Validation Engineer
Validation Engineer
Automated Systems, Inc. (ASI)
Round Lake, IL
See who Automated Systems, Inc. (ASI) has hired for this role
Job Description
Validation Engineer
Contract: 6+ month contract duration
Location: Round Lake, IL – Onsite
Automated Systems, Inc. is looking for a Validation Engineer for one of our global client’s Pharmaceutical Manufacturing Facility located in Round Lake, IL. The ideal candidate will handle the supporting system owners with the generation and management of documentation associated with Medical Products instrument validation and qualification activities. In this position the activity focus is on laboratory equipment and instrument systems (LE&IS) utilized in the engineering, chemistry, and information technology areas. All activities will be performed in compliance with the internal Quality System procedures and international/national regulations.
Essential Duties And Responsibilities
We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.
We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.
Validation Engineer
Contract: 6+ month contract duration
Location: Round Lake, IL – Onsite
Automated Systems, Inc. is looking for a Validation Engineer for one of our global client’s Pharmaceutical Manufacturing Facility located in Round Lake, IL. The ideal candidate will handle the supporting system owners with the generation and management of documentation associated with Medical Products instrument validation and qualification activities. In this position the activity focus is on laboratory equipment and instrument systems (LE&IS) utilized in the engineering, chemistry, and information technology areas. All activities will be performed in compliance with the internal Quality System procedures and international/national regulations.
Essential Duties And Responsibilities
- Applies knowledge or quickly learn cGXPs, relevant SOP curriculum, routine project procedures, project management, and other training as appropriate.
- Serves as project lead with projects of intermediate scope and cross-functional teams.
- Incumbent will be responsible for the management and archiving of approved package documents.
- Incumbent may be involved with supporting system change control requests.
- Mentors and provides leadership to junior team members.
- Handles routine tasks timely, accurately.
- Basic Knowledge about industry GMP/GDP
- Expertise with Instrument/Equipment validations
- Proficient in MS Word and Excel, Computer software
- Well organized & able to multi-task
- Team oriented
- Analytical mindset
- Able to summarize and easily explain complex situations
- Solid verbal and written communication skills, including technical/business writing
- BS in relevant Engineering/Science field.
- Other degrees acceptable with 3-5 years of relevant and recent validation/qualification experience.
- 3 years’ experience in GMP-regulated industry, preferably medical device or pharmaceutical.
- 2+ years’ experience performing instrument validations.
- GAMP experience is required.
We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.
We are a dynamic, project oriented consulting company offering individuals a wide variety of technical challenges. We are currently experiencing rapid growth, and are in need of talented individuals. ASI offers top wages and excellent benefits. ASI is an equal opportunity employer.
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Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Pharmaceutical Manufacturing
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