Process Engineer - Validation, Optimization & SOPs
$65k - $75kAmneal Pharmaceuticals LLC (J0P)
Description: The Process Engineer provides support to the operation Manager/Associate Director Operation/ Engineering in implementing improvements, validation and automation to the plant operations and assist in several functions such as writing standard operating procedures (SOPs), develop process flow, review design documents related to procurement of new equipment. Help with equipment validation. Essential Functions: Support process/validation engineer; for plant operations to suggest and implement improvements; for new manufacturing processes through process and equipment validation. This entails completing process simulations and optimization studies and implementing modifications and process installations at the manufacturing level Support day-to-day manufacturing operations by monitoring process performance and identifying improvement opportunities. Assist in process optimization to improve yield, efficiency, quality, and equipment reliability. Analyze manufacturing data using statistical and analytical tools to drive data-based decision making Help prepare and update Standard Operating Procedures (SOPs) and help execute equipment installation and operational qualifications, validation protocols, reports, and change controls. Supports technical services by troubleshooting activities in the operation department. Protocol review and Development process Help generate reports, charts, and tables based on established statistical methods to drive process enhancements. Investigate process deviations and non-conformances; perform root cause analysis (RCA) and support CAPA implementation. Assist process/validation engineer evaluate, improve and validate current manufacturing practices or processes and equipment’s with an effort for continuous improvement towards productivity, quality, reliability and consistency. Provide support on various manufacturing/engineering equipment uptime. Ensure compliance with FDA regulations, cGMP requirements, and internal quality standards. Collaborate with cross-functional teams to support continuous improvement initiatives and regulatory readiness. Communicate with vendors on possibility of material improvement. Additional Responsibilities: Other duties that management may from time to time assign Write deviation and CAPA (Corrective action and preventive action Assist review of process related documents Day Shift – 12-hour per day, rotating schedule (6:00am-6:30pm) 3 days on week 1 and 4 days on week 2 of pay cycle Education: Bachelors Degree (BA/BS) Engineering, Pharmaceutics, Industrial Pharmacy, or related field plus 3 years of experience in Industrial Pharmacy or Engineering in lieu of the Master’s degree. Master's degree in Engineering is preferable. - Required Master Degree (MS/MA) Engineering, Pharmaceutics, Industrial Pharmacy, or related field. - Preferred Experience: 3 years or more in Engineering, Pharmaceutics, Industrial Pharmacy, or related field plus 3 years of experience in Industrial Pharmacy or Engineering in lieu of the Master’s degree. no experience in Engineering, Pharmaceutics, Industrial Pharmacy, or related field plus 3 years of experience in Industrial Pharmacy or Engineering in lieu of the Master’s degree. he base salary for this position ranges from $65000 to $75000 per year. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities. Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws. #J-18808-Ljbffr Amneal Pharmaceuticals LLC (J0P)
$95.41k - $143.11k
MacDermid Alpha Electronics Solutions in Piscataway Township, New Jersey, is seeking an Engineer to optimize chemical processes within the Global Process Engineering Group. The ideal candidate will have at least 5 years of experience in chemical process development and...Suggested- A manufacturer of industrial equipment in Central New Jersey is seeking a Process Engineer to design, optimize, and maintain manufacturing processes. The ideal candidate will have a Bachelor's degree in Chemical Engineering and 6-10 years of experience in a relevant industrial...Suggested
$94.1k - $129.4k
...Process Engineer Edison NJ R26_0836 Full time Who We Are Johns Manville is... ...quality for the process, leading process optimization and equipment reliability. Your Day... ...management tools (e.g., set up sheets in MII, SOP's …) Actively support improvement of...SuggestedFull timeTemporary workFlexible hours- Amneal is looking for a Process Engineer to plan and execute process and cleaning validation assignments in Piscataway Township, New Jersey. The role requires a sound understanding of pharmaceutical engineering principles and the ability to manage multiple projects effectively...Suggested
- ...Mixers in Central New Jersey is seeking a Process Engineer. We are seeking a Process Engineer... ...candidate will be responsible for the design, optimization, and maintenance of our manufacturing... ..., standard operating procedures (SOPs) etc. Ensure processes comply with industry...Suggested
- Associate Process Engineer/Scientist- Drug Product, Biologics Manufacturing Science and Technology... ...Responsible for characterizing, optimizing and troubleshooting product and manufacturing... ..., specifications, process validations and launch. Provide assistance to sites...
$109k - $164k
...Revolutionizing wafer fabrication processes for enhanced efficiency and... ...Advanced Materials and Joining - Engineering polymer and metal joining solutions for optimally performing circuits Film &... ...support pilot studies, process validation, and troubleshooting Optimize...Local areaWorldwide- ...Description Objective The Process Engineer will provide technical... ...assess, and execute projects to optimize existing processes, raw materials... .... Write and execute validation protocols either acting as the... ...Operating Procedures (SOPs), Batch Records, Work Instructions...Temporary workPart timeLocal areaImmediate startRemote workRelocation
- ...The Process Engineer Intern is expected to support the director of process engineering to manage and lead process engineers to support day... ...technical support to engineers to drive the progress on all optimization and development projects as needed. Plan and execute new...Internship
- ...Job Description Job Description The Process Engineer I ensures manufacturing processes are... ...enhance process understanding, enable validation, and ensure manufacturing consistency.... .... Assist in developing and optimizing tooling and manufacturing processes to...
