JOB TITLE: Engineering - Associate Scientist

Location: Summit, NJ (100% onsite)

Duration: 6 months initial (possibility of extension for right candidate depending on performance)

Work Schedule: Wed-Sat- (4 pm- 2 am) EST or Wed-Sat- (7am-5pm) EST

PURPOSE AND SCOPE OF POSITION:

The Associate Scientist/Engineer is responsible for leading investigation reports in support of S12 CAR

T operations. This includes execution of thorough root cause investigations, interviewing personnel,

hypothesis testing and interpretation of results, authoring investigation reports, identifying corrective and

preventive actions (CAPA), and troubleshooting complex problems. The successful incumbent must

interface closely with different functional organizations, including Quality Assurance teams.

REQUIRED COMPETENCIES:

Knowledge, Skills, and Abilities:

• Working experience of deviation investigations utilizing root cause analysis tools.

• Working experience in the CAPA process and ability to identify and verify effectiveness.

• Technical writing skills and ability to collaborate effectively in cross functional teams.

• Proven ability to accurately and completely understand, follow, interpret, apply Global Regulatory

and cGMP requirements.

• Ability to support health authority inspections.

• Knowledge of data trending and tracking, including use of statistical analysis software a plus.

• Demonstrate advanced problem-solving ability / mentality, technical adeptness and logical thinking.

• Ability to set priorities, manage timelines and effectively react/manage changing priorities.

• Ability to work with management (global and site) and support corporate and departmental goals.

• Ability to communicate honestly, transparently and effectively with peers, department management

and cross functional peers.

• Ability to utilize electronic Quality systems such as eQRMs (Enterprise Quality and Regulatory

Management system) or Infinity.

• Hands on experience preferred with CAR-T or biopharmaceutical manufacturing and Quality

Control.

Education and Experience:

• Requires a Bachelor’s Degree in science or engineering, preferably

in Biochemistry, life sciences or related engineering discipline (advanced

degree preferred).

• Minimum 1 year of relevant work experience, preferably in a health

authority regulated environment.

• Previous experience working in a biopharmaceutical manufacturing

facility is preferred (CAR T a plus).

• An equivalent combination of education and experience may

substitute.

DUTIES AND RESPONSIBILITIES:

• Conduct thorough investigations (Environmental Monitoring, deviations, etc.) utilizing root

cause analysis tools.

• Lead investigations and cross functional investigation teams, and close reports in a timely

manner

• Perform GEMBA walks with stakeholders to better understand process steps and evaluate

Root Cause Analysis.

• Work with functional teams to propose effective CAPAs, develop CAPA plans and assure

CAPA effectiveness.

• Assess potential impact and risk to product or process associated changes may have upon

change implementation and develop an appropriate mitigation strategy.

• May Initiate change control documentation

• Identify functional area SMEs to perform impact assessments as part of the change

management process.

• Ensure all investigations are completed in a timely manner. Notify stakeholders of any

delays in a timely manner.

• Provide technical support for manufacturing investigations / CAPAs / change controls as

needed.

• Support deviation investigation defense during audits and site inspections related inquiries.

• Handle complex issues and solve problems with minimal guidance.

• Serve as author or technical reviewer of departmental procedures as appropriate.

• Employ lean manufacturing / six sigma principles to continuously improve products, processes and

systems.

• Continuously support S12, living the “patients first” mission and fostering a “Right First Time”

mindset.

WORKING CONDITIONS (US Only):

• The incumbent will be working 80% to 90% of the time in an office environment.

• The incumbent will be working 10% to 20% of the time in a manufacturing and/or laboratory

setting.

• The incumbent may travel between NJ sites for training, meetings or corporate events on

occasion.

• The incumbent will need to have flexibility to work extended hours (>8 hours/day),

weekend and/or holidays when required to meet deadlines.

If hired, you will enjoy the following Eclaro Benefits:

• 401k Retirement Savings Plan administered by Merrill Lynch
• Commuter Check Pretax Commuter Benefits
• Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro

If you feel you are qualified with the required skills and if you are interested , please free to send your word version most updated resume TAILORED to the job description above to June@eclaro.com or call (212)804-7476.

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.