• Conduct routine LC-MS/MS experiments based on established protocols
• Involved in general instrument maintenance
• Involved in protein expression, purification, modification via chemical conjugation, QC and biophysical and functional characterization of proteins
• Develop new protein functional assays, biochemical characterization of insects and insect resistance mechanisms, and mode of action studies of insecticidal proteins
• Review literature for technical support and consult with colleagues for advice on issues
• Recognize unexpected problems and readily communicate with the supervisor to address the issue

Skills: LC-MS/MS Operation, Instrument Maintenance, Protein Expression, Protein Purification, Chemical Conjugation, Protein Characterization, Assay Development, Literature Review

• Communicate effectively with both ATL and client staff
• Teach and mentor other staff members
• Remain flexible to ever-changing needs in a positive and professional manner
• Maintain mammalian cell culture lines
• Create cell line banks
• Generate media and other cell culture reagents
• Update and maintain biological inventories
• Perform experiment documentation
• Assist in any troubleshooting, operation, and maintenance of laboratory instrumentation
• Interact professionally with both internal and external clients
• Train and offer guidance to other ATL associates
• Maintain a high level of knowledge of various aspects of laboratory operations

Skills: Effective Communication, Staff Training, Flexibility, Mammalian Cell Culture, Cell Line Banking, Reagent Preparation, Inventory Management, Laboratory Instrumentation Maintenance

• Plan, develop and execute cellular, biochemical, and molecular assays for analysis of AAV-based gene therapies
• Support internal and external collaborations to increase team capabilities and address strategic needs
• Take initiative to identify and support emerging technical approaches and platforms that may drive increased value for pipeline programs
• Demonstrate initiative, teamwork, collaboration, and technical expertise as an independent and team player
• Maintain organized and detailed electronic records to support internal documentation needs and regulatory submissions
• Ability to multitask and contribute to multiple projects under demanding timelines
• Work as part of a multi-site team.
• Support and participate in R&D and project management meetings.

Skills: Assay Development, AAV Gene Therapy Analysis, Cross-functional Collaboration, Technical Innovation, Electronic Recordkeeping, Multitasking, Project Management, Teamwork

• Participating in conducting semi-complex tests or investigations about the development of new design methods, materials, or processes, and investigating possible applications of results
• Generating, correlating, and analyzing technical information needed to accomplish semi-complex tasks
• Verifying product performance (clinical evaluation) and executing validation studies, adhering to written protocols
• Taking part in the knowledge exchange with the R&D team to improve and further develop products and software solutions
• Performing laboratory experiments by executing them according to plan.
• Handling potentially biohazardous serum and plasma from human and animal sources

Skills: Experimental Design, Technical Data Analysis, Product Validation, Clinical Evaluation, Knowledge Sharing, Laboratory Experimentation, Protocol Adherence, Biohazard Handling

• Manufacture kit components, including antibody-bead coupling conjugations, antibody-biotin conjugation, and various formulations.
• Work with bottling, labeling, and storing components according to standard operating protocols
• Perform in-process testing to ensure the quality of components and kits
• Document, analyze, and review data
• Assemble and package kits and transfer with proper documentation
• Manage inventory, plan, and execute scheduled production work orders

Skills: Antibody Conjugation, Kit Component Manufacturing, SOP Compliance, Quality Control Testing, Data Documentation, Kit Assembly, Inventory Management, Production Planning

• Monitors TAT for testing and review to support batch release by providing input for effective analytical planning of scheduling of testing and data review.
• Responsible for Deviation management and final approval of investigations. 
• Helps to initiate effective CAPAs to reduce repeat deviations.
• Monitors and reports quality metrics.
• Encourages team members to seek out optimization and improvement opportunities
• Accountable for the personnel development and performance management planning of a team of specialists
• Supports the implementation of new products in the facility
• Manage projects or oversee team members managing projects
• Ensures personnel are qualified through proper training on appropriate SOPs
• Ensures personnel continue to grow professionally and technically by proper coaching and aiding in developing leadership skills
• Participates in regulatory and internal inspections and assures the team is inspection-ready at all times

