"The characteristic we admire most about Harba is their commitment to following through on their promises. If they say they will hit a deadline, they will."
HR Business Partner
"Harba is reliable and responsive. We had a need and they delivered as promised quickly and efficiently. The very fast turnaround of nine days exceeded my expectations and their attention to detail allowed me to focus on other things."
Vice President of Human Resources
"It is with great pleasure that I recommend Harba Solutions Inc. as a life science staffing supplier of choice. Harba's ability to provide quality candidates quickly that meet the needs of our organization has been instrumental in the success of our partnership."
Job Description:
Executing manufacturing procedures within an ISO Class 7 clean room, adhering to established SOPs, cGMPs, and safety regulations.
Conducting aseptic manipulations of cell culture lots and final product assemblies.
Recording production operations in corresponding batch records and log sheets in accordance with cGMPs and established SOPs.
Entering data from product...
Job Description:
This role entails providing operational support, covering tasks such as batch record review, media disposition, label issuance and reconciliation, archiving, and overseeing the final product packaging/release to the courier.
Requirements:
Bachelor’s Degree in a relevant field, with consideration for Biotechnology certification.
Minimum of 1 year of GMP exper...
Job
Responsibilities:
Promote cross-functional interactions to achieve quality outputs and to improve the CRMS
Provide vision, direction, development, and leadership to the Quality Assurance Team
Engage with Quality leadership to ensure development continues to be responsive to changing quality expectations
Formulates a justifiable stance on regulator...
Responsibilities:
Support development of CMC regulatory for submissions (e.g. IND/CTA/BLA/MAA) and identify regulatory risks
Provide guidance for regulatory CMC aspects of product development projects
Review documents for submission-readiness, to ensure that all submissions conform to health authority guidelines
Contribute in the Regulatory CMC discussions and interactions with health...
Responsibilities:
The Regulatory Affairs Specialist I is responsible for supporting the development and implementation of the overall objectives and regulatory strategies that impact the introduction of new products, and the market status of existing products
The Regulatory Affairs Specialist I will assist Regulatory Affairs management by supporting the activities and processes required to...
Responsibilities:
The Senior Regulatory Affairs Specialist is responsible for planning and executing global regulatory activities that are necessary in obtaining and maintaining regulatory clearance/certification for all international geographies for our company's surgical robotic device portfolio
This position is also responsible for developing global regulatory strategies for new p...