Biopharma Manufacturing Associate job in Rockville, USA

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Last Name*

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Job type: Contract

Discipline: Biological Sciences, Pharmacology

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a Biopharma Manufacturing Associate for a multinational pharmaceutical company located in Rockville, MD. Successful candidate will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep.

Job Responsibilities:

Applies company Values and Expectations into daily tasks by engaging positively with the team, using a patient and team-first mentality to achieve personal goals.
With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
Proactively works with senior staff to achieve competency in production operations
Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities
Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc)
During production transition times, support commissioning, decommissioning, validation, document revisions, engineering activities and execution of technical protocols.
Maintain a clean and orderly production area in accordance with good house keeping practices.
Proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success
Transparently participates in investigations that are the result of safety or compliance issues.
Applies company Values and Expectations into daily tasks by engaging positively with the team, using a patient and team-first mentality to achieve personal goals.
With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
Proactively works with senior staff to achieve competency in production operations
Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities
Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc)

Skills and Requirements:

BS/BA in life sciences/engineering, with 1 or more years of directly related experience preferred OR Associate's in life sciences/engineering.
Degree in other discipline (or lack of degree) may be considered if sufficient technical depth has been achieved from professional experience.
Excellent oral and written communication skills.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Sarah Beshara at (+1) 267-477-3355 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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