Position Summary For Material Handler 1 (Picking/Selecting & Checking/Quality Control). In general Material Handlers are broken into two groups Checking & Quality Control and Selecting & Picking materials. Responsibilities For Material Handler 1 (Picking/Selecting & Checking/Quality ...
Assist in execution of Quality records (i. ...
The Scientist, Analytical Development & Quality Control is responsible for analytical development, feasibility, method qualification, routine, and stability testing of antibody drug conjugates and intermediates. A minimum of 3-5 years in Analytical Development and/or Quality Control preferably in a ...
Quality Control Specialist - Marlborough, MA - Monday - Friday 8:00AM-5:00PM. Quality oriented employee who ensures that department maintains inspection readiness at all times. Suggest room for improvements, for the sake of quality. ...
Construction Quality Control Manager. Construction Quality Control Manager (CQCM). The CQCM reports directly to the Project Manager and/or Quality Assurance Manager to ensure that a conflict of interest does not occur among the project's productivity, schedule, and quality objectives. Create, update...
Responsible for the Company’s gas quality control programs. The employee is occasionally required to walk; use hands and fingers to operate, handle, or feel objects, tools, or controls; and reach with hands and arms. ...
As the Quality Control Technician for Rolls-Royce, you will be responsible for assisting with determining acceptability of products against standards, specifications and drawings. Report non-conformances and prepare Quality Notifications when required. ...
Your Impactful Responsibilities" or "Take the Lead with These Responsibilities" ) .What skills and capabilities will make you successful? .Candidate need to be successful?) .Managers title that the role reports to? Also give context of stakeholders, team environment, and if it is a leadership or sin...
Responsibilities and Requirements:.We're hoping to find someone with a strong GMP experience and previous QC background could really help.I'll say maybe like three to five years.But in terms of the work, somebody who can perform ELISA, Western, QPCR would be ideal.And with two different groups, so s...
Performs operations necessary for quality testing within quality control. Provides an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Monitors and/or performs inspection and control of products and materials. ...
The Quality Control Supervisor within mRNA Center of Excellence will be responsible for overseeing operations within the QC laboratory activities supporting mRNA vaccine development in the Analytical Development quality control laboratory. Earned Bachelor degree or Master degree with 8+ years of exp...
Quality Control in a GMP environment with specific experience in microbiological testing and sampling. Demonstrated understanding of quality systems including change control, deviations and CAPAs. Prepare and complete change control requests using electronic systems, e. Knowledge and control of lab ...
We are looking for Quality Control (QC) professionals to join our team as Senior Quality Control Analysts, supporting our internal GMP cell therapy manufacturing. Supports and assists TSCAN Quality Assurance and Quality Control projects. Quality Control and/or Analytical Development experience in Bi...
The Senior Analyst / Scientist will work cross-functionally with others in Quality Control, Analytical Development teams, Quality Assurance, and Manufacturing, as needed. The individual will also work on data trending, invalid assays investigations, quality events (investigations, deviations, Change...
Exciting pharmaceutical companyhas a contract QC Analyst II Biochemistry Position!.This is a 6 month contract role with potential for renewal.Lexington, MA-This is an onsite position.Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufactur...
Assist in execution of Quality records (i. ...
Documents data obtained during quality control activities, consistent with company policies and procedures. Communicates significant issues or developments identified during quality control and compliance activities and notifies supervisor and appropriate merchant team. QUALIFICATIONS: ** High schoo...
Analyst I, Quality Control, Microbiology. BS in a relevant scientific discipline with a minimum of 0 - 2 years (or MS in a relevant scientific discipline with 1 year) Quality Control experience in a cGMP organization. ...
This position will work with Quality management to author and review documents in support of ElevateBio's programs as well as routine QC operations. The primary focus will be tracking, writing, and reviewing quality events. The Technical Writer will be expected to use their expertise to work indepen...
Write and review investigations (Environment Control Notification, NCR, OOS, Planned Deviation). ...
Collects samples and performs accurate quality control testing to ensure product quality. Prepare required documents with test results to be presented to production personnel and quality control management. Assist in the investigation and testing, and sampling of raw materials and finished products ...
Quality Control Validation Scientist I is responsible for the qualification activities, following SOPs and regulations including Data Integrity, related to one or more of the following areas: IQ, OQ, PQ and requalification. ...
The Quality Control Analyst will be responsible for:. Author and support quality events; Change Controls, Deviation, CAPA, OOS Investigation, as needed. ...
Participate in authoring quality systems records such as deviations, change controls, CAPAs. General knowledge of industry standards and guidelines for quality control laboratory operation. Quality control, SOP, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System. Contr...
The Quality Control Microbiology Compliance Data Review Associate I is responsible for the review and verification of microbiological data to ensure accuracy, compliance with regulatory standards, and adherence to company policies. This role plays a crucial part in maintaining the integrity of the q...