Insmed

Manager, Quality Control Bioassay

Insmed$124K — $161K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 7 years of experience or MS with 5 years in the pharmaceutical industry
  • Experience in GMP testing focused on analytical methods and testing lifecycle
  • Proven background in optimizing cell-based potency and molecular biology assays
  • Familiarity with lab instrumentation/software for potency assays
  • Clinical experience in an FDA-regulated environment
  • Strong organizational and communication skills

Responsibilities

  • Oversee the execution of QC testing and data review
  • Supervise day-to-day activities of QC staff
  • Develop protocols and reports for assay transfers and validations
  • Act as a subject matter expert during CDMO interactions
  • Author and review QC SOPs, protocols, and reports
  • Manage quality deviations and investigations within the QMS
  • Maintain the QC lab and ensure equipment calibration

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Generous paid time off and family-forming benefits
  • 401(k) plan with competitive company match and equity awards
  • Access to learning and development programs
  • Employee resource groups and volunteer opportunities
Full Job Description
About the Role:
We're looking for a Manager, Quality Control - Bioassay on the Quality Control team to help us expand what's possible for patients with serious diseases. Reporting to the Associate Director, Quality Control, you'll participate in the transfer, qualification, and optimization of methods in a Quality Control environment throughout the lifecycle of the method. This individual shall also be able to author/implement Quality Control area procedures for an AAV based gene therapy laboratory.

What You'll Do:

In this role, you'll have the opportunity to provide oversight of cell-based biological potency assays, protein chemistry assays, and molecular biology assays for process monitoring, stability, and release in a GMP environment such as SDS-PAGE, western blot, ddPCR or qPCR, and culture of primary mammalian cells. You'll also:
  • Actively participate and manage in the timely execution of all routine QC testing, data review, and preparation of summary reports
  • Supervise and manage day-to-day activities of direct reports
  • Participate in developing timelines, protocols and reports for assay transfers, qualifications / validations.
  • Interact with CDMO's as a subject matter expert to support method transfer and testing activities.
  • Author and review QC analytical SOPs, protocols, and reports as needed
  • May act as an analytical lab representative on a CMC team.
  • Perform quality management activities such as deviation, CAPA, change control, investigation of OOS, OOT and anomalous results within the company QMS according to established procedures.
  • Maintain QC laboratory, track critical reagents and equipment logbooks, and ensure all the equipment is calibrated
  • Utilize the LIMS system to submit samples, enter data, and track samples.
  • Utilize statistical analysis software to generate assay control charts and recommend assay acceptance criteria.
  • Learn and become proficient in all laboratory instrument software to conduct testing.
  • Establish laboratory and participate in hiring QC staff


Who You Are:

You have a bachelor's degree along with 7 years or MS with a minimum of 5 years of experience of relevant industry experience.

You are or you also have:
  • Experience in pharmaceutical industry with a GMP testing focus, ideally covering the analytical method and testing lifecycle from development through commercial drug product testing, with experience in a GMP QC release testing role
  • Experience in optimizing methods with particular emphasis on cell-based potency assay, molecular biology assay, and protein chemistry assays.
  • Experience with related instrumentation and software used for cell-based potency assays such as JESS, droplet digital PCR systems, cell counters, PLA, etc.
  • Significant experience in an FDA-regulated environment
  • Entrepreneurial spirit, with strong willingness to take on new challenges required to bring novel medicines to the clinic
  • Excellent organizational and communication skills


Nice to have (but not required):
  • Experience with JMP statistical software a plus


Where You'll Work

This role is based out of our San Diego office and requires full-time, in-person presence to support hands-on collaboration, access specialized equipment, and/or operational needs.

Travel Requirements

Minimal travel expected

Pay Range:
$124,000.00-161,000.00 Annual

Life at Insmed

At Insmed, you'll find a culture as human as our mission-intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you work, how you grow, and how you show up for patients, your team, and yourself.

Highlights of our U.S. offerings include:
  • Comprehensive medical, dental, and vision coverage and mental health support, annual wellbeing reimbursement, and access to our Employee Assistance Program (EAP)
  • Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules with purposeful in-person collaboration
  • 401(k) plan with a competitive company match, annual equity awards, and participation in our Employee Stock Purchase Plan (ESPP), and company-paid life and disability insurance
  • Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities
  • Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back


Eligibility for specific programs may vary and is subject to the terms and conditions of each plan.

Current Insmed Employees: Please apply via the Jobs Hub in Workday.

About Insmed

Insmed is a biopharmaceutical company that develops drugs to treat serious and rare diseases. The company's lead product candidate is ARIKAYCE, which is being developed to treat patients with nontuberculous mycobacterial lung disease. Insmed is also developing drugs to treat other respiratory diseases, as well as rare diseases such as lipodystrophy. The company was founded in 1988 and is headquartered in Bridgewater, New Jersey.
Learn more about Insmed
Size
613 employees
Market Cap
$2.6 billion
Industry
Net Income
-$294 million
Revenue
$164.4 million
NASDAQ

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