5 Biochemical Engineering Jobs

As a Sales Manager at our client, a global leader in nutraceutical and pharmaceutical ingredients, you will play a crucial role in expanding the market presence in India. Reporting to the Head of Business APAC, based overseas, you will be based in Mumbai and responsible for driving growth and building strong relationships with key customers. Your responsibilities will include providing insights on market trends in the assigned segment, suggesting improvements in the sales strategy to the regional Sales Leader, and collaborating with internal technical and marketing departments to meet customer expectations around technical projects. You will also be expected to deliver regular activity reports, sales forecasts, and actively participate in conferences, events, and trade shows in the country. To excel in this role, you should ideally possess a Masters Degree in Biochemical Engineering, Biotechnology, or Bioprocessing. A background in life sciences will be advantageous. Additionally, a minimum of 5 years of sales experience in industrial Biotechnology (Pharma, Food, Feed, Bio-Ingredients) is preferred, with a proven track record in B2B technical product/ingredients sales. We are looking for a highly autonomous and hands-on individual with an energetic, self-driven attitude to consistently deliver results. If you are ready to take on this exciting opportunity and contribute to our client's growth ambitions in the APAC region, we look forward to receiving your application.,

Responsibilities: Develop and optimize upstream cell culture processes, including media formulation, feeding strategies, and bioreactor control parameters. Perform small-scale, bench-scale, and pilot-scale experiments to support process development and solving. Assess and incorporate single-use bioreactor systems and technologies to enhance process flexibility and efficiency. Design and complete experiments to enhance cell growth, productivity, and product quality attributes. Technology Transfer and Scale-Up Lead upstream process technology transfer to clinical and commercial manufacturing scales. Develop and document detailed process descriptions, standard operating procedures (SOPs), and batch records for scale-up activities. Collaborate with manufacturing to ensure smooth implementation of upstream processes in single-use production systems. Data Analysis and Documentation Analyze experimental data to evaluate process performance, identify trends, and recommend improvements. Prepare technical reports, presentations, and documentation for internal and external collaborators, following Good Documentation Practices (GDP). Maintain accurate records of process development activities and experimental results in electronic lab notebooks (ELNs). Collaboration and multi-functional Support Work closely with downstream processing, analytical development, quality assurance, and regulatory teams to ensure seamless integration into end-to-end biomanufacturing workflows. Participate in project meetings and contribute to strategy discussions, ensuring alignment with organizational goals and timelines. Support solving and resolution of upstream-related challenges during production. Stay informed on advancements in cell culture technologies, single-use systems, and bioprocessing methodologies. Identify and implement innovative approaches to improve upstream process efficiency, scalability, and sustainability. Actively contribute to fostering a culture of innovation and continuous improvement within the Bioprocess Design Center. Experience: Ph.D., M.S., or B.S. in Biotechnology, Biochemical Engineering, Molecular Biology, or a related field with a focus on cell culture and upstream processing. 3+ years of experience in upstream process development for biologics, including hands-on experience with mammalian or microbial cell culture systems. Proficiency in working with single-use bioreactor systems is highly preferred. Familiarity with fed-batch, perfusion, and continuous culture processes. Solid understanding of bioreactor design, operation, and process control strategies. Proficiency with process monitoring tools and analytical instrumentation for cell culture. Excellent problem-solving and analytical skills with the ability to manage sophisticated data sets. Strong written and verbal communication skills, with experience communicating technical data to diverse audiences. Experience with cGMP guidelines, regulatory standards, and technology transfer in biomanufacturing. Knowledge of cell line development and characterization. Familiarity with automation, PAT (Process Analytical Technology), and data-driven optimization tools. Lead numerous projects simultaneously and meet aggressive timelines. Demonstrated ability to lead multiple collaborators and conflicting goals. Business-level proficiency in English (verbal/written) and proficiency in Excel and presentation skills. Willingness to travel as required. Self-motivated, team-oriented, collaborative and skilled in working in a matrixed and multi-functional environment Good social skills (oral and written)

The Process Automation Engineer, reporting to the Business Process Excellence (BPE) team, requires a BE/B Tech in Chemical or Bio-chemical with 4 to 6 years of experience. You will be accountable for leading various project activities such as internal kick-off meetings, preparing functional design specifications, valve matrix, and equipment modules. Coordinating with third-party aggregators to ensure error-free deliverables and conducting bench tests with customers will be a crucial aspect of your role. Additionally, you will participate in pre-FAT activities and support on-site requirements when necessary. Participating in the standardization program, you will commit to finalizing the standardized P&ID, coordinating internal review meetings, and ensuring alignment with organizational objectives. Your behavioral skills should reflect a strong desire to stay updated on technological advancements worldwide and possess commercial awareness to meet customer and organizational requirements effectively. Key performance indicators include minimizing iterations in FDS and VM and effectively closing all points raised during simulation testing, bench tests, pre-FAT, and FAT activities.,

As a BPE (Process Automation Engineer), you will be accountable and responsible for various key tasks. These include planning and participating in Internal Kick-Off Meetings (KOM) and committing to delivery dates, preparing and closing Functional Design Specifications (FDS), Valve Matrix (VM), and Equipment Modules (EM). You will also need to coordinate with Third Party Aggregators to ensure error-free deliverables, conduct Bench Tests with customers, and participate in Pre-FAT activities. In addition to the above responsibilities, you will also be supporting the Standardization program of the organization. This involves participating in finalizing the Standardized Piping and Instrumentation Diagram (P&ID), coordinating internal review meetings, and ensuring the requirements for standardization are met. To excel in this role, you should possess behavioral skills such as an intense desire and passion to stay updated on technological developments worldwide. You should also have a strong commercial awareness, understanding both customer requirements and organizational objectives. Your performance will be measured based on key performance indicators such as minimizing iterations in the FDS and VM, as well as effectively closing points raised during Simulation Testing, Bench Test, Pre-FAT, and FAT activities. Overall, as a BPE (Process Automation Engineer), you will play a crucial role in ensuring the successful execution of projects and contributing to the standardization efforts of the organization.,

As a BPE (Process Automation Engineer), you will hold a BE/B Tech degree in Chemical or Bio-chemical with 4 to 6 years of experience. Your primary responsibilities will include planning and participating in Internal Kick-Off Meetings (KOM), committing to delivery dates, preparing and finalizing Functional Design Specifications (FDS), Valve Matrix (VM), and Equipment Modules (EM). You will also be responsible for coordinating with Third Party Aggregators to ensure error-free deliverables, conducting Bench Tests with customers, documenting Pre-FAT activities, and complying with FAT results. Additionally, you will provide support both online and on-site for customers when required. In relation to the standardization program of the organization, you will participate in finalizing the Standardized P&ID, commit to a plan, and delivery date. You will also coordinate internal review meetings to meet the standardization requirements. Your success in this role will depend on your behavioral skills, including a strong desire and passion to stay updated on technological developments globally, commercial awareness for both customer requirements and organizational objectives. Key Performance Indicators for this role include minimizing iterations in the FDS and VM and closing points raised during Simulation Testing, Bench Test, Pre-FAT, and FAT activities.,