104 Manufacturing jobs in Trenton
Manufacturing - Digital Manufacturing, Manager

Posted 9 days ago
Job Viewed
Job Description
**Industry/Sector:** Not Applicable
**Time Type:** Full time
**Travel Requirements:** Up to 60%
At PwC, our people in operations consulting specialise in providing consulting services on optimising operational efficiency and effectiveness. These individuals analyse client needs, develop operational strategies, and offer guidance and support to help clients streamline processes, improve productivity, and drive business performance.
In product development and manufacturing at PwC, you will specialise in improving product development and manufacturing processes. You will work closely with clients to analyse product development lifecycles, identify bottlenecks, and develop strategies to enhance speed to market, reduce costs, and improve quality. Working in this area, you will also provide guidance on implementing lean manufacturing principles, optimising supply chain integration, and leveraging digital technologies.
Enhancing your leadership style, you motivate, develop and inspire others to deliver quality. You are responsible for coaching, leveraging team member's unique strengths, and managing performance to deliver on client expectations. With your growing knowledge of how business works, you play an important role in identifying opportunities that contribute to the success of our Firm. You are expected to lead with integrity and authenticity, articulating our purpose and values in a meaningful way. You embrace technology and innovation to enhance your delivery and encourage others to do the same.
Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to:
+ Analyse and identify the linkages and interactions between the component parts of an entire system.
+ Take ownership of projects, ensuring their successful planning, budgeting, execution, and completion.
+ Partner with team leadership to ensure collective ownership of quality, timelines, and deliverables.
+ Develop skills outside your comfort zone, and encourage others to do the same.
+ Effectively mentor others.
+ Use the review of work as an opportunity to deepen the expertise of team members.
+ Address conflicts or issues, engaging in difficult conversations with clients, team members and other stakeholders, escalating where appropriate.
+ Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements.
Our Product Development & Manufacturing (PD&M) Team helps our clients leverage advanced strategies, operational approaches and technologies to innovate, develop and manufacture products and services in a manner that significantly increases operational efficiency and drives new levels of enterprise-wide growth in a connected world.
**Job Requirements and Preferences** :
**Basic Qualifications** :
**Minimum Degree Required** :
Bachelor Degree
**Minimum Years of Experience** :
5 year(s)
**Preferred Qualifications** :
**Degree Preferred** :
Master Degree
**Preferred Fields of Study** :
Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering, Computer Engineering, Engineering, Engineering Mechanics, Engineering Physics, Industrial and Operations Engineering, Industrial Engineering, Materials Science and Engineering, Mechanical Engineering, Production Engineering, Project Engineering & Management, Biomedical Science, Computer and Information Science, Data Processing/Analytics/Science
**Preferred Knowledge/Skills** :
Demonstrates extensive knowledge and experience with and a proven record of success in leading or facilitating project management or client consultations in the areas of product development and manufacturing, preferably for a global network of professional services firms, in one of the following core industry sectors including, but not limited to:
+ Industrial: Automotive; Aerospace; Chemicals; Industrial Manufacturing; or, Construction;
+ Technology: Hardware/Electronics; Systems; Software; Semiconductor; or, Telecommunications;
+ Life Sciences: Pharma, Bio Pharma, & Specialty Pharma; Medical Device, Medical Technology & Diagnostics; Generics; or, Animal Health; and,
+ Consumer Markets: Food & Beverage; Goods; or, Vertically Integrated Retail.
Functional Experience:
Demonstrates extensive knowledge and experience with and a proven record of success to deliver advisory services in the following capability areas:
+ Digital Manufacturing Application (MES, CMMS, QMS) Configuration and/or Deployment;
+ Digital Twin;
+ Digital Manufacturing Strategy Development;
+ Digital Manufacturing Blueprint & Design;
+ Digital Manufacturing Control Systems Design & Deployment;
+ Manufacturing Decision Support & Analytics;
+ Machine Connectivity; and,
+ Industrial IoT and Cloud Solutions.
