WuXi Biologics Jobs Hiring Now
WuXi Biologics is hiring for 12 open roles on Migrate Mate as of October 15, 2026, concentrated in engineering (Non-Software) and executive leadership & C-Suite, with listed salaries up to about $960,000. Migrate Mate updates WuXi Biologics's live openings daily. WuXi Biologics is a global contract research and manufacturing organization that provides biologics drug development and production services to pharmaceutical and biotechnology clients.
Find WuXi Biologics JobsOverview
WuXi Biologics hiring data on Migrate Mate, as of October 15, 2026.
- Open jobs
- 12
- Top team
- Engineering (Non-Software)
- Seniority
- Manager level or above
- Work type
- 8% remote or hybrid
- Top location
- Cranbury
- Salary range
- $50,000–$960,000
Listed salaries for WuXi Biologics roles on Migrate Mate range from about $50,000 to $960,000 per year across 12 open roles, as of October 15, 2026. One role lists an hourly contract rate.
Open Roles at WuXi Biologics
Showing 12 of 12+ WuXi Biologics jobs
Job Title – Senior Process Equipment and Reliability Engineer l
Job Location – Cranbury NJ
Job Summary
The Process Equipment and Reliability Engineer I will provide technical support to ensure safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. An Engineer I will assist with troubleshooting, preventive maintenance, and reliability initiatives while working within cGMP requirements, engineering systems, and reliability methodologies. This role is designed to build foundational skills in equipment engineering and reliability while contributing to daily operations and long-term asset improvement efforts.
Job Responsibilities
Equipment Reliability & Support
- Assist in monitoring equipment performance and identifying potential reliability risks.
- Support troubleshooting activities for processing and utility equipment under guidance from senior engineers.
- Participate in root cause investigations and contribute to corrective and preventive actions (CAPA).
- Collect and analyze basic equipment data (e.g., downtime, work orders, maintenance history) to support reliability assessments.Maintenance & Asset Management
- Support the execution of preventive and predictive maintenance programs.
- Assist in updating and maintaining accurate equipment records in the CMMS system.
- Help develop and revise maintenance procedures, work instructions, and SOPs.
- Learn and apply reliability tools such as Failure Modes and Effects Analysis (FMEA) and Reliability-Centered Maintenance (RCM).
Process Equipment Familiarization
- Gain exposure to upstream, downstream, and fill/finish equipment (e.g., bioreactors, chromatography skids, filtration systems, CIP/SIP systems, autoclaves).
- Work with operations, maintenance, and senior engineers to understand process-equipment interactions.
- Support commissioning, qualification, and validation activities for new or modified equipment as assigned.
Compliance & Documentation
- Ensure all work is completed in accordance with cGMP, FDA, EMA, and internal quality requirements.
- Draft, revise, and review technical documentation (SOPs, equipment logs, reports) under supervision.
- Support preparation for audits and inspections by providing accurate documentation and technical input.
Continuous Learning & Improvement
- Participate in training programs to develop knowledge of biopharma manufacturing equipment, reliability principles, and regulatory compliance.
- Contribute to continuous improvement projects focused on reducing downtime, improving equipment performance, and increasing operational efficiency.
- Collaborate with cross-functional teams to learn best practices and support improvement initiatives.
Job Qualifications
- Bachelor’s degree in mechanical, Chemical, Bioprocess, or related Engineering discipline.
- +2 years of engineering experience; internship or co-op in pharmaceutical, biotech, or regulated manufacturing environment preferred.
- Basic understanding of process equipment and maintenance concepts.
- Strong problem-solving and analytical skills with eagerness to learn reliability engineering practices.
- Ability to work effectively in a team environment and communicate technical information clearly.
- Familiarity with cGMP or other regulated manufacturing environments is a plus.
- Proficiency with Microsoft Office tools; exposure to CMMS or data analysis software is desirable.
- Experience with CMMS systems, asset management practices, and data-driven decision-making.
- Must work in a self-motivated, highly flexible, well-organized, and detail-oriented style with the requirement of some evening conference call time and occasional local or international travel.
- Must be able to wear appropriate PPE, ability to stand /sit/walk for long periods of time, ability to lift 50 lbs. occasionally.
Why This Role Matters
This position plays a pivotal role in safeguarding the performance of the facility’s most critical assets. Your support will directly influence manufacturing reliability, product quality, and the site’s long-term operational strategy. You will have the opportunity to shape how we work, modernize how we manage equipment, and build a culture that values innovation, accountability, and technical excellence.
The anticipated salary for this position is $70,000-110,000
The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs.
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
Job Title – Senior Process Equipment and Reliability Engineer l
Job Location – Cranbury NJ
Job Summary
The Process Equipment and Reliability Engineer I will provide technical support to ensure safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. An Engineer I will assist with troubleshooting, preventive maintenance, and reliability initiatives while working within cGMP requirements, engineering systems, and reliability methodologies. This role is designed to build foundational skills in equipment engineering and reliability while contributing to daily operations and long-term asset improvement efforts.
Job Responsibilities
Equipment Reliability & Support
- Assist in monitoring equipment performance and identifying potential reliability risks.
- Support troubleshooting activities for processing and utility equipment under guidance from senior engineers.
- Participate in root cause investigations and contribute to corrective and preventive actions (CAPA).
