Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases.

We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases. 

Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development.

Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

Industry: Biotechnology Research
Company Size: 1,001-5,000 employees

Vertex Pharmaceuticals

Savvy Admin PROD

**Job Description**

**General Summary**

Vertex is seeking a talented and motivated Scientist to join our Process Development team. The Process Development Engineering Scientist will lead projects focused on process development, optimization, and characterization of cell therapy products for current and future programs. This role involves hands-on work with large-scale bioreactors (50L and above) and will focus on developing scalable media and bioreactor processes to advance our Type 1 Diabetes program.

**Key Responsibilities**

- Design and execute experiments to develop robust manufacturing processes for cell therapy products and support programs in clinical development.

- Develop robust, scalable media and bioreactor processes for cell therapy manufacturing.

- Evaluate novel and emerging technologies to advance project strategies.

- Lead projects within the team and provide training and support to scientists and engineers in large-scale bioprocessing and media scale-up.

- Apply deep knowledge of cell culture, bioreactor operations, and scale-up principles to process development activities.

- Use scientific and engineering fundamentals to support process design, development, and process understanding.

- Apply statistical tools and design of experiments (DOE) to guide process optimization.

- Develop process development and optimization strategies for 50L scale and beyond.

- Drive development activities in a cross-functional team environment.

- Author and review batch records, technical reports, and supporting documentation.

- Troubleshoot and resolve process challenges through the application of technical expertise and scientific judgment.

- Troubleshoot process and equipment-related issues and apply a strong understanding of large-scale bioprocessing equipment to support operations.

**Knowledge And Skills**

- Experience in large-scale bioprocessing, including operation of 50L and above bioreactors.

- Strong understanding of large-scale bioprocessing equipment and demonstrated ability to troubleshoot equipment and process issues.

- Strong background in design of experiments (DOE) and statistical analysis.

- Strong understanding of cell culture processes and bioreactor scale-up.

- Excellent verbal and written communication skills, with the ability to communicate complex technical and scientific information clearly.

- Ability to manage multiple priorities, meet timelines, and adapt in a fast-paced environment.

**Qualifications**

- Bachelor’s degree in Chemical Engineering, Bioengineering, Biochemistry, Biology, or a related field with 6–8 years of relevant experience, or Master’s degree with 4–6 years of relevant experience, or PhD with 0–3 years of relevant experience.

**Pay Range**

$104,000 - $156,000

**Disclosure Statement**

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

**Flex Designation**

On-Site Designated

**Flex Eligibility Status**

In this **On-Site ** designated role, you will work **five days per week on-site **with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

**Company Information**

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Process Dev Engineering Scientist

At Jacobs, we're challenging today to reinvent tomorrow – delivering outcomes and solutions for the world's most complex challenges. With a team of approximately 45,000, we provide end-to-end services in advanced manufacturing, cities & places, energy, environmental, life sciences, transportation and water. From advisory and consulting, feasibility, planning, design, program and lifecycle management, we're creating a more connected and sustainable world.

Industry: Business Consulting and Services
Company Size: 10,001+ employees

Jacobs

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good.

Your impact

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good.

This job opportunity is available at **ANY ** location in the United States. Ideally, selected candidates will be near a JACOBS U.S. based office, but we intend to hire the "best" candidates.

At Jacobs, we’re transforming intangible ideas into innovative solutions designing the future - today. If you are someone who thrives in a fast-paced, collaborative work environment and who also enjoys working closely with clients in the Data Center market, this opportunity is for you!

As an EPC Telecom Engineer, you will be responsible for the full lifecycle of telecommunications systems, from initial technical design to field commissioning and project closeout.

**Core Responsibilities**

**Detailed Engineering ** Design voice and data systems, including detailed architectural schematics and network diagrams. Perform technical calculations and prepare deliverables like specifications, reports, and procedures.

-  Develop detailed telecom infrastructure designs, including structured cabling (fiber/copper), high-speed network circuits, and rack layouts.

-  Create technical specifications

-  Conduct Site Visits

-  Review technical documents

-  Sign and Seal Telecommunications Design packages

-  create Bill of Materials (BOM) from design drawings and specifications.

-  Work with BIM designers to prepare telecommunications design packages.

**Procurement Support ** Prepare technical requisitions for hardware, software, and cabling. Conduct technical evaluations of vendor bids, review vendor documentation, and oversee Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs).

-  Partner with supply chain teams to evaluate and select vendors for mission-critical hardware and cabling.

-  Coordinate equipment purchasing, shipping, and inventory management for large-scale deployments.

-  Manage vendor relationships and ensure materials meet quality and code standards.

**Construction & Field Oversight ** Provide technical support to construction teams, resolve field change requests (FCDs), and work with APM’s to manage subcontractors. Ensure installations comply with project specifications and safety (HSE) standards.

-  Oversee on-site installation activities, including fiber splicing, rack-and-stack, and network circuit turn-ups.

-  Track project milestones, manage change orders, and conduct site inspections to ensure "right first time" execution.

-  Support commissioning and testing to verify system readiness before operational handover.

**Project Management ** Interface with construction PM’s, design PM’s, Vendors, Clients and other engineering disciplines to ensure system consistency.

**Essential Skills & Job Requirements.**

Technical Proficiency Expertise in Fiber Optics, IP-based systems, wireless technology, and Cisco IOS/XR or Junos operating systems.

Problem Solving Ability to diagnose complex network issues and develop disaster recovery plans.

Coordination Strong communication skills for liaising between vendors, clients, and multidisciplinary engineering teams.

