Associate Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing (Onsite)
$71.9k - $113.2kFull-time
Merck & Co.
Job Description Job Description: The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) Drug Product development and clinical manufacturing facility in Rahway, New Jersey.- This team works with non-sterile formulations, typically oral solid dosage (blending, roller compaction, encapsulation, tableting) including spray dried intermediates, liquid suspension/bottle fills, and autoinjector assembly. We are part of the research division, focusing on development and clinical deliveries in a GMP piloting facility supporting our Company's research division. The Oral Solids Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for an Associate Specialist - Process Engineer to lead clinical supply manufacturing, scientific rigor of processes, and ultimately to enable flexibility and speed of our Company's pipeline. This person will: • Lead on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
• Draft and execute GxP documentation including but not limited to batch records, equipment qualification and cleaning, change records and deviations.
• Build partnerships by developing and leveraging relationships within and across work groups of formulators, engineers, safety and quality representatives.
• Foster culture of collaboration, learning and innovation.
Required Experience and Skills: • Experience executing GxP manufacturing in pilot plant environment.
• Experience of interest in supporting electronic batch records and MES systems.
• Knowledge and experience of drug product processing.
• Desire and willingness to learn and contribute through independent problem-solving.
• Experience in leading and supporting quality investigations and change management.
Education Minimum Requirements: • Associate's degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related field with a minimum of 3 years relevant experience
• Bachelor's in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field.
• Master's degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field
Preferred Experience and Skills: • Knowledge of Investigational drug regulatory requirements
• Understanding of Clinical Supply Chain Operations
• Experience with Commissioning, Qualification and Validation
• Experience with spray dried intermediates and/or hot melt extrusion
#EBRG #VETjobs #FLEX Required Skills:
Driving Continuous Improvement, Engineering Standards, Equipment Qualification, Estimation and Planning, GMP Compliance, GMP Validation, Lean Manufacturing, Manufacturing Quality Control, Manufacturing Scale-Up, Process Control, Process Optimization, Teamwork Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement
• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is:
USA - New Jersey - Rahway Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is:
$71,900.00 - $113,200.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at . Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. Additional location(s) Compensation Information: San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- Employee Status:
Regular Relocation:
Domestic VISA Sponsorship:
No Travel Requirements:
10% Flexible Work Arrangements:
Not Applicable Shift:
Not Indicated Valid Driving License:
No Hazardous Material(s):
Acetone, Iso-Propyl Alcohol Job Posting End Date:
11/6/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R423989
• Draft and execute GxP documentation including but not limited to batch records, equipment qualification and cleaning, change records and deviations.
• Build partnerships by developing and leveraging relationships within and across work groups of formulators, engineers, safety and quality representatives.
• Foster culture of collaboration, learning and innovation.
Required Experience and Skills: • Experience executing GxP manufacturing in pilot plant environment.
• Experience of interest in supporting electronic batch records and MES systems.
• Knowledge and experience of drug product processing.
• Desire and willingness to learn and contribute through independent problem-solving.
• Experience in leading and supporting quality investigations and change management.
Education Minimum Requirements: • Associate's degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related field with a minimum of 3 years relevant experience
• Bachelor's in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field.
• Master's degree in chemical engineering, Chemistry, Pharmaceutical Sciences or related scientific field
Preferred Experience and Skills: • Knowledge of Investigational drug regulatory requirements
• Understanding of Clinical Supply Chain Operations
• Experience with Commissioning, Qualification and Validation
• Experience with spray dried intermediates and/or hot melt extrusion
#EBRG #VETjobs #FLEX Required Skills:
Driving Continuous Improvement, Engineering Standards, Equipment Qualification, Estimation and Planning, GMP Compliance, GMP Validation, Lean Manufacturing, Manufacturing Quality Control, Manufacturing Scale-Up, Process Control, Process Optimization, Teamwork Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement
• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The primary location for this posting is:
USA - New Jersey - Rahway Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is:
$71,900.00 - $113,200.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at . Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. Additional location(s) Compensation Information: San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- Employee Status:
Regular Relocation:
Domestic VISA Sponsorship:
No Travel Requirements:
10% Flexible Work Arrangements:
