Downstream Process Development Engineer
Downstream Process Development Engineer
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Salary Not Disclosed
1 Vacancy
Job Description
The Downstream Process Development Engineer plays a critical role in the development and scale-up of purification processes for biopharmaceutical products. Working within the Downstream Process Development Pilot team this position supports pilot-scale operations technology transfer and the generation of non-GMP material to advance product development from early-stage research through to manufacturing readiness.
Key Responsibilities
- Execute pilot-scale downstream purification processes including chromatography ultrafiltration/diafiltration (UF/DF) and filtration techniques.
- Collaborate with scientists and engineers to design and implement experimental protocols that support process development and scale-up.
- Operate and troubleshoot equipment such as AKTA chromatography systems and TFF units; utilize software tools like Unicorn and JMP for data analysis.
- Draft and maintain technical documentation including SOPs batch records and experimental reports.
- Support technology transfer activities by preparing and consolidating technical documentation for internal and external stakeholders.
- Interpret experimental data independently and contribute to technical reports and presentations.
- Coordinate with cross-functional teams to ensure alignment on project timelines deliverables and process requirements.
Qualifications :
- Bachelors degree in Chemistry Biology Engineering or related field with 3 years of relevant industry experience or Masters degree with 1 year of experience.
- Hands-on experience with downstream purification processes and pilot-scale operations (501000L scale).
- Proficiency in chromatography UF/DF depth filtration and sterile filtration techniques.
- Familiarity with AKTA systems Unicorn software and other analytical tools.
- Strong documentation organizational and communication skills.
- Ability to work both independently and collaboratively in a fast-paced team-oriented environment.
- Experience with technology transfer and scale-up to GMP manufacturing is highly desirable.
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
What to Expect in the Hiring Process:
- 10-15 Minute Phone Interview with Region Recruiter
- 45-60 Minute Virtual Interview with Manager and/or Group Leader
- 45-60 Minute Site Visit to Meet the Team
The position is Full Time Monday-Friday 8 am-5 pm. Candidates currently living within a commutable distance of Lexington MA are encouraged to apply.
- Excellent full-time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins Lancaster Laboratories Professional Scientific Services (PSS) is a global award-winning insourcing solution that places our people at our clients sites dedicated to running and managing laboratory services while eliminating headcount co-employment and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise as well as HR and great place to work best practices to recruit hire train and manage highly qualified scientists to perform laboratory services using our clients quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories please explore our website .
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Employment Type
Full-time