Skills: Analytical Planning, Deviation Management, CAPA Implementation, Quality Metrics Monitoring, Process Improvement, Team Development, Project Management, Regulatory Compliance

• Support research efforts by providing expertise in novel nucleic acid chemistries for the synthesis and development of novel biomolecular machines
• Develop and implement analytical and biophysical methodologies to help analyze, characterize and evaluate nucleic acids for amplification
• Investigate methods to characterize and modify target nucleic acids.
• Conformational analysis of secondary structure, including sequence-specific conformations
• Investigate methods to characterize nucleic acid/enzyme interactions
• Manage projects by coordinating and prioritizing work streams, timelines and deliverables while driving project execution to meet corporate expectations

Skills: Nucleic Acid Chemistry, Biomolecular Synthesis, Analytical Method Development, Biophysical Characterization, Nucleic Acid Modification, Conformational Analysis, Enzyme Interaction Studies, Project Management

• Express, purify and characterize recombinant proteins and enzymes
• Develop functional assays capable of reporting on the efficacy of synthetic small-molecule effectors
• Develop molecular analysis tools to understand the mechanisms of new small molecules, including metabolite profiling and proteomics
• Establish target-based methods for the efficient discovery of novel crop protection leads
• Collaborate both internally and externally to develop new capabilities

Skills: Protein Expression, Protein Purification, Protein Characterization, Functional Assay Development, Molecular Analysis, Metabolite Profiling, Proteomics, Collaborative Research

• Perform all of the manufacturing processes independently in the Biochemistry Engineering group in the Process Integration department. 
• Execute purification and/or conjugation production orders and experiments following all Standard Operating Procedures (SOPs) and batch instructions. 
• Perform data review, summarize results, complete all required documentation and data entry in all required databases independently and accurately. 
• Complete assignments with good quality and in a given timeline. 
• Work independently and collaborate well in a team environment. 
• Participate in lab supply orders, reagent preparations, and equipment maintenance.
• Participate in validation/verification execution and support continuous improvement initiatives (5S blitz, shift start-up meeting, and Kaizen).
• Responsible for understanding and creating deviation notifications. 
• Provide technical training to junior associates or other functional groups on general lab equipment.
• Mainly perform routine and troubleshooting antibody purifications and/or conjugations with minimal supervision.
• Complete weekly assignments within the due dates.
• Proactively address any issues that may have arisen during production and provide timely updates to the supervisor.
• Participate in new product validation and verification execution.
• Prepare summary reports when performing process/product troubleshooting and optimization.
• Create engineering change requests for any specification and/or process changes
• Provide Technical training to junior associates or different functional groups.

Skills: Bioprocess Manufacturing, Protein Purification, Conjugation Production, SOP Compliance, Data Management, Equipment Maintenance, Process Validation, Technical Training

• Communicate effectively with both ATL and client staff
• Teach and mentor other staff members
• Remain flexible to ever-changing needs in a positive and professional manner
• Maintain mammalian cell culture lines
• Create cell line banks
• Generate media and other cell culture reagents
• Update and maintain biological inventories
• Perform experiment documentation
• Assist in any troubleshooting, operation, and maintenance of laboratory instrumentation
• Interact professionally with both internal and external clients
• Train and offer guidance to other ATL associates
• Maintain a high level of knowledge of various aspects of laboratory operations

Skills: Effective Communication, Staff Training, Flexibility, Mammalian Cell Culture, Cell Line Banking, Reagent Preparation, Inventory Management, Laboratory Instrumentation Maintenance

