Test Engineer - Manufacturing

19968 Milton, Delaware US Tech Solutions

Posted 1 day ago

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Job Description

**Internal ID:** ** **
Job Title: Test Engineer - Manufacturing
**Job Summary:**
As a Test Engineer in the manufacturing sector, you will play a crucial role in ensuring the quality and reliability of products through the development and implementation of effective testing processes. You will collaborate with cross-functional teams, including design, production, and quality assurance, to optimize testing methodologies and contribute to the continuous improvement of manufacturing processes.
**Responsibilities:**
1. **Test Planning and Strategy:**
2. Develop and implement comprehensive test plans for manufacturing processes.
3. Collaborate with design and production teams to understand product specifications and requirements.
4. **Test System Development:**
5. Design, develop, and maintain test systems and equipment to ensure accuracy and efficiency in the manufacturing testing process.
6. Integrate testing processes into the overall production workflow.
7. **Test Execution:**
8. Perform testing activities on manufactured products, ensuring adherence to quality standards and specifications.
9. Troubleshoot and resolve any issues encountered during the testing phase.
10. **Data Analysis and Reporting:**
11. Collect, analyze, and interpret test data to identify trends, patterns, and areas for improvement.
12. Prepare and present comprehensive reports on test results and findings.
13. **Collaboration:**
14. Work closely with cross-functional teams, including design, production, and quality assurance, to address testing requirements and challenges.
15. Participate in design reviews to provide input on testability and manufacturability.
16. **Continuous Improvement:**
17. Identify opportunities for process improvements and efficiency gains in the manufacturing testing phase.
18. Implement changes and updates to testing processes based on lessons learned and feedback.
19. **Documentation:**
20. Maintain accurate and up-to-date documentation of test procedures, equipment, and results.
21. Ensure compliance with regulatory standards and industry best practices.
22. **Quality Assurance:**
23. Contribute to the development and maintenance of quality standards for manufacturing processes.
24. Collaborate with the quality assurance team to address and rectify any non-conformities.
**Qualifications:**
+ Bachelor's degree in Electrical Engineering, Mechanical Engineering, or a related field.
+ Proven experience in test engineering within a manufacturing environment.
+ Strong knowledge of testing methodologies, equipment, and tools.
+ Familiarity with relevant industry standards and regulations.
+ Excellent problem-solving and troubleshooting skills.
+ Effective communication and collaboration skills.
+ Detail-oriented with a focus on accuracy and precision.
+ Ability to work independently and as part of a team.
**Preferred Qualifications:**
+ Master's degree in Electrical Engineering, Mechanical Engineering, or a related field.
+ Professional certifications related to test engineering and manufacturing.
+ Experience with automated testing systems.
+ Familiarity with Six Sigma or other process improvement methodologies.
**Note: This job description is not exhaustive and may be subject to change at the discretion of the employer.**
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Flexible Circuit Manufacturing Technician

19947 Georgetown, Delaware ZipRecruiter

Posted 8 days ago

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Job Description

Job DescriptionJob Description Flexible Circuit Manufacturing Technician

Shift: This opening is for a 2nd shift position only (swing shift).

What your 2nd-shift day looks like

You arrive ready to build high-conductance flexible circuits and intelligent wiring systems that power our customers' products. You review the work order, set up your station, and dial in the equipment to meet exacting customer specs. Throughout the shift, you inspect incoming materials, load them onto the machines, and keep a close eye on quality—performing basic checks and testing finished goods and packaging prior to shipment.

When something seems off, you pause the process, notify a lead or supervisor, and help troubleshoot. You keep production moving safely by operating electric and manual pallet jacks and other fixed or safety-sensitive equipment. Between batches, you prepare materials with safety knives, scissors, and tweezers, maintain accurate job-time and inventory entries in company systems, and move WIP efficiently between stations, onto carriers, and onto mobile racks. You don't leave a mess behind—your area stays clean, orderly, and compliant with safety procedures. Throughout the shift you contribute ideas to improve efficiency and recommend process tweaks to your supervisor.

