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Description: Has good troubleshooting capabilities, and is capable of developing methods and procedures. Works under direct supervision of Manager. Individual is well grounded in a scientific ...
Hours: 2PM – 10PM; Overtime will be possible; Weekends and Holidays are requiredWork Environment: Lab/ProductionThe technician roles will be mainly responsible to support production by testing ...
Description:Bring Your Own Device (BYOD)/Laptop Clinical Trial LeaderPlans, manages and monitors daily activities of clinical studies. Ensures that all activities are in compliance with ...
Description: Harvest Processing We have openings for energetic and committed team members to support breeding activities. This is an entry level position that would support soybean ...
THIS SITE WILL HAVE THE PPE AND INFRARED THERMOMETER This is a weekend only shift 16 hours 3pm – 11pm a shift- (4:45a - 9a) b shift- (9a - 6p) c shift- (7a - 7p) d shift- (7p - ...
The position is in the Pre-Pivotal Attribute Sciences group within the Process Development department. Emphasis focuses on the development and qualification of chromatography and capillary ...
Description: 1) Data Collection and reviewEnsuring Data is obtained from the required systems (LIMS, batch record data base) daily- this may require running queries in LIMS, downloading data, ...
75% Onsite, shift: 8-5 standard hours, and potential evenings as the process requires Manage the development and implementation of clinical and commercial product specifications, in process ...
The Medical Advisor - Advertising and Promotional Review Committee (RC) will be responsible for the medical review of promotional materials for transplant and established products in collaboration ...
The Assistant Clinical Inspection Readiness Leader (Assistant CIRL) is part of the Clinical Quality Performance Team, under the Quality umbrella, and supports the Clinical Inspection Readiness Leader ...
Candidate will be 100% remote throughout the contract MDR work Taken data from registries and studies to work on writing reports to feed into the MDR documentation Technical writing experience a ...
Job Title: Adverse Event Processing Pharmacovigilance AssociateFunctional Area Description The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The ...
Remote till the pendamic situation The Regulatory Affairs Analyst, reviews and assess’ incoming global regulatory information for entry into client’s registration and documentation ...
Position requires that the individual have a degree in science, preferably chemistry or chemical engineering with the following experience: B.SC. with 2 years, M.S. with 0 ...
Responsible for rearing insects and maintaining plants within greenhouse. Rearing responsibilities include preparing rearing materials, transferring and collecting insects, filling in data forms, and ...
Travel up to 30% of the time domestically and / or internationally may be required. Additional Main Responsibilities This field includes Main Responsibilities. Ensures compliance with ...
Conducts routine analyses based on written procedures Reviews data and results of testing to ensure compliance to appropriate specifications and protocols Performs maintenance and calibration of ...
The Regulatory Affairs CMC Sr. Associate will provide Regulatory CMC support for biologic and small molecule investigational drugs being evaluated for the treatment of oncology, HIV and liver ...
Assist the Clinical Research Scientist team to interface with project team members including: Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory ...
Serves as the key operational contact with external investigators and internal stakeholders Has ability to evaluate a scientific proposal or protocol to identify logistical, regulatory and safety ...
