problem-solving - Attention to detail and accuracy - Data collection and management - Adaptability - Ability to take initiatives - Stress tolerance You will play a crucial role in ensuring effective communication and coordination within the cross functional teams and providing satisfactory responses to inquiries and concerns related to pharmaceutical products and services.,
Position : AGM - Production Injectables. Experience : 14 to 18 years. Designation : Assistant General Manager Qualification : M. Pharmacy/Pharmacy Experience from sterile formulation industry (Injectable) No.of Vacancies : 1 Job Description Responsible to ensure all the activity in manufacturing area of lines. Approval of Indented Raw Materials, Primary Packaging Materials as per the production plan. Coordination with cross functional team in the batch planning and ensure the Process flow, Personnel flow; Material flow shall be done as per the procedures. To ensure compliance to the validation schedules - qualification, requalification of area, equipment, and facility. To Ensure Prior intimation to validation team regarding any qualification, requalification of area, equipment, and facility. Initiation, review, and timely closure of all QMS elements like Change control, PNC, Exceptions and CAPA as per procedure. Attending trainings like on job, cGMP, External and Giving training on process related SOPs. Updating cGMP related practices and recent regulatory up gradation to the personnel working in the shop floor to improve the systems. Co-ordination with training team and ensures the completion of training of all the production personnel working in respective areas. Following safety systems and GMP systems during the work execution. To ensure the compliance of all the observation of internal audits. Responsible for final review of in-process and Finished product batches To ensure air flow visualization study (smoke study) as per approved protocol/sop. Review and approval of CPV Monitoring Plan Responsible for guiding visitors and auditors for Plant visit/Audit. (ref:iimjobs.com)
Position : AGM - Production Injectables. Experience : 14 to 18 years. Designation : Assistant General Manager Qualification : M. Pharmacy/Pharmacy Experience from sterile formulation industry (Injectable) No.of Vacancies : 1 Job Description Responsible to ensure all the activity in manufacturing area of lines. Approval of Indented Raw Materials, Primary Packaging Materials as per the production plan. Coordination with cross functional team in the batch planning and ensure the Process flow, Personnel flow; Material flow shall be done as per the procedures. To ensure compliance to the validation schedules - qualification, requalification of area, equipment, and facility. To Ensure Prior intimation to validation team regarding any qualification, requalification of area, equipment, and facility. Initiation, review, and timely closure of all QMS elements like Change control, PNC, Exceptions and CAPA as per procedure. Attending trainings like on job, cGMP, External and Giving training on process related SOPs. Updating cGMP related practices and recent regulatory up gradation to the personnel working in the shop floor to improve the systems. Co-ordination with training team and ensures the completion of training of all the production personnel working in respective areas. Following safety systems and GMP systems during the work execution. To ensure the compliance of all the observation of internal audits. Responsible for final review of in-process and Finished product batches To ensure air flow visualization study (smoke study) as per approved protocol/sop. Review and approval of CPV Monitoring Plan Responsible for guiding visitors and auditors for Plant visit/Audit. (ref:iimjobs.com)
Manager Production QMS Experience : 13 - 18 years Role & Responsibilities Manage Manufacturing Operations: Lead and supervise all activities in the manufacturing section to ensure smooth and efficient operations. Production Planning & Execution: Plan and execute manufacturing schedules in coordination with Project Management and Supply Chain teams. Compliance & Quality Assurance: Implement and monitor adherence to current Good Manufacturing Practices (cGMP), quality standards, and documentation practices. Continuous Improvement & CAPA: Review and approve process deviations, non-conformances, and corrective/preventive actions in coordination with QA. Training & Team Development: Conduct training on standard operating procedures and promote a strong quality and safety culture within the team. Preferred Candidate Profile Bachelor's/Masters degree in Pharmacy, or related field. 13-18 years of experience in manufacturing/QMS roles within the pharmaceutical or related industries. Strong knowledge of GMP, QMS documentation, and audit compliance. Excellent leadership, communication, and problem-solving skills. (ref:iimjobs.com)
