Process Scientist Ii Jobs

PhD in chemistry with 0-5 years experience in the pharma industry.

Experience with applying biocatalysis in a laboratory setting.

Working experience designing and optimizing biocatalytic reactions, high-throughput screening in multi-well plates and developing new enzyme platforms.

Non-standard Work Schedule, Travel Or Environment Requirements

Responsible for coaching, mentoring, training, supervising, and developing staff when assigned; participate in recruiting when needed.

Prepares research reports and technical presentations and external publications.

10+ years of experience with database management systems such as MySQL, PostgreSQL, or MongoDB

6 years of experience analytical skills and the ability to extract insights from large sets of data

2-4 years of experience in building ML models

4-7 years of experience with programming languages such as Python or SQL

7-9 years of experience in data visualization tool such as Tableau, PowerBI, or Looker

3 years of experience with data-related libraries such as Pandas, NumPy, or Matplotlib

PhD in chemistry, chemical engineering, or a related field or MS +3 years of experience

Demonstrated experience with the design and synthesis of complex novel targets

Relevant laboratory experience in life science applications.

Experience executing molecular biology assays.

Experience in surface chemistry, polymer chemistry, bioconjugation and surface functionalization.

Experience with imaging of biological samples

The responsibilities listed are a general overview of the position and additional duties may be assigned.

Makes decisions and recommendations that have an impact on clinical research activities with minimal supervision from faculty

Formulates and conducts clinical research on problems of considerable scope and complexity

Provides clinical research expertise in an ongoing capacity

Independently interprets, organizes, executes, and coordinates clinical research assignments

Oversees the coordination of the Center’s journal club, works in progress meeting, guest lectures, and annual Alzheimer’s Disease Research Day

Offer guidance and lab-level leadership for incumbent associates, with possibility for 1-2 direct report(s)

May include approximately 20% remote work, with flexibility based on project needs

BS+8 / MS+6 / PhD+2 years minimum industry experience in a process development or MSAT role

Excellent communication and presentation skills. Capability to convey complex technical information in a clear, concise, and influential manner

Prior experience developing purification processes for virus, VLP, or gene therapy vectors for GMP clinical manufacturing.

Working knowledge of the GMP manufacturing environment, which may include involvement in process transfer, review of batch records/deviations/CAPAs, or ‘person-in-plant’ duties.

Demonstrated scientific writing skills and strong verbal communication skills.

Synthesis, purification and characterization of ADCs on mg to gram scale under minimal supervision.

Optimization and validation of conjugation protocols and formulation buffers.

Optimization of automated techniques for ADC synthesis and purification.

Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.

Demonstrated ability to learn, understand and master new experimental techniques.

Statistical analysis of data experience is preferred.

Must be willing to take a drug test and post-offer physical (if required).

Requirements for Scientist II BioProcess Sciences:

Assist in improving consistency, stability and yields.

Assist in optimizing current processes by conducting experiments to evaluate different growth parameters, medium components and new equipment.

Assist in setting up, operation and validation of new equipment. Ensures maintenance of equipment and it is kept in operational status.

Technical liaison including production/maintenance employees, plant technical and management resources, corporate engineering and R&D organizations.

Minimum of 3 years of experience with process operations in a manufacturing environment required.

Experience of continuous improvement methodology e.g. Lean Six Sigma tools.

Experience of successfully leading teams to make changes through capital projects or large operating changes.

Review existing operations and identify opportunities for improvement using sound engineering principles.

Use continuous improvement tools as the primary methodology to identify, quantify, direct and implement refinery improvements.

Excellent oral (including public speaking) and written communication skills

Experience building and/or working in collaborative, diverse and inclusive team environments

Strong interpersonal skills, demonstrated through mentorship, listening and good communication

The following qualifications are required:

Develop and/or refine existing open-source aquatic algorithms for SBG, and lead their validation

Lead SBG DEIA collaborations and activities with minority and underrepresented groups

Any years direct manufacturing and manufacturing engineering experience.

Closely manage quality, build sequence, and schedule of hardware throughout the entire manufacturing process.

Manage hardware configuration and maintain pedigree throughout the entire build and test process.

