Roles and Responsibilities Conduct patent infringement analysis using tools like PatentScope, Google Patents, and Thomson Innovation. Perform prior art search on granted patents to identify relevant documents. Analyze search results to determine potential infringement risks and provide recommendations for mitigation strategies. Collaborate with cross-functional teams to develop comprehensive intellectual property protection plans. Stay up-to-date with industry trends and regulatory changes related to pharmaceuticals. Desired Candidate Profile 8-12 years of experience in IP management, preferably in the API= pharmaceutical or life sciences sector. Strong understanding of analytics, chemical synthesis, compliance, data mining, document management, informatics, litigation support, prosecution processes. MS/M.Sc (Science) degree from a reputed institution; Ph.D. preferred but not mandatory.

Dear Respect Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation QA Department Job description -4 -7 Yrs Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs,BDRs, PDRs, MFRs and MPR) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audits for Cross functional Departments in Formulation Division and External Division. Conducting and Coordinating Employee Trainings. Responsible for Review and Approval of Vendor Qualification Please Share update resume: careers@biophore.com Ref to Friends or colleagues. Total Exp: Current CTC: Exp CTC : Notice Period: Designation:

Roles and Responsibilities Manage projects from concept to commercialization, ensuring timely delivery of high-quality products. Develop project plans, monitor progress, and identify potential roadblocks to mitigate risks. Collaborate with cross-functional teams to ensure effective communication and coordination across departments. Conduct market research and analyze data to inform product development decisions. Ensure compliance with regulatory requirements throughout the product lifecycle. Desired Candidate Profile 6-11 years of experience in pharmaceutical or life sciences industry as a Project Manager (R&D). MS/M.Sc(Science) degree in Chemistry or related field; MBA preferred. Strong understanding of project management principles, including planning, execution, monitoring & control. Proven track record of successfully managing multiple projects simultaneously while meeting deadlines.

Roles and Responsibilities Manage project timelines, milestones, and deliverables to ensure successful completion of projects within budget and scope. Develop detailed project plans, including resource allocation, budgeting, and risk assessment. Collaborate with cross-functional teams to identify potential roadblocks and develop mitigation strategies. Ensure effective communication among team members, stakeholders, and clients through regular progress updates and status reports. Identify opportunities for process improvements and implement changes to increase efficiency. Desired Candidate Profile 15-20years of experience in pharmaceutical industry with expertise in API development or related field. MS/M.Sc(Science) / M.Pharma degree from a recognized institution. Strong understanding of chemistry principles applied to pharmaceutical sciences. Proven track record of successfully managing complex projects from initiation to delivery.

Roles and Responsibilities Manage network infrastructure, including hardware installation, configuration, and maintenance of HPLC, GC, QC applications, empower and other server applications Provide technical support for desktop administration tasks such as troubleshooting and resolving issues related to software applications. Troubleshoot and resolve complex network problems using various tools and techniques. Collaborate with team members to ensure seamless operation of instrumentation systems. Perform routine maintenance tasks to prevent equipment failures and optimize system performance. Desired Candidate Profile 5-10 years of experience in Network Administration or pharma field. B.Tech/B.E. degree in Information Technology or a related field (or equivalent). Strong knowledge of networking protocols (e.g., TCP/IP), operating systems (Windows/Linux), and troubleshooting techniques. Experience working with industrial automation systems is an added advantage.

Roles and Responsibilities Develop novel organic synthesis routes through literature search, patent analysis, and technical discussions with team members. Execute experimental work on new projects, including planning, execution, and optimization of reactions. Collaborate with cross-functional teams to achieve project goals and deliverables. Conduct analytical testing and characterization of products using various techniques such as NMR, IR, GC-MS etc. Maintain accurate records of experiments, results, and data analysis. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Strong understanding of chemical principles and laboratory practices. Excellent communication skills for effective collaboration with team members.

