Frontage Laboratories

Manager/Senior Manager BGC Operations

Frontage Laboratories$100K — $130K *
Exton, PA 19341In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS, MS, or PhD in Biological Sciences, Biochemical Engineering, Chemistry, or related disciplines
  • Over six years of GMP testing and analytical development experience for biologics/gene therapy
  • Expertise in technical areas like binding assays (ELISA, SPR, etc.) and separation sciences
  • Knowledge of GMP laboratory operations and method validation
  • Familiarity with FDA, EU, USP, and ICH guidelines
  • Excellent communication skills for interactions with stakeholders
  • Ability to assess compliance risks and make informed decisions.

Responsibilities

  • Lead and oversee QC activities for biologics and gene therapy programs
  • Develop, qualify, validate, and verify analytical methods
  • Author/review/approve all validation documentation and data packages
  • Manage deviations, OOS/OOT issues, and CAPAs
  • Support regulatory inspections and client audits as a subject matter expert
  • Train and develop QC staff scientists
  • Manage budgets and allocate resources effectively.

Benefits

  • Health and dental insurance
  • 401(k) plan
  • Disability insurance
  • Life insurance
Full Job Description
Manager/Senior Manager for Biologics, Cell, and Gene Therapy Operations (BCGT)

Location: Exton, PA

Full Time

Position Summary

We are seeking a highly experienced CMC Quality Control (QC) leader to support biologics and gene therapy CMC programs in a contract research laboratory environment. The focus of the role is to closely collaborate with scientists from multi-disciplinary teams and to ensure Frontage consistently provides high quality of work for its clients.

This position requires strong expertise in phase-appropriate CMC QC strategy, analytical method lifecycle management, and regulatory compliance, along with the ability to operate effectively in a multi-client, fast-paced CRO setting.

Key Responsibilities
  • Lead and oversee QC activities supporting biologics and gene therapy programs in all phases
  • Lead method development, qualification, validation, verification, and transfer

  • Author/review/approve validation protocols, reports, and analytical data packages
  • Oversee deviations, OOS/OOT, CAPAs, change control, and data integrity investigations
  • Support regulatory inspections and client audits as CMC QC subject matter expert

• Train and develop staff scientists
• Manage budgets and balance resource allocation to meet project priorities.
• Closely interact with clients through various means of communication and ensure client satisfaction.

Education Requirements
  • BS, MS, or PhD in Biological Sciences, Biochemical Engineering, Chemistry, or related disciplines.

Required Experience

  • More than six years of experience in GMP testing and analytical development for biologics and/or gene therapy products.
  • Expertise in at least one of technical areas, such as binding assay (ELISA, SPR, BLI, etc.), potency assay (cell based), molecular biology (qPCR and dPCR), and separation sciences (RP-HPLC, HIC, HILIC, SE-HPLC, IEX, icIEF, and CE-SDS, etc.)
  • Knowledge of general GMP laboratory operations, method transfer, qualification, and validation.
  • Knowledge of FDA, EU, USP, ICH guidelines and regulations
  • Excellent communication skills for liaising and communicating with vendors, customers, and internal departments.
  • Able to quickly assess compliance risk of events and make decisions that are scientifically sound and compliant with the regulations.
  • Ability to collaborate effectively in a dynamic and cross-functional matrix environment.
  • Experience with ZENQMS and laboratory information systems, such as NuGenesis, is plus.


Salary and Benefits

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

About Frontage Laboratories

Frontage Laboratories is a contract research organization (CRO) that provides research and development services to pharmaceutical and biotechnology companies. The company was founded in 2001 and is headquartered in Malvern, Pennsylvania. Frontage Laboratories offers a wide range of services including drug discovery, preclinical and clinical development, bioanalysis, and regulatory affairs. The company has facilities in the United States and China. Frontage Laboratories is known for its expertise in drug development and its ability to provide customized solutions to its clients.
Learn more about Frontage Laboratories
Size
1,000 employees
Industry
Founded
2001

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