Associate Process Engineer - Manufacturing & Validation
$65k - $85kMerck
Merck & Co. is seeking an Associate Process Engineer to support plant operations in Piscataway Township, NJ. The role focuses on improving processes and ensuring compliance with regulatory standards, requiring a Bachelor's degree in Engineering or a related field and relevant experience. The ideal candidate will have a robust understanding of process optimization and quality assurance, with 3 years of experience in Industrial Pharmacy or Engineering. The position offers a competitive salary ranging from $65,000 to $85,000 annually, alongside a comprehensive benefits package. #J-18808-Ljbffr Merck & Co.
$80k - $90k
Merck & Co. is seeking a Process Engineer to report to the Manager of Technical Services. The... ...candidate will execute and manage cleaning validation and post-approval projects, working... ...of experience in the Pharmaceutical/Manufacturing Industry. Strong verbal and written communication...Suggested$80k - $90k
Description Process Engineer reports to the Manager of Technical Services and plans, executes... ...functionally directs Process/Cleaning Validation/Study assignments and projects, which... ...Prepare validation protocols & reports for manufacturing process and cleaning process...SuggestedFlexible hours$65k - $85k
Description: The Associate Process Engineer provides support to the operation Manager/Associate Director... ...in implementing improvements, validation and automation to the plant operations... ...and implement improvements; for new manufacturing processes through process and...SuggestedLocal areaFlexible hoursWeekend workDay shift3 days per week1 day per week$65k - $85k
Amneal Pharmaceuticals LLC is seeking an Associate Process Engineer in Piscataway Township, NJ. This role involves supporting the operation manager with improvements, validation, and automation in plant operations. Key tasks include writing SOPs, running process optimization...SuggestedDay shift- ...in electrified and internal combustion engine (ICE) powertrains, ensuring the delivery... ...solving. This role is responsible for the validation of production powertrain control modules... ...improvements in testing strategies and processes, including requirements traceability,...SuggestedFull timeImmediate start
- MEDVACON in Edison, New Jersey is seeking contractors for cGMP Quality Compliance Validation roles in a pharmaceutical setting. The company collaborates with leading pharmaceutical firms and offers positions available for W2 or direct 1099. Candidates with prior consulting...Permanent employmentContract workFor contractorsRemote work
- ...for all aspects of the computer system validation life cycle. Design, deliver, support and... ...systems and security of the associated data. Create and review validation plans... ...Master’s degree in Science, Technology, or Engineering (any) with 1 year of experience in the...
- ...regulatory compliance across the product lifecycle. This hybrid role involves managing the GxP IT Quality Assurance program, reviewing validation deliverables, and supporting inspections. Ideal candidates will have a strong background in the BioTech or Pharmaceutical...
$120k
...Validation Specialist Legend Biotech is a global... ...and address deviations associated with those activities... ...changes. Control Aseptic process validation and... ...process needs defined by Manufacturing or Tech Support.... ...rationales, and approval for engineering and process changes...Local areaWorldwide- Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology Key responsibilities Execution of post-market process change activities... ..., manufacturing, specifications, process validations and launch. Provide assistance to sites...
$109k - $164k
...looking for? We are seeking an experienced Process Engineer with deep expertise in chemical... ...efficient, cost‑effective, and high‑quality manufacturing processes while supporting continuous... ...and support pilot studies, process validation, and troubleshooting Optimize processes...Local area- ...mindset for computer system validation for GMP, GDP, GLP space. Regulatory... ...and coordinate activities associated with the GxP IT Quality... ...Development Life Cycle (SDLC) process such as incident, problem,... ...applications as well as commercial manufacturing processes. Good...Local area
- Katalyst CRO is looking for a CSV Consultant in Raritan, NJ to support system validation activities in a regulated environment. The consultant will ensure compliance with FDA guidelines, contribute to validation documentation, and work within the System Development Lifecycle...
