GE Analytical Development Analyst - Biomanufacturing Services in Marlborough, Massachusetts
Healthcare Life Sciences
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GE Healthcare Life Sciencesprovides products and services used as tools for biopharmaceutical manufacturing, drug discovery and the latest in cellular technologies, thereby enabling our customers around the world to be more productive, effective and creative. Our motivation is to create better health for more people. Through our five decades of supporting the biopharmaceutical industry and its research partners to become more productive, we are helping to reduce costs, increase access and improve quality in the healthcare system. We use our expertise and know-how in imaginative ways to work with our customers to provide what’s needed today and create products and solutions to enable the medical treatments of tomorrow. We add value to our customers by:
Providing cutting-edge research tools that give deeper insights into cell function to enable disease diagnosis and the development of treatments.
Enabling manufacturing productivity: we provide solutions for the entire bioprocess workflow (i.e. start-to-finish bioprocessing) helping our customers to develop and manufacture biopharmaceuticals more efficiently.
Providing high quality support and maintenance services.
We are the home of many famous brands, including Whatman, Amersham, Biacore, WAVE, Applied Precision, Xcellerex and more.
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GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is anEqual Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
Posted Position Title
Analytical Development Analyst - Biomanufacturing Services
Location(s) Where Opening Is Available United States
U.S. State, China or Canada Provinces
The Research Associate will perform analytical testing in support of the process development team and non GMP biomanufacturing runs. This position will also be involved in Assay Transfers and Qualifications.
Develop analytical methods and/or transfer assays in from outside labs to support process development and characterization testing of biologics.
• Write and review test methods, protocols, and reports.
• Participate in Assay Qualifications including writing protocols and reports and reviewing data.
• As part of the Analytical Development group this position will work closely with the upstream and downstream process development teams and the QC group.
BA/BS degree in a related scientific discipline (e.g. chemistry, biology)
2 to 5 years of analytical experience in the biotechnology industry
Relevant laboratory experience would include general experience in protein characterization work and experience with the following techniques: HPLC, CE, ELISAs, testing for residual DNA and HCP.
Quality Specific Goals:
Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
Complete all planned Quality & Compliance training within the defined deadlines
Identify and report any quality or compliance concerns and take immediate corrective action as required
Support compliance/closure of Regulatory and Quality requirements before completing Design Outputs/Program Deliverables
Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible
Bachelors degree in Life Sciences, Chemistry, Physics, Biomedical Engineering or related field
1 year relevant work experience
Masters degree in Life Sciences, Chemistry, Physics, Biomedical Engineering or related field
Demonstrated record of innovation in the area of scientific expertise
Excellent oral and written communication skills
Experience with research collaborations
Self-starter, energizing, results oriented, and able to multi-task
Demonstrated problem solving ability and results orientation
Additional Eligibility Qualifications
GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Ability to write clear technical documentation
Familiarity with aseptic technique and tissue culture is desirable.
Flexibility with scheduling – may include off-shift, weekend, and holiday coverage