• Experience in a Biotech/Life Science manufacturing environment
• Have some working knowledge in the science disciplines and the operation of basic lab equipment
• Demonstrated ability to use laboratory instruments and applicable computer software
• Knowledge of general laboratory safety 
• Effective interpersonal skills, verbal and written communication 
• Demonstrated ability to follow established policies and procedures
• Demonstrated ability to keep neat, accurate, complete, and legible records and logs
• Possesses analytical problem-solving skills

Qualifications: BS in Biological Sciences with 1 year of Experience

• Working experience in related biotech product development or manufacturing.
• Demonstrated ability to be detail-oriented, organized and work well in a group setting
• Able to perform basic computer operations such as MS Office and Outlook and other computer-based software
• Working experience in related biotech product development or manufacturing.
• Experience in using UV Monitor
• Experience in conjugated antibody
• Experience in manufacturing in an ISO/GMP environment

Qualifications: BS in Molecular Biology with 2 years of Experience

• Should be an expert in either DNA/RNA chemistry or biochemistry. 
• Be a highly motivated and independent individual who is also comfortable working collaboratively as part of a multi-disciplinary team.
• Experience in a fast-growth biotech
• Laboratory experience in nucleic acid/oligonucleotide biochemistry or chemistry (not including RNA extraction)
• A passion for science and learning
• Team oriented with good humour, friendly, and plenty of energy
• The ability to work under pressure and prioritise workload
• Experience in the synthesis or chemical modification of oligos/nucleic acids
• Knowledge of tertiary oligo structures, duplexes, or DNA/RNA origami approaches
• Knowledge of RNA therapeutics
• Understanding of the analysis of RNA degradation
• Background in oligonucleotide purification, assembly, and/or characterisation

Qualifications: BS in Biomedical Sciences with 5 years of Experience

• Experience with modern genomics and biotechnology approaches for gene discovery
• Significant experience in biochemistry and understanding of pathway dissection and how that impacts food sensory perception
• Experience in vegetable, fruit, and/or grain crops
• Previous experience in corporate research
• Demonstrated research experience in designing advanced genomic discovery projects that delivered target genes impacting consumer- and processing-relevant crop attributes
• Experience in modern flavor and taste science genetics across populations to drive personnel preference
• Excellent communication and networking ability with internal and external audiences that have a wide range of scientific expertise
• A proven ability to work closely with colleagues on complex projects with a high degree of flexibility and comfort with change
• Ability to balance the need to deliver aggressive business innovation goals with scientific excellence
• Demonstrated experience in team discovery with knowledge of both plant breeding practices and principles of agronomic investigation
• Personnel management experience
• An individual with extensive external discipline-based networks to foster collaboration and identify a mix of tactical and strategic partners to accelerate project delivery

Qualifications: BS in Cell Biology with 10 years of Experience

• Related industry laboratory experience
• Strong technical writing and verbal communication skills
• Demonstrates excellent interpersonal skills (written and oral) and the ability to work in a cross-functional, customer-focused environment
• Experience with ELISA, FRET, qPCR, cell culture and aseptic technique, cell-based potency assays, flow cytometry, or plate-based biochemical assays (impurity, HCP).
• Experience working in a cGMP environment
• Perform experiments and data review according to SOPs and protocols.
• Experience with an electronic laboratory notebook
• Excellence in bioassay troubleshooting 
• Ability to work with limited guidance to plan, execute, and follow through with studies
• Softmax Pro working experience

Qualifications: BS in Microbiology with 3 years of Experience

• Industrial experience in the production/quality control of in vitro diagnostic or similar products.
• Understanding of production operations, quality assurance/control, and cGMP/GLP requirements.
• Ability to show a high level of care and attention to all aspects of the role and show a desire to achieve excellence through own initiative.
• Proven team player capable of working within multiple areas whilst maximising performance.
• Excellent communication skills (both written and verbal) and be team-focused.
• Willingness and ability to collaborate with and influence other groups in a positive, team-based environment.
• Pays attention to detail and works with a sense of urgency, and can be impartial and objective.
• Excellent organisation, planning and judgement skills, and will be able to positively achieve results through others.
• Flexible and willing to work overtime
• Ability to read, analyze and interpret technical data, technical procedures or governmental regulations.
• Ability to use Microsoft Word, Excel, PowerPoint, and Outlook.

