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- Tasks: Join a dynamic team to design and automate biopharmaceutical processes.
- Company: ADVENT Engineering is a leading firm in biotech and pharmaceutical consulting.
- Benefits: Enjoy competitive pay, medical insurance, and flexible work options.
- Why this job: Make an impact in life sciences while working with cutting-edge technology.
- Qualifications: Bachelor's or master's degree in engineering with 3+ years in biotech.
- Other info: Experience with CFD and AutoCAD is a plus.
The predicted salary is between 60000 - 84000 £ per year.
Direct message the job poster from Trinity Consultants – Advent Engineering
Life Sciences Talent Acquisition Specialist
PROCESS ENGINEER
Onsite
ADVENT Engineering Life Science Solutions, a Trinity Consulting Co., is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Located across the US, ADVENT participates in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system projects.
ADVENT\’s services include process engineering, automation engineering, project engineering, HVAC/facility system design, process development, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies.
The successful candidate will work with a group of engineers involved in the design, automation, commissioning & qualification and start-up of various processes, systems, and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. This is an outstanding opportunity to join our growing team!
Responsibilities
- Lead and/or participate in client meetings to discuss technical issues, project updates, project progress.
- Interact with project management, vendors and clients in coordination, design, review, start-up and CQV of biopharmaceutical process, facilities/utilities systems and Process equipment.
- Generation and review of engineering design specifications, documentation, and drawings for upstream, downstream bulk processing equipment (fermenters, chromatography skids, bioreactors, TFF, UFDF, centrifuge etc.) and critical utilities (WFI, process gases etc.)
- Responsible for the design review to ensure the design is consistent with industry-accepted and best practice, leading edge technologies and client requirements.
- Review Master Batch Records and build out operational data repository
- Excellent understanding of applicable industry codes and standard practices (e.g., ASME BPE, etc.)
- Participate in construction activities as needed, including reviewing RFI’s, submittals, responding to design change notices, issuing field change bulletins, attend site walk-throughs and issue field observation reports, develop operational and functional acceptance tests, develop drawings, and produce other system documentation.
- Perform engineering studies for expanding, improving, or automating existing facilities with limited supervision.
- Assume ownership of the process-related aspects of a portion of a large project or an entire small project and provide technical support to the design team.
- Establish and maintain excellent working relationships with clients and members of the design team.
- Must be able to demonstrate the ability to work independently.
- CFD and Autocad experience a plus
Qualifications
- Requires a bachelor’s or master’s degree in Mechanical Engineering, Chemical Engineering, Biochemical Engineering, or related discipline. Engineering degree is preferred.
- Three (3) plus years of experience in the biotech-pharmaceutical environment with a demonstrated foundational understanding of large molecule biologics and/or cell and gene therapy manufacturing processes.
- Basic understanding of utilities and equipment required to support drug substance and drug product manufacturing.
- Basic knowledge of Commissioning, Qualification and Validation (CQV)
- Familiarity with ASME BPE.
- Direct experience in the design or commissioning/qualification in any of the following systems: upstream / downstream bulk process equipment, lyophilization, formulation / fill vial and syringe forms, sterilization, Clean-In-Place, clean utilities (WFI/PW, Pure Steam, Clean Gases).
- Strong knowledge on review, understanding P&IDs drawings, ISA symbology is important.
- Strong knowledge of hygienic process components and instruments is required.
- Strong knowledge of Master Batch records.
- Basic knowledge of automation narratives and architecture of various platforms, including PLC/SCADA, DCS (e.g., DeltaV) and BMS/BAS experience is a plus.
- Basic knowledge of regulatory compliance inclusive of cGMP, OSHA, EPA, FDA regulations. Familiarity with ICH guidelines and EMA regulations is a plus.
- Basic technical writing with proficiency in Excel, PowerPoint, Visio, Word, SharePoint, etc. in addition to experience working within shared work environments.
Seniority level
-
Seniority level
Associate
Employment type
-
Employment type
Full-time
Job function
-
Job function
Engineering and Consulting
-
Industries
Manufacturing, Engineering Services, and Pharmaceutical Manufacturing
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Inferred from the description for this job
Medical insurance
Vision insurance
401(k)
Paid maternity leave
Paid paternity leave
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Process Engineer, RMTO – Process Engineering
Process Engineer, Manufacturing Innovation and New Technology
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Process Engineer employer: Trinity Consultants - Advent Engineering
Contact Detail:
Trinity Consultants - Advent Engineering Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Engineer
✨Tip Number 1
Network with professionals in the biotech and pharmaceutical industries. Attend industry conferences, webinars, or local meetups to connect with potential colleagues and learn about the latest trends in process engineering.
✨Tip Number 2
Familiarise yourself with the specific technologies and equipment mentioned in the job description, such as bioreactors and chromatography skids. Having hands-on experience or knowledge of these systems can set you apart during interviews.
✨Tip Number 3
Prepare to discuss your previous projects in detail, especially those related to commissioning and qualification processes. Be ready to explain your role, the challenges faced, and how you contributed to the project's success.
✨Tip Number 4
Showcase your technical writing skills by preparing a portfolio of relevant documentation you've created, such as engineering design specifications or Master Batch Records. This will demonstrate your ability to communicate complex information effectively.
We think you need these skills to ace Process Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in process engineering, particularly in the biotech and pharmaceutical sectors. Emphasise any specific projects you've worked on that align with the responsibilities listed in the job description.
Craft a Strong Cover Letter: Write a cover letter that directly addresses the key qualifications mentioned in the job description. Discuss your technical skills, such as automation engineering and technical writing, and how they relate to the role at ADVENT Engineering.
Showcase Technical Skills: In your application, clearly outline your technical skills, especially those related to design specifications, engineering codes, and software tools like AutoCAD. Mention any experience you have with commissioning and qualification processes.
Highlight Soft Skills: Don't forget to mention your ability to work independently and maintain excellent working relationships with clients and team members. These soft skills are crucial for the collaborative environment at ADVENT Engineering.
How to prepare for a job interview at Trinity Consultants - Advent Engineering
✨Know Your Technical Stuff
Make sure you brush up on your knowledge of process engineering, especially in the biotech and pharmaceutical sectors. Be prepared to discuss specific equipment like fermenters and bioreactors, as well as industry standards like ASME BPE.
✨Showcase Your Experience
Highlight your previous experience in the biotech-pharmaceutical environment. Be ready to share examples of projects you've worked on, particularly those involving commissioning, qualification, and validation (CQV) processes.
✨Prepare for Technical Questions
Expect technical questions related to P&IDs, automation narratives, and regulatory compliance. Practise explaining complex concepts clearly, as this will demonstrate your communication skills and technical aptitude.
✨Demonstrate Teamwork and Independence
ADVENT values collaboration and the ability to work independently. Prepare examples that showcase your ability to lead projects while also being a team player, highlighting any successful client interactions or project management experiences.
