Job Description Physical verification and readiness of equipment and instrument for process. Arranging the process accessories and consumables in process area before batch execution. Coordination for dispensing of raw material required for the production processes. Preparation of process, equipment and area related SOPs and EOP s. Preparation of process, area and equipment qualification/ validation protocols. Preparation and execution of various reports like process, equipment, area qualification and validation. Request and Issuance of BPR. Preparation and review of BPR. Preparation and execution of study protocols, URS as and when required Work Experience Four to Seven Years Education Masters in Biotechnology or Biochemistry B.Tech in Biotechnology or Biochemistry Competencies

Role & responsibilities To work as a study physician. Assessing the eligibility of the volunteers for participating in the study. Training of SOPs of Clinical Staff. Supervise Administration of investigational product, ICF process and all study activities from check in to check out as per applicable protocol and GCP guidelines. Management of medical emergencies during studies. Management of post study adverse event. Reveiweing of documents generated during study. Assist the CI/PI in medical aspect of the study. Preferred candidate profile Immediate to 1month joinees preferable

Long Description Collate field force training requirements identified through training needs analysis. Formulate a training framework, training plan, and road map for different levels (ME’s & AM’s)with clear objectives and KPIs for structured and integrated development of the field force. Organize and deliver field force training programs interactively and timely. Collaborate with Business unit to develop product refresh training, handling objections, presentations for current and new brands/indication launches. Reinforce the application of skills by participating in field activities, coaching, team role-play, and presentations. Provide in-field training support for Sales team in alignment with Organizational priorities. Run annual field force skills assessments, disease/product knowledge assessments, and generate insight reports incorporating performance against benchmarks and required remedial actions through Digital tools (SMART WINNR). Conduct or participate in other departmental training programs where appropriate, such as the Trainee Program. Prepare Field forces for current and future field related challenges through Proactive approach. Develop internal team members through structured Individual Development Plans (IDPs). Competencies Innovation & Creativity Process Excellence Collaboration Customer Centricity Developing Talent Strategic Agility Stakeholder Management Result Orientation Education Post Graduation in Business Management Graduation in Pharmacy Work Experience Minimum 5-10 years of Pharma Sales Training

Job Description Comply with all cGMP, GxP, and any other applicable regulatory requirements, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/managers. Daily planning, job allocation of departmental activities to fulfill the market requirement and commitment. Monitoring of IMS, Blister, Strip, Bulk, powder, and batch split-up activity. Responsible for shipper labeling as per EMO & all the transactions in SAP for finished products. Packing and documentation of assigned products as per instruction given in the BPR, SOP, and cGMP. Ensuring the movement of bulk, packing material, semi-finished, and finished goods as per SOP. Updating and monitoring of Overall Equipment Efficiency (OEE). To upkeep cleanliness of area and machine as per GMP requirement. Operation, washing, and cleaning of equipment and accessories used in related production activities as per SOP. Performing in-process checks as per respective BPR and recording of results of in-process checks in BPR. Monitoring of differential pressure, temperature, and relative humidity as per SOP. Ensure calibration and preventive maintenance of equipment and instruments as per approved schedule and the results of same meeting the standards. To initiate and review the request like additional material requisition, material return note, packing material carry forward stereo request and screen request, etc. Area and equipment usage documented as per SOP. Procurement, receipt nomenclature, issuance, retrieval, and destruction of change parts for packing. Online reconciliation and review of batch packing record. Preparation and review of Standard Operating Procedures and batch packing record. Preparation and review of validation and qualification of process and equipment. To organize and implement on-job training of employees and contractual workmen in the department. Handling of change controls, deviations, and CAPA through QAMS. To perform the investigation related to market complaints, deviations, nonconformities, and implementation of suitable corrective and preventive actions (outcomes of the investigations) within the proposed timelines. Coordination between PPC, PM, Engineering, and QC department to have smooth functioning of production activity. To ensure proper self-hygiene before entering the production area and follow all the rules and regulations set by the HR department. Plan for dispensing activities in accordance with the plan and to coordinate with production planning and control department for timely availability of P.M. To ensure effective control on usage of manpower, machine, and material in the department and maintain proper inventory of operating supplies in the department. To support Quality Management System and to report any discrepancy, abnormality, non-conformance, or any incidence observed to the department head and QA head. Checking of label, insert/outsert with batch packing record and also retention of all required packing material proof with batch packing record for packing section. Troubleshooting: Handling, ensuring, verifying, and troubleshooting of software like bar-coding (1D, 2D), ACG Inspection System for label, blister inspection system, inkjet coding, Data Acquisition System (DAS), and Caliber QAMS. Any additional responsibility delegated by the department head. Work Experience 2 to 5 Years Education Graduation in Pharmacy Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