Qualifications: BS in Molecular Biology with 2 years of Experience

• Strong initiative and enthusiasm to complete ambitious tasks and learn new technologies related to CAR T products.
• Work experience in GMP quality control or manufacturing
• Strong understanding of applicable USP, ICH, and Ph Eur regulations related to intermediate, release, and stability testing.
• Excellent verbal and written communication skills.
• Extensive experience with scheduling, testing, and data review of QC bioassays for in-process, release, and stability samples.
• Experience with QMS systems, including OOT/OOS/invalid investigations and working cross-functionally to support CAPA and proactive initiatives.
• Experience in training and mentoring laboratory analysts, with a focus on team building.
• Experience troubleshooting analytical equipment and methods.
• Ability and desire to work in a fast-paced environment, manage large projects, and implement microbiology programs.
• Experience interacting with hosting internal and external auditors

Qualifications: BS in Biochemistry with 8 years of Experience

• Hands-on experience in immunoassay development
• Experience with protein or small molecule conjugation techniques, particle chemistry, particle size analysis, and flow cytometry.
• Proficient in analytical techniques such as HPLC, Size Exclusion Chromatography, capillary electrophoresis (e.g., reduced and non-reduced CE-SDS, icIEF), spectroscopic analysis.
• Experience with the development of in vitro diagnostics for biomarkers in the Point of Care setting
• Diagnostic (IVD) assay development experience 
• Familiarity with creating and reviewing formal documents such as protocols, reports, QC specifications, and manufacturing documents.
• Experience in the handling of chemical materials and biological samples, including plasma.
• Experience with microparticle-antibody conjugation
• Demonstrated skills in carrying out innovative research with minimal guidance in an accurate, effective manner
• Proven experience supervising scientific staff, coordinating interdepartmental efforts, generating research hypotheses, analyzing complex problems and data, and bringing products to market
• Experience identifying and implementing new technologies or improvements of existing technologies for any of marker discovery, marker validation, product development, DFM, and product manufacturing
• Knowledge of scientific principles and concepts
• Experience in product development and experimental design
• Knowledge of advanced methods for statistical experimental design and data analysis
• Strong analytical and problem-solving skills
• Team player with excellent organizational, communication skills, and ability to manage multiple tasks/projects simultaneously
• Ability to plan and execute experiments to prove feasibility, develop new processes and set specifications, characterize materials and set specifications, and troubleshoot problems

Qualifications: BS in Cell Biology with 11 years of Experience

• Expertise with stable isotope analysis, especially compound-specific stable isotope analysis.
• Expertise in one or more of isotope-ratio mass spectrometry, coding in R, and application of mixing models.
• Demonstrated experience working with large data sets.
• A documented producer, such as authorship of a peer-reviewed publication and/or report.
• Demonstrated ability to give oral presentations such as conference presentations (oral and/or poster) or other public presentations.
• Proven analytical chemistry experience.
• Experience using isotope-ratio mass spectrometry for stable isotope analyses.
• Experience using R statistical software

Qualifications: BS in Microbiology with 3 years of Experience

• Eager to work in a challenging experimental environment
• Experience in hands-on chemical laboratory work (able to handle chemical reagents)
• In-depth understanding of chemical and biochemical reactions, i.e, extraction, separation, sedimentation
• Research or industry experiences with downstream processing
• Experience in DoE or any experiment design tools
• Able to adapt and thrive in a rapid pace and a quickly changing environment.
• Strong passion to innovate and go the extra mile to achieve beyond expectations.
• Good team-play spirit with the ability to listen and communicate with others.

Qualifications: BS in Molecular Biology with 2 years of Experience