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ZL01-051325 Biologic Operator II

Validation & Engineering Group00617, PR, US

Hace más de 30 días

Descripción del trabajo

Job Description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position :

Biologic Operator II

Qualifications :

Associate Degree in Science, Mechanics, Electricity, Instrumentation or related field. No previous experience required. Basic knowledge of laboratory techniques.

Basic knowledge of computerized systems such as Delta V, MES and SAP preferred.

Basic mechanical and mathematical skills.

Basic verbal and written communication skills in English and Spanish.

Third shift position, trainings will be taken for 1-2 months on First shift.

Candidate must be available to work any shift based on business needs.

Responsibilities :

Operate manufacturing equipment and instruments, such as tanks, autoclaves, filtration systems, washers, filter integrity testing, pH, amongst others.

Conduct equipment setup (CIP, PT, SIP) operations according to the established procedures.

Manufacture of bulk biologics operations in Media & Buffer Formulation (Central Services), Inoculum or Fermentation (Upstream) and Capture or Purification (Downstream) areas according to approved and effective procedures.

Conduct equipment and facility inspections and advise of situations that affect operating and environmental conditions.

Monitor critical parameters and elevate any deviation that could impact operations to address accordingly.

Provide technical assistance to manufacturing areas, specifically the troubleshooting support of equipment and process events.

Receive, inspect and verify materials availability to be used for the production activities.

Document, audit and timely correct manufacturing electronic or paper batch record discrepancies.

Document process and equipment status in electronic or manual records.

Sample collection and processing as required by the process.

Strict adherence to current Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP) and accurately complete process-associated documentation.

Provide assistance to operations in accordance with environmental management, occupational health and safety (EHS) systems and promote continuous improvement.

Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.

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Biologic Operator Ii • 00617, PR, US