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WuXi Biologics

Bioprocess Technician l/ll MFG DSP

WuXi Biologics, Cranbury, New Jersey, United States

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WuXi Biologics is a leading global open‑access biologics technology platform offering end‑to‑end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing. We employ over 12,000 people worldwide and serve more than 600 customers, including top 20 biopharmaceutical companies.

Base Pay Range $28.00/hr - $34.00/hr

Job Location – Cranbury NJ

Job Summary Reporting to the Manufacturing Supervisor, Downstream, the Bioprocessing Associate II will work with the wider Manufacturing teams to support the production of biological products at the MFG18 Cranbury facility. The role is responsible for procedures and processes associated with the manufacture of Drug Substance.

Responsibilities

Assist in maintaining a safety‑oriented, cGMP compliant work environment at all times.

Support facility and equipment start‑up activities as needed.

Contribute to the Production team’s delivery of production output targets and quality levels on schedule.

Prepare shift duties, including checking buffer and material/consumable requirements.

Carry out all production operations in the assigned area as directed by SOPs and Manufacturing Batch Records.

Support MFG efforts in Continuous Improvement through Lean/Six Sigma tools (Standard Work, TPM, 5S, Method 1, 2, etc.).

Immediately notify the Supervisor or Senior Team Member of any deviation from SOPs or the standard production process.

Perform housekeeping duties as assigned to maintain facility at a high standard.

Complete all required training in a timely manner and maintain compliance at all times.

Adhere fully to all safety policies, procedures and regulations.

Ensure highest quality and compliance standards.

Perform all duties in accordance with GMP requirements, SOPs and controlled documents.

Be flexible to take on additional tasks and responsibilities as directed by the MFG Supervisor.

Adhere to WuXi corporate core values and PROUD culture.

Qualifications

Certificate, Diploma, Degree or equivalent experience in Science/Engineering, or related field is essential.

0‑2 years’ experience in biopharmaceutical cGMP manufacturing.

Direct experience in biopharmaceutical manufacturing and/or clinical phase manufacturing is an advantage.

Thorough knowledge of current Good Manufacturing Practices (GMP).

Knowledge of biotech manufacturing processes and translation of that knowledge into documentation such as batch records and SOPs.

Basic understanding of bioprocessing/biotechnology.

Ability to work within and adapt to complex electronic systems such as process automation, SAP and Trackwise investigation system.

Basic understanding of biopharmaceutical equipment and systems such as bioreactors, centrifuges, autoclaves / glass washers, media/buffer systems, and purification systems.

Excellent communication, interpersonal and presentation skills.

Collaborative and inclusive approach to work with colleagues.

Excellent problem solving and troubleshooting skills.

Flexible approach to work and a positive attitude that fits within the team dynamic.

Engage cross‑functionally with a site‑based team.

Autonomous self‑starter who uses initiative to drive actions forward.

Demonstrate strong ethics in adhering to company procedures and policies, regulatory standards, and customer expectations.

This role may initially be day‑based to support onboarding and training but will migrate to a permanent shift schedule as per business requirement.

Employment Details Seniority level:

Entry level

Employment type:

Full‑time

Job function:

Manufacturing

WuXi Biologics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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