56 cqv opportunities in Boston updated today
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· Page 1 / 3Job Summary: We are seeking a detail-oriented Validation Engineer to support validation and calibration activities for critical pharmaceutical manufacturing and sterile processing equipment. This role requires strong expertise in regulatory compliance, including GMP and 21 CFR Part 11, along with ha
The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development,
A leading consulting firm is seeking a motivated US - CQV Consultant in Boston, MA. The role involves writing critical CQV documents, reviewing protocols for compliance, and leading efforts in biopharmaceutical manufacturing. Candidates should hold a Bachelor's in Engineering with 3-4 years of relev
ElektrofiA biopharmaceutical company in Boston is seeking an experienced Associate Director for Manufacturing Science and Technology. This role involves leading equipment design and facility readiness initiatives for proprietary technologies. Candidates should have a minimum of 10 years in the biopharmaceuti
BioSpace, Inc.A leading biopharma company in Waltham, Massachusetts, is seeking a Validation Engineer with 4–7 years of experience. The role involves generating and executing validation documentation and ensuring compliance with GMP standards. The ideal candidate will have hands-on experience in a regulated envir
CAIPosition Description: The CQV Senior Project Manager is responsible for leading services delivered to life sciences clients in all aspects of CQV-project execution and capital project Operational Readiness. Skills and Characteristics Required: - Significant experience in Project Management Principle
The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development,
A consulting company in life sciences seeks a Consultant/Senior Consultant to join their Boston office. This full-time position involves leading small project teams, managing client relationships, and ensuring project delivery in biomanufacturing settings. Candidates should possess 5-7 years of cons
A leading biotechnology firm in Norwood is seeking a Validation Specialist to execute qualification activities in compliance with industry standards. The successful candidate will perform commissioning and validation at a GMP manufacturing facility, ensuring all processes are in compliance. A degree
MENTOR Technical Group CorporationA leading technical solutions provider in Boston is seeking a qualified professional to develop and validate biotech process equipment, ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor’s degree in Chemical Engineering or a related field, along with 3–5 years of
A leading biotechnology company located in Marlborough, Massachusetts, is seeking a Validation Engineer to lead commissioning and validation activities within a cGMP environment. The role involves developing validation strategies, documenting compliance activities, and providing technical leadership
A leading biopharma company in Waltham, Massachusetts, is seeking a Validation Engineer with 4–7 years of experience. The role involves generating and executing validation documentation and ensuring compliance with GMP standards. The ideal candidate will have hands-on experience in a regulated envir
A leading engineering consultancy is seeking a Project Engineer/Senior Project Engineer in Boston, MA. Responsibilities include supporting biomanufacturing projects, maintaining client relations, and ensuring high-quality deliverables. Candidates should have a Bachelor's degree in Life Science or En
Trinity Consultants - Advent EngineeringIMPORTANT: We are only considering W2 candidates at this time. Applications from third-party vendors or C2C arrangements will not be considered. ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Headquartered near San Fra
MENTOR Technical Group CorporationMentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and
Overview Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and op
The Role Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development,
**The Role:**Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and
The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Marlborough, Massachusetts, a key hub for research, development,
ModernaThe Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and o
Location: Framingham, Massachusetts, United States Employment Type: Full-Time Reference Code: TSO822815MA Date Posted: 01/Nov/2022 Years of Experience Req.: 0 Years Summary DPS is looking for a CQV Engineer to work for a client in New Bedford, MA Key Responsibilities Become familiar with the user, f
BioSpace*The Role** Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and
The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and o
The Role The individual in this role leads commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within cGMP manufacturing environments. This role provides technic
InteProsThis range is provided by IntePros. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $60.00/hr - $70.00/hr Direct message the job poster from IntePros Senior Recruiter Specializing in Life Sciences and Engineering The purpose of the
CQV Engineer III page is loaded## CQV Engineer IIIlocations: Marlborough, Massachusetts: Norwood, Massachusettstime type: Full timeposted on: Posted Todayjob requisition id: R18865**The Role**The individual in this role leads commissioning, qualification, and validation (CQV) activities to ensure fa
A leading biopharmaceutical company is seeking a CQV Specialist to work on-site in Norwood, Massachusetts. This role involves executing validation activities, authoring technical documentation, and ensuring compliance within a cGMP environment. Candidates must have a B.S. in Engineering and 2-5 year
Validation & Engineering Group, Inc. (V&EG) is a leading service supplier that provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and related services. We are seeki
A leading biotech company in Norwood, Massachusetts, is looking for a skilled individual to support commissioning, qualification, and validation (CQV) activities in a cGMP manufacturing environment. The role requires a B.S. in Engineering and 2-5 years of relevant experience. You will author and rev
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Boston. Actual salaries may vary depending on experience, company, and area.
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