Manager Production QMS Experience : 13 - 18 years Role & Responsibilities Manage Manufacturing Operations: Lead and supervise all activities in the manufacturing section to ensure smooth and efficient operations. Production Planning & Execution: Plan and execute manufacturing schedules in coordination with Project Management and Supply Chain teams. Compliance & Quality Assurance: Implement and monitor adherence to current Good Manufacturing Practices (cGMP), quality standards, and documentation practices. Continuous Improvement & CAPA: Review and approve process deviations, non-conformances, and corrective/preventive actions in coordination with QA. Training & Team Development: Conduct training on standard operating procedures and promote a strong quality and safety culture within the team. Preferred Candidate Profile Bachelor's/Masters degree in Pharmacy, or related field. 13-18 years of experience in manufacturing/QMS roles within the pharmaceutical or related industries. Strong knowledge of GMP, QMS documentation, and audit compliance. Excellent leadership, communication, and problem-solving skills. (ref:iimjobs.com)
As a Manager - Production Derma (Ointment, Cream, Lotion, Gel), your role involves overseeing various activities related to production operations in a Pharmaceutical Manufacturing facility. Your responsibilities include: - Responsible for all activities from Raw Material dispensing to the product reaching the packing stage. - Approval and strict implementation of production operations instructions, including SOPs and Batch manufacturing. - Ensuring production operations comply with cGMP regulations, providing initial and ongoing training to department personnel. - Documentation management such as monthly stock statements and production reports. - Scheduling and overseeing calibrations and preventive maintenance activities. - Coordination with Production Planning and Inventory Control (PPIC) for production schedule. - Collaborating with Quality Assurance (QA), Quality Control (QC), and Stores for planned production schedule implementation. - Maintaining plant hygiene through cleaning and sanitation practices. - Implementation of Safety, Health, and Environment policy requirements within the plant. - Carrying out Environmental Management System related activities. - Vendor coordination to ensure smooth manufacturing process functioning. - Review and approval of risk assessments. Qualifications required for this role: - Education: B. Pharmacy or M. Pharmacy. - Experience: 15-20 years in Pharmaceutical Production with a focus on Derma (Ointment, Cream, Lotion, Gel) Regulatory Manufacturing facility. - Strong leadership skills, people management abilities, and experience in regulated markets (USFDA) are essential for this position.,
Job Title: EHS Officer (Experienced Only) Company: AUROBINDO PHARMA LTD Location: Jadcherla, Telangana, India (On-site) Employment Type: Full-time Job Function: Environment, Health & Safety (EHS) Industry: Pharmaceuticals About the Role We are immediately hiring an experienced EHS Officer to join our team at the Aurobindo Pharma Unit 7 facility in Jadcherla. This critical role ensures operational safety and environmental compliance within our Active Pharmaceutical Ingredients (API) and Formulations manufacturing units. We are looking for dedicated professionals with hands-on industry experience. Key Responsibilities: Ensure site compliance with all applicable EHS regulations, including the Factories Act and PCB norms. Conduct regular hazard identification, risk assessments, and implement robust corrective and preventive actions (CAPA). Manage safe systems of work for hazardous activities, including confined space entry, electrical safety, and chemical handling. Coordinate EHS training programs, induction sessions, and emergency response drills (e.g., fire drills). Lead incident investigations, prepare detailed Root Cause Analysis (RCA) reports, and track safety metrics. Maintain accurate EHS documentation and support internal/external audits (ISO 14001, ISO 45001, USFDA). Required Qualifications & Experience Experience: Minimum of 2-6 years of direct EHS experience is required. Must have worked within a pharmaceutical API or Formulations manufacturing unit . Education: Candidates must possess one of the following qualifications: B.Sc. in Chemistry. Diploma in Mechanical Engineering (or a related engineering field). SBTET (State Board of Technical Education and Training) Diploma or Certification in Industrial Safety. Skills: Strong knowledge of EHS management systems and legal requirements. Excellent problem-solving, communication, and interpersonal skills. Proficiency in maintaining EHS records and documentation. You can send your updated CV with the subject line "Application for EHS Officer – Jadcherla Unit 7" to PavanKumar.Gurramkonda@Aurobindo.com #EHS #SafetyOfficer #AurobindoPharma #Jadcherla #Hiring #Pharmaceuticals #API #Formulations #IndustrialSafety #TelanganaJobs #HSE #NowHiring #JobOpening
