Associate Scientist, Downstream – Biologics Drug Substance Commercialization Full-time

Bioprocess Drug Substance Commercialization Scientist/Engineer

We aspire to be the premier research-intensive biopharmaceutical company. Our manufacturing division is at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases. We are seeking a motivated scientist/engineer to join our Bioprocess Drug Substance Commercialization (BDSC) group. This role offers an exciting opportunity to work on late-stage process development, technology transfer, and in-line support of biologics.

Responsibilities

• Execute hands-on experiments in biologics downstream processing, including lab-scale process characterization, pilot-scale process development, and process scale-up/scale-down model development.
• Collaborate with commercial manufacturing teams as a process sciences representative to support facility start-up and in-line support activities, including on-the-floor support for drug substance manufacturing as needed.
• Author and/or review technical documents to support Process Performance Qualification (PPQ) and licensure.

Qualifications

Required

• Bachelor's Degree or higher in Chemical Engineering, Chemistry, Biology or comparable discipline.
• Experience executing lab activities, including authoring study protocols, planning and performing experiments, performing data analysis, and writing technical reports.
• Ability to execute experiments independently in a manner that meets quality and timeline expectations.
• Well-developed communication, organizational, and problem-solving skills, with an attention to detail.

Preferred

• Experience with downstream processing of monoclonal antibody (mAb) products or similar products in a laboratory or manufacturing setting, including unit operations such as membrane filtration, preparative chromatography, ultrafiltration or tangential flow filtration, and viral clearance.
• Large molecule drug substance technology transfer experience.
• Collaboration with analytical teams, pilot-scale, and/or manufacturing environments.
• Experience authoring technical documentation in support of the following: process description, process characterization, process performance qualification, risk assessment, control strategy, process comparability reports, and/or regulatory submissions.
• Current Good Manufacturing Practice (cGMP) awareness or experience.

The salary range for this role is $71,900.00 – $113,200.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.