Validation Engineer II
MEDVACON
POSITION OVERVIEW:
The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications. ESSENTIAL JOB FUNCTIONS:
VALUES:
SUPERVISORY RESPONSIBILITIES:
This position does not have supervisory responsibilities. CERTIFICATES, LICENSES, REGISTRATIONS:
Certified Quality Engineer Preferred.
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to View email address on click.appcast.io.
The Validation Engineer II ensures compliance and operational excellence by managing validation processes across sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications. ESSENTIAL JOB FUNCTIONS:
- Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site Acceptance Testing, Installation Qualification, Operational Qualification, Performance Qualification, and Process Qualification for sterile and non-sterile manufacturing.
- Oversees multiple validation projects, ensuring timely budget-compliant completion while driving continuous improvement to boost manufacturing efficiency.
- Prepares, reviews, and approves technical documents, including Standard Operating Procedures and current Good Manufacturing Practice (cGMP) records, while managing change control, Corrective and Preventive Action, and quality investigations.
- Operates and manages critical equipment, executing cleaning, sterilization, and lyophilization cycles.
- Provides training, supports Research and Development and product development, manages contractors for Commissioning, Qualification, and Validation (CQV) activities, and assists with audits to ensure compliance.
- Bachelor of Science degree in a scientific or engineering discipline.
- 7 years Validation experience in the pharmaceutical or biotechnology industries.
- Advanced knowledge of cGMP, CQV, sterilization process validation, and regulatory compliance, including Good Automated Manufacturing Practice and 21 Code of Federal Regulations Part 11.
- Strong problem-solving, project management, and attention to detail, with proficiency in Microsoft Office Suite, Quality Management Systems, and experience in Computer System Validation and Cleaning Validation preferred.
- Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.
- Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.
- Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.
- Resourcefulness: Secures and deploys resources effectively and efficiently.
- Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.
- Ensures Accountability: Holds self and other accountable to meet commitment.
- Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.
- Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.
VALUES:
- People: Our people define who we are as a company, and we believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth.
- Quality: Quality stands at the core of our mission, reflecting our commitment to excellence in every medication we produce.
- Service: We are here to serve others. Every interaction with our patients, providers, employees, and other stakeholders comes from a place of service.
- Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care.
SUPERVISORY RESPONSIBILITIES:
This position does not have supervisory responsibilities. CERTIFICATES, LICENSES, REGISTRATIONS:
Certified Quality Engineer Preferred.
Important Notice: Protecting Your Information
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to View email address on click.appcast.io.
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Validation Engineer II in East Windsor, Middlesex County, NJ vacancy
- ...Group is a fully integrated architecture, engineering, construction, system integration, and... ...to build a better world.Job Description:Validation Engineer Who You’ll Work With You will join... ...Design Group as a Validation Engineer II, you are joining a team that will...SuggestedFull timeWork at officeFlexible hours
$80k - $120k
...Compensation $80,000.00 - $120,000.00 / Yearly Hours Per Week 40 Number Of Positions 1 Job Description The Validation Engineer will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance...SuggestedFull time$71.3k - $97.75k
Integra LifeSciences is seeking a Process Engineer in Plainsboro Township, NJ, to optimize and sustain manufacturing processes. The role involves cross-functional collaboration to enhance workflow and efficiency while ensuring compliance with FDA regulations and other...Suggested- ...related to system start up, commissioning, qualification, and validation. They will work towards ensuring compliance and quality... ...cycle development and PQ. Qualifications: Experience in Engineering, Commissioning, Qualification, and Validation processes Knowledge...SuggestedFull time
$72.8k - $80.1k
...workDirect small teams in document development and/or executionQualifications and Experience- Bachelor's degree in a science or engineering field (or equivalent experience)- 2–4 years' experience in commissioning and qualification in a regulated industry- Familiarity with...SuggestedWorldwide$71.3k - $97.75k
...patient outcomes and set new standards of care. The Process Engineer is responsible to understand, optimize, and sustain manufacturing... ..., etc. Lead & execute engineering studies, IQ/OQ/PQ/TMV validations, manufacturing process requirements, specifications, Engineering...Contract workTemporary workImmediate start$71.3k - $97.75k
INTEGRA LIFESCIENCES CORP is seeking a Process Engineer in Plainsboro Township, New Jersey. The role focuses on optimizing manufacturing processes using lean and six sigma methodologies. You'll work cross-functionally to implement solutions and improve operational efficiencies...$71.3k - $97.75k
...outcomes and set new standards of care. The Quality Assurance Engineer II will provide Quality compliance support on all aspects of the... ...by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed...Temporary work$71.3k - $97.75k
...new standards of care. Summary The Global Supplier Quality Engineer II will play a vital role supporting Supplier Quality by conducting... .../assessments, inspection technique support, verification /validation activities, CAPA and change management. FDA CFR part 820 and...Contract workTemporary work3 days per week$94.3k - $129.95k
...advance patient outcomes and set new standards of care.The Sr Engineer II, Lean Six Sigma Black Belt is a key practitioner within Integra... ...chain, distribution, and supporting functions to deliver validated improvements in cost, quality, throughput, and service. Conduct...Full timeTemporary workWork at officeImmediate start$80k - $120k
...October 2017 About the Job: The position reports to the Sr. Validation Manager and is responsible for supporting commissioning,... ...activities. Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external vendors. Participate in...Temporary workWork experience placementFlexible hours- Integra LifeSciences is seeking a Global Supplier Quality Engineer II to support supplier quality at our Plainsboro, NJ site. You will lead supplier audits, maintain supplier quality requirements, and provide QA leadership to contract manufacturers and raw material suppliers...Contract work3 days per week
- Integra LifeSciences is seeking a Staff Engineer - Supplier Quality Validation Engineer in New Jersey with hands-on experience in IQ/OQ/PQ validation to drive continuous improvement and supplier quality across surgical and tissue technologies divisions. The role requires...
