Quality Control (Immediate Joiners only) Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Raw Materials, Packaging Materials. To ensure that the proper maintenance of department, premises and equipment. Preferred candidate profile B. Pharm / M. Sc in Chemistry or Organic Chemistry or General Chemistry or Pharmaceutical Chemistry or Industrial Chemistry Experience: 3 to 8 years
QUALIFICATIONS: Bachelors degree in Computer Science, Information Systems, Statistics, or a related field. Proficiency in Advanced Excel is mandatory. Familiarity with data visualization tools (e.g., Power BI, Tableau) is a plus. KEY RESPONSIBILITIES: Advanced Excel: Proficient in using functions, pivot tables, VLOOKUP/XLOOKUP, Power Query, and data visualization tools for efficient data management and reporting. MIS Operations: Expertise data analysis, report generation, and maintenance of Management Information Systems to support business decision-making. Data Accuracy & Integrity: Ensure consistency, accuracy, and timeliness of data across reports and dashboards. Communication Skills: Strong verbal and written communication abilities for effective collaboration with cross-functional teams and presentation of data insights. EXPERIENCE: 6 Months to 2 Year of relevant experience in MIS, business analysis, or data reporting. Role & responsibilities
Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Raw Materials, Packaging Materials. To ensure that the proper maintenance of department, premises and equipment. Preferred candidate profile B. Pharm / M. Sc in Chemistry or Organic Chemistry or General Chemistry or Pharmaceutical Chemistry or Industrial Chemistry Experience: 3 to 6 years
Roles & Responsibilities: Develop and execute regulatory strategies for the registration and lifecycle management of pharmaceutical products in ROW markets. Compile, review, and submit high-quality regulatory dossiers (CTD/eCTD format) in compliance with regional authority requirements. Interact with local affiliates, regulatory agencies, and distributors to ensure timely approvals and resolve queries or deficiencies. Maintain regulatory documentation and product information to ensure compliance with health authority regulations. Monitor and analyze changing regulatory landscapes in ROW regions and update stakeholders on impact. Support cross-functional teams including R&D, QA, Supply Chain, and Commercial in regulatory matters related to ROW. Manage post-approval changes (variations), renewals, and other lifecycle submissions. Participate in audits and inspections, ensuring regulatory readiness and compliance. Train and mentor junior regulatory staff, if applicable. EXPERIENCE: 8 10 years of experience in Regulatory Affairs in ROW markets. Strong knowledge of regulatory guidelines (ICH, WHO, local agency requirements). Experience with dossier preparation (CTD/eCTD) and handling agency queries. Understanding of regulatory requirements across key ROW territories. Project management and stakeholder communication skills. SKILLS: Familiarity with registration processes for both generics and branded formulations. Experience in working with third-party manufacturers and CROs. Hands-on experience with regulatory tracking tools and systems.
Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Raw Materials, Packaging Materials. To ensure that the proper maintenance of department, premises and equipment. Preferred candidate profile B. Pharm / M. Sc in Chemistry or Organic Chemistry or General Chemistry or Pharmaceutical Chemistry or Industrial Chemistry Experience: 2 to 5 years
JOB DESCRIPTION: JOB CODE: BIOPLUS/MEDCOMM/WH/020 DATE OF CREATION: 7th Feb 2025 Department Marketing/ Medico-marketing Communications Position Scientific Writer / Sr. Scientific Writer Reports to General Manager Marketing Communications Qualification Ph. D/ M. Pharm / B. Pharm / MBBS / BDS / MDS / BAMS / BHMS/ PG in life sciences. Experience Total 4 Years experience in Medico-Marketing in the Pharmaceutical Industry. 3+ years experience in developing scientific and medico-marketing content development for pharmaceutical companies Strong written and verbal communication/presentation skills Ability to translate complex medical concepts into easy-to-understand marketing messages. Ability to collaborate effectively across departments (e.g., Sales, Medical Affairs, Regulatory). Knowledge of the healthcare industry, medical products, and healthcare trends. Location Whitefield Road, Bangalore Type of Work Full time, work from office Company Description: With over 75 years of experience, Bioplus Life Sciences is a pharmaceutical company based in Bengaluru. We focus on advanced Biotechnology and have programs in late-stage clinical phases for global unmet needs. Our pipeline includes pre-clinical programs and blockbuster Novel therapeutics, with a strong emphasis on R&D and Clinical Development. We