Demonstrates extensive knowledge and experience with and a proven record of success to deliver advisory services in the following capability areas:
+ Manufacturing Strategy & Operations;
+ Operations Excellence;
+ Maintenance & Reliability Management; and,
+ Digital Automation.
Demonstrates extensive abilities to lead and manage a diverse team including:
+ Demonstrates the ability to build, maintain, and utilize networks of client relationships;
+ Possesses advanced problem solving and analysis skills;
+ Possesses advanced spreadsheet, presentation and document development skills;
+ Possesses detailed value case development skills;
+ Possesses the ability to interpret financial statements;
+ Possesses engaging interpersonal skills;
+ Possesses a collaborative and 'can-do' mindset;
+ Possesses financial modeling skills;
+ Possesses the ability to influence and shape thinking of peer level and Director level client resources;
+ Possesses Program/Project leadership skills - ability to lead complex multi-workstream projects;
+ Effectively manages unstructured situations, anticipating client needs and developing solutions;
+ Possesses the ability to develop/coach resources and guide careers of team members;
+ Possesses client presentation skills; and,
+ Possesses proposal & pricing development skills.
Learn more about how we work: does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: PwC is an?equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law?
For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all.
Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: salary range for this position is: $99,000 - $232,000, plus individuals may be eligible for an annual discretionary bonus. For roles that are based in Maryland, this is the listed salary range for this position. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link:
Manufacturing Manager
Posted 9 days ago
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Job Description
You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients.Company InformationOur client is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing.Job SummaryReporting to the Manufacturing Director, the Manufacturing Manager will play a pivotal role in establishing the Manufacturing Department by supporting operational readiness and leading the manufacturing team to consistently deliver on specific Key Performance Indicators (KPIs). The Manufacturing Manager will work closely with the MSAT (Manufacturing Science & Technology) teams to ensure the effective and efficient tech transfer of products and processes to the facility.Key Responsibilities Member of the Manufacturing leadership team. Support the execution of the overall Manufacturing strategy aligned with the facility's strategic business plans and global Manufacturing strategy. Lead a team of Supervisors and Manufacturing Bioprocessing Associates to execute routine manufacturing activities of therapeutic proteins in a mammalian cell culture facility. Manage daily downstream manufacturing activities and ensure production timelines are met. Collaborate with MSAT and engineering teams on technical transfer, process validation, etc. Collaborate with QC & QA groups to ensure GMP compliance, manage deviation investigation and CAPA implementation, and support client auditing and agency inspections. Provides working knowledge and technical leadership in Downstream operations. Schedules and/or delivers training to manufacturing personnel to ensure staff can perform manufacturing operations safely and compliantly. Motivate, retain, develop existing group members and recruit new staff to build a strong Downstream manufacturing team. Contribute to continual improvement of all manufacturing documentation (SOP's, MBR's, OJT's) to ensure they are current, accurate, and clear. Communicate operational status regularly to senior management, as required, at the appropriate level of detail. Assist the Manufacturing Director to coordinate the work between the Downstream groups and other functional groups to meet the production objectives and timelines. Perform all duties in accordance with GMP requirements, SOPs, and controlled documents. Will be flexible to take on additional tasks and responsibilities at the discretion of the Manufacturing Director. Will act as a role model for the Manufacturing function and also the wider organisation in adherence to corporate core values and company culture.Qualifications Comprehensive knowledge and experience of relevant cGMP, safety and environmental regulations within the biopharmaceutical industry. Ideally, experienced in establishing a Manufacturing department and building a team of similar size and scale. 10+ years in biopharmaceutical manufacturing with extensive experience in Downstream processing. Experience in the large-scale chromatography, ultrafiltration/diafiltration, viral inactivation, filtration, etc. Experience in dealing with FDA, and/or EMA, and have a solid understanding of quality system in terms of deviation, investigation, CAPA and change control. Experience in working with cross-functional teams. Experience in troubleshooting and investigation of the critical deviation, and making the risk analysis on the development, technical transfer and process validation. Must be quality-focused with knowledge and understanding of cGMP quality systems and how they apply to manufacturing operations.Experience 10+ years in biopharmaceutical manufacturing.Skills Technical skills relevant to downstream processing operations. Strong leadership abilities and the ability to adapt to a dynamic manufacturing environment. Excellent verbal and written communication and presentation skills. Strong interpersonal skills to work effectively with all levels of staff. Ability to work independently and proactively. Results-oriented, with the ability to manage multiple priorities in a short period of time. Excellent organizational and planning skills, strong attention to detail.Education Certificate, Diploma, Degree in Science, Engineering or related field, or equivalent experience in the biopharmaceutical industry is essential. BSc, MSc, or PhD in Chemical Engineering, Bioscience, or Biotechnology is advantageous.Additional Requirements Must be willing to travel as required internationally to fulfill the responsibilities of the position.Medix Overview:With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we're dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.
