Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, we live by our
Creative Solutions Services, LLC is seeking a Validation Specialist in Framingham, MA. The candidate will support cleaning validation activities and perform equipment qualifications required by GMP standards. The ideal candidate will have a Bachelors degree in Engineering or
Replimune Group in Framingham, MA is seeking a Validation Engineer II to join a dedicated CQV team. The role focuses on qualifying facility equipment, utilities, instrumentation, and computerized systems, ensuring they remain in a validated state per regulatory
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, we live by our
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care becauseAt Replimune, We Live By Our Values United: We Collaborate for a
Replimune is seeking a Validation Engineer II for its Framingham, MA facility to qualify and maintain equipment, utilities, and computerized systems in a validated state under cGMP. You will coordinate CQV campaigns, work with internal customers and contractors,
Replimune in Massachusetts is seeking a Senior Validation Engineer to join the validation team at the Framingham site. You will lead qualification of facilities, utilities, equipment and computerized systems, coordinating protocols, reviews and project executions to maintain a validated
Replimune Group, Inc. in Framingham, MA is seeking a Senior Validation Engineer to lead qualification of facilities, utilities, equipment and computerized systems in a cGMP environment. You will partner with internal teams and external contractors to plan, execute
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, we live by our
QUALITY CONSULTING GROUP, LLC is seeking a talented engineer to join its team in Puerto Rico & USA, focusing on computer software validations within the pharmaceutical, biotech, medical devices, and manufacturing space. The role requires experience with software
Replimune Group, based in Framingham, MA, seeks a Senior Validation Engineer to qualify and maintain biotech facility equipment, utilities, instrumentation and computerized systems in a validated state. You will coordinate with internal customers and contractors to plan, execute
The Sr Quality Engineer, Computer System Validation (CSV) is responsible for QA oversight of the validation and compliance of GxP-regulated computerized systems and any associated GMP equipment ensuring they are implemented, maintained, and retired in accordance with global regulatory
Quality Consulting Group, LLC is seeking a talented individual for a manufacturing engineering role in Puerto Rico. This position involves designing manufacturing processes, collaborating on new products, and ensuring quality standards are met. Qualifications include a
Quality Consulting Group, LLC is seeking a motivated professional to join our team in Puerto Rico & USA. You will oversee change control, equipment qualification, and process validation for terminally sterilized medical devices. You’ll engage in design
A leading ophthalmology company is seeking a Quality Engineer in Northbridge, MA to oversee the quality engineering functions of drug product validation and qualification. The successful candidate will work closely with multiple departments to ensure compliance with regulatory
Initial Therapeutics, Inc. is seeking a Sr Quality Engineer for Computer System Validation (CSV). This role ensures compliance with GxP regulations, overseeing the validation and maintenance of computerized systems and associated equipment in alignment with global standards. The ideal
A global EPCM firm is seeking a CQV Engineer to support projects in New Bedford, MA. The role involves developing and executing equipment validation protocols within a cGMP and FDA regulated environment. Candidates should have 3-5 years of
A leading consulting firm in Puerto Rico is seeking a highly motivated individual for a role focused on process validation, equipment IQ, and computer software validation. The ideal candidate will have a Bachelors degree in Engineering and at
A global pharmaceutical solutions company in Villalba, PR is seeking an individual contributor to provide engineering support and manage projects. The ideal candidate should possess a Bachelor’s degree in Engineering and have proven experience in Process
Quality Consulting Group, LLC is seeking a talented engineer to design manufacturing processes in Puerto Rico and USA. Responsibilities include developing manufacturing layouts, supervising equipment performance, and managing validation processes for tools and equipment throughout production. The ideal