- Gemco is seeking a Process Engineer in Middlesex, New Jersey, to optimize manufacturing processes and ensure regulatory compliance. The ideal candidate will have a Bachelor's degree in mechanical or chemical engineering and at least 5 years of relevant experience. Key...
- ...Job Description Job Description Process Engineer Reports to: Process Improvement Engineering... ...shift (3 PM - 11 PM) to ensure optimal performance of processes, effective support... ...(NPI) activities, including process validation, work instruction development, and ramp...Work at officeShift workAfternoon shift
- Validation Engineer**Who You’ll Work With**You will join one of our 45 offices in the US, be part... ...assist in the design of manufacturing processes, help manage projects, develop facilities... ...environments* Authoring CAPA's, deviations, SOP's is a plus* Strong technical writing...Work at officeFlexible hours
- ...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,...Full timeImmediate start
- Job Position Summary Process Engineer is responsible for the process design, operation, and implementation of manufacturing operations. You... ...Safety culture and wear PPE when required. Create, configure, and optimize manufacturing processes from inception through start up to...Work at office
- A leading technology services company is looking for an Associate Process Engineer/Scientist specializing in Drug Product within Biologics Manufacturing. Responsibilities include executing process changes, troubleshooting manufacturing processes, and serving as a technical...
- ...to ask for an accommodation or an alternative application process. Process Engineer Reg Full Time 6 Technical New Jersey, Somerville, NJ, US 3... ...regulatory/environmental requirements. Develop, configure and optimize industrial processes from inception through to start up...Full timeFlexible hours
- ...Technologies LLC is seeking a Quality/Validation Engineer with hands‑on expertise in GxP‑regulated... ...regulations and Computer System Validation (CSV) processes. Lead and manage validation activities... ...review Standard Operating Procedures (SOPs) and Work Instructions (WIs) for...Full time
- ...rigorous approach, field-tested processes, and elite expertise... ...Commissioning, Qualification, and Validation (CQV) activities with a strong... ...related documents, including SOPs, master plans, and execution... ...Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences...For contractorsWorldwide
- ...Job Description We are seeking a Senior Validation Engineer with solid hands-on validation... ...lifecycle activities across all manufacturing process streams, but also have the ability to apply... ...impact assessments, summary reports, SOPs and other technical documents. This...Contract workFor contractorsFlexible hours
$127.31k - $167.1k
...myeloma. Legend Biotech is seeking a Sr. QA Validation Specialist, CSV & Equipment as part of... ..., systems, computer systems, and processes within a cell therapy manufacturing plant... ...Site. Review and approve change controls, SOPs, non‑conformances, and CAPAs associated...Permanent employmentFull timeTemporary workFor contractorsWork experience placementWork at officeLocal areaWorldwideFlexible hours$93.46k - $122.67k
Job Overview QA Validation Specialist III role at BioSpace, based in Raritan, NJ. Exempt level... ..., systems, computer systems, and processes within a cell therapy manufacturing plant... ...Raritan Site. Approve change controls, SOPs, non‑conformances, and CAPAs associated...Work at officeFlexible hours$109k - $164k
Element Solutions is looking for a Senior Process Engineer in Piscataway Township, NJ. The ideal candidate will focus on chemical process... ...requiring 11+ years of experience. Responsibilities include process optimization and cross-functional collaboration. This position offers a...- ...standards and precision-driven processes. Key Responsibilities:... ...deploy process enhancements to optimize yield and reduce production... ...sites to perform detailed engineering audits and collaborate on developing... ..., including process validation, work instruction development...
- ...preparing documentation for all aspects of the computer system validation life cycle. Design, deliver, support and maintain GxP... .... Qualifications Master’s degree in Science, Technology, or Engineering (any) with 1 year of experience in the job offered or related...
- ...innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly... ...directly from customers Lead Master Validation Plan creation in order to support PPQ... ...development and review of relevant SOPs for manufacturing operations and...Flexible hours
$90k - $100k
...Automation Engineer The Automation Engineer is responsible for overseeing and optimizing automation systems to improve production efficiency... ...upstream and downstream processing equipment, including Mixers... ..., qualification and validation of digital process automation...Full timeTemporary workLocal areaFlexible hours$90k - $210k
...are seeking an Automation Engineer to support the development, validation, and day-to-day... ...transferring, scaling, and optimizing automated QC test methods... ..., and robust end-to-end processes for high-throughput QC testing... ...Operating Procedures (SOPs), documentation, and...Flexible hours- Energy Jobline ZR is looking for a Process Engineer in Westfield, New Jersey. This role involves improving manufacturing processes, ensuring safety, and creating optimized process documentation. Candidates should have an associate degree in a related field and relevant...
- ...The Automation Engineer is responsible for designing, implementing... ...Programs, debugs, and optimizes robotic and automated systems... ...development and execution of IQ/OQ/PQ validation activities to ensure systems... ..., repeatable manufacturing processes that meet defined run rates,...
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