Upstream Biotechnologist

About No deviation At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation. We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally. Position Overview We are looking for an Upstream Biotech personnel to support upstream biologics manufacturing activities in a GMP environment. The role will focus on cell culture operations, seed train expansion, bioreactor operations, media preparation, process monitoring, sampling, batch record execution, and GMP documentation. The candidate should have hands-on experience in upstream biologics or biopharmaceutical manufacturing and be comfortable working in a GMP cleanroom environment. Key Responsibilities • Support daily upstream biologics manufacturing operations, including cell culture, seed train, inoculation, bioreactor operation, harvest, and related activities. • Perform media preparation, filtration, transfer, and material handling in accordance with approved procedures. • Operate upstream process equipment such as bioreactors, single-use systems, mixers, pumps, filters, and harvest equipment. • Monitor process parameters such as pH, dissolved oxygen, temperature, agitation, gas flow, viable cell density, viability, osmolality, and metabolites. • Perform in-process sampling and coordinate with QC for testing requirements. • Execute production steps according to approved batch records, SOPs, GMP, and safety requirements. • Complete GMP documentation accurately, including batch records, logbooks, equipment records, and cleaning records. • Support basic troubleshooting of process or equipment issues during manufacturing operations. • Support deviation reporting, investigation inputs, CAPA, and change control activities where required. • Maintain manufacturing areas in a state of GMP readiness, including housekeeping, equipment status checks, material reconciliation, and cleanroom discipline. • Work closely with Manufacturing, MSAT, QA, QC, Engineering, Automation, and Validation teams to ensure smooth production execution. • Support facility start-up, process transfer, engineering runs, PPQ, or validation activities where required. Required Qualifications • Diploma / Degree in Biotechnology, Life Sciences, Bioprocess, Pharmaceutical Science, Chemical Process Technology, or related discipline. • Minimum 1–5 years of relevant experience in upstream biologics manufacturing, cell culture, or biopharmaceutical production. • Good understanding of GMP, GDP, aseptic practices, contamination control, and cleanroom behaviour. • Experience with single-use bioreactors, wave bags, stainless-steel bioreactors, filtration systems, pumps, and automated manufacturing systems will be advantageous. • Familiarity with DeltaV, MES, SCADA, electronic batch records, or LIMS will be an added advantage. • Able to work independently and as part of a shift or manufacturing team. • Willing to work in a GMP cleanroom environment and follow strict gowning requirements. • Strong attention to detail and good documentation discipline Why join us? • Generous Leave Policy. • Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs. • Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company. • Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated. • Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career. How to apply Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team! Please submit your resume, outlining your qualifications and experience relevant to the role, here.