Position : AGM - Production Injectables. Experience : 14 to 18 years. Designation : Assistant General Manager Qualification : M. Pharmacy/Pharmacy Experience from sterile formulation industry (Injectable) No.of Vacancies : 1 Job Description Responsible to ensure all the activity in manufacturing area of lines. Approval of Indented Raw Materials, Primary Packaging Materials as per the production plan. Coordination with cross functional team in the batch planning and ensure the Process flow, Personnel flow; Material flow shall be done as per the procedures. To ensure compliance to the validation schedules - qualification, requalification of area, equipment, and facility. To Ensure Prior intimation to validation team regarding any qualification, requalification of area, equipment, and facility. Initiation, review, and timely closure of all QMS elements like Change control, PNC, Exceptions and CAPA as per procedure. Attending trainings like on job, cGMP, External and Giving training on process related SOPs. Updating cGMP related practices and recent regulatory up gradation to the personnel working in the shop floor to improve the systems. Co-ordination with training team and ensures the completion of training of all the production personnel working in respective areas. Following safety systems and GMP systems during the work execution. To ensure the compliance of all the observation of internal audits. Responsible for final review of in-process and Finished product batches To ensure air flow visualization study (smoke study) as per approved protocol/sop. Review and approval of CPV Monitoring Plan Responsible for guiding visitors and auditors for Plant visit/Audit. (ref:iimjobs.com)
Company Description Aurobindo Pharma Limited, headquartered in Hyderabad, India, is a leading global pharmaceutical company operating in over 150 countries. The company specializes in developing, manufacturing, and marketing a comprehensive range of generic pharmaceuticals, branded specialty drugs, and active pharmaceutical ingredients (APIs). Recognized as the largest generic pharmaceutical company in the United States and prominent in Europe, Aurobindo Pharma operates over 30 advanced manufacturing and packaging facilities approved by major regulatory authorities like USFDA, UK MHRA, and more. With a diverse portfolio spanning eight major therapeutic areas and a robust R&D infrastructure, Aurobindo is dedicated to innovation, quality, affordability, and accessibility in the healthcare space. Role Description The Assistant Manager role is a full-time, on-site position located in Naidupeta. The primary responsibilities include overseeing daily operational activities, ensuring compliance with regulatory standards, and managing production or process operations within the assigned department. The Assistant Manager will monitor and improve production efficiency, implement best practices, and ensure adherence to quality and safety standards. Additional duties include coordinating with cross-functional teams, preparing reports, and supervising a team to achieve organizational goals effectively. Qualifications Strong understanding of pharmaceutical production processes, manufacturing operations, and compliance regulations Leadership and team management skills to supervise and guide team members effectively Proficiency in process monitoring, quality assurance, and optimization techniques Excellent communication, problem-solving, and decision-making abilities Educational qualifications in Pharmacy, Chemistry, or a related field; advanced degree preferred Familiarity with regulatory standards such as USFDA, WHO, and GMP guidelines Relevant experience in a managerial role within the pharmaceutical or manufacturing industry is a plus Strong organizational and time-management skills to handle multiple tasks and meet deadlines
Manager Production QMS Experience : 13 - 18 years Role & Responsibilities Manage Manufacturing Operations: Lead and supervise all activities in the manufacturing section to ensure smooth and efficient operations. Production Planning & Execution: Plan and execute manufacturing schedules in coordination with Project Management and Supply Chain teams. Compliance & Quality Assurance: Implement and monitor adherence to current Good Manufacturing Practices (cGMP), quality standards, and documentation practices. Continuous Improvement & CAPA: Review and approve process deviations, non-conformances, and corrective/preventive actions in coordination with QA. Training & Team Development: Conduct training on standard operating procedures and promote a strong quality and safety culture within the team. Preferred Candidate Profile Bachelor's/Masters degree in Pharmacy, or related field. 13-18 years of experience in manufacturing/QMS roles within the pharmaceutical or related industries. Strong knowledge of GMP, QMS documentation, and audit compliance. Excellent leadership, communication, and problem-solving skills. (ref:iimjobs.com)