Replimune Group, Inc.

Senior Validation Engineer

Replimune Group, Inc.$152K — $197K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Scientific, Engineering or similar subject required; MSc or MS preferred.
  • Minimum of seven years professional experience in validation, engineering, or operations.
  • At least seven years relevant experience in a cGMP environment.
  • Experience with GMP utilities and equipment is essential.
  • Demonstrates professionalism and ability to build effective working relationships.
  • Strong attention to detail and technical writing skills required.
  • Familiarity with cGMP, GDP, and applicable regulatory requirements.

Responsibilities

  • Serve as a validation technical leader, providing expertise in qualification and validation activities.
  • Act as a key member of project teams for design, procurement, and installation of new equipment.
  • Establish and maintain validation project plans for cGMP compliance.
  • Manage validation procedures within areas of expertise.
  • Develop, review, and execute validation lifecycle documents in line with regulatory standards.
  • Maintain qualified systems in a validated state through ongoing assessments and documentation.
  • Author and support investigations of deviations and CAPAs.

Benefits

  • Eligible for an annual performance incentive bonus.
  • Access to new hire equity and ongoing performance-based equity.
  • Medical, dental, and vision insurance.
  • 401k matching program.
  • Flexible time off policy and paid holidays including year-end shutdown.
Full Job Description
Summary of job description:

The Senior Validation Engineer will work as part of a larger validation team to ensure the biotech facility equipment, utilities, instrumentation and computerized systems are qualified and maintained in a validated state in accordance with appropriate regulatory guidance. The individual will work with internal customers and external contractors to coordinate scheduling, execution, and review of qualification protocols / reports. The individual will project manage validation campaigns to support maintaining validation through change control, assessments, performance monitoring and requalification assessments.
  • This position is based in our Framingham location and typically has a 5-day on-site expectation.


Key responsibilities:
  • Serve as a validation technical leader, providing subject matter expertise in qualification and validation activities across facilities, utilities, equipment, processes, and computerized systems.
  • Act as key member of project teams for design, procurement and installation of new equipment and facility expansion projects. Responsibilities will include support of design, selection, commissioning and qualification of utilities and equipment, vendor oversight and documentation review.
  • Establish, revise, and maintain validation project plans for qualification of equipment required for cGMP compliance.
  • Own and maintain validation procedures within area(s) of subject matter expertise.
  • Develop, review, approve, execute, and maintain validation lifecycle documents, including validation procedures, qualification/requalification protocols, and reports, in accordance with cGMP, GDP, and ALCOA principles.
  • Maintain qualified systems in a validated state through requalification, periodic review, continued verification, change control assessments, and evaluation of validation impacts resulting from proposed changes and deviations related to validated systems and processes.
  • Author and support investigation of deviations and CAPAs.
  • Assist with troubleshooting equipment / system failures.
  • Deliver training on validation program elements to Validation Engineers.
  • Maintain a strong understanding of the current regulatory landscape and proactively stays informed of evolving regulations, industry guidance, and compliance expectations applicable to validation activities


Other responsibilities
  • Ensure that all work is performed in accordance with Standard Operating Procedures (SOPs), ALCOA principles, Current Good Manufacturing Practices (cGMP), quality standards, and safety procedures.
  • Support equipment and process related non-conformance investigations and change control activities.
  • Assist with internal and regulatory agency audits / inspections.
  • Ensure training is kept in GMP compliant state.
  • Accountable for managing assigned deliverables, maintaining project milestones, and ensuring proactive, accurate communication with cross-functional teams and stakeholders.


Educational requirements:
  • Bachelor's degree in Scientific, Engineering or similar subject required, MSc or MS preferred.


Experience and skill requirement:
  • A minimum of seven years professional experience in validation, engineering, or operations.
  • A minimum of seven years relevant experience in a cGMP environment is required.
  • Experience with GMP utilities and equipment is required.
  • Demonstrates professionalism, emotional intelligence, and the ability to build effective working relationships across functional teams.
  • Strong attention to details, flexibility and technical writing skills are important for this position.
  • Good knowledge of cGMP, GDP, and applicable regulatory requirements
  • Ability to work independently or in a team environment, while demonstrating initiative and accountability.

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 $152,000- $197,000. 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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