are delighted to invite you to explore an opportunity of learning, contributing and discovering science and medicine with us as part of our global research team. Bioplus Life Sciences and its subsidiaries Theialife Inc, USA & Akeso Biopharma, Singapore have a novel portfolio of first in class and best in class novel therapeutics in discovery stage to Phase 3 clinical stage. Theialife is currently building a global leadership team in Boston, as a prerequisite to list on NASDAQ. Our lead molecule ND 10 for early onset paediatric myopia control will be applying for EU Marketing Authorization in Q1-2025 and US FDA pre submission meeting NDA meeting also in Q1-2025. As you are probably familiar with the drug discovery journey you will appreciate that is the culmination of 18 years of effort, perseverance, and devotion to a single-minded goal of creating a global biopharmaceutical company. The myopia drug opportunity is itself over USD 20 billion and there is no other therapeutic in clinical development except Atropine which has had efficacy endpoint issues. We are adding new large manufacturing capability including a 2-million-liter microbial fermentation bio foundry and significant dosage form capacity. By 2030 we intend to be amongst the Worlds top 5 Ophthalmology innovation led global companies. To support, build and develop our pipeline we are looking to add Scientists, Doctors and Engineers and Technical People to our team of likeminded dedicated science warriors who have devoted their lives to pursue excellence and contribute to finding medical solutions for significant global unmet medical needs. Job Summary: A Medico Marketing Specialist plays a crucial role in developing and executing Pharma marketing strategies aimed at healthcare professionals, medical organizations, and consumers. This position requires a blend of marketing expertise and a strong understanding of the healthcare industry to promote medical products, services, or solutions effectively. The Medico Marketing Specialist is responsible for creating marketing materials, managing campaigns, and building relationships with healthcare stakeholders, ensuring that marketing efforts align with industry regulations and standards. Key Responsibilities: Responsible to define, develop and execute medico marketing strategies and tactics for various product segments in collaboration with cross-functional stake holders. Analyze market trends, customer needs, and competitors to position products effectively. Define product attributes, go-to-market strategy, product positioning, key benefits, and target customers in association with the Marketing & Sales team. Collaborate with product development teams to align marketing strategies with new medical offerings. Plan, execute, and optimize multi-channel marketing campaigns, including digital, print, events, and healthcare conferences. Manage content creation for promotional materials such as brochures, presentations, website content, and product brochures. Ensure all marketing materials comply with regulatory standards Conduct educational webinars and product demos to engage medical professionals and increase awareness. Respond to inquiries from healthcare professionals and stakeholders in a timely manner. Provide medico marketing tools to field force to enable them for effective communication on promotions. Generate and provide medical content for official websites/ portals. New Product development and launch strategy and support. Regular training and flow of latest medical developments in the given field. Scientific Support and Technical Training to internal and external customers. Identify new opportunities for growth and suggest innovative marketing approaches. Soft Skills: Strong communication and interpersonal abilities to effectively engage with cross-functional teams and stakeholders. High level of analytical thinking, problem-solving, and strategic planning Excellent in people management skill What We Offer: A collaborative, innovative, and supportive work environment. Career advancement opportunities in a leading company at the forefront of biotechnological advancements. Why Join Bioplus? Bioplus offers a unique opportunity to make a significant impact on global healthcare by shaping the commercial success of novel, life-changing therapies. As part of our team, youll collaborate with passionate professionals committed to improving patient outcomes worldwide. Equal Employment Opportunity (EEO) Policy: Career opportunities at Bioplus are provided without discrimination on the basis of race, sex/gender, religion/caste/creed, social or ethnic origin, colour, age, differently abled (including physical medical conditions), sexual orientation, domestic partnership status, gender identity or expression, marital status, ancestry, genetic information or any other reason prohibited by laws in India.