Understanding of engineering fundamentals for mechanical design and manufacturing including working knowledge of GD&T.

Experience prioritizing hardware procurement and fabrication and communicating these priorities to the team.

Strong written, personal, technical, and software skills (CAD, Scheduling, Issue Tracking, Excel, Word, PowerPoint, Outlook, etc).

Prior experience supporting investigations, change controls, process monitoring, process validation, and routine commercial support in a GMP setting.

Preferred experience in working with CMOs.

Strong communication skills: clear, concise communication and resolution of complex technical issues across broad audiences and functional teams.

Excellent organizational skills, with the ability to multi-task in an extremely fast-paced environment with changing priorities.

Collaborates with Manufacturing and Quality counterparts within bluebird to ensure robust supply and support CMO performance.

Ensures timely review of process data and supports the resolution of deviations, investigations, change controls, and updates to regulatory documents.

Extensive experience in upstream, downstream, analytical development, and continuous manufacturing for vaccines/biologics, with in-depth domain knowledge in one of these areas.

Strong knowledge of global regulatory requirements for vaccines.

Demonstrated scientific and communication capability to strongly influence senior management across functional areas and steer scientific strategy and policy.

Demonstrated expertise in addressing complex challenges in pipeline and life cycle management through critical thinking, innovation, scientific rigor, and cross-functional collaboration.

Experience in CMC or program direction, leading to multiple successful submissions for vaccines/biologics.

Working knowledge on DPI and adjuvant development and innovation.

Experience with organic structural analysis and its interpretation in petrological and mineralogical context.

Experience in UV flight instrument operation and development.

This position requires the following qualifications:

The following qualifications are preferred:

For further benefits information click Benefits and Perks

PhD in geomicrobiology, or a related field.

iota offers a very competitive benefits package that includes the following:

Maintains in-depth scientific knowledge in relevant therapeutic areas

Bachelor's degree with 2+ years research experience in biology, oncology, or immunology

Experience with molecular and/or cell-based assays or histopathology

Experience in independently optimizing experimental methods and assays

Experience working in interdisciplinary environments and building relationships with key external partners

Ability to manage multiple priorities and comply with deadlines.

Maintains their certifications as needed for assigned job tasks.

Demonstrates strong analytical skills and logical thought processes.

Assists in troubleshooting multi-discipline problems.

Applies scientific/engineering principles applicable to assigned tasks and problem-solving.

Independently design, execute and interpret critical experiments to answer scientific questions.

Bachelor's degree in Engineering and 2 years of relevant experience, or

Master’s degree in Engineering and 1 year of relevant experience

Engineer in Training (EIT) certification

Click here for benefits information: HNTB Total Rewards

Completes assigned work within the schedule and number of hours provided.

Responsible for preparation and/or modification for select portions of project reports, plans, designs, and calculations.

Strong project management and organizational skills.

Leads technical support activities related to maintaining commercial product supplies through management of internal and external resources.

Knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing is preferred.

Contributes to user requirement specification and provides expert process technical support to utilize and validate new and improved technologies.

Experience with statistical data analysis tools is preferred.

Excellent troubleshooting skills and ability to solve complex technical issues.

Engage in stakeholder meetings to identify business objectives and scope solution requirements.

Use, maintain, share and collaborate through Truist internal code repositories to foster continual learning and cross-pollination of skillsets.

Working knowledge of calculus/differential equations, including use of stochastic processes.

Data Analysis techniques, EDA, Data Visualization to effectively communicate to stakeholders, clarify requirements and make effective suggestions.

Natural Language Processing techniques and other related Deep Learning knowledge.

Utilizing experience with: SQL, SAS, Hadoop, Hive, NoSQL, Spark, Python, and R.

Collaborates with Process Development Scientists and Management during technical transfer and experiment design.

Responsible for reviewing executed documentation for accuracy and completeness prior to submission to management.

Assists with the implementation of Process Development strategies as directed by management

Expected to adhere to all procedures, including gowning and safety requirements, at all times

Strong oral and written communication skills

Knowledge of Current Good Manufacturing Processes (cGMP), Regulatory Guidelines, Aseptic Manufacturing, as well as bulk intermediate and medical device manufacturing.