Thorough knowledge of industry standards such as BICSI, ANSI/TIA, and NEC.

Excellent project management skills.

Familiarity with responding to RFP’s

Proficiency with Bluebeam.

Proficiency in optical transport systems (10G-100G).

Proficiency with reading and interpreting testing results for different telecommunications technologies.

Experience in providing Quality Assurance and checking of telecommunications systems designed by others

Experience with start-up and commissioning of telecommunications systems

Experienced in creating a budget for a project.

Experienced in creating and maintaining a project schedule

**Experienced In Identifying And Mitigating Company Risk**

Here's what you'll need

**Education ** Bachelor’s degree in electrical engineering, Telecommunications, or Computer Science from an ABET-accredited institution.

**Experience ** 6 – 8 years’ experience working on EPC projects or a combination of experience working for MEP design firm and installation contractor.

**Travel ** This position will require at least 25% travel.

**Certifications**

-  Professional Engineering (PE) license

**Ideally, you’ll also have**

-  CCNA (Cisco Certified Network Associate)

-  PMP (Project Manager Professional)

-  RCDD (Registered Communications Distribution Designer)

-  CompTIA Network+

Our health and welfare benefits are designed to invest in you, and in the things you care about. Your health. Your well-being. Your security. Your future. Employees have access to medical, dental, vision, and basic life insurance, a 401(k) plan, and the ability to purchase company stock at a discount. Eligible employees may also enroll in a deferred compensation plan or the Executive Deferral Plan. Jacobs has an unlimited U.S. Personalized Paid Time Off (PPTO) policy for full-time salaried/exempt employees, seven paid holidays, and caregiver leave. And certain roles may be eligible for additional rewards, including merit increases, performance discretionary bonus, and stock.

The base salary range for this position is $155,600.00 to $272,300.00. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Job posted on February 06, 2026. This position will be open for at least 3 days.

Your application experience is important to us, and we’re keen to adapt to make every interaction even better. If you require further support or reasonable adjustments with regards to the recruitment process (for example, you require the application form in a different format), please contact the team via Careers Support.

EPC Telecom Engineer

**Job Description**

**General Summary:**

The Principal Scientist/Engineer, Manufacturing Science and Technology (MSAT) – Biologics & Cell Therapy is a key technical role within the **Commercial Manufacturing and Technology Operations (CMTO) ** organization. This position supports late‑stage clinical and commercial programs across the Vertex Biopharmaceutical Sciences and Manufacturing Operations (BSMO) network, with a focus on **manufacturing process support, lifecycle management, and technical execution for biologics.**

Based at the Boston Seaport site, this role partners closely with cross‑functional internal teams and external manufacturing partners to ensure robust, compliant, and scalable manufacturing processes that enable reliable clinical and commercial supply to patients.

**Key Responsibilities**

- Provide MSAT support across biologics manufacturing processes, spanning development, technology transfer, validation, and commercial lifecycle management.

- Plan, prioritize, and execute MSAT deliverables by developing and managing timelines aligned with program milestones and supply requirements.

- Contribute as a technical team member on cross‑functional project teams, ensuring manufacturing readiness and alignment across development, manufacturing, quality, regulatory, and supply chain functions.

- Apply strong process understanding and data‑driven decision‑making to support manufacturing performance, troubleshoot process issues, and assess risks to supply.

- Author and review technical reports and process data summaries to support deviations, investigations, change controls, CAPAs, and continuous improvement initiatives.

- Support technology transfer activities between development, internal manufacturing sites, and external partners, ensuring effective knowledge transfer and process understanding.

- Serve as a technical interface with contract manufacturing organizations (CMOs) and external partners, supporting execution, issue resolution, and alignment to program objectives.

- Provide manufacturing process expertise to support regulatory submissions and respond to technical questions from global health authorities.

- Contribute to process validation, continued process verification (CPV), and ongoing process monitoring activities in support of commercial operations.

- Drive a culture of continuous improvement, supporting initiatives to enhance process robustness, efficiency, and compliance.

- Work on site a minimum of 3 days per week; approximately 10% travel is expected.

**Required Experience And Qualifications**

- Minimum of 8 years of relevant experience in the biopharmaceutical industry, or an equivalent combination of education and experience.

- Bachelor’s degree in science or engineering (e.g., chemical engineering, biochemical engineering, biology, biotechnology) or equivalent; advanced degree preferred.

- Experience supporting late‑stage and/or commercial biologics products in a cGMP manufacturing environment.

- Broad understanding of manufacturing process development, scale‑up, and lifecycle support for complex biological products.

- Working knowledge of cGMP regulations and guidance across major global health authorities (e.g., FDA, EMA).

- Experience with technology transfer, process validation, and process performance monitoring.

- Direct experience working with contract manufacturing organizations (CMOs) and/or external technical service providers.

- Experience supporting manufacturing quality systems, including deviations, investigations, change controls, and CAPAs.

- Strong written and verbal communication skills, with the ability to convey complex technical concepts to cross‑functional stakeholders.

- Demonstrated ability to work independently, manage multiple priorities, and exercise sound scientific and technical judgment.

**Pay Range**

$145,500 - $218,300

**Disclosure Statement**

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

**Flex Designation**

Hybrid-Eligible Or On-Site Eligible

**Flex Eligibility Status**

In this Hybrid-Eligible role, you can choose to be designated as:

-  Hybrid: work remotely up to two days per week; or select

-  On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

**Company Information**

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

MSAT Principal Scientist, Biologics

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