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Process Engineer, Biotech Drug Substance Technology (JP11861)
Thousand Oaks, CA · Biotech/PharmaceuticalJob Title: Process Engineer, Biotech Drug Substance Technology (JP11861)
Location: Thousand Oaks, CA. (Local/hybrid)
Employment Type: Contract
Business Unit: Commercial DP - Process Eng
Duration: Initial 9 months with likely extensions and/or conversion to permanent
Posting Date: 10/09/23
Rate: $38-42/HR W2
Notes: Must be local (1-2 days a week). Masters Degree is highly preferable, Pharma industry experience, Independent worker
3 Key Consulting is hiring an Engineer, Drug Substance Technology for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple products to various aseptic fill finish manufacturing plants and production lines. The candidate will support senior staff in the planning, execution and documentation of characterization, process validation and technology transfer projects. The candidate will be primarily responsible for executing characterization studies and other experiments at the lab scale and production scale to generate technical data packages using complex technology, while organizing data and analyzing results under supervision of senior staff. The candidate will be responsible for liaising with various drug product teams to ensure successful technology transfer, with associated documentation, of client’s products. The candidate will assist to establish the experimental design, develop and execute protocols, obtain reproducible and reliable results, analyze and document experimental results, and communicate results to cross functional groups.
Basic Qualifications
Top Must Have Skills:
Day to Day Responsibilities:
Responsibilities include, but are not limited to, the following:
Red Flags:
Phone screening followed by video call (panel interview)
We invite qualified candidates to send your resume to recuiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA. (Local/hybrid)
Employment Type: Contract
Business Unit: Commercial DP - Process Eng
Duration: Initial 9 months with likely extensions and/or conversion to permanent
Posting Date: 10/09/23
Rate: $38-42/HR W2
Notes: Must be local (1-2 days a week). Masters Degree is highly preferable, Pharma industry experience, Independent worker
3 Key Consulting is hiring an Engineer, Drug Substance Technology for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple products to various aseptic fill finish manufacturing plants and production lines. The candidate will support senior staff in the planning, execution and documentation of characterization, process validation and technology transfer projects. The candidate will be primarily responsible for executing characterization studies and other experiments at the lab scale and production scale to generate technical data packages using complex technology, while organizing data and analyzing results under supervision of senior staff. The candidate will be responsible for liaising with various drug product teams to ensure successful technology transfer, with associated documentation, of client’s products. The candidate will assist to establish the experimental design, develop and execute protocols, obtain reproducible and reliable results, analyze and document experimental results, and communicate results to cross functional groups.
Basic Qualifications
- Master’s degree OR Bachelor's Degree and 2 years of relevant experience.
- Preferred Qualifications/Educational background in Chemical Engineering, Biomedical Engineering, Biotechnology correlated technical field of study in biotechnology, life sciences or related discipline.
- Knowledge in scientific principles of freeze/thaw, formulation/mixing, filtration, filling, lyophilization, capping, and visual inspection.
- Ability to work on multiple projects simultaneously, learn new techniques, keep accurate records, follow SOP’s and instructions in compliance with company policies, and comfortable to operate in a very flexible, agile environment
- Ability to independently design and execute characterization studies, author characterization protocols, process transfer documents, application notes and technical reports.
- Proficiency in technical problem solving, critical thinking, and delivery of technical solutions with some oversight
- Strong knowledge of Quality systems and Drug Product Manufacturing (GMP).
- Demonstrated ability to use interpersonal skills to build strong technical relationships.
- Self-motivation, adaptability, and a positive attitude.
- Excellent communication skills, both oral and written.
Top Must Have Skills:
- Masters Degree HIGHLY PREFERABLE
- Familiarity with cGMP and experience in drug product / drug substance manufacturing or process development in pharmaceutical industry setting and manufacturing
- Knowledge of and hands-on experience with various drug product technologies
- Ideal candidate:
Must have at least a Masters Degree
Pharma industry experience
Independent worker
Day to Day Responsibilities:
Responsibilities include, but are not limited to, the following:
- Apply fundamental engineering and scientific principles to resolve issues and evaluate effects of process improvements, equipment, scale, and raw materials
- Assist in the design and execution of experiments in order to characterize and enable implementation of new capabilities and process changes such as filling, lyophilization and analytical technologies
- Support technology transfer leads during the transfer of drug products into manufacturing sites (clinical and commercial), including make-a-batch exercises, process transfer documents, and change control assessments
- Support development of technology transfer tools (clinical and commercial)
- Effectively communicate results of characterization studies, experimental execution and technology transfer initiatives
- Author/review technical documents, such as technical protocols, technical assessments, technical reports and draft standard operating procedures
- Conduct analysis of data generated, including statistical analysis using Minitab, JMP etc.
- Development of digital tools and models by leveraging data analytics and programming skills
Red Flags:
- No pharma experience
- Must have experiment experience
- Not an entry level role
Phone screening followed by video call (panel interview)
We invite qualified candidates to send your resume to recuiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team