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Production Control Associate Jobs in Passaic, NJ

Workforce 1

Retail Shortage Control

Staten Island, NY

$17/hr

Join Burlington as a Part-Time Retail Shortage Control Associate and help create a safe, secure ... Excellent leadership skills that support fostering productive business relationships. * Candidates ...

New

Workforce 1

Retail Shortage Control

Staten Island, NY · On-site

$17/hr

Position OverviewJoin Burlington as a Part-Time Retail Shortage Control Associate and help create a ... Excellent leadership skills that support fostering productive business relationships. * Candidates ...

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Production Control Associate information

See Passaic, NJ salary details

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How much do production control associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for production control associate in Passaic, NJ is $17.42, according to ZipRecruiter salary data. Most workers in this role earn between $14.95 and $18.89 per hour, depending on experience, location, and employer.

What are some typical challenges a production control associate faces and how can they be effectively managed?

Production Control Associates often encounter challenges such as coordinating schedules across multiple departments, managing last-minute changes in production plans, and ensuring timely delivery of materials. These challenges can be effectively managed by staying organized, maintaining clear communication with team members and supervisors, and utilizing software tools to track progress and inventory. Being proactive and adaptable is key, as priorities can shift quickly in a manufacturing environment.

Is production control associate a stressful job?

Production control associates often work in fast-paced manufacturing or logistics environments, where meeting deadlines and managing inventory can create pressure. The job requires attention to detail, organization, and sometimes working under tight schedules, which can contribute to stress levels depending on workload and company culture.

What is the difference between Production Control Associate vs Production Planner?

AspectProduction Control AssociateProduction Planner
CredentialsHigh school diploma or equivalent; some roles may require technical certificationsTypically requires a degree in manufacturing, logistics, or related field
Work EnvironmentManufacturing or warehouse settings, coordinating daily production activitiesOffice-based, focusing on scheduling and planning production runs
Employer & Industry UsageUsed across manufacturing industries to monitor and control production flowCommonly used in manufacturing to develop production schedules and optimize resources

The Production Control Associate primarily manages daily production activities and ensures smooth operations, while the Production Planner focuses on creating and maintaining production schedules to meet demand. Both roles are essential in manufacturing but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a production control associate?

To thrive as a Production Control Associate, you need strong organizational, analytical, and problem-solving skills, often supported by a background in supply chain management or manufacturing operations. Familiarity with ERP/MRP systems, inventory management software, and Microsoft Excel is typically required. Attention to detail, effective communication, and the ability to work under pressure distinguish top performers in this role. These skills ensure efficient production scheduling, timely material flow, and smooth coordination between departments to meet organizational goals.

What does a production control associate do?

A Production Control Associate is responsible for coordinating and overseeing the flow of materials and products through a manufacturing process. Their tasks typically include scheduling production activities, tracking inventory levels, ensuring materials are available for production, and communicating with various departments to resolve issues. They play a key role in ensuring that production targets are met efficiently and that any disruptions to the workflow are minimized. This role often requires strong organizational and communication skills, as well as the ability to work with production management software.
Production Control Associate jobs near you

HTP Analytical QC Associate Scientist

GenScript/ProBio

Piscataway, NJ • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago

Job description

About GenScript
Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Genscript is seeking a motivated and detail-oriented HTP Analytical QC Associate Scientist to join our dynamic US Protein Department in Piscataway, New Jersey.
The estimated salary range is $60,000 - $75,000, depending on experience.
Reporting to: Supervisor of HTP Platform
Employment Type: Full-time
Role Description:
We are seeking a detail-oriented and proactive Associate Scientist to join our High-Throughput Protein Analytical QC Laboratory. This role is responsible for performing analytical characterization and quality control testing of recombinant proteins generated from high-throughput production workflows.
The successful candidate will play a critical role in ensuring protein identity, purity, and overall quality through robust analytical methodologies. This position operates in a data-driven and quality-focused environment where accuracy, reproducibility, and data integrity are essential. The ideal candidate will have hands-on experience with protein analytical techniques and familiarity with laboratory data management systems such as ELN, LIMS, or equivalent platforms.
Key Responsibilities:
  1. Perform routine and non-routine analytical and QC testing to evaluate protein identity, purity, and quality attributes.
  2. Execute a range of protein characterization assays, including:
  3. HPLC / UPLC (e.g., SEC, RP, IEX)
  4. Capillary Electrophoresis (CE, iCE/cIEF)
  5. SDS-PAGE
  6. Western blot
  7. LC-MS
  8. Endotoxin assays
  9. Prepare samples, reagents, buffers, and standards in accordance with established protocols and assay requirements.
  10. Perform sample preparation workflows, including use of automated liquid handling systems where applicable.
  11. Analyze, interpret, and document experimental data in ELN, LIMS, or equivalent systems, ensuring compliance with data integrity standards (e.g., ALCOA+ principles).
  12. Support method troubleshooting and optimization, ensuring assay robustness, reproducibility, and consistency across runs.
  13. Maintain laboratory instruments and ensure proper calibration and performance, supporting compliance with quality and safety standards.
  14. Collaborate with cross-functional teams (e.g., protein production, process development) to support project timelines and deliverables.
  15. Contribute to continuous improvement initiatives, including method refinement, workflow efficiency, and data quality enhancement.

Qualifications:
  1. BS or MS in Biochemistry, Analytical Chemistry, Biotechnology, or a related field with 2+ years of relevant experience in protein analytical characterization or QC.
  2. Hands-on experience with protein analytical techniques such as HPLC/UPLC, CE, SDS-PAGE, Western blot, LC-MS, or endotoxin assays.
  3. Familiarity with protein characterization workflows, including purity, aggregation, and identity analysis.
  4. Experience with laboratory data systems (ELN, LIMS, or similar) and strong documentation practices.
  5. Strong attention to detail and commitment to data integrity, accuracy, and reproducibility.
  6. Experience in a CRO/CDMO or regulated QC environment is preferred.

#LI-EB1
#GS
Benefits:
Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

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