- ...Responsibilities Apply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures,... ..., and Excel spreadsheet validation. Bachelor's degree in Computer Science, Engineering, Biological Sciences, or a related field....
$104.8k - $192.2k
...wherever you want it to go. Join EY and help to build a better working world. We are seeking an experienced Identity Verification Engineer with hands-on expertise in 1Kosmos or Microsoft Verified ID Identity Platform , identity proofing, passwordless authentication,...For contractorsSummer holidayFlexible hours- As the Engineer - Industrial, you will be responsible for supporting the Engineering team in driving operational efficiency, labor productivity... ...improvement initiatives by embedding labor standards and validating performance against benchmarksAnalyze data to support labor...Immediate startWorldwideShift work
$95.6k - $130.6k
...Description BeOne Medicines is seeking highly motivated and organized engineer, to join our team at the Hopewell, NJ site. The successful... .... Provide SME input for the commissioning, qualification and validation of responsible systems. Develop and maintain technical,...Hourly payWork at officeLocal area- ...profilers. In addition, AID runs its own soils, asphalt, and concrete materials testing laboratory. Job Description The “Senior Engineer” position will involve performing engineering tasks, in the field, office, and lab, under the supervision of more senior engineers...Full timeWork at officeImmediate start
- ...Job Title : Test Engineer, Hardware Location: Cranbury, NJ Division: Photonics Department: OptoGration, Inc. About Us Quantum Computing Inc. (QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable...Local areaRemote work
$118k - $158k
...(MS&T) function is seeking a highly motivated Senior Process Engineer to be responsible for early and late stage AAV development, commercialization... ...transfer, process improvement implementation, process validation and technical support of late phase and commercial GMP...Full timeTemporary workLocal areaShift work$90k - $110k
...related issues and update business rules as needed. Conduct all other job-related activities.Supervision received: Senior Manager, Engineering.Qualifications & Skills Required:Minimum 3 years experience in a distribution center or similar industryAdvanced knowledge in...Full timeRemote work1 day per week- ...Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&... ...and Experience - Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute...For contractorsWorldwide
$28.76 - $38.48 per hour
...minimum of 2 to 4 years as a Maintenance Technician / Building Engineer or equivalent field experience required including working knowledge... ...hand tools, including but not limited to, a snow blower. • Valid driver’s license and satisfactory driving record when required....Contract workFor contractorsTraineeshipWork at officeLocal areaImmediate startShift workNight shiftWeekend work- RBC Bearings is a well-known international manufacturer and marketer of highly engineered precision plain, roller and ball bearings. We have been providing bearing solutions to our customers since 1919. Over the past ten years, under the leadership of our current management...Full time
$95k - $171k
..., Kubernetes, and ensuring reliability for AI workloads within Akamai's serverless inference platform. As an Site Reliability Engineer II, you will be responsible for: Building and maintaining dashboards, alerts, and monitoring for inference workloads using Akamai...Permanent employmentWork experience placementWork at officeRemote workWork from homeWorldwideFlexible hours$140k - $155k
...business by fusing threat intelligence, monitoring, detection engineering, and response into one proactive, intelligence-led defense capability... ...States of America), IFTECH202.2 - Middle Professional Tier II (EEO Job Group)SummaryLocation: New York, NY; Princeton, NJ;...Full timeSecond jobLive inWorldwideFlexible hours$75k - $100k
Electrical Engineer At Salas O'Brien we tell our clients that we're engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That's why we're committed to living our values every day: inspiring, achieving,...For contractorsLocal area$90k - $95k
...Job Description: The Automation Engineer will primarily support and troubleshoot plant automation systems, including but not limited to: Programmable Logic Controllers (PLCs) Human Machine Interfaces (HMIs) Servo systems and servo drives AC and DC...Permanent employmentFlexible hours$105k - $115k
...headquarters is located in Monroe Township, New Jersey and has an additional office in Richmond, California.The Role:The Manufacturing Engineer is responsible for the development, implementation and documentation of the manufacturing process. They will serve as the link...Work at officeLocal areaRemote work- ...Hope all is well, Please find the job description given below and let me know your interest. Position: Site Reliability Engineer II Location: Pennington, NJ | Onsite (2 Virtual Rounds | Onsite Interview May Be Requested) Contract: 12+ Months Contract...Contract work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Validation Engineer II. Be the first to apply!
Related searches
- process validation engineer
- analog mixed signal ams verification engineer
- hil validation engineer
- pharmaceutical validation engineer
- senior design verification engineer
- validation officer
- cleaning validation specialist
- software verification engineer
- senior validation engineer
- entry level verification engineer


