Senior Scientist I, Cell Culture Process Development

Posted 14 Days Ago
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Worcester, MA, USA
In-Office
97K-184K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Lead development and characterization of high‑productivity CHO cell culture processes for cGMP biotherapeutic manufacturing. Own high‑throughput upstream experiments, SOPs, data collection/formatting, and digital system enhancements. Serve as SME, support technical transfer and manufacturing, ensure GMP compliance, and liaise cross‑functionally to translate operational needs into system requirements.
Summary Generated by Built In
Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

We are seeking a detail-oriented and technically driven Senior Scientist to join the Cell Culture Process Development group within PDS&T Biologics at AbbVie Bioresearch Center in Worcester or Waltham, MA. As part of the Cell Culture Development organization, you will play a central role in the execution, data management, and continuous improvement of high content experimental workflows. You will leverage and help enhance digital platforms to optimize team efficiency, and partner cross-functionally to expand our analytical and operational capabilities. This is an excellent opportunity for a scientific professional who thrives at the intersection of laboratory operations, data-driven process improvement and cell culture development. 

Key Responsibilities: 

  • Develop and characterize highly-productive CHO cell culture processes suitable for cGMP biotherapeutic manufacturing within project timelines, performing technical transfer, and manufacturing support activities. 

  • Serve as the upstream subject matter expert for high-throughput systems, executing and supporting experiments to ensure consistent, high-quality scientific output. Develop and maintain SOPs and best practices related to high-throughput system usage and experimental workflows 

  • Lead data collection and formatting activities for high-throughput processes, utilizing existing digital platforms to ensure timely, structured, and analysis-ready outputs. 

  • Drive enhancements to cell culture process development digital systems to improve overall team efficiency and operational effectiveness by identifying gaps in current upstream workflows. 

  • Act as a liaison between scientific and technical stakeholders to translate operational needs into functional system requirements. 

  • Understand and adhere to corporate standards regarding code of conduct, safety, documentation and GMP compliance.  

Qualifications

  • Bachelor’s Degree or equivalent education with minimum 10 years of experience, or Master’s Degree or equivalent education with minimum 8 years of experience. Or PhD with no minimum years of experience, in chemical engineering, biochemical engineering, or a related discipline.  

  • Demonstrated experience with high-throughput laboratory systems and associated experimental workflows 

  • Hands-on experience with mammalian suspension cell culture at different bench-top scales: deep-well plates, shake flasks, bioreactors. 

  • Experience in statistical data analysis tools such as design of experiments, multivariate data analysis and data modeling.  

  • Hands-on knowledge in programming languages and cloud platforms is a plus 

Additional Information

​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​
  • This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Skills Required

  • Bachelor's degree + 10 years, Master's degree + 8 years, or PhD (no minimum) in chemical, biochemical engineering, or related discipline
  • Demonstrated experience with high-throughput laboratory systems and experimental workflows
  • Hands-on experience with mammalian suspension cell culture across scales (deep-well plates, shake flasks, bioreactors)
  • Experience developing and characterizing CHO cell culture processes suitable for cGMP manufacturing, including technical transfer and manufacturing support
  • Experience with statistical data analysis tools such as design of experiments, multivariate data analysis, and data modeling
  • Knowledge of GMP compliance, laboratory documentation, and SOP development
  • Hands-on knowledge in programming languages and cloud platforms

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support Retirement programs are portrayed as a standout, with a dollar‑for‑dollar 401(k) match up to 6% and an additional annual company contribution based on age and service. Feedback suggests this materially boosts perceived total compensation for many U.S. employees.
  • Parental & Family Support Paid parental and caregiver leave are emphasized, including up to 12 weeks of fully paid parental leave for all parents and 4 weeks of paid caregiver leave in the U.S. Feedback suggests these policies are a meaningful differentiator for employees balancing family needs.
  • Leave & Time Off Breadth Time off is described as extensive, with tiered vacation that scales with tenure, 17 company holidays, and two paid volunteer days in the U.S. Feedback suggests the breadth of leave contributes notably to overall benefits satisfaction.

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The Company
HQ: North Chicago, IL
50,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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