What are the responsibilities and job description for the Engineer Senior, Biotechnology - (JP11209) position at 3 Key Consulting?
Job Title: Engineer Senior, Biotechnology - (JP11209)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Physical Testing Systems Development
Duration: 15 months (with likely extensions and/or conversion to permanent)
Posting Date: 01/03/23
Notes: Only qualified candidates need apply. 100% onsite. Monday - Friday 8am - 5pm (flex)/ 7- 4pm
3 Key Consulting is hiring an Engineer Senior for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Senior Engineer is responsible for engineering activities required for development / qualification / validation and transfer of GMP physical test methods for combination products, devices, primary container, and secondary packaging components, as required. This individual shall have the ability to work on multiple projects at one time that may involve either new or changed product, process, tooling or equipment introduction to improve product quality and reliability.
Top Must Have Skills:
Day to Day Responsibilities:
Basic Qualifications:
Preferred Qualifications:
Red Flags:
Interview process:
We invite qualified candidates to send your resume to resumes@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.
Employment Type: Contract
Business Unit: Physical Testing Systems Development
Duration: 15 months (with likely extensions and/or conversion to permanent)
Posting Date: 01/03/23
Notes: Only qualified candidates need apply. 100% onsite. Monday - Friday 8am - 5pm (flex)/ 7- 4pm
3 Key Consulting is hiring an Engineer Senior for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Senior Engineer is responsible for engineering activities required for development / qualification / validation and transfer of GMP physical test methods for combination products, devices, primary container, and secondary packaging components, as required. This individual shall have the ability to work on multiple projects at one time that may involve either new or changed product, process, tooling or equipment introduction to improve product quality and reliability.
Top Must Have Skills:
- Test Method development/validation experience, Equipment qualification and implementation
- Experience with regulated industry, preferred
- Experience with data analysis, preferred
- BS or Masters Degree with a minimum of 3-4 years of experience
Day to Day Responsibilities:
- Assure transfer of new combination product test methods to QC or manufacturing, by developing six sigma processes and compiling all required documentation.
- Implement projects per Combination Product Operations (CPO) and company procedures to ensure projects are completed on schedule and within established budget.
- Apply core engineering principles to develop physical test methods for medical device and combination product systems.
- Perform data analysis to support method development, qualification, validation, and transfer
- Provide expert support in the design or redesign of tools and/or equipment required for manufacturing processes.
- Provide expert support for investigations as well as new processes development required to improve manufacturing operations. Improvements may be required for a variety of reasons (i.e. quality, reliability, new product introduction, cost saving).
- Coordinate gauge and equipment development and delivery with selected contractors.
- Ensure that qualification parameters are met for product assembly and performance requirements.
- Support development of cost estimates for new processes, gauges and equipment development used in generation of capital request documentation.
- Generate procedures necessary to support department and new product equipment.
- Provide expert training to individuals in the operation and maintenance of processes, gauges and equipment introduced to the manufacturing department (i.e. production operator, mechanics, process engineers).
- Participate in and assume responsibilities of team functions as assigned (i.e. Product Improvement Teams). Supervise work of support staff during development and manufacture of system.
- Excellent communication (written and verbal) and organizational skills
- Develops and maintains integrated timelines capturing appropriate cross functional details and deliverables which are aligned with the functional and project deliverables
- Networks with manufacturing, quality and regulatory organizations both internal and external to client
- Facilitates robust horizontal communication to ensure all functions are aware of changes in deliverables and impacts to risk.
- Proactively identifies issues and/or risks and develops mitigation options to resolve or escalate efficiently
- Integrates partner/vendor timelines with timelines as appropriate
Basic Qualifications:
- Doctorate Degree OR
- Master's Degree and 3 years of Engineering experience OR
- Bachelor's Degree and 5 years of Engineering experience OR
- Associate's degree and 10 years of Engineering experience OR
- High school diploma/GED and 12 years of Engineering experience.
Preferred Qualifications:
- M.S. or Ph. D. in Mechanical, Aerospace, Mechatronics, Chemical or Biomedical engineering
- Excellent written and verbal communication skills together with demonstrated ability to work in a highly matrixed team environment
- Experience with managing technical teams, including setting priorities and leveling resources
- Technical writing experience
- Spanish language skills preferred
- Experienced with SolidWorks (or other 3D-CAD software)
- Familiar with equipment and software IOQ
- Experience with process characterization, scale-up, technology transfer experience, pFMEAs and dFMEAs
- Experience with change controls, deviations, CAPA
- Experience with combination products and device regulatory requirements
- Understanding of the six sigma process, utilizing Minitab (or other statistical software packages) to solve statistical problems
- Work history with cGMPs, regulatory filings and compliance issues for sterile injectable products manufactured by aseptic processing
- Experience with machine controls (PLC, HMI) and vision systems
Red Flags:
- No formal engineering training
- Job Jumping - multiple job changes in a year
Interview process:
- Phone
- In Person/webex panel
We invite qualified candidates to send your resume to resumes@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.