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Validation Engineer
Job Description
Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve.
Title: Validation Engineer
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
Description:
We are currently looking for an experienced Validation Engineer to join a growing team at a production-scale facility focused on testing reagents. The company is expanding its fill lines and implementing several new processes, which will involve validation work across both manufacturing and lab scales. As part of a small, agile team, you will help manage complex and fast-paced validation projects that support equipment testing, process validation, and the qualification of custom systems.
This is an exciting opportunity to work in a dynamic, collaborative environment where priorities can shift quickly, and deadlines are ever-changing. Flexibility, strong organizational skills, and a keen eye for detail are essential to succeed in this role.
Key Responsibilities:
Required Qualifications:
Additional Skills:
Onboarding Requirements:
Compensation & Benefits:
If you're an experienced Validation Engineer ready to take on exciting challenges in a fast-paced setting, this is the role for you. Please submit your resume to be considered!
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Title: Validation Engineer
Hiring Organization: Connexion Systems & Engineering
Compensation, Benefits, and Employment Type
- Duration: 5+ month contract
- Pay rate: $55-$80/hr
- Job Location: San Diego, CA
- Schedule: M-F, 8am-5pm, expected overtime, some weekends required
- Job#: bh18051
Description:
We are currently looking for an experienced Validation Engineer to join a growing team at a production-scale facility focused on testing reagents. The company is expanding its fill lines and implementing several new processes, which will involve validation work across both manufacturing and lab scales. As part of a small, agile team, you will help manage complex and fast-paced validation projects that support equipment testing, process validation, and the qualification of custom systems.
This is an exciting opportunity to work in a dynamic, collaborative environment where priorities can shift quickly, and deadlines are ever-changing. Flexibility, strong organizational skills, and a keen eye for detail are essential to succeed in this role.
Key Responsibilities:
- Ensure adherence to all site validation policies and procedures.
- Lead and support validation/qualification activities for process, cleaning, equipment, computer software, and facilities.
- Develop, execute, and approve qualification protocols in collaboration with internal and external project teams.
- Coordinate with equipment manufacturers and internal teams to ensure proper execution of validation activities.
- Maintain up-to-date validation documentation and ensure accuracy in project files.
- Provide expert guidance to resolve technical issues during qualification activities.
- Split responsibilities 50/50 between process validation and equipment validation.
- Collaborate with cross-functional teams to deliver validation projects on time and within scope.
Required Qualifications:
- Bachelor’s degree in Mechanical or Chemical Engineering, Science, or related field.
- 5-7 years of experience in pharmaceutical/biotech operations.
- Minimum 5 years of hands-on experience with validation in regulated environments (process, cleaning, equipment, computer software, or facilities).
- Solid experience in cGMP, OSHA, and EPA compliance.
- Strong understanding of biotech unit operations and validation principles.
- Design or owner experience in manufacturing processes and utility systems (e.g., purified water, WFI, CIP, SIP, compressed air).
- Knowledge of processes in fermentation, purification, and/or formulation.
- Excellent project management and organizational skills.
- Proficiency in MS Word, Excel, and Project.
- Experience writing validation protocols, executing studies, and analyzing data.
Additional Skills:
- Ability to multitask in a fast-paced, changing environment.
- Strong communication skills, both written and oral.
- Collaborative team player who can manage cross-functional relationships.
- Must be flexible and open to working weekends and overtime when needed to meet project deadlines.
Onboarding Requirements:
- 9-panel drug screen (no THC)
- Criminal background check (7 years)
- Employment and education verification
- OIG Sanctions check
- System for Award Mgmt (SAM) Exclusion check
- GDS Training Checklist
- Competitive pay rate: $55-$80/hr
- 5+ month contract with potential for extension
- Opportunity to contribute to important projects in a cutting-edge environment
Please use the apply button to submit your resume for consideration. A Connexion Representative will contact you shortly.
You may also send your resume and cover letter via email to the recruiter listed below. You MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to jobpostings@csetalent.com. We would be glad to help you find the perfect job!
Meet Your Recruiter
Caroline Driscoll
Account Manager & Sr. Technical Recruiter
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