Not Applicable Shift:
Not Indicated Valid Driving License:
No Hazardous Material(s):
Acetone, Iso-Propyl Alcohol Job Posting End Date:
11/6/2026
*A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R423989
Vacancy posted 5 hours ago
Similar jobs that could be interesting for youBased on the Associate Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing (Onsite) in Rahway, NJ vacancy
$71.9k - $113.2k
...is a GMP (Good Manufacturing Practices)... ...Small Molecule Process Research and Development... ...Operations Specialist will provide... ...(API) for clinical use and drug product... ...: - Associate in Science, Associate... ...the year. Onsite presence is... ..., Shift Work, Solids Handling Preferred...SuggestedFull timeFor contractorsCasual workLocal areaRelocationVisa sponsorshipFlexible hoursShift workRotating shiftDay shiftAfternoon shift$30.6 - $35.6 per hour
...are seeking an Associate Scientist to support oral solid dosage formulation development... ...studies, batch processing, data analysis,... ...and/or manufacturing work and 10%–20%... ...arrangement: 100% onsite; Schedule: Monday... ...chemistry, science, engineering, or a related discipline...SuggestedHourly payContract workFor contractorsWork experience placementWork at officeVisa sponsorshipMonday to Friday$71.9k - $113.2k
...Product development and Good Manufacturing Practice (GMP) clinical manufacturing plant in... ...with the formulators, engineers, Quality... ...scientific rigor of the processes, and ultimately to enable... ...motivated candidates for Associate Specialist positions within the Operations...SuggestedFor contractorsInternshipWork at officeFlexible hours$65.1k - $102.5k
Associate Specialist, Packaging Summary:- Global Clinical Supply Operations (CSO) is seeking a motivated... ...of areas and processes to identify opportunities... ...operations management, engineering, supply chain, or related... ...Continuous Improvement, Good Manufacturing Practices (GMP),...SuggestedFor contractorsWork at officeLocal areaRelocationVisa sponsorshipFlexible hoursShift work$71.9k - $113.2k
...direction of the applicable management, the Clinical Data Manager (CDM) is responsible for... ...key performance indicators according to process expectations at the protocol level.- Monitors... ...planning and time management.- Fluent oral and written English skills.- Good sense...SuggestedFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work$71.9k - $113.2k
...Activities: Assumes the responsibilities for all clinical programming (including reporting and... ...SAS, etc. along with AI related tools. Solid knowledge of MS Windows/Office software... ...skills. Desire and ability to learn new processes and technologies Ability to multi-task,...For contractorsSecond jobLocal areaRelocationVisa sponsorshipFlexible hoursShift work$65.1k - $102.5k
...Merck's Global Clinical Supply Operations seeks an Associate Specialist to support clinical supply packaging operations. The role involves coordinating with... ...Requirements Bachelor's degree in operations management, engineering, supply chain, or related technical field One...Work at office$65.1k - $102.5k
...Job Description Associate Specialist, Packaging Summary:- Global Clinical Supply Operations (CSO... ...walkthroughs of areas and processes to identify... ...operations management, engineering, supply chain, or related... ...Continuous Improvement, Good Manufacturing Practices (GMP),...Full timeFor contractorsWork at officeLocal areaRelocationVisa sponsorshipFlexible hoursShift work$71.9k - $113.2k
...Merck seeks an Associate Specialist in Engineering for a new sterile clinical manufacturing facility in New Jersey. The role combines hands-on manufacturing operations... ...technical support for equipment commissioning, process development, and regulatory readiness during facility...Work at officeAfternoon shift$10k
...Summary: The Chemical Engineering Research & Development department... ...seeking an engineering associate specialist for the Equipment... ...Substance development and GMP clinical manufacturing facilities located in... ...facility compliance, new processing technologies, and production...Full timeFor contractorsWork at officeLocal areaRelocationVisa sponsorshipFlexible hoursShift work$71.9k - $113.2k
...Merck's Chemical Engineering R&D department seeks an engineering associate specialist to support API Development facilities... ...substance development and GMP clinical manufacturing labs. Responsibilities... ...knowledge ~ Proficiency with process flow diagrams and mechanical...Work at office$117k - $184.2k
...Plant is a Good Manufacturing Practices (GMP) facility... ...within the Process Research and Development... ...scale-up of clinical supplies... ...degree in Chemical Engineering, Materials Science... ...manufacturing facility - OR- Associates degree with at... ...the year. Onsite presence is required...Contract workFor contractorsCasual workLocal areaRelocationVisa sponsorshipFlexible hoursShift workRotating shiftDay shiftAfternoon shift$71.9k - $113.2k
...within the Chemical Engineering Research &... ...MACS Operations Specialist position will report to the Associate Director, Engineering... ...development and GMP clinical manufacturing plant under... ...the Small Molecule Process Research & Development... ...weekly.- Onsite presence is required...Full timeFor contractorsWork experience placementCasual workLocal areaRelocationVisa sponsorshipFlexible hoursShift workRotating shiftDay shiftAfternoon shift$87.3k - $137.4k
