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Computer System Validation Csv Pharmaceutical Jobs in Delaware

Basic understanding of computer systems, networks, and common software applications. * Strong ... Valid driver's license may be required for travel between agency locations. * Must successfully ...

Closes out orders in the computer system to maintain accurate records. * Conforms with all safety ... Valid state driver's license in good standing and minimum state-required automobile insurance. #J ...

New

Pharmacist

Milford, DE · On-site

$56.25 - $67.50/hr

... the automated dispensing system. Reviews technician preparation of intravenous admixtures ... Ensures and validates processes are followed for dispense prep of medications. At a minimum ...

Pharmacist

Milford, DE · On-site

$56.25 - $67.50/hr

... the automated dispensing system. Reviews technician preparation of intravenous admixtures ... Ensures and validates processes are followed for dispense prep of medications. At a minimum ...

PHARMACY TECH II - CERTIFIED

Lewes, DE · On-site

$18.75 - $29.06/hr

... and prepackaged pharmaceuticals and assist staff pharmacists as directed ... Computer SkillsQualifications 1 year hospital experience preferred or other relevant experience as ...

Pharmacy Technician

Bear, DE · On-site

$16.75 - $20.50/hr

... computer system and hands-on training with our teams. Bring your flavor: Building the future of ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...

Pharmacy Technician

Dover, DE · On-site

$17.50 - $21.25/hr

... computer system and hands-on training with our teams. Bring your flavor: Building the future of ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...

Pharmacy Technician

Bear, DE · On-site

$16.75 - $20.50/hr

... computer system and hands-on training with our teams. Bring your flavor: Building the future of ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...

Pharmacy Technician

Dover, DE

$17.50 - $21.25/hr

... computer system and hands-on training with our teams. Bring your flavor: Building the future of ... S. We operate over 2,200 stores, 1,732 pharmacies, 405 fuel centers, 22 distribution facilities ...

Computer Skills Qualifications 1 year hospital experience preferred or other relevant experience as ... Valid DL With No More Than 3 Moving Violations Credentials Education Essential: * High school ...

PHARMACY TECH II - CERTIFIED

Lewes, DE · On-site

$18.75 - $29.06/hr

... and prepackaged pharmaceuticals and assist staff pharmacists as directed ... Computer SkillsQualifications 1 year hospital experience preferred or other relevant experience as ...

Showing results 41-60

Computer System Validation Csv Pharmaceutical information

What is computer system validation (CSV) in the pharmaceutical industry?

Computer System Validation (CSV) in the pharmaceutical industry is a process used to ensure that computerized systems used in drug manufacturing and related processes work as intended and comply with regulatory standards, such as FDA 21 CFR Part 11. CSV involves planning, testing, documenting, and maintaining systems to guarantee the accuracy, reliability, and integrity of data. This is critical for patient safety and product quality, as well as for meeting legal and regulatory requirements. The process typically includes risk assessment, validation planning, protocol execution, and ongoing monitoring of system performance.

What are common challenges faced by computer system validation (CSV) professionals in the pharmaceutical industry?

CSV professionals in the pharmaceutical industry often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for audits, and ensuring thorough validation of complex systems within tight project timelines. Collaboration with cross-functional teams, such as IT, quality assurance, and manufacturing, is essential to address technical and compliance issues. Additionally, balancing the need for robust validation with operational efficiency requires strong communication and project management skills.

What are the key skills and qualifications needed to thrive as a computer system validation (CSV) professional in the pharmaceutical industry?

To thrive as a Computer System Validation (CSV) professional in pharmaceuticals, you need a strong background in life sciences or engineering, knowledge of regulatory standards (such as FDA 21 CFR Part 11), and experience with validation protocols. Familiarity with validation lifecycle management tools, quality management systems (QMS), and industry guidelines like GAMP 5 is typically required, along with certifications such as ISPE or PMP being advantageous. Outstanding attention to detail, analytical thinking, and strong communication skills help ensure compliance and effective coordination with cross-functional teams. These competencies are vital for maintaining regulatory compliance, data integrity, and patient safety in pharmaceutical operations.

What is the difference between Computer System Validation Csv Pharmaceutical vs Quality Assurance Specialist?

AspectComputer System Validation Csv PharmaceuticalQuality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, Validation certificationsGxP, ISO, QA certifications
Work EnvironmentPharmaceutical manufacturing, regulated labsQuality departments across industries, including pharma
Employer & IndustryPharmaceutical companies, biotech firmsPharma, biotech, healthcare organizations
Primary FocusEnsuring computer systems meet validation and compliance standardsMaintaining quality standards and process improvements

Computer System Validation Csv Pharmaceutical specialists focus on validating computer systems to ensure compliance with industry regulations, while Quality Assurance Specialists oversee overall quality processes. Both roles require GxP knowledge and are vital in pharmaceutical environments, but their core responsibilities differ in scope and focus.

What are popular job titles related to Computer System Validation Csv Pharmaceutical jobs in Delaware?

For Computer System Validation Csv Pharmaceutical jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Csv Pharmaceutical jobs in Delaware look for?

