Biopharmaceutical Associate I job in Rockville, USA

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Job type: Contract

Discipline: Manufacturing

Location: United States

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

Biopharmaceutical Associate I - Contract - Rockville, Maryland

Support the production of life‑changing biopharmaceuticals through hands‑on, high‑quality manufacturing operations.

��ý is seeking a Biopharmaceutical Associate I to support the production and delivery of high-quality biopharmaceutical drug substances. This position involves hands-on operations with process equipment, media preparation, and monitoring systems, ensuring the highest standards of quality and efficiency.

Primary Responsibilities:

The successful candidate will contribute to safe, compliant, and reliable manufacturing processes while adhering to best practices in documentation and safety.

Skills & Requirements:

High school diploma or equivalent.
Ability to follow detailed instructions and document processes accurately.
Familiarity with good documentation and data integrity practices.
Commitment to safety procedures and promoting a strong safety culture.
Proficiency in English (speaking, reading, writing, and understanding).
Strong verbal and written communication skills.
Demonstrated ability to work effectively in a team environment.
Willingness and ability to work rotating 24/7 shifts.

The Biopharmaceutical Associate I's responsibilities will be:

Prepare, clean, sterilize, batch, pasteurize, filter, and deliver media and solutions for cell culture and purification operations.
Set up, operate, clean, and break down process equipment.
Perform sampling procedures using analytical instruments to analyze cell culture solutions and product concentration characteristics.
Operate filter integrity equipment to confirm the integrity of filters pre- and post-use.
Monitor and trend process operations, equipment, and instruments to proactively identify and escalate issues for resolution.
Set up fixed and mobile process equipment and parts with Clean-In-Place (CIP) skids to execute validated cleaning and sterilization processes.
Follow standard operating procedures (SOPs), protocols, and batch records/logbooks to perform operations safely and document accurately.
Adhere to safety policies and procedures, actively identifying and correcting unsafe behaviors and conditions.

If you are having difficulty in applying or if you have any questions, please contact Hannah Cihlar at h.cihlar@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

��ý is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��ý is acting as an Employment Agency in relation to this vacancy.

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