6585 - Project Engineer

veristainc; Thousand Oaks (CA); Presencial; USD 85.000 - 127.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive pay

Medical, Dental & Vision insurances

401(k) Retirement Plan with company‑M

Paid Time Off and Holidays

Tuition Reimbursement

Onsite work in Thousand Oaks

Descripción de la vacante

Verista is a leading life sciences solutions provider with a strong customer focus in pharmaceutical and biotechnology manufacturing. We are seeking a Project Engineer to support analytical equipment, CQV activities, and ongoing operations across multiple facilities.

The role requires a Bachelor's degree in Engineering or related discipline and 5+ years of hands-on experience in GMP environments. Onsite work in Thousand Oaks, CA, five days a week, with a competitive salary and benefits package.

Formación

• Bachelor's degree in Engineering, Biotechnology, Chemistry, or related technical discipline preferred.
• 5+ years of relevant experience supporting analytical equipment in a pharmaceutical, biotechnology, or GMP-regulated manufacturing environment.
• Demonstrated hands-on experience troubleshooting analytical or in-process testing equipment.
• Experience supporting commissioning, qualification, and validation (CQV) of analytical instrumentation.
• Strong understanding of GMP requirements, preventative maintenance, and equipment documentation.
• Proven ability to perform root cause analysis and coordinate technical troubleshooting with equipment vendors.
• Experience providing direct equipment support within an active manufacturing environment.

Responsabilidades

• Perform hands-on troubleshooting, root cause analysis, and technical support for analytical equipment used in pharmaceutical and biotechnology manufacturing.
• Lead and support commissioning, qualification, validation (CQV), and decommissioning activities for analytical equipment.
• Coordinate with equipment vendors to resolve technical issues, perform repairs, and improve equipment reliability.
• Execute and manage preventative maintenance activities, equipment inspections, and spare parts inventory.
• Review and maintain qualification documentation, SOPs, equipment records, and associated GMP documentation.
• Perform user access audits, password management, and other equipment compliance activities.
• Collaborate with Analytical, Engineering, Instrumentation, and Manufacturing teams to ensure equipment availability and operational efficiency.
• Develop and execute project plans, schedules, and equipment improvement initiatives.

Conocimientos

Troubleshooting equipment

Root cause analysis

Project management

Strong communication

GMP compliance

Educación

Bachelor's degree in Engineering, Biotechnology, Chemistry or related technical discipline

Herramientas

CQV

Descripción del empleo

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Project Engineer Responsibilities

• Perform hands-on troubleshooting, root cause analysis, and technical support for analytical equipment used in pharmaceutical and biotechnology manufacturing.
• Support a variety of analytical instruments, including cell counters, metabolite analyzers, blood gas analyzers, osmometers, spectrophotometers, endotoxin analyzers, TOC analyzers, and filter integrity testers.
• Lead and support commissioning, qualification, validation (CQV), and decommissioning activities for analytical equipment.
• Coordinate with equipment vendors to resolve technical issues, perform repairs, and improve equipment reliability.
• Execute and manage preventative maintenance activities, equipment inspections, and spare parts inventory.
• Review and maintain qualification documentation, SOPs, equipment records, and associated GMP documentation.
• Perform user access audits, password management, and other equipment compliance activities.
• Collaborate with Analytical, Engineering, Instrumentation, and Manufacturing teams to ensure equipment availability and operational efficiency.
• Develop and execute project plans, schedules, and equipment improvement initiatives.
• Support analytical equipment across multiple manufacturing buildings while managing competing project priorities.

Requirements

• Bachelor's degree in Engineering, Biotechnology, Chemistry, or a related technical discipline preferred.
• 5+ years of relevant experience supporting analytical equipment in a pharmaceutical, biotechnology, or GMP-regulated manufacturing environment preferred.
• Demonstrated hands-on experience troubleshooting analytical or in-process testing equipment.
• Experience supporting commissioning, qualification, and validation (CQV) of analytical instrumentation.
• Strong understanding of GMP requirements, preventative maintenance, and equipment documentation.
• Proven ability to perform root cause analysis and coordinate technical troubleshooting with equipment vendors.
• Experience providing direct equipment support within an active manufacturing environment.
• Strong communication, organizational, and project management skills.
• Ability to manage multiple technical projects in a deadline-driven environment.

Onsite job requirement in Thousand Oaks, CA five days per week.

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range

$85,470 - $127,144 USD

Benefits

Why Choose Verista?

• High growth potential and fast-paced organization with a people-focused culture
• Competitive pay plus performance-based incentive programs
• Company-paid Life, Short-Term, and Long-Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.

For more information about our company, please visit us at Verista.com