Technical Development Associate; Analytical

Shift

Monday through Friday, 8:00AM - 5:00PM

This lab-based role provides hands‑on support for Biopharma Analytical Technical Development by executing critical experiments and advancing the science of animal health.

$21.00 - $25.00 per hour

• Execute sample testing using basic analytical tools including RP‑HPLC, SEC, icIEF, CE‑SDS, and ELISA.
• Organize, interpret, and present experimental data to peers to support project advancement.
• Design, execute, analyze, and evaluate experiments that meet R&D product development objectives.
• Ensure experiments are well designed and documented with clear objectives.
• Technically manage small‑scale laboratory projects as required.
• Identify process improvement opportunities through data analysis, observation, and technical report writing in collaboration with senior scientists and technicians.
• Organize and execute routine experimental work in accordance with established methods, SOPs, and applicable regulatory guidelines.
• Ensure high‑quality data and documentation practices by authoring technical reports and contributing to the creation of SOPs.
• Independently operate and perform basic troubleshooting of laboratory equipment relevant to assigned work.
• Recognize and communicate atypical results/deviations and support investigation and resolution as needed.
• Accurately document work in batch records and/or electronic laboratory notebooks.
• Collaborate with scientists and cross‑functional teams to share key learnings to advance portfolio projects and drive new platform innovations.
• Adapt to new procedures and evolving project needs in a dynamic R&D environment.
• Maintain a safe, clean, and organized laboratory work environment and encourage safe behaviors by coworkers.
• Contribute to a cohesive team environment and maintain a positive attitude.

• Bachelor's degree in Chemistry preferred.
• Bachelor's degree in Biology, Molecular Biology, Microbiology, Chemical Engineering, or a related scientific discipline also considered.
• Strong problem‑solving skills, attention to detail, technical curiosity, and high learning agility.
• Ability to work independently and collaborate within cross‑functional teams.
• Effective written and verbal communication skills for documenting and presenting technical data.
• Solid organizational skills with the ability to prioritize and deliver results.
• Demonstrated ownership with the ability to prioritize and manage multiple tasks efficiently.
• Interest in pharmaceutical science and drug product manufacturing, with a willingness to learn and grow in this area.

• Hands‑on experience with basic analytical tools (RP‑HPLC, SEC, icIEF, CE‑SDS, and ELISA).
• Previous experience in analytical development.
• Demonstrated ability to work effectively in a cross‑functional, team‑oriented environment.
• Self‑motivated and able to work with minimal supervision.

• Competitive salaries
• Medical, dental, and vision coverage
• 401K retirement savings plan (100% vested immediately in the employer match)
• Life and disability insurance
• Voluntary benefits
• Paid time off for holidays
• Sick and vacation days
• HSA
• Wellness program
• Flexible spending accounts
• Tuition reimbursement
• Employee Assistance program
• Parental leave
• Optional legal coverage
• protection

PACE provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.