The top searched job categories for Computer System Validation Csv Pharmaceutical jobs in Delaware are:

What cities in Delaware are hiring for Computer System Validation Csv Pharmaceutical jobs?

Cities in Delaware with the most Computer System Validation Csv Pharmaceutical job openings:

Infographic showing various Computer System Validation Csv Pharmaceutical job openings in Delaware as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution.

Chemical Operator I & II (Pharmaceutical)

Synerfac Technical Staffing

Wilmington, DE

$28 - $32/hr

Full-time

Re-posted 21 days ago


Job description

Job Description:
We are seeking Manufacturing Operators for our client in Wilmington, DE. The Manufacturing Operator is responsible for the batch-wise manufacture of active pharmaceutical ingredients in a safe and GMP compliant manner. The Manufacturing Operator carries out tasks associated with chemical manufacturing utilizing batch logs, standard operating procedures, and work instructions under cGMP guidelines. The Manufacturing Operator adheres to all safety, quality, and compliance regulations, procedures, and guidelines, with special care given to protect the environment in which we operate.
Responsibilities:
* Complies with company policies and procedures, established safety procedures, and maintains a safe and clean working environment.
* Oversees manufacturing process composed of steps such as set-up, loading, unloading, processing, drying, documentation, and follow-up.
* Accurately completes batch logs and other documentation to produce product efficiently and in compliance with cGMP and standard operating procedures.
* Proper operation of process controls, DCS systems, pneumatic, hydraulic and electrical equipment as detailed in procedures to product materials in a safe and cGMP environment.
* Recognizes and documents 'abnormal' operating conditions with proper response including immediate notification of supervision.
* Inspects components and products of the production cycle for compliance with applicable standards.
* Ability to use SAP to electronically document transactions.
* Inspects components of the production cycle for compliance with standards.
* Makes good use of hold periods for subsequent processing steps. Utilizes idle processing time to perform other production related activities (housekeeping, lean initiatives, training, etc.)
* Understand and participate in operator asset care initiatives.
* Other duties as assigned.
* Carries out duties in compliance with all state and federal regulations and guidelines including FDA, EPA, OSHA and DEA. Complies with all company and site policies and procedures. Recognizes and reports unsafe conditions and procedures to supervisors immediately with relevant documentation.
* Successfully completes regulatory and job training requirements on time.
* Participates on investigative teams and site group initiatives (PHAs, PSSR, etc.).
* Understands and responsibly performs duties with attention to safety, environmental matters, quality, compliance, and controlled substances handling. Items include; wearing appropriate personal protective equipment, recognizing, reporting and appropriately responding to hazards in the work area (spills, accidents, near misses, etc.), maintaining proper housekeeping at all times, properly labeling and storing chemicals, plus all other relevant job requirements.
* Assists in training operators.
* Makes positive contributions demonstrated by:
* Making suggestions for improvement and recommending solutions
* Providing overtime as needed
* Learning new skills and processes
Job Requirements:
* High school diploma or general education degree (GED).
* Work experience in a chemical and/or pharmaceutical environment.
* Two to four years related experience and/or training or equivalent combination of education and experience.
* Read, understand, and interpret documents such as safety procedures, batch logs, operating and maintenance instructions, government regulations and procedure manuals.
* Write routine reports, operating procedures, and correspondence with supervisory assistance if required.
* Add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
* Compute rate, ratio, and percent and be able to create and interpret bar graphs.
* Calculate figures and amounts such as proportions, percentages, area, and volume.
* Mechanical aptitude of production equipment and processes.
* Ability to safely operate a forklift.
* Use computer software applications including Microsoft Office suite.
* Work well with others in a team environment, influencing people in opinions and behaviors consistent with good leadership examples.
* Perform a variety of tasks, changing tasks frequently, staying focused, maintaining attention to detail, with a focus on Safe and Right First Time production
* While performing the duties of this job, the employee is regularly required to stand, walk, climb, band, and stoop. The employee uses hands to handle and feel and must reach with hands and arms.
* The employee frequently is required to talk, hear, taste, and smell.
* The employee must occasionally lift and/or move up to 50 pounds.
* The employee is frequently exposed to weather conditions including occasional extreme heat and cold.
* The employee must be able to qualify for and use respiratory protective equipment.
* Specific vision abilities required

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About Synerfac Technical Staffing

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Since 1987, Synerfac has served three groups, Our Clients, Our Candidates and Our Staff. We treat all three with equal importance because we recognize the synergy of success when one group succeeds, We all succeed. Synerfac is in the business of providing opportunities and adding value. We strive to create extraordinary experiences. For our clients we provide staffing services that enable them to focus on their core competencies which will add value to their businesses. For our employees we provide permanent and temporary assignments that complement their job skills and experience while providing professional and financial rewards. For our staff –we provide careers that are balanced, uplifting and carry the highest rewards by continually improving our business process. Our goal is to enhance the lives and enterprises of all those we touch to make them better off for having known us.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Cherry Hill, NJ, US

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