JOB DESCRIPTION: EXECUTIVE ASSISTANT (PROJECT MANAGEMENT) JOB CODE: BIOPLUS/EAP/WH/022 DATE OF CREATION: 28/02/2025 Department Corporate Position Executive Assistant (Project Management) Reports to AVP - BD Qualification Bachelors degree in business administration, Management, or a related field (preferred) Experience Minimum 2-3 years in an Executive Assistant or similar role, preferably with project management responsibilities Location Whitefield Road, Bangalore Type of work: Full time, work from office Company Description: With over 75 years of experience, Bioplus Life Sciences is a pharmaceutical company based in Bengaluru. We focus on advanced Biotechnology and have programs in late-stage clinical phases for global unmet needs. Our pipeline includes pre-clinical programs and blockbuster Novel therapeutics, with a strong emphasis on R&D and Clinical Development. We are delighted to invite you to explore an opportunity of learning, contributing and discovering science and medicine with us as part of our global research team. Bioplus Life Sciences and its subsidiaries Theialife Inc, USA & Akeso Biopharma, Singapore have a novel portfolio of first in class and best in class novel therapeutics in discovery stage to Phase 3 clinical stage. Theialife is currently building a global leadership team in Boston, as a prerequisite to list on NASDAQ. Our lead molecule ND 10 for early onset paediatric myopia control will be applying for EU Marketing Authorization in Q1-2025 and US FDA pre submission meeting NDA meeting also in Q1-2025. As you are probably familiar with the drug discovery journey you will appreciate that is the culmination of 18 years of effort, perseverance, and devotion to a single-minded goal of creating a global biopharmaceutical company. The myopia drug opportunity is itself over USD 20 billion and there is no other therapeutic in clinical development except Atropine which has had efficacy endpoint issues. We are adding new large manufacturing capability including a 2-million-liter microbial fermentation bio foundry and significant dosage form capacity. By 2030 we intend to be amongst the Worlds top 5 Ophthalmology innovation led global companies. To support, build and develop our pipeline we are looking to add Scientists, Doctors and Engineers and Technical People to our team of likeminded dedicated science warriors who have devoted their lives to pursue excellence and contribute to finding medical solutions for significant global unmet medical needs. POSITION OVERVIEW: The Executive Assistant will play a pivotal role in managing executive priorities, driving strategic projects, and ensuring seamless operations. This role demands exceptional organizational skills, a high degree of confidentiality, and the ability to manage multiple projects with a hands-on approach. KEY RESPONSIBILITIES: Executive Support: Provide high-level administrative support to the executive team, including calendar management, meeting coordination, and travel arrangements. Project Management: Lead and support critical projects from inception to completion using modern Project Management Systems (PMS). Stakeholder Coordination: Liaise with internal and external stakeholders, ensuring timely communication and follow-ups. Data Management: Prepare, analyze, and present data-driven reports and dashboards using advanced Excel techniques. Process Improvement: Identify opportunities for operational efficiencies and implement solutions. Confidentiality: Handle sensitive information with the utmost discretion and professionalism. KEY SKILLS: Out of box thinker. Excellent administrative knowledge and experience. Adept at building relationships both internally and externally to leverage resources when needed. Sound judgement regarding confidential and sensitive matters. Strong communications / project management background to manage the complexity of the role. Proven ability to meet multiple and/or unexpected deadlines in a demanding environment. 2-3 years experience providing support for upper-level management in a related organization Proficiency in Windows, including MS Word, EXCEL, and PowerPoint. Good knowledge on new technical software and tools. Ability to learn new software quickly. Excellent writing, editing, grammatical, organizational, and research skills. Strong interpersonal skills and the ability to build relationships with stakeholders, including staff, board members, external partners, and donors. Excellent management, time-management, and problem-solving skills. Previous experience working with and managing teams. Ability to conduct research and present data in a concise and well-written manner. Ability to work with a broad range of people, including Board members, colleagues of the CEO/Chairman, and others. A background in Communications is ideal SOFT SKILLS: Strong communication and interpersonal abilities to effectively engage with cross-functional teams and stakeholders. High level of analytical thinking, problem-solving, and strategic planning WHAT WE OFFER: A collaborative, innovative, and supportive work environment. Career advancement opportunities in a leading company at the forefront of biotechnological advancements. WHY JOIN BIOPLUS? Bioplus offers a unique opportunity to make a significant impact on global healthcare by shaping the commercial success of novel, life-changing therapies. As part of our team, youll collaborate with passionate professionals committed to improving patient outcomes worldwide. EQUAL EMPLOYMENT OPPORTUNITY (EEO) POLICY: Career opportunities at Bioplus are provided without discrimination on the basis of race, sex/gender, religion/caste/creed, social or ethnic origin, colour, age, differently abled (including physical medical conditions), sexual orientation, domestic partnership status, gender identity or expression, marital status, ancestry, genetic information or any other reason prohibited by laws in India.
