Quality Control Analyst (Reference Standards)

Regeneron Pharmaceuticals, Inc (USA); United States; On-site; USD 35,000 - 54,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension benefits

401(k)

Health programs

Fitness centers

Insurance benefits

Paid time off

Family support

Job summary

Regeneron Pharmaceuticals, Inc. in Rensselaer, NY is seeking a QC Analyst, Reference Standards to manage the lifecycle of reference standards and reference materials in support of the company’s quality program.

The role involves data gathering, test result documentation, and ensuring compliance with standards. Calibration of instruments and collaboration with internal and external stakeholders are key parts of the job.

Qualifications

• BS/BA in Life Sciences or related field; substitution with relevant experience allowed.

Responsibilities

• Responsible for life-cycle management of reference standards and reference materials.
• Gathers data and documents test results.
• Reviews test results to ensure compliance with standards; reports any quality anomalies.
• Aligns with all pertinent regulatory agency requirements.
• Participates in required training activities.
• Maintains laboratory supplies.
• Writes and revises control test procedures and SOPs.
• Completes test records and reviews data.
• Calibrates or verifies calibration of instruments/devices prior to use.
• Interacts with outside customers or functional peer groups.
• May be responsible for maintaining a specific project.
• May assist in validation of methods.
• May be involved in establishing the transfer of methodology from R&D.

Skills

Life sciences

Data collection

Documentation

Calibration

Education

BS/BA in Life Sciences or related field

Tools

Laboratory instruments

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently looking for a Quality Control (QC) Analyst, Reference Standards, to manage the life cycle of reference standards and reference materials in support of the company’s quality program.

When & where: Location: Rensselaer, New York, United States. Work model: 1st | Mon-Fri | 08:00a-04:30p.

Responsibilities

• Responsible for life-cycle management of reference standards and reference materials
• Gathers data and documents test results.
• Reviews test results to ensure compliance with standards; reports any quality anomalies.
• Aligns with all pertinent regulatory agency requirements.
• Participates in required training activities.
• Maintains laboratory supplies.
• Writes and revises control test procedures and SOPs.
• Completes test records and reviews data.
• Calibrates or verifies calibration of instruments/devices prior to use.
• Interacts with outside customers or functional peer groups.
• May be responsible for maintaining a specific project.
• May assist in validation of methods.
• May be involved in establishing the transfer of methodology from R&D.

Education and Experience

Requires BS/BA in Life Sciences or related field; will substitute relevant experience for education. Level is settled based on qualifications relevant to the role.

We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

Benefits

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (hourly) $25.24 - $39.47

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.

Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.