What you'll do

  • Read work orders; set up, run, and reset production equipment to meet customer requirements and internal quality standards.
  • Inspect raw materials; prepare product using safety knives, scissors, and tweezers; carry out basic quality checks and testing of product and packaging before shipment.
  • Escalate equipment failures or process issues to leads/supervisors; recommend process improvements.
  • Locate, stock, build, and manage WIP; load/unload materials to and from fixed equipment, carriers, and mobile racks; move WIP safely across the line; prepare outbound shipments.
  • Operate safety-sensitive and heavy equipment including electric/manual pallet jacks and fixed machinery.
  • Perform system tracking activities per customer and departmental guidelines; enter accurate job time and inventory data.
  • Identify and report defective materials or questionable conditions.
  • Report accidents, injuries, and unsafe conditions immediately to your supervisor or area lead.
  • Maintain a clean, orderly work area and follow prescribed safety regulations.
  • Support your teammates and pitch in wherever needed to meet goals.

What you bring

  • High school diploma or equivalent .
  • Previous production operations, material handling, or technician experience in manufacturing or warehouse settings (not required).
  • Comfort communicating in English, written and verbal.
  • 18+.
  • Punctual, professional, and solutions-oriented.
  • Able to notice process issues and respond to safety signals via sight, touch, or hearing.
  • Open to schedule flexibility (days, nights, weekends) as needed; available for overtime and short-notice schedule changes.

PPE

You may be required to wear PPE such as safety glasses, safety shoes, bump caps, gloves, hair nets, masks, and clean-room frocks while following all safety procedures.

Physical demands and environment

Physical Demands – Manufacturing Environment
Expect physically demanding work for extended periods, up to 12 hours per day. You will frequently use hands and fingers to handle tools and controls; stand, walk, sit, reach, push/pull; climb or balance; and stoop, kneel, crouch, or crawl for extended durations. You must be able to lift and move up to 35 lbs without assistance (including carrying 20 lbs up and down stairs). Vision needs include close, distance, , and peripheral vision, plus the ability to adjust focus.

Work Environment – Manufacturing/Shop Environment
Work in a shop setting with high noise from operating machines, moving equipment and machine parts, nuisance dust, and potential skin exposure to hazardous materials used during material prep.

Proficiencies

  • Material Handler Experience
  • Experience in a Manufacturing Environment

Compliance and classification Essential Duties and Responsibilities

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Minimum Qualifications (Knowledge, Skills and Abilities):

To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions.

Working Conditions/Hours:

Hourly/Non-Exempt- shift work

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Security Professional - Manufacturing Facility - Part Time