- Collect and analyze basic equipment data (e.g., downtime, work orders, maintenance history) to support reliability assessments.Maintenance & Asset Management
- Support the execution of preventive and predictive maintenance programs.
- Assist in updating and maintaining accurate equipment records in the CMMS system.
- Help develop and revise maintenance procedures, work instructions, and SOPs.
- Learn and apply reliability tools such as Failure Modes and Effects Analysis (FMEA) and Reliability-Centered Maintenance (RCM).
Process Equipment Familiarization
- Gain exposure to upstream, downstream, and fill/finish equipment (e.g., bioreactors, chromatography skids, filtration systems, CIP/SIP systems, autoclaves).
- Work with operations, maintenance, and senior engineers to understand process-equipment interactions.
- Support commissioning, qualification, and validation activities for new or modified equipment as assigned.
Compliance & Documentation
- Ensure all work is completed in accordance with cGMP, FDA, EMA, and internal quality requirements.
- Draft, revise, and review technical documentation (SOPs, equipment logs, reports) under supervision.
- Support preparation for audits and inspections by providing accurate documentation and technical input.
Continuous Learning & Improvement
- Participate in training programs to develop knowledge of biopharma manufacturing equipment, reliability principles, and regulatory compliance.
- Contribute to continuous improvement projects focused on reducing downtime, improving equipment performance, and increasing operational efficiency.
- Collaborate with cross-functional teams to learn best practices and support improvement initiatives.
Job Qualifications
- Bachelor’s degree in mechanical, Chemical, Bioprocess, or related Engineering discipline.
- +2 years of engineering experience; internship or co-op in pharmaceutical, biotech, or regulated manufacturing environment preferred.
- Basic understanding of process equipment and maintenance concepts.
- Strong problem-solving and analytical skills with eagerness to learn reliability engineering practices.
- Ability to work effectively in a team environment and communicate technical information clearly.
- Familiarity with cGMP or other regulated manufacturing environments is a plus.
- Proficiency with Microsoft Office tools; exposure to CMMS or data analysis software is desirable.
- Experience with CMMS systems, asset management practices, and data-driven decision-making.
- Must work in a self-motivated, highly flexible, well-organized, and detail-oriented style with the requirement of some evening conference call time and occasional local or international travel.
- Must be able to wear appropriate PPE, ability to stand /sit/walk for long periods of time, ability to lift 50 lbs. occasionally.
Why This Role Matters
This position plays a pivotal role in safeguarding the performance of the facility’s most critical assets. Your support will directly influence manufacturing reliability, product quality, and the site’s long-term operational strategy. You will have the opportunity to shape how we work, modernize how we manage equipment, and build a culture that values innovation, accountability, and technical excellence.
The anticipated salary for this position is $70,000-110,000
The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs.
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
Job Roles at WuXi Biologics
Working at WuXi Biologics
WuXi Biologics's 12 open roles are manager level or above, and about 8% are remote or hybrid. The most active teams are engineering (Non-Software), executive leadership & C-Suite, and biotech & life sciences. WuXi Biologics provides contract biologics development, manufacturing, and testing services across the drug development lifecycle, supporting clients from early-stage research through commercial production. The company operates large-scale GMP manufacturing and laboratory facilities and hires across scientific, engineering, quality, and operations functions. Most WuXi Biologics roles are based in Cranbury.
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Browse jobs by roleWuXi Biologics Jobs: Frequently Asked Questions
How many jobs is WuXi Biologics hiring for right now?
WuXi Biologics is hiring for 12 open roles on Migrate Mate as of October 15, 2026, updated daily, concentrated in engineering (Non-Software) and executive leadership & C-Suite. Roles span laboratory science, process engineering, manufacturing operations, and quality functions, covering both contractor and full-time positions.
What kinds of roles does WuXi Biologics hire for?
The most active teams are engineering (Non-Software), executive leadership & C-Suite, and biotech & life sciences. WuXi Biologics recruits across biological sciences, process and facilities engineering, manufacturing production, quality control, and corporate functions such as legal and commercial operations. Most postings are manager level or above, ranging from bench-level technician and scientist roles to senior scientists, principal scientists, and executive leadership positions.
Are WuXi Biologics jobs remote or in-person?
Mostly on-site. About 8% of WuXi Biologics's open roles on Migrate Mate are remote or hybrid as of October 15, 2026, with the rest based in Cranbury. Each WuXi Biologics listing shows its work location so you can filter before applying.
How do I apply to a job at WuXi Biologics?
Find a WuXi Biologics role on Migrate Mate and follow the listing link through to WuXi Biologics's own careers portal to submit your application directly. WuXi Biologics manages its own hiring process, including application review, interviews, and offers, independent of Migrate Mate.
What do WuXi Biologics jobs pay?
Listed salaries for WuXi Biologics roles on Migrate Mate range from about $50,000 to $960,000 per year as of October 15, 2026, with most postings at manager level or above. One role lists an hourly contract rate. Exact pay is set by WuXi Biologics and shown on each listing.
Does WuXi Biologics hire entry-level?
Most of WuXi Biologics's open roles on Migrate Mate are manager level or above as of October 15, 2026. Entry-level openings are limited. Check individual WuXi Biologics listings for stated experience requirements.
Where is WuXi Biologics hiring?
Most WuXi Biologics roles are based in Cranbury, and about 8% offer remote or hybrid work as of October 15, 2026. Migrate Mate shows the location on each listing.