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Description

This person will be part of the cleanroom and inspecting all receiving and afinal products

Responsibilities:

• Manage the equipment calibration and maintenance program. Maintain the inventory and status of measuring devices.

• Provide help and support for all aspects of testing related to manufacturing.

o First article inspections

o In-process release inspection.

o Final QC release of finished goods.

o Document review.

• Ensures that all inspections and procedures are properly completed and documented.

• Supports the environmental monitoring of cleanrooms and bioburden results. Provides solution for microbial failures.

• Review all quality assessment results and determine whether to accept or reject manufactured products during the inspection process.

• Participates on investigation of source materials for products and components.

• Responsible for completing customer surveys and questionnaires.

Preferred Skills:

High School Diploma with 1-3 years of experience in quality assurance.

Experience:

• Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820.

• Experienced in the areas of the Quality System including corrective actions, change control, quality audits and validation of manufacturing processes, or product development in a pharmaceutical or medical device environment.

• Solid organizational and planning skills required.

• Ability to communicate effectively, verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors.

• Must be able to work effectively and efficiently in a team environment.

• Must have passion to innovate and drive for solutions.

• Must display personal accountability for results and integrity.

• Must display eagerness to learn and continuously improve.

• Must have uncompromising dedication to quality.

• Good general mathematical skills.

• General computer skills.

Skills

labeling, Quality control, Quality assurance, Blueprint, GMP, documentation, quality, inspection, deviation, attention to detail, document control, bachelors, Calipers, Quality inspection, Assembly

Top Skills Details

labeling,Quality control,Quality assurance,Blueprint

Additional Skills & Qualifications

Looking for someone who can work in a high pace environment in the clean room.

Small measuring and computer skills

Experience Level

Intermediate Level

Job Type & Location

This is a Permanent position based out of Camarillo, CA.

Pay and Benefits

The pay range for this position is $49920.00 - $49920.00/yr.

Medical, Dental, Vision, FSA, Life and AD&D, 401(k)

Workplace Type

This is a fully onsite position in Camarillo,CA.

Application Deadline

This position is anticipated to close on Dec 4, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.