19947 Georgetown, Delaware Allied Universal

Posted 1 day ago

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Job Description

Allied Universal®, North America's leading security and facility services company, provides rewarding careers that give you a sense of purpose. While working in a dynamic, diverse, and inclusive workplace, you will be part of a team that fuels a culture that will reflect in our communities and customers we serve. We offer medical, dental, and vision coverage, life insurance, retirement plans, employee assistance programs, company discounts, perks, and more for most full-time positions!
As a **Security Professional - - Manufacturing Facility - Part Time** in **Georgetown, DE** , you will serve and safeguard clients in a range of industries such as Food/Beverage and more .
Join a leading team where flexibility meets opportunity. As a Part-Time Security Officer, you'll use our exclusive Claim a Shift platform to view and Pick up open shifts based on your availability-giving you the freedom to build a schedule that works for you, while gaining valuable site experience across various industries. Whether you're looking to supplement your income or take the first step toward a full-time role, this position offers unmatched access to hands-on experience and growth opportunities. As a Security Officer with Allied Universal at a leading food and beverage facility, you will play a key role in helping to maintain a secure environment by managing access control and monitoring the premises. Your responsibilities include conducting routine patrols, remaining visible to help deter security-related incidents, and assisting with the flow of personnel and visitors throughout the location. You will utilize your customer service skills to provide a welcoming experience while maintaining a focus on security-related protocols. This role offers the opportunity to work in a dynamic setting where teamwork, integrity, and a people-first approach are valued. Join our team and help create a positive and secure environment for everyone at the site.
**Position Type: Part Time**
**Pay Rate: $19.75 / Hour**
**Job Schedule:**
**Day** **Time**
Fri03:00 PM - 11:00 PM
Sat03:00 PM - 11:00 PM
Sun03:00 PM - 11:00 PM
**What You'll Do:**
+ Use our proprietary scheduling platform to claim open shifts at client sites
+ Support operations across a range of environments including commercial real estate, healthcare, and education
+ Receive site-specific training and guidance from experienced teams
+ Deliver consistent, professional security presence and customer service
+ Be ready to fill in at short notice when urgent needs arise
**Responsibilities:**
+ Monitor and control access to the location by verifying identification and credentials of individuals entering or exiting the premises.
+ Assist in implementing site-specific security-related procedures and protocols to help to deter unauthorized access.
+ Provide customer service by interacting with employees, visitors, and vendors in a professional and courteous manner.
+ Respond to incidents and critical situations in a calm, problem-solving manner, following established protocols.
+ Conduct regular and random patrols throughout the location, including production areas and perimeter, to observe for any unusual activity or potential security-related concerns.
+ Document and report all security-related incidents, observations, and actions taken according to Allied Universal and client site requirements.
+ Support emergency response activities as directed, including assisting with evacuations or other site-specific procedures as needed.
**What We're Looking For:**
+ Availability across various days and shifts
+ Reliability and ability to adapt to different post assignments
+ A desire to gain broad experience and grow within the company
+ Interest in transitioning into full-time roles when available
**Minimum Requirements:**
+ Customer service experience is preferred.
+ Loss prevention experience is preferred.
+ Comfortable using a computer or tablet is preferred.
+ Access control or badge experience is preferred.
+ A valid Guard Card or license is preferred.
+ Be at least 18 years of age for unarmed roles; 21 plus years of age for armed roles.
+ Possess a high school diploma or equivalent.
+ As a condition of employment, applicants will be subject to a background investigation in accordance with all federal, state, and local laws.
+ Allied Universal will consider qualified applications with criminal histories in a manner consistent with applicable laws.
+ As a condition of employment, applicants will be subject to a drug screen to the extent permitted by law.
+ Licensing requirements are subject to state and/or local laws and regulations and may be required prior to employment.
+ A valid driver's license will be required for driving positions only.
**Why Join Us:**
+ Flexible Scheduling: Choose from a variety of open shifts that align with your availability and lifestyle.
+ Career Growth: Clear path to full-time roles and ongoing advancement through paid training programs.
+ Smart Tools: Access exclusive technology for real-time shift visibility and claiming.
+ Full-Time Benefits: Health insurance, 401(k) plans, and a comprehensive benefits package for full-time employees.
+ Employee Perks: Enjoy discounts at restaurants, entertainment venues, and more through our perks program.
**Allied Universal® is an Equal Opportunity Employer.** All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: .
If you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: .
**Allied Universal® is an Equal Opportunity Employer.** All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: .
If you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: .
**Job ID:**
**Location:** United States-Delaware-Georgetown
**Job Category:** Security Officer, Part Time Security
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Associate Director, Integrated Process Team (IPT) Lead - Millsboro, DE (Animal Health, Global Man...

