Associate Scientist, Process Development II

Society for Conservation Biology; Massachusetts; On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in biotherapeutics seeks a motivated junior Scientist for its CHO Cell Line Development team. The role involves advancing development of cell lines for cGMP production, requiring expertise in mammalian cell culture, communication, and technical skills. The position promises a collaborative environment with opportunities for growth in a vital area of bioprocess development.

Benefits

Comprehensive benefits package

Paid time off

Participation in short-term incentive programs

Qualifications

• 3+ years experience with a Bachelor's Degree or a Master's Degree.
• Strong interest in a collaborative environment.
• Ability to prioritize and multi-task across projects.

Responsibilities

• Develop CHO cell lines for cGMP biotherapeutic manufacturing.
• Participate as CLD lead in cross-functional CMC teams.
• Author technical reports and present scientific data.

Skills

Attention to details

Strong time management

Communication skills

Education

Bachelor's Degree or Master's Degree

Job description

Company Description

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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

The Bioprocess Development at the AbbVie Bioresearch Center in Worcester, MA is seeking a highly motivated junior Scientist to join the CHO Cell Line Development team. The Scientist will advance AbbVie's biotherapeutics pipeline through the development and characterization of highly productive CHO cell lines suitable for cGMP protein manufacturing. The selected candidate will have good experience in mammalian cell culture and demonstrate good aseptic technique history, following standard protocol to generate and analyze precise, reliable, and reproducible data in a timely manner. The candidate will also need to demonstrate good communication, presentation, and technical writing skills, team-working spirit, and strong scientific thinking approach in problem solving. The position is based in AbbVie Bioresearch Centre, Worcester, MA.

Key Responsibilities includes:

• Develop a highly productive stable CHO cell line suitable for cGMP biotherapeutic manufacturing for various Biologics projects following standard protocols
• Participate and contribute to cross functional CMC team as CLD lead to ensure the success of CMC timeline
• Participate new technology improvement projects
• Perform routine tasks competently, independently and generate reliable and consistent results.
• Author technical reports detailing standard procedures used and results. Effectively present scientific data and concepts to various audiences Analyze and critique results, noting significant deviations.
• Learn and effectively implement new experimental protocols and/or techniques. Maintain laboratory equipment and optimize laboratory operations for efficient use of time and laboratory supplies and reagents, when appropriate.
• Consult literature to understand scientific purpose of assignments. Impact projects predominantly through lab activity.
• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.

Qualifications

• Bachelor's Degree, or equivalent education, with typically 3 or more years' experience or Master's Degree or equivalent education (no additional experience).
• Attention to details, careful record-keeping, strong time management skills with executing multi-step experiments
• Strong interest in working in a highly collaborative environment
• Ability to prioritize and multi-task across projects while keeping deliverables within timelines
• Good verbal and written communication skills.

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