Investigation Specialist

Regeneron Pharmaceuticals, Inc; New York (NY); On-site; USD 59,000 - 127,000; Full time

Job summary

An established industry player is seeking Investigation Specialists to join their dynamic team. In this role, you will be pivotal in ensuring compliance and driving quality in manufacturing operations. Your day-to-day will involve investigating non-conformances, preparing detailed reports, and collaborating with cross-functional teams to implement corrective actions. This role is perfect for organized individuals with a keen eye for detail and a passion for quality assurance. Join a company that values diversity and offers comprehensive benefits, including health programs and equity awards, while making a significant impact in the field of biologics manufacturing.

Benefits

Health and wellness programs

Fitness centers

Equity awards

Annual bonuses

Paid time off

Qualifications

• Bachelor’s degree in Life Sciences or Engineering required.
• Experience in biologics manufacturing operations preferred.

Responsibilities

• Investigate non-conformances and prepare reports with findings.
• Review batch records and ensure compliance with cGMP standards.
• Train new employees on investigative processes.

Skills

Attention to Detail

Organizational Skills

Analytical Skills

Communication Skills

Education

Bachelor’s degree in Life Sciences

Bachelor’s degree in Engineering

Related field

Tools

Computerized Systems

Job description

We are currently looking to fill multiple Investigation Specialist positions. These positions perform all compliance related tasks vital to complete investigations and implementation of robust corrective actions for supporting manufacturing operations.

Current Department with Openings:

• Global Manufacturing

• Quality Control

• Technical Operations

In this role, a typical day might include the following:

• Independently investigating non conformances and preventing reoccurrences in support of manufacturing operations

• Preparing investigation reports that include recommendations on investigation findings for medium/high severity non conformances

• Analyzing and evaluating information captured through investigations, summarizes information and trends in investigation reports

• Communicating findings and recommendations at group meetings

• Reviewing completed batch records and logbooks in accordance with cGMP standards in support of investigations

• Reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures

• Monitoring production processes to acquire vital data in support of investigations and track efficiency of changes

• Participating in and/or leading cross-functional study teams to get results, support and or author investigations

• Gathering, trending, and analyzing process related data to drive consistency and timeliness

• Documenting all training

• Training new employees on investigative processes and techniques

• Coordinating and/or leading cross-functional meetings with multiple departments.

This role may be for you if you:

• Excel in a quality driven organization

• Have an understanding of biologics manufacturing operations

• Are organized and have an attention to detail

• Can prioritize multiple assignments and changing priorities

• Are able to learn and utilize computerized systems for daily performance of tasks

To be considered for this role you must hold a Bachelor’s degree in Life Sciences, Engineering, or related field and the following minimum amounts of relevant experience for each level:

• Associate Specialist – 0-2+ years

• Specialist – 2+ years

• Senior Specialist – 5+ years

May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$59,700.00 - $126,800.00