- ...rigorous approach, field-tested processes, and elite expertise... ...Commissioning, Qualification, and Validation (CQV) activities with a... ...’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences... ...experience in a GMP (Good Manufacturing Practice) environment - Outstanding...For contractorsWorldwide
- ...Description We are seeking a Senior Validation Engineer with solid hands-on validation experience... ...for execution activities for QC and Manufacturing equipment. In addition to many of the... ...lifecycle activities across all manufacturing process streams, but also have the ability to...Contract workFor contractorsFlexible hours
- Initial Therapeutics, Inc. is looking for a Validation Specialist to execute site validation activities and ensure compliance... .... You will oversee equipment qualifications, manage manufacturing controls, and support process validation in a dynamic biopharma environment. The...
- Creative Solutions Services, LLC is seeking a qualified candidate for a role focusing on validation in the pharmaceutical industry. Candidates should have over 3 years of experience in Computer System Validation and a strong background in FDA regulations. The position...
- A growing consulting firm in New Jersey is seeking a Validation Engineer II to develop and execute validation documents and assist in FDA compliance... ..., along with at least 3 years of experience in validation processes within pharmaceutical or medical device sectors. Collaborate...
- Piper Companies is seeking an experienced CQV Validation Engineer in Raritan, NJ, to assist with the IQ/OQ/PQ of new instruments/equipment. This role involves developing validation protocols, conducting testing, and providing technical support to ensure compliance with...
- ...into new sectors and steadily grow. Job Description Responsibilities: Investigates and troubleshoots validation problems for equipment and/or performance processes and conducts equipment qualification activities. Conducts analyses of testing results and process anomalies...
- ...currently looking for an experienced CQV Validation Engineer in Raritan, NJ to work for an... ...new instruments/equipment in support of manufacturing operations. Responsibilities for the... ...Experience with IQ/OQ/PQ protocols, process validation, and risk assessment. Excellent...
- Validation Engineer**Who You’ll Work With**You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals... ...clients across the country to assist in the design of manufacturing processes, help manage projects, develop facilities, and impact...Work at officeFlexible hours
$50 - $55 per hour
...Role: Life Sciences : Computer System Validation Engineer Location: Raritan, NJ- Onsite Experience: 8 & Above Duration: 12+ Months... ...Computer System Validation (CSV)Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience...$20 per hour
...Mental Health Associate - Full-Time / Part-Time / Per-Diem Somerset, NJ ( Description The Center for Great Expectations (CGE) offers... ...role, candidates must be at least 21 years old and possess a valid driver’s license. This position is ideal for individuals who...Daily paidFull timePart timeFlexible hoursShift workNight shiftWeekend workDay shift$20.45 - $30.7 per hour
...opportunity for a portable sanitation Equipment Associate ready to grow their career with the... ...High School Diploma or equivalency A valid driver's license Diligent attention to... ...accommodation at any point of the application process, please email ****@*****.*** for...Hourly payFlexible hours$65k
...of Love Veterinary Hospice! Join Lap of Love as an In-Home, Associate Veterinarian in the Central New Jersey area. Imagine a veterinary... ...Doctor of Veterinary Medicine (DVM/VMD/BVMS) Must possess a valid U.S. driver's license Availability to work some weekends...Full timeTemporary workPart timeFlexible hoursWeekend work2 days per week$93.46k - $122.67k
Job Overview QA Validation Specialist III role at BioSpace, based in Raritan,... ..., systems, computer systems, and processes within a cell therapy manufacturing plant in a sterile GMP environment... ..., non‑conformances, and CAPAs associated with qualification/validation execution...Work at officeFlexible hours$62.23k - $75.56k
...assessment, and public policy. Postdoctoral Associate (2) positions will investigate how... ...environmental nanoparticles influence disease processes. Posting Summary Position:... ...publications. Experience in developing and validating advanced cellular models such as induced...Full timeDay shift$60.01k - $65k
...seeking a motivated and resourceful Project Associate to actively contribute to successful... ...efficiency programs. They perform a variety of processing activities in support of energy... ...information from contractors and customers. They validate contractor/customer reports to ensure...Full timeContract workPart timeFor contractorsWork experience placementWork at officeLocal areaFlexible hours- ...A leading technology organization in Raritan, New Jersey, seeks a skilled professional to document software and validate specifications for lab instrumentation. Key tasks include gathering requirements, creating infrastructure and data flow diagrams, and performing risk...
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