Manufacturing Engineer
Posted 4 days ago
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Job Description
Insight Global is looking to hire a Manufacturing Engineer for an electronic component manufacturing client in north Philadelphia supporting aerospace, defense, and medical industries. This person will be responsible for developing and implementing custom tools, jigs, and fixtures for connector assembly processes. They will work closely with the design engineer, manufacturing, and quality teams to ensure designs meet specifications, tolerances, and safety standards. They will also identify opportunities for improvement for both product and process efficiency.
This is an on-site position Monday-Friday but offers flexible working hours if needed. We can pay between $90-110k salary + full benefits including health, dental, vision, life, disability, HSA/FSA, 401k match, PTO, and tuition reimbursement.
We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form ( . The EEOC "Know Your Rights" Poster is available here ( .
To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: .
Skills and Requirements
Required Skills & Experience
-5+ years of experience in small scale manufacturing
-Familiar with AS9100 quality standards
-Experience developing and implementing custom tools, jigs, and fixtures for connector assembly
-Knowledge of GD&T
-Solidworks null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to
Manufacturing Technician
Posted 4 days ago
Job Viewed
Job Description
One of our manufacturing clients is seeking a Manufacturing Technician to join their growing team. This would be working for a startup company who is creating propulsion systems for the commercial and defense aerial space. They are seeking a self-motivated Manufacturing Technician who has a high attention to detail and is process-driven and able to work in small, cross-disciplinary teams. Their primary focus will be to perform assembly and calibration of propulsion systems.
We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form ( . The EEOC "Know Your Rights" Poster is available here ( .
To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: .
Skills and Requirements
2+ years of experience in hardware assembly
2+ years of experience with soldering
Experience following standard operating procedures and work instructions as part of an ISO-compliant Quality Management System Associates Degree in a manufacturing or electronics engineering
Experience working with drone propulsion systems or other robotic actuation systems
Experience with PCBA electronics assembly or contract manufacturing of electronic products null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to
Manufacturing Painter
Posted 4 days ago
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Job Description
Pay: $18-22/hr based on experience
Shift: 730am-4pm (Mon-Friday)
Please review the information below and if interested apply by submitting your resume with the best contact information included so we can reach out and speak further about this opportunity.
**Description:**
- Perform paint prep on products prior to paint work
- Perform in process quality inspections utilizing precision measuring tool
- Gather materials to complete daily production
- Complete spray coating on each product
- Maximize efficiency with tooling and fixtures
**Qualifications:**
- Comfortable with working in a manufacturing environment
- Strong mechanical aptitude
- Attention to detail
**Benefits:**
- 100% paid benefits for the individual
- Clean environment
- Temperature controlled
- 401k match
- Profit sharing plan
- Life Insurance
**- PTO**
**Pay and Benefits**
The pay range for this position is $8.00 - 22.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
**Workplace Type**
This is a fully onsite position in Horsham,PA.
**Application Deadline**
This position is anticipated to close on Jul 21, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Quality Control Inspector
Posted 1 day ago
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Job Description
As a Quality Control Inspector , you will play a vital role in ensuring that all semi-finished and finished parts meet the highest quality standards of the industry, our customers, and our company.
