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Biotech Validation Jobs in Littleton, Massachusetts

Currently, there are no Biotech Validation jobs available in Littleton, Massachusetts which match this search. You may wish to explore similar job titles on the Biotech jobs in Massachusetts page or view related jobs below.
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CyberCoders Search. Apply. Done. Learn more about CyberCoders Senior Product Manager Apply Lexington, MA Unspecified Job Details If you are a Senior Product Manager with Biotech experience, please read on! Top Reasons to Work with Us - Small but Mighty Biotech company who invented blood panel detection test that has changed the lives of millions! - Comprehensive benefits and compensatio...
VALIDATION ENGINEER Our client is seeking a Validation Engineer who will be responsible for manufacturing process and equipment validation and have experience with highly complex capital equipment as well as commissioning, qualification, and validation of equipment and processes. They will also need to understand the quality impact on the product from a validation standpoint. The candidate select...
IPS is hiring! We have multiple needs for Validation Engineers to join our industry leading Commissioning, Qualification and Validation (CQV) team on-site with our client in Portsmouth, NH. Performs cGMP compliance based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS’ clients. Follows IPS and client standards and requi...
MilliporeSigma's Provantage Laboratory Services Group seeks a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being the technical liaison for laboratory scale validation studies performed by the Provantage Laboratory Services Group. The Validation Project Manager i...
MilliporeSigma's Provantage Laboratory Services Group seeks a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being the technical liaison for laboratory scale validation studies performed by the Provantage Laboratory Services Group. The Validation Project Manager i...
MilliporeSigma's Provantage Laboratory Services Group seeks a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being the technical liaison for laboratory scale validation studies performed by the Provantage Laboratory Services Group. The Validation Project Manager i...
MilliporeSigma's Provantage Laboratory Services Group seeks a self-motivated Project Coordinator to coordinate validation testing on Biopharmaceutical/Pharmaceutical formulations of customer products and solutions. Candidate is responsible for being the technical liaison for laboratory scale validation studies performed by the Provantage Laboratory Services Group. The Validation Project Manager i...
The position is responsible for working as a member of a cross functional team, providing hands-on support for applicable validation projects. The Validation Engineer will be responsible for writing and executing validation, qualification, commissioning, and/or engineering test plans as necessary. This individual will work with relevant LFB USA departments to schedule and perform validation activi...
Hello! New Contract Opportunity Senior Statistical Programmer Major Pharmaceutical Company 12 Month Contract Lexington MA 02421 Senior Statistical Programmer Responsibilities: The Senior Statistical Programmer II will support the Clinical Development teams by: - Creating / Updating / Supporting / Validating Standard Reporting Macros for Standard tables, listings and figures. - Support th...
Essential Function This role is within the eClinical Platform Solutions group and focuses on developing functional requirements specifications and delivering eClinical solutions for eCPS owned products and integration services. It has a number of key requirements that include working in partnership with global functional, engineering and operational groups as well as external customers. The eClin...
Job ID: 258537 Contract Length: 4 Months-Contract to Hire Face to face interview required Our client is one of the oldest independent biotech companies in the world. They are currently looking for a MDM Consultant/Data Analyst for a role with their dedicated team. Every day that you work is a day that you will be working towards making a difference in people’s lives. What You'll Do: Interface...
Sr. ManufacturingTechnician-POS_75036715-0002JC Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare dis...
Auto req ID 31615BR Position Title QA/QC Scientist II Job Description Job Title: QA/QC Scientist II Requisition ID: 31615BR When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving...
Company Overview Alkermes plc is a fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquart...
Position Summary: We have a unique opportunity to join our world-class Data Management Team in a long-term contract role. The Contract Clinical Data Manager will be responsible for coordination and oversight of data management activities in support of the clinical trials/programs Duties and Responsibilities: Clinical sub-team team leader: works closely with the Clinical Trial Manager and is resp...
Alkermes plc is a fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ir...
Alkermes plc is a fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ir...
Senior Clinical Data Programmer (contract) The Sr. Clinical Data Programmer is r esponsible for SAS programming to support data management cleaning activities on global projects with competing priorities, and a ssists with management of external data vendor integrations. Essential Duties: Create standard and/or custom programs/ reports for use by data management in data analytics tools such as ...
As the Manager of International Support, Bioprofile, you will be responsible for supporting all international dealer and subsidiary activities relating to the BioProfile line of instruments. This will include heavy interface with Nova’s international dealers, trouble shooting, providing administrative and logistical support, as well, as instrument training and product management. You will provide ...
Job Description The process engineer is responsible for site based cGMP engineering support of biotech clients. They will act as process engineering lead for developing cleaning development strategy and perform risk assessment and gap analysis for site cleaning programs. Since 1993, Hyde E+C has worked as an integral part of project teams for clients and equipment vendors in the pharmaceutical a...