R

Rentschler Biopharma

CDMO delivering biopharmaceutical development and manufacturing

Analytical Project Coordinator - Quality Control

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMilford, MA, USAIn-person

About the Job

Requirements

  • A Master's degree in biochemistry, biotechnology, or a comparable field and at least 5 years of experience in Analytical Process Sciences, Analytical Development, and/or project management in a pharmaceutical, biotechnology, CDMO, or other healthcare-related field; alternatively, a Bachelor's degree and at least 7 years of such experience.
  • Solid experience in common biological and protein chemical analytical methods.
  • Knowledge of GMP-compliant analytics and a strong understanding of GMP requirements in a commercial GMP environment.
  • Effective verbal and written communication with directors and peers, including full competence in following detailed written instructions and creating or revising SOPs and reports.
  • Advanced knowledge of the development, approval, manufacturing, and testing of biopharmaceuticals.
  • Proficiency in Microsoft Office applications, including Outlook, Word, Excel, PowerPoint, and Project.

Responsibilities

  • Serve as the primary QC contact for the complete analytical methods portfolio and link project teams, international customers, and internal and external laboratories.
  • Represent QC laboratories and Rentschler quality standards on assigned client projects; collaborate with QC departments (AD, Microbiology, Raw Materials, and Release), and potentially Process Development Analytics, to gather information for clients and relay client feedback and requests to the appropriate departments.
  • Determine client needs for requested work packages and collaborate internally to assess capabilities and capacity.
  • Prepare for client-facing meetings by consulting subject matter experts, reviewing work-package data, and generating presentations as appropriate.
  • Plan analytical work packages, including method development, qualifications, validations, specification development, and sampling plans.
  • Assess new projects for QC activities and capabilities.
  • Coordinate analytical support and timelines among development, production, and QC departments.
  • Provide organizational and technical support for analytical method development within projects; initiate and own change controls related to client requests for SOPs, specification documents, and scope of analytical methods.
  • Compile, evaluate, and document analytical data across laboratories, and collaborate in lifecycle management of analytical methods for assigned projects.
  • Collaborate on and potentially author SOPs, laboratory investigations, out-of-specification investigations, and deviations related to assigned projects.
  • Escalate quality-critical issues in customer projects within the Rentschler Quality Unit.
  • Review or collaborate on development, validation, and qualification of analytical methods under ICH and USP guidelines.
  • Research new methods and techniques and initiate and organize laboratory testing.
  • Ensure department readiness for internal and external audits and serve, as needed, as a contact person for analytical laboratories during inspections.
  • Work in a laboratory environment as needed, including using chemical reagents and analytical equipment, and wear required personal protective equipment.
  • Perform work involving frequent lifting up to 10 pounds, frequent standing and walking in the laboratory for extended periods, and frequent sitting for extended periods while using a computer.

About the Company

Rentschler Biopharma

CDMO delivering biopharmaceutical development and manufacturing

What the company does: Rentschler Biopharma provides contract development and manufacturing services for biopharmaceuticals, helping other pharmaceutical companies develop and produce complex medicines. How its products work: It offers end-to-end services in biopharma development and manufacturing, backed by facilities and staff that design, optimize, and produce biologic drugs at scale for clients, including a major site in Milford, MA that has expanded capacity to serve the international market. How it differs from competitors: It has a long heritage in biopharma, a dedicated CDMO focus since 1997, and a global footprint with a major U.S. site and expanded capacity, positioning itself as a reliable partner for developing and manufacturing complex biologics. What its goal is: To be a trusted partner for pharmaceutical companies by providing development and manufacturing services at scale, supporting clients as they bring biologic medicines to market.

Company size
501-1,000
Company stage
Series A
Total funding
$1.6M
Headquarters
Laupheim, Germany
Founded
1927

Recently Posted Jobs

Explore more opportunities at Rentschler Biopharma

See more jobs