- Evaluate semi-finished and finished parts to verify compliance with industry standards, customer requirements, and company quality standards.
- Utilize your knowledge of drawings, specifications, and relevant standards (e.g., ASME) to assess parts and ensure they meet design and quality criteria.
- Apply preventive action techniques to identify potential issues and address them proactively, minimizing the impact on the production process.
- Utilize continuous improvement methodologies and root cause analysis techniques to identify and address the underlying causes of errors or defects.
- Maintain accurate and detailed records of all calibrations, tests, inspections, results, findings, and any other required information.
- The ideal candidate will have experience in a manufacturing facility and quality control processes, as well as the ability to read and work from blueprints and mechanical drawings.
- The candidate will also have excellent critical thinking and problem-solving skills, and the ability to work effectively independently and within a team environment.
- Additionally, the candidate will have experience with standard Microsoft Office and related technology, and the ability to work in a constant state of alertness and in a safe manner.
To apply, please submit your resume to
Pikemann is a recruiting company that was founded by three partners with over 40 years of experience providing contingent staffing and permanent placement services in the greater Seattle area. We partner with our clients to bring the right technology and finance candidates that meet their workforce needs.
Quality Control Inspector
Posted 2 days ago
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Job Description
MACOM designs andmanufactures semiconductor products for Data Center, Telecommunication, andIndustrial and Defense applications. Headquartered in Lowell, Massachusetts,MACOM has design centers and sales offices throughout North America, Europe,and Asia. MACOM is certified to the ISO9001 international quality standard andISO14001 environmental management standard.
MACOM has more than 65years of application expertise with multiple design centers, Si, GaAs and InPfabrication, manufacturing, assembly and test, and operational facilitiesthroughout North America, Europe, and Asia. In addition, MACOM offers foundry servicesthat represents a key core competency within our business.
MACOM sells anddistributes products globally via a sales channel comprised of a direct fieldsales force, authorized sales representatives, and leading industrydistributors. Our sales team is trained across all of our products to give ourcustomers insights into our entire portfolio.
Title: Quality ControlInspector
Asa Quality Inspector, you will be responsible for verifying all requireddocuments that are involved/required with the parts/products you areinspecting. Document any non-conformances in detail on the Company's Q-notesystem. This includes all areas of quality control, incoming inspection, in-processinspection and final inspection. When not working with the microscope, you willbe verifying measurements with handheld measuring tools.
Key Responsibilities:
- Perform incoming inspection, in-process inspection, first article inspection and final inspection of electronic and mechanical components with little to no assistance.
- Schedule source inspections as required.
- Generate internal and external reports.
- Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers.
- Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications.
- Perform routine SAP transactions to move, disposition, and route material.
- Safe handling of ESD sensitive materials.
- Working knowledge of SAP, Agile, Excel, MSWord and Outlook.
- Ability to prepare oral and written reports clearly and concisely.
- Excellent internal and external communication skills.
- Advanced understanding of quality control standards and testing techniques.
- Knowledge of statistical sampling techniques.
- Able to lift up to 20 pounds.
- Able to sit for periods of time working with a microscope.
- High School diploma (or equivalent) or AS degree (preferred).
- Minimum 2 years Quality Control inspection experience (preferred).
- Self-motivated with the ability to evaluate complex issues in a high-pressure environment.
- Knowledge of all aspects of inspection and testing.
- Experience with Mil-PRF-38534, class H & K; Hybrids, Mil-STD-883; methods 2008, 2009, 2010, 2017 Semiconductors and Passive devices.
- Knowledge of IPC-600 and 610, J-STD-001.
- Knowledge and experience in performing mechanical and electronic inspections.
- Ability to work from technical drawings, sketches and specifications.
- Due to ITAR regulations, U.S. citizenship or permanent residency required.
The Salary Range for this position is $25.00-$28.00.Actual salary offered to candidate will depend on several factors, includingbut not limited to, work location, relevant candidates' experience, education,and specific knowledge, skills, and abilities.
Benefits: This position offers a comprehensive benefits packageincluding:
Health, dental, and vision insurance.
