Replimune Group, Inc.

Director, Manufacturing

Replimune Group, Inc.$188K — $243K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BA in relevant science field plus 10+ years or Master's with 8+ years of experience.
  • 6+ years of experience in sterile product development and operations in a cGMP environment.
  • Proven leadership skills in a regulated environment preferred.
  • Technical expertise in control implementation and visual inspection required.
  • Strong problem-solving and decision-making capabilities.
  • Effective communication skills with health authorities.

Responsibilities

  • Oversee aseptic operations, ensuring best-in-class product quality.
  • Lead risk management for aseptic controls and establish contamination strategies.
  • Manage day-to-day operations, including scheduling and document planning.
  • Support investigations and implement documentation for sterile operations.
  • Collaborate with Engineering and Facilities for equipment maintenance standards.
  • Drive the deployment of new technologies for continuous improvement.
  • Develop and retain staff, ensuring commercial readiness for product launches.
  • Engage in industry forums to influence aseptic strategy and regulations.

Benefits

  • Annual performance incentive bonus opportunity.
  • Equity options for new hires and performance-based stock options.
  • Medical, dental, and vision insurance coverage.
  • 401k match to support retirement planning.
  • Flexible time off and numerous paid holidays, including year-end shutdown.
Full Job Description
Summary of job description:

Replimune is a fast-paced growing innovative company that is in the process of bringing on-line a new production facility purposefully designed to manufacture our Oncolytic Immunotherapies. This multi-product facility in Framingham contains cGMP manufacturing suites and Quality Control testing laboratories. Director Manufacturing is responsible for defining and overseeing drug product manufacturing operations and ensuring sterile quality assurance and compliance to international standards at the Framingham, MA facility. The position will have the overall responsibility for monitoring and maintaining aseptic operations and systems consisting of technologies required for product formulation, filtration, vial filling and visual inspection. Reporting to the Senior Director of Manufacturing, the incumbent works closely with internal stakeholders (Operations, Engineering, Validation, Facilities, Quality Control and Quality Assurance) to ensure an aseptic program that adheres to contamination control strategy (CCS) and focuses on continuous improvement including providing support for GMP document management as part of day-to-day operations.
  • This position is based in our Framingham location and typically has a 5-day on-site expectation.


Key responsibilities:
  • Aseptic operations at Framingham facility including process controls, ensuring environmental monitoring systems are adequately staged, best practices and training are established to ensure the site maintains best-in-class sterile product quality assurance.
  • Leads risk management efforts for aseptic operational controls and defines and maintains the facility's cross-contamination and particulate control strategy
  • Work effectively with department leads to manage day to day operations involving scheduling of activities and staff, planning, batch record creation, execution and revision for DP formulation and filling.
  • Support investigations, CAPA closure and implementation, protocol execution and overall documentation to support sterile operations
  • Partners with Facilities, Engineering and Validation groups to ensure effective standards are maintained for preventative maintenance and calibration of equipment/facilities to support sterile manufacturing.
  • Support and/or lead deployment of new technology as part of continuous improvement to existing systems or build out of future manufacturing suites
  • Ensure the hiring, development, and retention of staff including engagement of the Sterile Operationsteam to ensure commercial readiness in support of product launch
  • Works externally in industry forums to establish relationships and help shape strategy and regulations for the requirements of aseptic operations using existing and new technologies
  • Safety as highest priority - ensure staff comply with all Safety Standards, OSHA and environmental requirements at all times. Proactively evaluate safety issues and address. Encourage a working environment which encourages input from all personnel

Educational requirements:
  • BA in Engineering/Biology/Chemistry/Biochemistry/Microbiology or other related science with minimum 10 years of work experience or Master's degree with 8 years of work experience

Experience and skill requirement:
  • Minimum 6 years of experience in sterile product development and operations / aseptic facility controls or relevant cGMP environment.
  • Experience leading teams and / or staff in a GMP-regulated environment is preferred.
  • Technical experience in sterile product development, control implementation (e.g. CCS) and visual inspection is required
  • Strong problem-solving skills; attention to detail and track record of excellent decision making and issue resolution
  • Demonstrated ability to work in cross-functional teams and across the business, persuasive and effective negotiation
  • Experience in written and oral communication with health authorities (e.g. FDA, EMA)


Salary Range

Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $188,500- $243,500. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate's unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.

At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.

About Replimune Group, Inc.

Replimune Group, Inc. is a clinical-stage biotechnology company focused on the development of oncolytic immunotherapies to treat cancer. The company's lead product candidate, RP1, is a selectively replicating version of herpes simplex virus 1 (HSV-1) that is designed to infect and destroy cancer cells. RP1 is currently being evaluated in multiple clinical trials for the treatment of various solid tumors. Replimune is also developing a pipeline of other oncolytic immunotherapies, including RP2, RP3, and RP-Abl, which are designed to target different types of cancer. The company was founded in 2015 and is headquartered in Cambridge, Massachusetts.
Learn more about Replimune Group, Inc.
Size
170 employees
Market Cap
$1.5 billion
Industry
Net Income
-$75.1 million
Founded
2015

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