COMPANY: • MANA PHARMA, S.L. is a fast growing Spanish Pharmaceutical Company holding a Pharmaceutical Wholesaler authorisation (WDA). We are specialised in exportation and commercialisation of medicines, medical devices, cosmetics and other pharmaceutical products outside the EU. • Our reputation throughout the past years is based on the quality of our work, and the confidence placed in MANA PHARMA by our clients and partners. SERVICES: MANA PHARMA has a great experience in both Registration and Commercialisation of medicines, medical devices and other pharmaceuticals outside the European framework. Furthermore, MANA PHARMA offers consultancy services. • Commercialisation: We fulfil all enquiries received from our customers optimising the procedure sourcing the products from trustworthy and duly authorised suppliers. • Registration: The knowledge gained throughout the years in different markets makes us experts in registering pharmaceutical products. Thus ensuring continuous supply of products in those territories where we are present and therefore increasing the turnover of our partners. • Consultancy: We believe that the adaptation to European Quality Standards is paramount nowadays. We assist our clients throughout this procedure and ensure full compliance with all Guidelines in force. Furthermore for pharmaceutical plants we offer advisory services for guaranteeing that processes and facilities meet European GMP rules.
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
? Experience : 1 to 2 years ? Roles and responsibilities ? Inorganic Salt Recovery: Lead the development and optimization of processes for recovering inorganic salts like Sodium Bromide, Lithium Coronides, Sodium Sulphate and similar compounds from industrial effluents. ? Effluent Treatment: Design and implement sedimentation processes for the treatment of aqueous effluents, ensuring effective removal of inorganic contaminants and compliance with environmental regulations. ? Process Optimization: Continuously improve recovery and sedimentation processes to reduce waste and improve overall efficiency. ? Laboratory Analysis: Perform qualitative and quantitative analysis of recovered salts and effluents to ensure purity, composition, and compliance with required standards. ? Collaboration: Work with cross-functional teams, including environmental, R&D, and operations teams, to support the scaling and application of inorganic salt recovery and effluent treatment methods. ? Regulatory Compliance: Ensure that all processes meet industry-specific regulations and environmental safety standards related to chemical handling, waste disposal, and effluent treatment.
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
? Experience : 1 to 2 years Experience in Bio-Catalysis Reactions ? Qualification: MSc Organic Chemistry ? Roles and responsibilities ? Bio-Catalysis Reactions: Design, develop, and optimize enzymatic processes for the synthesis, modification, and transformation of organic compounds. Work with various types of enzymes (e. g. , hydrolases, oxidoreductases, transferases) to catalysed reactions efficiently. ? Process Development: Implement and optimize bio-catalytic processes, ensuring high efficiency, selectivity, and yield of enzymatic reactions. Work on large-scale applications where applicable. ? Biocatalyst Screening: Conduct screening of different enzymes and biocatalysts for specific reactions, including enzyme engineering or mutation to improve reaction efficiency and selectivity. ? Research and Development : Stay up to date with the latest advancements in bio-catalysis, enzymology, and related technologies. Contribute to research projects aimed at discovering and developing new biocatalytic applications.
Hyderabad
INR 10.0 - 14.0 Lacs P.A.
Work from Office
Full Time
Our mission is to ensure the generation of accurate and precise findings. Please enter subscribe form shortcode CHEACK INSTAGRAM POST Please enter instagram feed shortcode Assistant Manager (Finance Accounting) Assistant Manager (Finance Accounting) MANA PHARMA Pvt Ltd is a fast-growing pharmaceutical company committed to sustainable development and manufacturing of APIs and intermediates. While our greenfield manufacturing facility is under development, we currently operate through strategic partnerships with contract manufacturing organizations (CMOs). We are focused on building strong internal capabilities to support compliant, scalable, and sustainable growth. Employee Value Proposition: This is a high-impact role offering autonomy, leadership visibility, and the opportunity to shape the finance function of a growth-stage pharma company. To manage and oversee the organization s day-to-day financial operations including reconciliations, taxation, compliance, and reporting. Support budgeting, forecasting, and financial analysis to aid business decision-making. Drive process improvements and ensure adherence to financial controls and statutory requirements. Key Responsibilities: Financial Reporting Compliance Prepare and analyse monthly, quarterly, and annual financial statements. Ensure compliance with accounting standards and statutory regulations. Coordinate with auditors during internal and external audits. Manage timely and accurate reconciliations of bank accounts, ledgers, GST returns, and intercompany accounts. Resolve discrepancies and ensure data accuracy. Budgeting Forecasting Support Assist in preparing annual budgets and forecasts in collaboration with departments. Monitor budget variances and report findings to senior finance leaders. Accounts Payable Receivable Manage daily accounting transactions and ledger management. Ensure timely invoicing, collections, and payments. Taxation Regulatory Filings Ensure accurate computation and timely payment of taxes (GST, TDS, PT, Income Tax). Ensure timely filing of statutory returns and compliance documentation. Cost Management Controls Assist in analysing cost structures and support cost control initiatives. Implement and maintain internal financial controls and policies. Cash Flow Treasury Management Monitor cash flows to maintain operational liquidity. Coordinate banking transactions and funding requirements. CMA Data Preparation for Bank Loans Prepare CMA data and related financial documentation for bank credit facilities. Liaise with banks and financial institutions for credit assessments. Team Management Development Supervise and mentor junior finance staff. Promote continuous improvement and adherence to processes within the team. Cross-Functional Collaboration Work closely with operations, procurement, and sales teams to gather financial inputs and align on budgets and forecasts. Key Skills Competencies: Sound knowledge of accounting standards, reconciliations, and taxation Experience preparing financial statements and CMA data Proficient in ERP systems (Tally, SAP, Oracle) and MS Excel Strong analytical and problem-solving skills Effective communication and interpersonal abilities Ability to manage deadlines and work under pressure Experience in the pharmaceutical industry preferred
Hyderabad
INR 5.0 - 9.0 Lacs P.A.