19966 Millsboro, Delaware Merck

Posted 1 day ago

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Job Description

**Job Description**
Join our Millsboro Senior Leadership team and lead a high-impact Integrated Process Team that directly influences site performance, product quality and cost-of-goods for life-changing animal vaccines. Your leadership will shape manufacturing systems and release processes that enable reliable, efficient vaccine production at scale. If you are a people-first leader with deep technical experience in aseptic filling and vaccine production, this is an opportunity to drive operational excellence, develop teams, and deliver measurable results.
**What you own:**
+ Lead and grow the Integrated Process Team (IPT) - coach managers and individual contributors, build capability, and create a high-performance, inclusive culture focused on continuous improvement.
+ Be accountable for IPT performance against site and division goals, including quality, safety, delivery, cost of goods, and budget forecasts.
+ Translate site strategy into IPT annual plans and priorities (hoshin kanri / scorecard) and drive execution using MPS/Lean principles and scientific problem solving.
+ Provide subject matter expertise for product release, aseptic operations, formulation and fill/finish activities.
+ Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits, inspections, validations and corrective actions.
+ Author, review and approve SOPs, Quality Notifications and technical documentation; collaborate cross-functionally with QA, Regulatory Affairs, EHS, Engineering, BTS, ATS and HR.
+ Direct technical troubleshooting and process improvements across antigen production, formulation, filling, and freeze-drying operations.
+ Manage IPT budget, resource planning and capital/project work aligned with site priorities.
**Who you are:**
+ A proven people leader who gets results by developing others: you have experience coaching managers, performance managing teams and building capabilities that last.
+ Technically strong across vaccine manufacturing: hands-on experience with aseptic filling, antigen/formulation processes, and fill/finish operations.
+ Operationally minded: you use Lean/MPS methods and scientific problem-solving to reduce variability, increase throughput and lower cost of goods.
+ A confident communicator who can convey strategy and expectations to leaders and frontline teams, and who works effectively across functional partners.
+ Quality- and compliance-focused with practical experience supporting regulatory inspections, validations and cGMP operations.
**Required qualifications:**
+ Bachelor's degree in a life sciences or related field AND ~8 years of relevant vaccine or pharmaceutical manufacturing experience, including at least 5 years in leadership roles (people, budget and operational accountability).
+ Demonstrated experience in aseptic techniques and operations, antigen production, formulation, filling and freeze-drying.
+ Strong knowledge of cGMP and USDA manufacturing requirements.
+ Proven track record of team building, coaching, and people development.
+ Experience applying Lean/MPS methodologies and scientific problem solving to deliver measurable operational improvements.
+ Excellent written and verbal communication skills; proficient with standard computer systems and applications.
**Preferred qualifications:**
+ Advanced degree in a relevant field.
+ Lean Six Sigma Green Belt or higher (LL2/LL3), or equivalent experience.
+ Experience with SAP and inventory control systems.
+ Familiarity with kata and other lean coaching tools.
**Required Skills:**
Antigens, Aseptic Filling, Aseptic Operations, Communication, Decision Making, Empowering People, Freeze Dry, Good Manufacturing Practices (GMP), Lean Six Sigma Process Improvement, Management Process, Manufacturing Quality Control, Motivating People, Packaging Processes, People Development, People Leadership, Problem Solving, Process Improvements, Production Ramp Up, Strategic Thinking, Team Leadership, Technical Problem-Solving, USDA Regulations, Vaccine Manufacturing, Vaccine Production
**Preferred Skills:**
Lean Coaching, SAP Systems
Current Employees apply HERE ( Contingent Workers apply HERE ( 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 ( 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 ( Hybrid Work Model**
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote".
The salary range for this role is
$126,500.00 - $199,100.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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 .
You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
**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:**
No relocation
**VISA Sponsorship:**
No
**Travel Requirements:**
10%
**Flexible Work Arrangements:**
Not Applicable
**Shift:**
1st - Day
**Valid Driving License:**
Yes
**Hazardous Material(s):**
yes
**Job Posting End Date:**
10/17/2025
***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:** R
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Senior Technician, Quality Control

