Quality Control Analyst

Regeneron Pharmaceuticals, Inc

City of Saratoga Springs (NY)

On-site

USD 34,000 - 61,000

Full time

7 days ago
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Benefits offered by this job

Student loan paydown
Tuition reimbursement
Relocation assistance
Well-being programs

Job summary

Regeneron Pharmaceuticals, Inc. is hiring multiple Quality Control (QC) Analysts for our new highly automated drug substance manufacturing facility in Saratoga Springs.

The QC Analyst performs a variety of chemical/biological/microbial analyses or sampling on raw materials, products, in-process materials, utilities, environmental monitoring, or stability samples in support of the company’s quality program. Initial schedule is full time, on-site with a 1st shift Mon-Fri, 8am-4:30pm; permanent

Qualifications

  • Requires B.S in Life Sciences or related field; or equivalent combination of education and experience.
  • Associate Quality Control Analyst: 0-2 years of experience.
  • Quality Control Analyst: 2+ years of experience.
  • Senior Quality Control Analyst I: 4+ years of experience.

Responsibilities

  • Gather data and documents test results.
  • Review test results to ensure compliance and report anomalies.
  • Comply with regulatory agency requirements.
  • Participate in GMP training activities.
  • Maintain laboratory supplies.
  • Conduct testing and sampling on raw materials, in-process, product, stability, and research samples.
  • Write and revise control test procedures and SOPs.
  • Calibrate or verify calibration of instruments prior to use.
  • Interact with outside customers or functional peer groups.
  • Develop new analytical methods and techniques.
  • Assist in validation of methods.
  • Transfer methodology from R&D with internal teams.

Skills

Quality Control
Laboratory Testing
GMP Training
Data Review
SOP Writing
Method Development

Education

B.S in Life Sciences or related field
Associate Quality Control Analyst option

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're hiring multiple Quality Control (QC) Analysts to join our team at our new highly automated drug substance manufacturing facility in Saratoga Springs. The QC Analyst performs a variety of chemical/biological/microbial analyses or sampling on raw materials, products, in-process materials, utilities, environmental monitoring, or stability samples in support of the company’s quality program.

When & where:
  • Location:
    • Initial: Rensselaer, New York, United States
    • Permanent: Saratoga Springs, New York, United States
  • Work model:
    • Initial: full time, on-site 1st, Mon-Fri, 8am-4:30pm
    • Permanent: full time, on-site, rotating 12-hour shifts, 7am-7:30pm , 3–4 days per week, includes 1 weekend day
    • Transition: candidates must be able to work both schedules. The permanent shift start date will be communicated with reasonable advance notice and is subject to business needs.
What you'll do:
  • Gather data and documents test results
  • Review test results to ensure compliance with standards; reports any quality anomalies
  • Comply with all pertinent regulatory agency requirements
  • Participate in required GMP training activities
  • Maintain laboratory supplies
  • Conduct testing and sampling on raw materials, in-process, product, stability, and/or research samples
  • Write and revise control test procedures and standard operating procedures (SOPs)
  • Complete test records and reviews data
  • Calibrate or verify calibration of instruments/devices prior to use
  • Interact with outside customers or functional peer groups
  • Engage in exciting projects aligning to our scientific initiatives
  • Devise or develop new analytical methods and techniques
  • Assist in validation of methods
  • Partner with internal teams on establishing the transfer of methodology from R&D
The environment and physical rhythms of the role:
  • Gowning: Full cleanroom attire (examples may include: laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)
  • Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire
  • Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment
  • Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs
Let's find out if we're a fit:
  • Requires B.S in Life Sciences or related field; or equivalent combination of education and experience
    • Associate Quality Control Analyst: 0-2 years of experience
    • Quality Control Analyst: 2+ years of experience
    • Senior Quality Control Analyst I: 4+ years of experience
  • Level will be determined based on experience
Thrive today. Grow Tomorrow.
  • Student loan paydown program & tuition reimbursement
  • Family care benefits
  • Relocation assistance
  • Inclusion, culture and well-being programs (including physical & mental health)

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. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: 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, and 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/.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.

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) $24.76 - $44.42

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