Senior Associate Scientist - Analytical Development

Reposted Yesterday
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Madison, WI, USA
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Support development, optimization, and transfer of analytical methods for biologics (mRNA, proteins, mAbs). Perform biochemical/biophysical assays (SDS-PAGE, ELISA, HPLC, CE, cIEF, qPCR, Sanger), develop assays using DoE/AQbD, record and review data under GMP/GDP, write SOPs, mentor colleagues, manage shipments and timelines, and maintain lab housekeeping. On-site with occasional weekend work.
Summary Generated by Built In
Job Description

Senior Associate Scientist - Analytical Development

Position Summary:

  • Work Schedule: M-F 8am-5pm

  • 100% on-site

Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast-growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer’s.

Catalent Pharma Solutions in Madison, WI is hiring a Senior Associate Scientist - Analytical Development. The Analytical Development team is responsible for evaluating client analytical methods and/or optimizing/developing methods required to support cell line, upstream, and downstream development, and transferring them to the QC department for phase appropriate validation. The team is also responsible for characterizing primary and high order structures; confirming product comparability across scale and establishing product degradant profiles and specifications for reference standards of mRNA proteins/mAbs generated at Catalent’s, Madison site. The team executes on this by applying the concepts of analytical quality by design (AQbD) in compliance with FDA and other regulatory agency requirements and in conformance with the sites GMP quality systems. The team’s role is therefore central to the success of projects that enter cell line and process development and technology transfer workstreams and also ensures that analytical methods can be applied in establishing product critical quality attributes (CQA) and supporting IND-enabling studies and applications that are essential in providing high quality drug products for our clients and their patients.

The Role:

  • Understand and apply biochemical/biophysical and immunological concepts associated with macromolecules including proteins, nucleic acids, and lipids and the methods for analysis

  • Execute all activities related to the analysis of proteins and other biological macromolecules from mammalian cell culture and process development ranging from SDS-PAGE/Agarose Gel analysis, ELISA and Western Blot analysis, various HPLC based methods, CE, cIEF, product binding/activity assays, qPCR, and Sanger Sequencing with a preferred focus on LCMS peptide mapping, intact mass analysis, and released N-glycan

  • Independently support developing robust assays, including use of experimental design (DoE) and applying the principles of AQbD

  • Accurately record experimental data/observations in data sheets or lab notebooks

  • Review and verify analytical data and reports ensuring accuracy and consistency

  • Accurately support shipments of samples to clients with appropriate information/paperwork

  • Maintain project timelines

  • Perform general lab housekeeping, including cleaning/sterilizing of lab and lab materials, disposal of trash and recyclables, autoclaving, ordering and stocking supplies, etc.

  • Actively participate in team meetings

  • Become fully trained on departmental SOPs, write procedural SOPs as necessary

  • Strong understanding of GMP documentation and guidelines

  • Follow Good Documentation Practices (GDP)

  • Mentor or train others, as assigned

  • Some weekend work required

  • Seek out guidance as necessary

  • Other duties as assigned

The Candidate:

  • High School Diploma/GED with 10+ years of experience

  • Associate’s degree in STEM discipline with 6-9 years of experience

  • B.S/B.A. in any STEM discipline with at least 3-6 years' experience in a laboratory environment

  • MS in STEM discipline with 0-3 years of industry laboratory experience

Why you should join Catalent:

  • Defined career path and annual performance review and feedback process 

  • Diverse, inclusive culture 

  • Positive working environment focusing on continually improving processes to remain innovative

  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives 

  • 152 hours of PTO + 8 paid holidays

  • Generous 401K match 

  • Medical, dental and vision benefits effective day one of employment 

  • Tuition Reimbursement - Let us help you finish your degree or start a new degree!

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

    

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Skills Required

  • Education/experience: High School Diploma/GED +10 years OR Associate's degree (STEM) +6-9 years OR B.S. (STEM) +3-6 years OR M.S. (STEM) +0-3 years of laboratory experience
  • 100% on-site work in Madison, WI; M-F 8am-5pm
  • Practical experience analyzing proteins and biological macromolecules using SDS-PAGE and Agarose Gel electrophoresis
  • Hands-on experience with ELISA and Western Blot assays
  • Experience with various HPLC-based methods
  • Experience with capillary electrophoresis (CE) and cIEF
  • Experience with product binding/activity assays, qPCR, and Sanger sequencing
  • Experience developing robust assays using experimental design (DoE) and applying AQbD principles
  • Strong understanding of GMP documentation, guidelines, and Good Documentation Practices (GDP)
  • Accurate recording of experimental data/observations in data sheets or lab notebooks and reviewing/verifying analytical data and reports
  • Ability to prepare and support shipments of samples to clients with appropriate paperwork
  • Ability to write procedural SOPs and become fully trained on departmental SOPs
  • Mentor or train others as assigned
  • Perform general lab housekeeping, ordering/stocking supplies, autoclaving, and waste disposal
  • Some weekend work required
  • Preferred: experience with LC-MS peptide mapping, intact mass analysis, and released N-glycan characterization

Catalent, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Catalent, Inc. and has not been reviewed or approved by Catalent, Inc..

  • Leave & Time Off Breadth Paid time off is commonly described as roughly 152 hours per year plus about eight paid holidays for U.S. roles. Eligibility and exact counts vary by location, but the allotment is positioned as competitive.
  • Retirement Support A 401(k) with a company match (often described as dollar‑for‑dollar up to 6%) is part of the package. The match level is commonly referenced as a meaningful component of total rewards.
  • Inclusive Benefits Coverage Medical, dental, vision, life/disability, HSA/FSA, EAP, tuition reimbursement, adoption assistance, commuter and dependent‑care benefits, and wellness programs are offered. Some roles indicate benefits eligibility begins on the first day for direct hires.

Catalent, Inc. Insights

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The Company
HQ: Tampa, FL
13,715 Employees
Year Founded: 2007

What We Do

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. For more information, visit www.catalent.com.

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