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Danaher Biotech Biochem Life Sciences Technician Job Opening, Apply Online

Danaher Biotech, Biochem & Life Sciences Technician Job Opening, Apply Online. Looking for opportunities as a Technician II at Danaher, Interested and eligible candidates can check out all the details given the same below.

Job title: Technician II

Job ID: R1246931

Job Location: Bangalore, Karnataka, India

Technical operations Technician II support the technical operations reagent team in product transfer from different parts of the globe and setting up the new process or validating the processes.

Summary of responsibilities:

Contributes to the support of development, implementation and maintenance of manufacturing methods, techniques, processes, and product. Interfacing as appropriate with Development, Quality, Manufacturing, Purchasing and suppliers. The incumbent assists with coordinating the release of new and enhancements to existing products; participates in design reviews, inspections, and product quality processes; aids the development product structures and ensures manufacturing documents are created, updated and in compliance with company standards, ISO and GMP as required.

Boundary Conditions/Authority Levels: Receives instruction on routine work, instructions on new assignments.

Essential Duties and Responsibilities:

  • Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained.
  • Ensures strict adherence to good laboratory and good documentation practices throughout the design and development cycle.
  • Involve in study planning to align with requirements standards and regulatory requirements and ensures the studies are conducted in agreement with approved plans.
  • Flexible to take up new challenges & performs other related duties as required.
    Should perform experiments to control or to manufacture reagents according to procedures, technical protocols in respect of QA and RA regulation and GMP rules.
  • Analyze results, solve simple technical issue/problem, and inform in an appropriate ways issues identified.
  • Organize tasks by taking into an account priority defined by Team Leader.
  • Responsible to follow all company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
  • Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.

Education and/or Experience:

  • Hands on Experience with various modes of Preparative or Analytical chromatography (Affinity, IEC, MMC, SEC) and advanced laboratory measurement systems are desired (AKTA, HPLC, Spectrophotometer, Protein estimation techniques, FRET analysis).
  • Advanced degree in Biochemistry, Biotechnology and Life sciences or related discipline, for example bachelor’s or master’s degree with 2-4 years’ experience in field.

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve.  Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you’ve ever wondered what’s within you, there’s no better time to find out.

APPLY ONLINE

Possible Interview Questions may be asked for Technician II at Danaher

1.  Can you describe your experience with Preparative or Analytical chromatography techniques such as Affinity, IEC, MMC, and SEC? Answer: During my previous roles, I have gained extensive hands-on experience with various modes of Preparative and Analytical chromatography, including Affinity, IEC (Ion Exchange Chromatography), MMC (Mixed-Mode Chromatography), and SEC (Size-Exclusion Chromatography). I have successfully utilized these techniques for purifying and analyzing biomolecules in research and manufacturing processes.

2. How do you ensure strict adherence to good laboratory and documentation practices during the design and development cycle? Answer: I prioritize adherence to good laboratory practices (GLP) and good documentation practices (GDP) throughout the entire design and development cycle. I maintain accurate and detailed records of experiments, ensuring proper documentation to meet company standards, ISO, and GMP (Good Manufacturing Practice) requirements.

3. Can you explain your experience in study planning and alignment with regulatory requirements? Answer: As a Technician II, I have actively participated in study planning, ensuring alignment with regulatory requirements and approved plans. I pay meticulous attention to detail while designing experiments and follow the relevant guidelines and standards to conduct studies in compliance with regulatory requirements.

4. How do you handle new challenges and prioritize tasks to meet deadlines? Answer: I am highly adaptable to new challenges and excel in organizing tasks effectively. When faced with new challenges, I evaluate their significance, collaborate with my team leader, and allocate time and resources accordingly to ensure timely completion of tasks. This approach has helped me handle multiple responsibilities efficiently.

5.  Can you provide an example of a technical issue you encountered during an experiment, and how did you resolve it? Answer: In one experiment, I encountered an unexpected variation in the results due to an equipment malfunction. To resolve the issue, I promptly notified the team and technical support, and we identified the root cause. By calibrating the equipment and repeating the experiment, we successfully obtained accurate and reliable data.

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