...the Chemical Engineering Research & Development... .... The Specialist - Automation Engineer... ...systems and associated IT-OT... ...Small Molecule Process Research & Development... ...of clinical and research materials... ...SSO is a Good Manufacturing Practice (GMP)... ...along with a solid working knowledge...Full timeFor contractorsWork at officeLocal areaRelocationVisa sponsorshipFlexible hoursShift work$87.3k - $137.4k
...Job Description This Engineer position provides on-... ...filling activities for clinical, stability, and developmental supplies for Oral Solid Dosage (OSD) products, including process development, scale-up,... ...facility, utilities, and manufacturing equipment in compliance...Full timeFor contractorsLocal areaRelocationVisa sponsorshipMonday to FridayFlexible hoursShift workAfternoon shift$71.9k - $113.2k
...Associate Specialist supporting daily production activities in a GMP-regulated pilot... ...small-molecule pharmaceutical manufacturing. Responsibilities include batch processing, equipment operation, process... ...first and second shift, onsite five days weekly Pilot plant...Work at officeRotating shiftAfternoon shift$71.9k - $113.2k
...Rahway, New Jersey seeks Associate Specialists for Technical Operations... ...involves supporting sterile clinical manufacturing startup, equipment... ...support for formulation, process development, scale-up, and... ...Bachelor's degree in engineering, chemistry, biological sciences...Work at officeFlexible hours$142.4k - $224.1k
...Position Title (Short Title): Associate Principal Scientist... ...Department: Translational Medicine, Clinical Operations Brief Description... .../biomarker collection processes. Represents Early-Stage... ...Effective communication (written and oral), problem solving and...Full timeFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- ...enthusiastic and experienced leaders in Process Engineering to support exciting GMP Drug Substance... ...in pharmaceutical or biotech manufacturing industry with a preference for experience... ...closure with teams. Location: Rahway, NJ Onsite Requirements: This is an onsite role....Full timeTemporary workFor contractors
$112k - $179k
...candidate to work closely with engineering, scientific and technical... ...role is focused primarily on process control and plant interfaces... ...reviews for design, and manufacture. Review design document packages... ...Ability to be onsite five days a week when required...Contract workShift work- Merck & Co. in Rahway, NJ is seeking a qualified SSO Process Supervisor to oversee daily GMP production in the Small Scale Organics pilot... ...teams to meet SSO objectives and customer requirements. Onsite five days a week with potential overtime. #J-18808-Ljbffr Merck...
$94.1k - $129.4k
...Johns Manville is a leading manufacturer and marketer of premium-... ...bonus. The purpose of the Process Engineer's role will be to provide technical... ...In collaboration with the specialists at JMTC, process modeling... ...climbing, etc.#LI-KL1 #LI-ONSITE #P #DPlease Keep in Mind If...Full timeTemporary workFlexible hours$88.9k - $139.7k
...Summary Qnity is seeking a Process Engineer. This individual will be... ...for supporting Polyimide manufacturing operations within a batch production... .... This is a 100% onsite position located in our... ...qualifications. Each role has an associated pay range (or an...Work at office- ...Process Engineer Orion Innovation is a premier, award-winning, global business and technology services firm. Orion delivers game-changing business transformation and product development rooted in digital strategy, experience design, and engineering, with a unique combination...
- Merck & Co. in Rahway, New Jersey, seeks a Senior Specialist to lead process design, execution and startup for Small Molecule High Potency/API/Containment projects. The role focuses on capital project delivery within GES and exposure to multiple business areas, including...
- Merck in Rahway, NJ is seeking a Senior Specialist in Process Design, Execution and Startup for Small Molecule HPAPI containment projects. You... ...and regulatory compliance, and collaborate with IPT, Engineering Firms, and Vendors to deliver end-to-end solutions. The role...
- ...insurance ~ Paid time off Process Engineer II - EDI Edison, New... ...In collaboration with the specialists at JMTC, process modeling... ...flexibility to address urgent manufacturing challenges. May be... ...innovation and adaptability Solid project management skills...Full time
- Position Title: Associate Specialist, Value Stream Cryo Operations Department... ..., storage, control of manufacturing patient materials, and support... ...to identify and implement process efficiencies. Maintaining... ...biology, chemistry, medical or clinical practices is a plus. #J-18...Shift workDay shift
- Parexel is seeking a Scientist II or III - Metrology Specialist for a full-time, long-term assignment onsite at a client site in Rahway, NJ. The role requires GMP lab experience and hands-on work with HPLC, GC, UV-Vis, and dissolution systems, as well as SOP development...Full time
- Synerfac Inc. is seeking a Technical Support Engineer for the Energy/Utilities sector in Union, NJ. This onsite role supports power metering, energy management, and related systems, working Mon-Fri, 9am-5pm, with a focus on rapid issue resolution and customer satisfaction...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing (Onsite). Be the first to apply!
Related searches
- recruiting associate Rahway, NJ
- trading associate Rahway, NJ
- cleaning associate Rahway, NJ
- drug safety associate Rahway, NJ
- transportation associate Rahway, NJ
- general maintenance associate Rahway, NJ
- call center associate Rahway, NJ
- psychology associate Rahway, NJ
- credit associate Rahway, NJ
- associates biology Rahway, NJ