Department: Formulation Development. Job Title: Research Associate / Sr. Research Associate - Formulation Development Experience: 2 - 4 Years Reporting to: Manager Formulation Development Location: Hosur, Tamil Nadu. Qualification M. Pharm in Pharmaceutics Candidate should be from English medium. Job Description: Preparation of product initiation from (PIF). Literature search/ Patent search/ Formulation strategy for formulation. Interpretation of stability study reports. Leading team in effective manner. Market sample / innovator sample procurement in coordination with the marketing team, providing training to team members. Reference/comparator product procurement and evaluation. Test license application. Preparation of costing formula. Execution of Bio batches. Procurement of Raw materials, Packing materials & Lab equipment. Preformulation studies / Drug excipient compatibility study review and further plans. Monitoring formula development activity for lab scale batches / pilot batches. Providing costs for new product development. Preparation of documents viz product development report, stability protocols, product specifications, formulation certificate, master formula record. Resource organization and coordination with relevant departments viz. purchase, R&D, Analytical, Quality Control, Quality Assurance, production and Engineering etc. Organizing seminars by internal staff and external vendors. Providing justification and response to queries received from regulatory authority. Formulation development and scale up. Stability Studies. Analytical data and stability data compilation. Maintenance of Lab Notebooks and Project files.
JOB DESCRIPTION: ASSISTANT MANAGER - ACCOUNTS JOB CODE: BIOPLUS/ACCOUNTS/WH/017 DATE OF CREATION: 31/01/2025 Department Finance & Accounts Position Assistant Manager - Accounts Reports to DGM Finance & Accounts Qualification CA Inter (Chartered Accountant - Intermediate) qualification Experience Minimum 7 - 10 yrs of experience in Strong knowledge of accounting standards and tax regulations (GST, Income Tax, TDS and TCS etc.). Minimum 4 -5 years of experience in accounts in the pharmaceutical or manufacturing industry. Strong knowledge of Indian GAAP, Ind AS, IFRS. Hands on experience in accounting software (Tally, SAP Business One, etc.). Good understanding of pharma industry-specific accounting practices and regulatory compliance. Strong analytical, problem-solving, and organizational skills. Should be able to handle B4 Audit Firms at the time of Statutory Audit. Should be able to prepare MIS Reports to management. Should be able to prepare the stand-alone and consolidated financial statement of the Company. Sound knowledge on SAP Business One would be an added advantage. Exposure in accounting and understanding of foreign currency transactions and should be able to prepare financial statements in foreign currency. Location Whitefield Road, Bangalore Type of Work Full time, work from office Company Description: With over 75 years of experience, Bioplus Life Sciences is a pharmaceutical company based in Bengaluru. We focus on advanced Biotechnology and have programs in late-stage clinical phases for global unmet needs. Our pipeline includes pre-clinical programs and blockbuster Novel therapeutics, with a strong emphasis on R&D and Clinical Development. We are delighted to invite you to explore an opportunity of learning, contributing and discovering science and medicine with us as part of our global research team. Bioplus Life Sciences and its subsidiaries Theialife Inc, USA & Akeso Biopharma, Singapore have a novel portfolio of first in class and best in class novel therapeutics in discovery stage to Phase 3 clinical stage. Theialife is currently building a global leadership team in Boston, as a prerequisite to list on NASDAQ. Our lead molecule ND 10 for early onset paediatric myopia control will be applying for EU Marketing Authorization in Q1-2025 and US FDA pre submission meeting NDA meeting also in Q1-2025. As you are probably familiar with the drug discovery journey you will appreciate that is the culmination of 18 years of effort, perseverance, and devotion to a single-minded goal of creating a global biopharmaceutical company. The myopia drug opportunity is itself over USD 20 billion and there is no other therapeutic in clinical development except Atropine which has had efficacy endpoint issues. We are adding new large manufacturing capability including a 2-million-liter microbial fermentation bio foundry and significant dosage form capacity. By 2030 we intend to be amongst the Worlds top 5 Ophthalmology innovation led global companies. To support, build and develop our pipeline we are looking to add Scientists, Doctors and Engineers and Technical People to our team of likeminded dedicated science warriors who have devoted their lives to pursue excellence and contribute to finding medical solutions for significant global unmet medical needs. Job Summary: We are looking for a highly motivated and detail-oriented Accounts Executive to join our finance team in the