Associate Specialist, Bio Technology Solutions (BTS)

MSD • De Soto, KS

12d • $71,900 - $113,200 • Onsite

About The Position

This position offers a unique opportunity for an early-career engineer or scientist to apply technical knowledge in a manufacturing environment while developing expertise in biologics production, process troubleshooting, investigations, validation, and continuous improvement. Our Animal Health Manufacturing teams are responsible for delivering high-quality vaccines and biopharmaceutical products that protect animal health around the world. We operate with a "Safety First, Quality Always" mindset and are committed to continuous improvement, scientific excellence, and collaboration across a global manufacturing network.

Requirements

• Bachelor of Science degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Biological Systems Engineering, Biomedical Engineering, Mechanical Engineering, Biochemistry, Microbiology, Protein Chemistry, or other related engineering or life science disciplines.
• Demonstrated technical aptitude through academic, internship, co-op, undergraduate research, or professional experiences.
• Strong analytical and problem-solving skills.
• Ability to evaluate issues from multiple perspectives including safety, compliance, equipment, process, and operational considerations.
• Effective written and verbal communication skills.
• Strong organizational skills and attention to detail.
• Ability to learn new technologies and manufacturing processes quickly.
• Ability to work independently while contributing effectively within team environments.
• Demonstrated collaboration and interpersonal skills.
• Proficiency in Microsoft Office applications and technical documentation practices.
• Commitment to safety, quality, and continuous improvement.
• Demonstrated integrity and scientific rigor in decision making.

Nice To Haves

• Internship, co-op, undergraduate research, or industry experience in biotechnology, biologics, pharmaceuticals, vaccines, or related manufacturing environments.
• Experience with fermentation, cell culture, purification, filtration, or sterile manufacturing processes.
• Knowledge of cGMP manufacturing environments.
• Familiarity with statistical analysis and data-driven decision making.
• Experience supporting investigations, validation, or process improvement projects.
• Understanding of process monitoring and control concepts.
• Familiarity with USDA or other regulated manufacturing requirements.
• Exposure to Lean, Six Sigma, or continuous improvement methodologies.

Responsibilities

• Support day-to-day manufacturing operations by providing technical assistance for vaccine and biopharmaceutical production processes.
• Assist with troubleshooting process, equipment, and operational issues to support uninterrupted manufacturing operations.
• Participate in technical investigations, root cause analyses, and corrective and preventive action (CAPA) activities.
• Analyze manufacturing data and process performance metrics to identify trends and opportunities for improvement.
• Support process improvement initiatives focused on safety, quality, reliability, productivity, and cost effectiveness.
• Collaborate with Manufacturing, Engineering, Quality, BTS Analytical, and BTS Process Development teams to resolve technical issues and improve process performance.
• Support lifecycle management of commercial manufacturing processes through data collection, analysis, and documentation.
• Assist in qualification, validation, and verification activities associated with manufacturing processes and equipment.
• Author and revise technical documents, including protocols, reports, investigations, risk assessments, operating procedures, and manufacturing support documentation.
• Support implementation of engineering controls, process analytical technologies, and standardized work practices.
• Participate in laboratory-scale and production-scale studies that support process understanding and continuous improvement.
• Contribute to technical evaluations associated with process changes, manufacturing deviations, and new technology implementation.
• Ensure all activities are performed in accordance with site safety requirements, current Good Manufacturing Practices (cGMP), and applicable regulatory standards.
• Present technical findings and project updates to team members and stakeholders.
• Effectively collaborate in cross-functional teams while fostering an inclusive and respectful work environment.
• Perform off-shift support or routine coverage activities as needed.

Benefits

• medical, dental, vision healthcare and other insurance benefits (for employee and family)
• retirement benefits, including 401(k)
• paid holidays
• vacation
• compassionate and sick days
• annual bonus
• long-term incentive

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level