Work from Office
Full Time
? Job Description: ? ? We are seeking for a motivated and detail-oriented QC Trainee / Executive to join our quality team. The ideal candidate will be responsible for supporting quality control operations in method development, routine analysis, and documentation for APIs and intermediates under development. ? ? Key Responsibilities: ? ? Perform sampling and testing of raw materials, intermediates, and finished products. ? ? Conduct instrumental analysis (HPLC, UV, IR, GC) as per approved methods. ? ? Prepare and maintain Certificates of Analysis (COAs), logbooks, and test records ? ? Maintain lab notebooks, data integrity, and QC documentation ? ? Support in creating analytical method to identify, quantify and monitor impurities and the quality of the product ? ? Work closely with R&D and QA teams ensure compliance ? ? Requirements: ? ? 0 1 years of relevant experience in QC role. ? ? Familiarity with laboratory instruments and quality systems. ? ? Basic understanding of analytical techniques and GLP/GMP concepts ? ? Basic understanding of data integrity and GLP practices and Willingness to work in shifts (if required). ? ? Strong attention to detail and documentation skills. ? ? Willingness to learn, good observation skills, and attention to detail ?
Hyderabad
INR 8.0 - 12.0 Lacs P.A.
Work from Office
Full Time
? Job Description: ? ? We are looking for a skilled and proactive QA/QC professional with 2 5 years of experience to join our quality team. The candidate will be responsible for executing and overseeing quality assurance and quality control activities in compliance with regulatory and company standards. ? ? Key Responsibilities: ? ? Quality Control? ? Perform analytical testing of raw materials, in-process samples, and finished products. ? ? Operate, calibrate, and troubleshoot instruments such as HPLC, UV-Vis, GC, FTIR, and KF. ? ? Prepare and review analytical documentation including test reports, COAs, and calibration records. ? ? Guide and Mentor QC Executives / Trainees for analytical testing ? Quality Assurance? ? Review batch manufacturing and packaging records (BMR/BPR). ? ? Investigate and document deviations, OOS, OOT, and implement CAPA with timely closure. ? ? Review and manage controlled documents (SOPs, protocols, forms) issuance, retrieval, and archival. ? ? Perform internal audits; support regulatory audits (e. g. , WHO, ISO, etc. ). ? ? Oversee GMP, GLP, hygiene training for production and QA/QC staff. ? ? Coordinate stability studies, analyze trends, and maintain stability protocols and logs. ? ? Ensure data integrity in documentation and electronic systems. ? ? Participate in risk assessment and mitigation for quality events. ? ? Support technology transfer, scale-up, and cross-functional quality activities. ? ? Evaluate and audit vendors and suppliers as part of QA oversight. ? ? Requirements: ? ? 2 5 years of hands-on experience in analytical techniques and instruments in a regulated environment. ? ? Strong understanding of cGMP, GLP, and ICH regulatory requirements. ? ? Proficient in analytical instrumentation and documentation practices. ? ? Ability to handle audits, deviations, and quality systems independently. ? ? Excellent communication, collaboration and organizational skills. ? ? Team player with attention to detail and accuracy. ?
Visakhapatnam, Hyderabad
INR 2.0 - 5.0 Lacs P.A.
Work from Office
Full Time
Our mission is to ensure the generation of accurate and precise findings. Please enter subscribe form shortcode CHEACK INSTAGRAM POST Please enter instagram feed shortcode Experience: 0-2 Years Location: Hyderabad Employment Type: Full-time Qualification: B. Tech / B. E (Chemical, Mechanical) or B. Sc/MSc (Chemistry or relevant field) Roles and responsibility: Assist in the execution of batch manufacturing processes as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs) Monitor and operate equipment such as reactors, centrifuges, dryers, and filters Support charging, reaction, separation, and drying stages in production Perform high vacuum distillation(HVD), Crystallization in production. Record process parameters (temperature, pressure, pH, etc. ) and escalate deviations to shift in-charge Ensure proper documentation and compliance during all stages of production Maintain shift logs and production records Follow cGMP guidelines and Good Documentation Practices (GDP) Adhere to safety protocols including PPE usage, equipment cleaning, and area hygiene Participate in safety drills and training sessions Ensure readiness of equipment before starting any batch Coordinate with Quality Control (QC), Quality Assurance (QA), and Engineering departments during routine activities Report abnormalities or equipment breakdowns to supervisors Attend training sessions on SOPs, EHS, cGMP, and new processes Continuously improve skills in process understanding and documentation
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Pharmaceutical Manufacturing
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