Dear Respect Applicants. Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) or Inject able We have opening for Formulation R&D Department. 1) Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. 7) Good Communication Skills. Role & responsibilities Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation Project Management- (OSD - Exp) J ob Description: 1) Project Management / Formulation R&D , 2) Manage the R&D projects with Internal stakeholders & partners from project Kick off to dossier filing . 3) Job role and provide all the critical activities to be performed, prepare micro plan for very major milestone based on project plan and ensure timely. 4) Coordinating for indenting raw material for prototype development till validation and co-ordination's-ordinating for Licensing Documents. 5) Preparing API Approval forms for API &WS requirement and coordinating for management approval. 6) Follow ups for the logistic (API,IMP,WS,RS) requirements for projects under development and validation with Alliance team. 7) Coordination with API Team availability PSD,GC/RID. 8) Coordination with Dispatch team . 9) Co-ordination with RA Team and Tech Pack and DMF for Formulation Team. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

Roles and Responsibilities Manage legal documentation, including contracts, agreements, and other legal documents. Oversee litigation matters related to real estate disputes and ensure compliance with relevant laws and regulations. Develop and implement effective strategies for managing risk exposure through contract drafting and negotiation. Collaborate with internal stakeholders to resolve non-litigation issues such as property transactions, lease negotiations, and licensing agreements. Ensure timely completion of all legal tasks while maintaining high-quality standards. Desired Candidate Profile 10-15 years of experience in a similar role within the Real Estate industry. LLB degree from a recognized university. Strong understanding of contractual, corporate law, due diligence processes, legal documentation, litigation management, regulatory requirements (RERA), and statutory compliances.

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation Research & development for Injections/sterile dosage forms. Job Openings: 3 Nos Position : Executive or Sr Executive Exp 3 - 6 Yrs. Job Location : Pashamylaram - Patancheruv. Hyderabad. Salary : As Per Company Norms Qualification : M .Pharmacy-Pharmaceutics Job Description : Product development of Injectables/Sterile dosage forms- liquid injection, Lyophilized products, suspensions & emulsions for regulated and semi regulated markets. Candidate must have knowledge on compatibility studies, filter validations & PDR preparation. Candidate must have experience on trouble shooting during technology transfer to plant Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

Dear All, Greetings from Biophore !! This is an opportunity with Biophore in Regulatory affairs -API Department . Please go thorough the JD. Interested candidates share your CV's to "recruitments@biophore.com". Location : Pashamylaram, Patancheruvu . Job description : Roles and Responsibilities DMF submissions, Annual Reports, Variations, Renewals etc. for US and Europe market. Compilation and publishing in eCTD/CTD format for Submission to health agencies like EDQM, USFDA etc. Oversee final technical quality review and technical validation (PDF/eCTD/NeeS) Review all regulatory agency submission materials for accuracy, comprehensiveness, or compliance with regulatory standards. Provide deficiencies responses to HA regulatory agencies for deficiencies and comments Evaluation of change controls for post-approval changes (PAC) Compilation, review and submission of Variations Keeping up to date with changes in regulatory legislation and guidelines Conduct Pre-submission and Initial Submissions meetings Preparation of gap analysis report of CMC regulatory submission including recommendations to facilitate the review of application by HA Gaps in manufacturing and controls, assessment of regulatory risk and strategy Providing gap analysis against applicable HA requirements and standards and communicate cross functional team to comply the samezCharacterization of the API and Raw materials used to manufacture the API Description of the product and process development Analytical methods and specifications used for testing Release and stability testing data for both the API Preparation of responses to HA,comment letters&assessment reports Initial assessment of the submission (initial / post approval submissions) E.g., initial validation comments, response to the completeness assessment report, response to the Information Requests

Roles and Responsibilities Co-ordinate with site personnel for timely corrections to troubleshoot And handling and managing lab equipment. Diploma / Degree in chemical Engineering, Should be prompt in attending all types of alarms and effectively, oil, gas, process, production, quality, reserch Chemical engineers research, design, and develop chemical processes and equipment, oversee the operation and maintenance of industrial chemical, environmental protection and biochemical or bio technical engineering. A person who has process control experience will be preferred. Overseeing the construction of new plants. Ensuring that equipment works to its specification and to appropriate capacities. Desired Candidate Profile Degree from a reputed institution with high academic achievements.Only Male candidates Job Benefits & Perks Free transportation & Subsidized meal ,Bonus etc