Employer-sponsored 401(k) plan.
Potential for performance-based bonus.
Paid time off.
Professional development opportunities.
EEO:
MACOM is an EqualOpportunity Employer committed to a diverse workforce. MACOM will not discriminateagainst any worker or job applicant on the basis of race, color, religion, sex,gender identity, sexual orientation, national origin, age, disability, geneticinformation, veteran status, military service, marital status, or any othercategory protected under applicable law.
Reasonable Accommodation:
Reasonable Accommodation. MACOM is committed to working with and providingreasonable accommodations to qualified individuals with physical and mentaldisabilities. If you have a disability and are in need of a reasonableaccommodation with respect to any part of the application process, please call or email Provide your name, phone number andthe position title and location in which you are interested, and nature ofaccommodation needed, and we will get back to you. We also work with currentemployees who request or need reasonable accommodation in order to perform theessential functions of their jobs.
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Quality Control Supervisor
Posted 4 days ago
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Job Description
Looking for a quality professional with over 10 years of experience in the pharmaceutical and biotechnology industry, specializing in **Quality Control (QC), Quality Systems, Analytical Method Validation** , and **Global Specification Management** . Demonstrates proven expertise in leading laboratory operations, managing cross-functional teams, and driving global standardization and digital transformation initiatives within highly regulated environments.
**Education Requirement:**
bachelor's degree or higher in **Chemistry** or a related scientific discipline is required.
**Key Responsibilities:**
+ Oversee and coordinate **daily equipment qualifications** in QC laboratories, collaborating with cross-functional teams to ensure timely execution.
+ Lead **analytical method validations** , managing project timelines, resource allocation, and testing execution.
+ Author and review technical documentation, including **SOPs, test methods, validation master plans** , and analytical reports in compliance with regulatory requirements.
+ Support **IQ/OQ/PQ execution, calibration activities** , and overall lab readiness in coordination with internal departments.
+ Provide oversight for **change control processes** , including authoring and reviewing documentation in systems such as **TrackWise** and **Veeva Vault Quality Docs** .
+ Lead the **digital transformation of QC systems** as Product Owner for **Empower CDS** , managing a global cross-functional team using **Agile project management** practices.
+ Manage operations in a high-throughput **stability testing lab** , leading a team of analysts and implementing **Lean Lab** and **5S** principles to increase productivity and reduce costs.
+ Conduct **investigations (OOS, deviations)** , perform **risk assessments** and **root cause analyses** , and implement **CAPAs** in alignment with **cGMP** and **data integrity** standards.
+ Oversee **data review and documentation compliance** , developing and maintaining SOPs to meet evolving regulatory requirements.
+ Coordinate **stability programs** end-to-end, including protocol updates, change control evaluations, and cross-functional collaboration with Regulatory, QA, and Supply Chain.
+ Perform hands-on **analytical testing** for finished products, stability studies, and technical transfer, while reviewing data for regulatory filings and batch release.
+ Provide technical leadership for **LIMS** and **electronic data archiving systems** , ensuring compliance with **FDA** and **ICH** guidelines during audits and inspections.
+ Contribute to the creation and maintenance of **product specifications** for raw materials, APIs, packaging components, and finished products in accordance with **USP, ICH** , and **CFR** standards.
**Tools & Systems:**
+ **Empower CDS (Waters), TotalChrom**
+ **TrackWise** , **LIMS** , **Veeva Vault Quality Docs, ComplianceWire**
**Key Areas of Expertise:**
+ Analytical Method Validation & Transfer
+ Equipment Qualification (IQ/OQ/PQ); Change Control & CAPA Management
+ Stability Program Oversight
+ Data Integrity & ALCOA+ Principles
+ GMP/GLP Compliance; Regulatory Submissions & Audit Readiness
+ Laboratory Operations & Team Leadership
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
Chemist, Quality Control

Posted 9 days ago
Job Viewed
Job Description
Responsibilities:
