Biotech Jobs in Massachusetts

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905 Massachusetts Biotech jobs found on Monster.

Jobs 1 to 20 of 905
. We are looking to hire a Quality Complaints Specialist (Medical Device/FDA/Complaints) for a global Q&R group in Andover, MA. Please email your resume to ***** for review. Responsibilities: Responsible to take assigned complaint investigations from evaluation to closure in accordance with internal and external (FDA, Canadian and European) regulatory requirements. Investi...
Johnson & Johnson companies are equal opportunity employers. Principal R&D Engineer, New Product Development – Mitek Sports Medicine-5770141001 Description DePuy Synthes, a member of Johnson & Johnson's Family of Companies, is recruiting for a Principal R&D Engineer, New Product Development – Mitek Sports Medicine to be located in Raynham, MA. DePuy Synthes is a Johnson & Johnson company that ...
The QA Specialist Temp (Quality Systems) is the responsible person for representing QA in a supporting role for the Supplier Management and Quality Risk Management Programs at the Allston Landing Facility. This position will report to the QA Manager, Quality Systems. He/she will work closely with the site subject matter experts, Supplier Management Team and Quality Risk Management ensuring that th...
Ocean Spray is a vibrant agricultural cooperative owned by more than 700 cranberry and grapefruit growers in the United States, Canada and Chile who have helped preserve the family farming way of life for generations. Formed in 1930, Ocean Spray is now the world's leading producer of cranberry juices, juice drinks and dried cranberries and is the best-selling brand in the bottled juice category. T...
Johnson & Johnson companies are equal opportunity employers. Product Development Engineer, Spine-4463141017 Description DePuy Synthes Spine is currently recruiting for a Product Development Engineer, Spine located in Raynham, MA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological business in the world. DePuy Synthes Compa...
ACCOUNTABILITIES: - Responsible for collaborating with PDD Global Compound Support Quality Assurance function to develop and implement a strategic audit plan for the development of all assigned TDC US compounds. Ensure that activities are conducted and reports written according to applicable regulations and Takeda SOPs. - Lead domestic and international audits of clinical investigator sites, doc...
Primary Role As a key member of the Manufacturing Science & Technology group in Process Development department. This individual will be responsible for providing technical and scientific leadership to support downstream processes of commercial productions and late stage clinical productions, including process and product investigations/troubleshooting, process continuous improvement and life-cycle...
Primary Role The Lead Investigator's responsibilities will be to lead and manage major/critical deviations and related reports to closure within the established timelines for the manufacturing department. Will conduct comprehensive investigations to determine potential product impact, identify root cause and implementation of corrective and preventative actions in accordance with established proce...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Saint-Gobain, the world leader in the habitat and construction markets, designs, manufactures and distributes building materials, providing innovative solutions to meet growing demand in emerging economies, for energy efficiency and for environmental protection. Saint-Gobain is a welcoming, solid, open-minded company that offers long-term career opportunities. The Northboro R&D Center focusing on...
About Us: Gyrus ACMI, Inc is a dynamic medical device company whose vision is to anticipate the needs of surgeons through powerful see and treat procedure solutions that are safe, simple, cost efficient and produce the highest quality patient outcomes. Gyrus ACMI is focused on Minimally Invasive procedures in Urology, Gynecology, General Surgery and ENT. Gyrus ACMI, believes its people are its gr...
Description Job Description / Capsule The Senior Director of Clinical Pharmacology Scientist is a strategic and scientific job which works closely with clinicians to create clinical pharmacology development plans that will fulfil requirements to reach Proof of Concept and registration. Key deliverables will be the design of the Clinical Pharmacology programme, to be delivered to the project team...
Client: Pharmaceutical MUST HAVE: - Bachelors degree in scientific/clinical related discipline - 3-5 years Clinical Project Management experience in the pharmaceutical industry with a minimum of 2 years working with observational research studies - CRO management experience Description: The Clinical Study Manager position is one of demonstrated expertise in understanding and coordinating the...
: Pall is a Fortune 1000 materials science and engineering company with the broadest filtration, separation and purification capabilities in the world. Our process and product enabling technologies help our customers make good products better, safer and even possible. We provide innovative products to customers in health care, biotechnology, pharmaceutical, semiconductor, municipal drinking water...
Technical Product Development – Manager Lab R&D Pall is a Fortune 1000 materials science and engineering company with the broadest filtration, separation and purification capabilities in the world. Our process and product enabling technologies help our customers make good products better, safer and even possible. We provide innovative products to customers in health care, biotechnology, pharmaceu...
The Quality Assurance Auditor will be responsible for conducting internal/external quality audits (including, but not limited to: Departmental, Process, Vendor qualification, and Clinical Site audits). The Quality Assurance Auditor must prepare audit plans, agendas and reports. He/she is responsible for assisting in various quality improvement initiatives in order to comply with Good Clinical Prac...
. TITLE: BioMed Compound Manager LOCATION: Cambridge, MA DURATION: 6 Month Contract PAY RATE: Open DESCRIPTION: This medical science professional will be a key contributor in the Sample Management Group and be primarily responsible for processing new compounds and inventory requests through the Compound Hub process. The primary responsibilities for this individual will include: Handling ne...
. TITLE: BioMed Compound Associate LOCATION: Cambridge, MA DURATION: 6 Month Contract PAY RATE: Open DESCRIPTION: This medical science professional will be a key contributor in the Sample Management Group and be primarily responsible for processing new compounds and inventory requests through the Compound Hub process. The primary responsibilities for this individual will include: Handling ...
. TITLE: Manufacturing Associate LOCATION: Cambridge, MA DURATION: 6 Month Contract PAY RATE: Open DESCRIPTION: Collaborating to formulate reagents for development Pilot manufacturing operations process validations Calculation of molar concentrations for dilutions, batch aliquotation, product labeling. Documentation, compliance, and standards (21 CFR 820, ISO 13485, 93/42/EEC, 98/79 EC, a...
Eppendorf, a leader in the bio-tech industry sales, marketing, manufacturing and distribution facilities located in North America, develops, produces and distributes systems for use in life-science research laboratories worldwide. Its product range includes pipettes, dispensers and centrifuges as well as consumables such as micro test tubes and pipette tips. In addition, Eppendorf provides instr...

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