Job Description EPO entries -Creation of SO. (LATAM, EUROPE, MENA, US, CANADA & SOUTH INDIA REGION) SAP - Creation of Free Sample orders & LL-LMSL (INTER PLANT) order punching. MWT - Creation of Customer master, up-dation of Customer master, enhancement of credit limit. Coordinating with logistics / Demand planning / plant team for dispatch & documentation Coordinating with Factory for dispatches of sample as per customer requirement. Co-ordinating with Customer for back office support . Payment follow up for LATAM, EUROPE & few India Customers. Uploading CDA in system. Any other office job as per requirements of SBU. Good communication skills knowledge of MS office, SAP software, etc. Work Experience- 5 years and above Education- Graduation Competencies Strategic Agility Innovation & Creativity Developing Talent Collaboration Stakeholder Management Customer Centricity Result Orientation Process Excellence 3. Customer Centricity 5. Result Orientation 7. Collaboration Communication Computer Skills

Open Positions: Officer / Executive / Sr Executive Quality Assurance & Quality Control : Analytical Skill on HPLC, Electrophoresis, Microbiology, Document Review, IPQA, Quality Systems, GMP Compliance, QA-QMS Biosimilars Manufacturing: Downstream (Operation of Chromatography systems) & Upstream (Handling of Single use and Stainless-steel bioreactors) Experience: 2 to 10 years of relevant experience in Biopharmaceutical Qualification: B Sc / B. Pharm/B Tech / M Sc in Microbiology / Biotechnology / Chemistry/M. Pharm Date : 01st June 2025, Sunday Time : 08:30 AM to 06:00 PM (Registration will be closed by 12:00 PM) Venue : Hotel Pride , 5, University Rd, Narveer Tanaji Wadi, Shivajinagar, Pune, Maharashtra 411005, India Note: All positions are based out at Pune, Gotawade.

Job Description The Executive, Corporate Communications works with a wide array of stakeholders including internal and external partners/vendors to achieve pre-defined goals. This position requires a high level of attention to detail, responsiveness, critical thinking skills, professionalism, and the ability to manage and prioritize multiple simultaneous requests in an effective manner. DUTIES AND RESPONSIBILITIES Acts as a key partner to stakeholders and is responsible for designing and implementing communication programs for social media audiences. Works closely with the Manager to roll out refresh of websites as and when needed. Supports the Manager on key strategic projects for various initiatives. Works with Data Analytics and website/social media teams to improve ROI on all campaigns. Contributes to development of creatives, graphics and videos for various campaigns. Work Experience 2-3 years experience in communications, media, and/or public relations in a professional services environment. Education Graduation Post Graduation in Mass Media or Marketing Competencies Result Orientation Customer Centricity Stakeholder Management Innovation Creativity Developing Talent Process Excellence Collaboration Strategic Agility

Job Description Conduct monthly MIS and variance analysis. Lead budgeting and MTP forecasting activities. Develop presentations for management review. Perform cost analysis and identify opportunities for cost reduction or savings. Analyze margins and assess the impact of changes in price and cost. Prepare business cases and propose key financial metrics to support decisive decision-making. Prepare capex budget Review and approve capex requistion Work Experience 8 - 10 years of experience Education Post Graduation in Chartered Accountancy Competencies Developing Talent Result Orientation Customer Centricity Strategic Agility Process Excellence Innovation Creativity Stakeholder Management Collaboration