1. Analytical support to all departments.
1. Support to regular QC activities, as required.
1. Method development, including validation and documentation.
1. Writing concise and timely reports to management on projects and regular activities.
1. Responsible for customer complaint investigations.
1. Assisting with technician training.
1. Other duties, as assigned.
Qualifications:
1. Bachelor of Chemistry degree (or related degree)
2. Knowledge of basic chemistry principles and analytical methods.
3. Working knowledge of cGMP as they relate to lab activities.
4. Careful attention to detail.
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Quality Control Sampler

Posted 9 days ago
Job Viewed
Job Description
The QC Sampler is responsible for sampling all incoming materials such as raw materials, packaging components, printed material and all other GMP materials using established Standard Operating Procedures (SOPs) and working in accordance with current Good Manufacturing Practices (cGMP). Collect, sample, and prepare QC Chemical test samples for various analysis laboratories when required.
**Area Of Responsibility**
+ Sample all incoming materials and packaging materials per procedures.
+ Inspect all incoming GMP materials per materials specifications Inspect all incoming GMP materials per materials specifications including Identify non-conforming materials cleanliness and defects.
+ Follow work-flow procedures from receiving test samples, monitoring inventories, to waste disposal
+ Train towards Visual Inspection qualifications
+ Accurately sample and weigh Chemical test samples according to Material Specifications and SOPs using, at times, sterile operating procedures
+ Perform QC Release testing for Visual Inspection of cosmetic defects and dimensional inspection of product container closure components
+ Initiate product non-conforming reports (UPD) as required (Track Wise) and investigate any problems noted with sampling/inspection process.
+ Issue/Dispense and receive labels and packaging materials per production batch record. Keep inventory of all product label/packaging materials
+ Enter transactions/transfers into SAP inventory control system
+ Maintain records/manual log books per good documentation practices (GDPs)
+ Coordinate scrap removal of rejected product
+ Update Raw Material Specifications (RMS)/(SOPs) as needed
+ Work under general supervision and follows established procedures and instructions
+ Operate and maintain the QC Chemical Sampling laboratory to GMP compliance and safety compliance
+ Operate, maintain and clean, and calibrate balances
+ Maintain laboratory supplies, reagents, chemicals, and equipment inventories for Sampling and Inspection laboratories
+ Manage calibration of instruments and equipment used for inspection and perform monthly equipment/ instrument maintenance and cleaning.
+ Other duties as assigned
**Work Conditions:**
Warehouse Environment
Laboratory environment:
+ Exposure to noise, bio-hazardous (live cultures), and chemicals
+ Exposure to non-hazardous and hazardous chemicals and materials
+ Moderate noise, oven heat, open flame, chemical fume hoods areas requiring wearing appropriate safety equipment (i.e. gloves, lab coat, safety glasses and respirator)
**Physical Requirements:**
+ Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands, talk or hear, stoop, kneel, crouch or crawl.
+ Able to operate basic mechanical tools (i.e.:) calipers, micrometers, and go no-go gages
+ Able to drive a fork truck/tow motor/operate forklift
+ Close vision; depth perception; ability to adjust focus
+ Use of repetitive motion
+ Able to operate computer/office machines
+ Able to lift and carry up to 50 lbs.
**Travel Estimate**
Up to 5 %
**Education and Job Qualification**
+ Minimum of High School/Trade School/Vocational School Diploma, GED, or equivalent. B.S. degree preferred.
+ The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
+ Good oral and written communication skills and ability to use these skills to follow specific instruction and report assay results (i.e. written SOPs)
+ Proficient with wet chemical methods and tests (USP, ACS, Titration, Limit tests, etc.)
+ Fundamental knowledge of chemical principles
+ Proficient with basic laboratory instrumentation.
+ Use of Track Wise software and knowledge of SAP is preferred.
+ Use of Lotus Notes software
+ Working knowledge of Microsoft Office Applications.
+ A self-starter with a hands-on approach and a can-do attitude.
**Experience**
+ Minimum of two (2) years of experience required in a Pharmaceutical/drug (FDA Regulated) industry preferred
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.