JD : Formulation-Project Management A. Project Initiation & Planning: 1. Preparing Project Charters as per Project Initiation forms from Business Development. 2. Preparing Project plan/schedule based on the scope as per customer requirement. 3. Conducting the Project kick off meetings. B. Project Management: Monitoring & control: 4. Coordinating with the all the internal HODs on the macro level of the project activities. 5. Conducting review meetings with the cross functional team members and senior management for tracking the project to ensure timely finished delivery. 6. Customer communication through meetings and circulating the MOM to stakeholders. 7. Reviewing project status and identifies early warning signals & on -time Escalations. C. Project Closure: 8. Coordinating with accounts for invoicing upon completion of each milestone of the respective project. 9. To organise project learnings upon completion of exhibit batch with CFT members. Please share me update resume: careers@biophore.com Total Exp : Current CTC : Exp CTC : Notice Period:

optimum utilization of available Man, Machine & Materials production Planning as per the targets inventory Management in premises. follow-up with both Internal & external Clients for the achieving Target regular update of charts Update of MIS adherence to the batch Schedules as per the timelines coordinate with SCM, R&D, QC, QA, TSD and other for new batch execution adherence to CGMP and GMP processes

Roles and Responsibilities Conduct HAZOP, HIRA, HAZID studies to identify potential hazards in processes. Develop and implement process safety management systems (PSMS) for API manufacturing and bulk drug production. Ensure compliance with regulatory requirements related to environment health & safety (EHS). Collaborate with cross-functional teams to design new products and processes that meet industry standards. Provide training on EHS procedures and best practices to employees. Desired Candidate Profile 4-7 years of experience in Process Safety Management System (PSMS), HAZOP/Hazid/Hira/LOTO etc. Diploma or B.Sc degree in Any Specialization; relevant certifications like NEBOSH IGC would be an added advantage. Strong understanding of pharmaceutical regulations such as GMPs, OSDs, Injectables etc.

Over see the development, implementation, and validation of analytical methods used for the testing of Active Pharmaceutical Ingredients (APIs) in compliance with internal standards, industry regulations, and customer requirements. The role requires leadership skills to manage a team, ensure compliance with good laboratory practices (GLP), and drive continuous improvement in method validation processes. This position also involves close collaboration with various cross-functional teams including R&D, Regulatory Affairs, and Quality Assurance.

Job Description: 1.Candidate must have knowledge Product Development, Characterization, Literature Search, Prototype Development, Scale-up Batches, Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D.Role & responsibilities Position : Executive/Sr Executive/Asst Manager Experience : 3 12 Yrs. Qualification: M. Pharm -Pharmaceutics Total Exp: Current CTC: Exp CTC : Notice Period: Current Designation:

Roles and Responsibilities Conduct quality control analysis of bulk drugs, APIs, and pharmaceutical products using techniques such as HPLC, GC, and method validation. Perform stability studies to ensure compliance with GMP guidelines. Calibrate instruments accurately and maintain records of instrument maintenance schedules. Ensure accurate documentation of test results, reports, and certificates of analysis. Collaborate with cross-functional teams to resolve quality issues. Only male candidates

Primary responsibilities of this role include the following: Identify new product opportunities (NCE, 505b2, first Gx) and manage the cross-functional evaluation including technical evaluation, clinical data review and commercial assessments Develop business cases through collaboration with technical, regulatory, IP and commercial. Understand business case drivers, including competitive landscape, clinical requirements, and other potential external factors which may impact valuation Review product lists of external partners for new product ideas and guidance of the licensing manager Portfolio support for strategic partnerships negotiation and BD-licensing talks Portfolio support to business teams in therapy understanding and product potential Ensure that the Company has the most competitive portfolio Update portfolio information tools, reports and databases as new information becomes available. Monitor pharma space and track new product approvals globally and prepare monthly report on opportunities

Roles and Responsibilities Develop new business opportunities through strategic partnerships and alliances with key stakeholders. Identify potential customers, understand their needs, and develop targeted sales strategies to drive revenue growth. Collaborate with cross-functional teams to launch new products or services in the US market. Manage relationships with existing clients to ensure customer satisfaction and retention. Analyze market trends and competitor activity to inform business development decisions. Desired Candidate Profile 6-10 years of experience in Business Development or related field (Pharmaceutical & Life Sciences industry preferred). MBA/PGDM degree from a reputable institution (Marketing specialization preferred). Proven track record of success in developing new business opportunities through partnerships, alliances, or direct sales efforts. Strong understanding of international marketing principles and practices; ability to adapt quickly to changing global markets.