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Process Engineer, Downstream Tech Transfer
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What they do
A Process Engineer solves problems related to the manufacturing and use of products, including chemicals, fuel, food, and clothing. Designs new products, improves existing ones, or develops new processes for better use of existing materials. May specialize in a chemical engineering process, such as making plastics, or in an industry such as health care.
$112,767 / year median in the U.S.
+6% projected growth
Job Description
- Support downstream process tech transfer activities from sending site or process development into GMP manufacturing, including protocol and report support, batch record review, and technical input to run readiness.
- Author deviation technical impact assessments: evaluate process excursions against validated ranges and product quality attributes, and write the technical justification that supports disposition.
- Draft, compile and support review of manufacturing summary reports, pulling together batch data, process performance and deviation outcomes into a coherent technical narrative.
- Author and review material specifications for downstream raw materials, buffers, resins and consumables.
- Perform process data review and trending across downstream unit operations, and support technical investigations arising from campaign execution.
- Interface with manufacturing, QA and process development to close documentation on schedule.
- BS or MS in chemical engineering, biochemical engineering, biotechnology or a related discipline.
- 5 or more years of process engineering or MS&T experience in biologics drug substance manufacturing, in a GMP environment.
- Hands-on technical knowledge of downstream unit operations: chromatography, depth and sterile filtration, viral clearance, tangential flow filtration and bulk drug substance handling.
- Demonstrated authoring of deviation technical impact assessments or equivalent investigation documentation that passed QA review.
- Direct tech transfer experience, either sending or receiving site, on at least one biologics process.
- Strong technical writing. This role is documentation-heavy and writing quality is a primary screening criterion. Preferred qualifications
- CDMO or multi-client manufacturing experience, where transfers run in parallel and timelines are externally driven.
- Experience authoring or supporting manufacturing summary reports for client-facing delivery.
- Familiarity with material specification systems and downstream raw material qualification.
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Woburn,MA.
San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.Benefits
- Paid Time Off (PTO)
- Sick Leave
- 401(k) Plans
- Other Retirement and Savings