pharmaceutical sector. The ideal candidate will possess CA Inter qualification and have a strong understanding of accounting principles, with the ability to manage financial records, reports, and compliance in a fast-paced industry. Key Responsibilities: Accounting & Financial Reporting: Prepare, analyze, and maintain accurate financial records for the company, including the balance sheet, P&L statements, and cash flow reports. Taxation & Compliance: Assist with indirect and direct tax calculations (GST, TDS etc.), ensuring timely filing of returns and compliance with applicable tax laws. Reconciliation: Perform monthly and quarterly bank reconciliations, accounts payable/receivable reconciliations, Statutory reconciliation like GST, RPT Reconciliations and other financial reconciliations as required. Audit Preparation: Assist in internal and external audits by providing necessary documentation and explanations. Inventory & Stock Management: Assist with inventory valuation and ensure accurate reporting of stock levels in coordination with the operations team. Vendor & Payment Management: Ensure proper vendor management, timely payments, and maintenance of records. Financial Analysis: Provide financial analysis and forecasting to senior management to support decision-making. Annual and monthly Returns: - Preparation of XBRL Returns, verifying ITR Forms of the company, assisting the auditor for preparation and verification of GSTR 1, GSTR 3B and Annual GST Returns etc., Income tax Assessments : - Assisting the auditors in submitting the required documents as per the Income tax notices and make sure that all the data submitted is accurate. Ad hoc Reports: - Should be able to provide the ad hoc reports and assist the management which helps to take right decisions. Soft Skills: Strong communication and interpersonal abilities to effectively engage with cross-functional teams and stakeholders. High level of analytical thinking, problem-solving, and strategic planning Excellent in people management skill What We Offer: A collaborative, innovative, and supportive work environment. Career advancement opportunities in a leading company at the forefront of biotechnological advancements. Why Join Bioplus? Bioplus offers a unique opportunity to make a significant impact on global healthcare by shaping the commercial success of novel, life-changing therapies. As part of our team, youll collaborate with passionate professionals committed to improving patient outcomes worldwide. Equal Employment Opportunity (EEO) Policy: Career opportunities at Bioplus are provided without discrimination on the basis of race, sex/gender, religion/caste/creed, social or ethnic origin, colour, age, differently abled (including physical medical conditions), sexual orientation, domestic partnership status, gender identity or expression, marital status, ancestry, genetic information or any other reason prohibited by laws in India.
Are you looking for exciting career opportunity. We are hiring talented professionals with 3-5 years of relevant experience. Responsibilities Experience in organic synthesis/multi-step synthesis Handling reactions in mg to gram scale Sound knowledge of isolation, separation, purification techniques Experience in characterization and identification of organic molecules using spectroscopic techniques like NMR, HPLC, LCMS, GC, GCMS Positive and confident individual with a strong work ethics Team player and good communication skills. Qualifications MSc in organic chemistry/Medicinal chemistry with 3-5 years of experience. Medium of study in English Post graduation from premium institutes is preferred Interested candidates may please write to nageswararao.i@bioplus.in
Handling and monitoring of Quality system monitoring, HACCP Activity, cGMP implementation, Audit & Compliance, Analytical QA, Vendor management, Qualification & Validation, Artwork, Recall, Training, IPQA and Document Management systems. Oversee QA documentation, QMS events, and GMP compliance. Manage deviations, CAPA, complaints, OOS/OOT, and APQR. Approve batch records, specifications, validations, and analytical reports. Lead vendor audits, technical agreements, and audit readiness. Drive training programs on GMP/GDP/GLP and quality systems. Preferred Profile: Experience: 818 years in API Quality Assurance. Education: MSc in Chemistry/related Proven track record in HACCP, cGMP implementation, analytical QA, vendor management, validation, recalls, training, and documentation systems. Location: Hosur, Tamil Nadu
Role & responsibilities Manage end-to-end technology transfer of OSD formulations to commercial sites. Drive process validation, optimization, and evaluation in line with regulatory standards. Ensure accurate documentation and compliance with global regulatory requirements. Coordinate cross-functional activities and respond to regulatory deficiencies. Preferred candidate profile Qualification: M.Pharm Experience: 1015 years in formulation technology transfer (OSD). Strong expertise in process validation, optimization, site transfers & commercial validation