19966 Millsboro, Delaware Merck

Posted today

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Job Description

**Job Description**
A Senior Laboratory Technician, Quality Control/Senior QC Lab Tech is responsible for performing advanced laboratory procedures independently for the testing of veterinary biologicals according to strict government and company-imposed guidelines. Technicians may work with a variety of technical equipment while completing Quality Testing. At all times technicians must follow Good Manufacturing Practices and Standard Operating Procedures (SOPs) and adhere to all safety and company policies, perform duties assigned by department management. A Senior QC Lab Tech must possess thorough knowledge of the underlying principles used in testing procedures and understand the material being evaluated, i.e. virus, bacteria, cell line, etc.
**Primary Responsibilities, but are not limited to:**
+ Demonstrates, at all times, safe work habits and maintains a safe work environment.
+ Understands and complies with all safety and company policies and procedures.
+ Perform testing methods using various types of cell culture, substrates, and viruses, per Quality Control Procedures.
+ Manage raw material schedule and perform inspection and release of raw materials in SAP
+ Write laboratory investigations as needed
+ Perform troubleshooting of test methods, with the ability to evaluate and implement new procedures.
+ Maintain and evaluate the sequential analysis of the testing standards used in the area of the assignment.
+ Performs data review
+ Clean work areas including floors, walls, tables, etc.
+ Equipment set-up and operations
+ Concurrent record keeping including charts, logbooks, and all pertinent documentation
+ Report all unusual, non-routing occurrences when performing tasks
+ Perform more advanced mathematical calculations, conversions and formulations
+ Responsible for waste accumulation, labeling and management of hazardous, universal and/or infectious wastes.
+ Participation in project teams and/or complete design of special projects.
+ Train others on methods and procedures
+ Effectively interacts with co-workers and others as needed. Demonstrates teamwork within own group and other internal groups
**Education Minimum Requirement:**
+ High school diploma or equivalent plus four (4) years of relevant experience required.
**Preferred Education:**
+ Associate degree in a science plus two (2) years of experience OR Bachelor's degree in the sciences preferred.
**Required Experience and Skills:**
+ Experience with analytical instrumentation
+ Experience with microscopic analysis and microbiological assays.
+ Experience with wet chemistry methods
+ Proven analytical aptitude and critical thinking skills
+ Strong written and verbal communication skills
+ Good Documentation Practices
+ Pipetting
+ Weighing
+ Troubleshoot / Problem solving beyond method defined action
+ Good Communication
+ Familiar with good laboratory techniques
**Preferred Experience and Skills:**
+ In-depth working knowledge and application of GMPs/GLPs
+ Knowledge of USP and EP monographs
+ Experience working with Cell Culture in biological operations or testing setting
+ Experience in use of root cause analysis tools
+ Experience using SAP
**Required Skills:**
Accountability, Accountability, Analytical Instrumentation, Cell-Based Assays, Cell Cultures, Compound Management, Discipline Management, Enzyme Linked Immunosorbent Assay (ELISA), GMP Compliance, GMP Laboratory, Keen Observation, Laboratory Analytical Techniques, Laboratory Information Management System (LIMS), Laboratory Investigations, Laboratory Operations, Laboratory Techniques, Mammalian Cell Culture, OOS Investigations, Primary Cell Culture, Proper Documentation, Quality Control Management, Quality Standards, Recordkeeping, SAP Enterprise Resource Planning (ERP), Standard Operating Procedure (SOP) Writing {+ 5 more}
**Preferred Skills:**
Current Employees apply HERE ( Contingent Workers apply HERE ( 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 ( 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 ( Hybrid Work Model**
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as "remote".
**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:**
No relocation
**VISA Sponsorship:**
No
**Travel Requirements:**
No Travel Required
**Flexible Work Arrangements:**
Not Applicable
**Shift:**
1st - Day
**Valid Driving License:**
No
**Hazardous Material(s):**
n/a
**Job Posting End Date:**
10/13/2025
***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:** R
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