Role & responsibilities 1) Candidate should have understanding and experience in development of different types of oral dosage forms like immediate release formulation/delayed release formulations/ pellet coating and controlled release formulation,hard gelatin capsule, soft gelatin capsules, solutions, suspensions, dry powders and syrups for different Regulated and semi regulated markets. 2) Carry out pre-formulation and formulation development experiments for new chemical entities and ANDA formulations. 3) Develop new technology platforms and conduct feasibility studies for novel formulations such as microspheres, pellets, and spherules, aqueous and non-aqueous suspensions, ophthalmic and spray coated particles using various polymers. This includes preparation of prototype formulations for bio/clinical studies, analyzing experimental data and preparation of technical reports. Follow existing or prepare new SOPs and equipment operating procedures. 4) Design, develop and conduct appropriate dissolution studies for the novel dosage forms. Prepare stability protocols and collect the stability data. As per ICH guidelines, set specifications for raw materials and finished products. Organize tech transfer of developed products to plants for the manufacturing of scale up, exhibit, clinical or bio study batches. Review bio study and clinical study designs and protocols. Support clinical supply manufacturing and labeling activities along with drug supply inventory control and reconciliation. 5) Maintain inventory and reconciliation of Innovator products. Maintenance and up keeping of the lab and pilot areas. Give timely support in resolving regulatory queries. 6) Analyze and interpret significance of bio/clinical study results. Preparation and review of registration lot documents, technical reports and submission related documents in accordance with the applicable FDA and ICH guidelines such as CMC and CTD sections of IND, 505(b)2, NDA and Para III and IV certified ANDA. Interact with QC, QA, Regulatory, Marketing, Clinical, Purchasing and Commercial departments for the successful development of new products. Maintain and follow safety standards as issued by the Company.

Long Description Job Description: 1. Adheres to departmental policies, protocols and procedures along with objectives, quality and assurance programs 2. Ability to work in Multidisciplinary team 3. To work under the guidance of senior practitioner in providing physiotherapy assessments,treatments and goal settings for patients 4. To write reports and attend multidisciplinary team meetings to plan and review on going treatment 5. To facilitate better recovery for patients by providing goal-based care resulting in better outcomes Competencies Result Orientation Process Excellence Customer Centricity Collaboration Stakeholder Management Education Work Experience Qualification - BPTH Experience - 0-3 YEARS

srikakulam vizianagaram districts covered diabetes care products Show more Show less

Job Description Candidate should the exposure for handling the Bottle packing line. Should have the work experience in Regulatory plant. Faced the USFDA, MHRA,TGA inspection. Good Communication skill. Having the SAP knowledge. Work Experience 3 to 05 years' Experience. Education Graduation in Pharmacy Competencies

Job Description Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Packing and documentation of assigned products as per instruction given in the BPR, SOP and cGMP. Handling the movement of bulk, packing material, semi-finished and finished goods as per SOP. Maintaining Overall equipment efficiency (OEE)/Productivity. To up keep cleanliness of area and machine as per GMP requirement. Operation, washing and cleaning of equipment and accessories used in related production activities as per SOP. Monitoring and recording of differential pressure, temperature & relative humidity as per SOP. Ensure calibration and preventive maintenance of equipment and instrument as per approved schedule and the results of same meeting the standards. Performing in-process checks as per respective BPR and recording of results of in process checks in BPR. Receipt, issuance, retrieval, maintenance and disposal of change parts. Area and Equipment Usage documented as per SOP. To attend the required cGMP/On job/Functional training activities as per planner. To ensure proper self - hygiene before entering in the production area and follow all the rules and regulation set by HR department. To initiate and review the request like additional material requisition, material return note, packing material carry forward Stereo request and screen request etc. To ensure the effective control on usage of manpower, machine and material in the department and maintain proper inventory of operating supplies in the department. To support Quality Management system and to report any discrepancy, abnormality, non -conformance or any incidence observed to the department head. Handling of Omnidoc, Data Acquisition system (DAS). Checking of strip/blister foil proof with batch packing record and also retention of all required packing material proof with batch packing record for packing section. To attend the trouble shooting of machine. Trouble shooting: Handling, ensuring, verifying and trouble shooting of software like, Blister inspection system, inkjet coding. Any additional responsibility delegated by department head. Work Experience 2 to 5 years of experience Education Diploma in Pharmacy Graduation in Science Competencies Strategic Agility Process Excellence Innovation & Creativity Developing Talent Customer Centricity Collaboration Result Orientation Stakeholder Management

