Associate or Snr Associate Scientist

Minaris; Philadelphia (Philadelphia County); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

Dental insurance

401(k) plan

Tuition assistance

Job summary

Minaris is seeking an experienced Downstream Process Development Associate Scientist to advance viral vector processes—from design to manufacturing transfer—ensuring robust, scalable production. The role emphasizes collaboration, rigorous documentation, and GMP-compliant practices to deliver high‑quality therapies.

Ideal candidates will have hands-on experience in chromatography, filtration, and fill/finish steps, plus strong analytical and problem‑solving skills.

Qualifications

• Master or Bachelor's in Biological/Chemical Engineering or Biological Sciences.
• Experience in GLP/GMP environments desirable.
• Strong written and verbal communication skills in a GMP setting.

Responsibilities

• Contribute to design and independently execute experiments to improve recovery, consistency, and robustness.
• Support development and troubleshooting of analytical methods.
• Coordinate and interpret analytical testing to generate reports and present in client meetings.
• Support technology transfer to manufacturing and provide floor support during GMP runs.
• Maintain accurate and organized experimental records.
• Regular and reliable attendance on a full-time basis.
• Maintain professional behavior reflecting company policies and practices.
• Align actions with Minaris Advanced Therapies values.

Skills

Downstream processing

Chromatography

TFF

Viral filtration

Fill/finish

GMP documentation

Analytical methods

Cross-functional collaboration

Technical problem-solving

Report generation

Communication skills

Education

Master or Bachelor's in Biological/Chemical Engineering or Biological Sciences

Job description

Be part of something bigger at Minaris — where every role contributes to creating hope for patients around the world. As a global leader in cell and gene therapy development, manufacturing, and testing, we turn breakthrough science into real‑world treatments that change lives. Our team of over 1,000 experts across North America, Europe, and Asia has helped bring transformative therapies to market.

At Minaris, you’ll join a purpose‑driven community focused on innovation, collaboration, and patient impact. Whether you’re in the lab, in the cleanroom, or behind the scenes, your work will directly support life‑saving therapies and make a lasting difference. If you're passionate about advancing cutting‑edge science and believe in the potential of cell and gene therapies, we invite you to help shape the future of medicine—one patient at a time.

Position Summary

The Downstream Process Development Associate Scientist will support viral vector process development activities, including process optimization, scale‑up, technology transfer to manufacturing, and on‑the‑floor production support. This role is responsible for integrating downstream process development with analytical evaluation to ensure robust, scalable, and high‑quality viral vector manufacturing processes. The successful candidate will possess strong written and verbal communication skills and will actively contribute to technical problem‑solving, cross‑functional collaboration, technical training, report generation, and GMP‑compliant documentation. The individual will play a key role in supporting process development, manufacturing readiness, and continuous improvement initiatives.

Essential Functions And Responsibilities

• Contribute to design and independently execute experiments with supervision to improve recovery, consistency and robustness.
• Support development and troubleshooting of analytical methods as needed.
• Coordinate and interpret analytical testing to generate reports and present in client meetings.
• Support technology transfer activities to manufacturing and provide floor support during GMP runs.
• Maintain accurate and organized experimental records.
• Regular and reliable attendance on a full‑time basis.
• Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
• Embodies Minaris Advanced Therapies values and aligns daily actions with department and company culture.
• Other duties as assigned.

Knowledge, Skills & Ability

• Demonstrated hands‑on experience with downstream processing operations, including chromatography, clarification, tangential flow filtration (TFF), viral filtration, and fill/finish activities.
• Strong attention to details with a demonstrated eagerness to learn and apply new techniques and technologies.
• Motivated to thrive in a dynamic, fast‑paced, and rapidly growing environment while effectively managing multiple priorities.
• Demonstrated critical thinking, innovation, and problem‑solving skills, with the ability to troubleshoot complex technical challenges.
• Excellent verbal and written communication skills, along with strong organizational, planning, and documentation capabilities.
• Ability to work effectively both independently and collaboratively within cross‑functional teams.

Education & Experience

• Master or Bachelors’ degree with major in Biological or Chemical Engineering, Biological Sciences or other science‑related major.
• 2-5 years of relevant experience with a Bachelors’ degree.
• 0-3 years of relevant experience with a Masters’ degree.
• Experience working in GLP and/or GMP environments, particularly with viral vector process development is highly desirable.

Quality Requirements

• Ensure compliance with all FDA and Worldwide Quality & Compliance regulations in all aspects of your work.
• Adhere to established procedures and protocols, prioritize continuous training and skill development, and uphold the highest standards of data integrity to ensure accuracy, compliance, and operational excellence.

Working Environment

Describe the environment in which the position will operate as it relates to the essential functions of the role. Depending on the work location, copy the applicable section below to include under work environment. For Hybrid roles, include both the remote and onsite sections. If changes are needed, partner with HR.

Onsite Employees: Employee will work with moderate noise level. Employee will perform tasks while experiencing numerous interruptions. Employee may travel by car and airplane to work at different locations and may occasionally be required to travel overnight. The work environment is fast paced. This position has the utmost responsibility for compliance with the rules and regulations regarding a safe and healthy work environment relative to their actions and conduct. Off‑shift, weekend and overtime duties may be required. While performing the job duties of this job, the employee is regularly required to use English written and oral communication skills.

Physical Requirements

The physical and mental demands described below are representative of those required to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

While performing the duties of this role, the employee is required to:

• Constantly work in a laboratory environment in proximity to biological materials, chemicals, and technical equipment.
• Constantly wear appropriate personal protective equipment (PPE) in accordance with safety and regulatory requirements.
• Constantly distinguish colors accurately (e.g., interpreting pH strips, test indicators, or assay results).
• Constantly sit and reach while operating computers and other standard office equipment.
• Constantly stand for extended periods, up to four hours at a time.
• Constantly perform tasks involving repetitive motions, including hand and wrist movements.
• Frequently lift and/or move materials weighing up to 20 pounds.
• Constantly use close and distance vision, depth perception, and hand–eye coordination to perform detailed analytical work.
• Frequently communicate verbally and in writing with colleagues and cross‑functional partners.

This position requires the ability to work safely in a laboratory setting with potential biological, chemical, ergonomic, and physical hazards while adhering to all safety policies and procedures.

Special Working Conditions

• May be required to work overtime

Disclaimer

The above information in this description is intended to describe the general nature and level of work performed. It does not contain nor is it intended to be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. Duties, responsibilities, and activities may change at any time with or without notice.

The estimated base salary range for each open position based in the United States of America is included for all our current openings. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) as part of the compensation package. Minaris Advanced Therapies employees are eligible for a comprehensive benefits package, including medical insurance, vision insurance, dental insurance, 401(k), paid time off, tuition assistance, and more.