Job Description Basic knowledge GDP & Data Integrity. Online monitoring & recording of batch observation. Optimum Utilization of equipment & material. Set & Operate BQS & de-foiling machine. Co-ordination with engineering for PM of BQS & other machine. To intimate requirement of spare parts/change parts. Follow safety, health & environment policies of company. To ensure that total shift operation performed with adherence to cGMP. Work Experience 2-5 years experience in BQS machine operation & troubleshooting. Education Vocational in Mechanical Engineering or Packaging Technology Diploma in Electrical or Mechanical Engineering Competencies Strategic Agility Innovation & Creativity Customer Centricity Developing Talent Result Orientation Process Excellence Collaboration Stakeholder Management

Job Description Experiment planning of downstream process development of therapeutic proteins, execution of planned experiments and data recording. Documents compilation and management when and where required Equipment calibration, verification, maintenance and daily routine activities. Lab compliance and timely delivery of any assigned work with appropriate quality. Work Experience For PHD - 2-5 years For MSc. - 5-7 years Education Doctorate in Biotechnology or Biotechnology Masters in Biotechnology or Biotechnology Competencies Collaboration Customer Centricity Developing Talent Innovation Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility

Long Description 1. Analyst required in executive role for analysis of development, trial batches, Scale up and QbD samples. 2.To carry out investigation of laboratory incidences and Out of Expectation test results. 3.Responsible for analysis of stability samples, intermediates, in process and finished products samples. Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence Education Graduation in Pharmacy Post Graduation in Pharmaceutical Chemistry Work Experience 4- 8 Years.

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

Job Description 1 Should have knowledge of dispending of RAW materials. 2. Should have exposure to SAP system. 3. Should have exposure to regulatory plant. 4. Should be able to read & write English. Work Experience 3- 6 year Education Graduation in Arts Competencies

Having 2-5 years of experience in Project/Program management. To assist in Project feasibility assessment, planning, scheduling & tracking. Responsible for Crossfuncational coordination for BA/BE studies with internal and external stakeholders Responsible to monitor progress of study and update respective stakeholders Responsible for keep of project tracker and existing database and dashboards upto date Responsible for creation of Purchase requisitions, Service order and ensuring payment delivery to vendors in timely manner Responsible for performing all the study activities in compliance with current GCP and GDP requirements and company policy. Executive-Project Manager preferred PMP certified candidate Competencies 1. Strategic Agility Building Positive Working Relationships Collaboration Communication Computer Skills Decision making through strategic thinking Decision Making/Judgment Integrity Education Masters Graduation in Pharmacy

Planning /Analysis (Routine and stability and QBD analysis) of ongoing projects by performing analysis of various tests (e. g. Dissolution, assay, Related substances test, or as per requirement) within given Time. Analytical Method development as per current SOP/guideline wherever required. Regulatory query/Plant Query related analysis for different products. To follow Good Laboratories practice while working. Documentation and compliance and review of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean. Method transfer at plant. Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method. Preparation/review of various documents like method transfer waiver, method equivalency report, cleaning validation report SOP, T-STP/FP STP etc. Coordination with team members, superiors and subordinates within the group and across all relevant groups (customers) to achieve target timelines. Procuring of columns, reagents and miscellaneous items for analytical product development/support. Whenever required give training to subordinates/colleagues to upgrade their knowledge and current requirements. Education Masters in Analytical Chemistry or Analytical Chemistry Post Graduation in Pharmacy or Analytical Chemistry