25 Pfizer jobs in Collegeville

Quality Operations Inspector -I

Position Summary

The Quality Assurance Inspector is responsible for providing on-the-floor quality oversight and support to ensure the compliance of manufacturing, packaging, labeling, and distribution operations with Piramal Standard Operating Procedures (SOPs) and applicable regulatory requirements. This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining product quality, safety, efficacy, and regulatory compliance across operations.

Key Responsibilities

• Issue batch records in alignment with the production schedule to support timely manufacturing activities and Perform potency calculations as applicable.
• Conduct line clearance and batch readiness assessments, including verification of concurrent documentation, equipment status, and preventive maintenance records.
• Review and evaluate Environmental Monitoring (EM) data for compliance with internal standards and regulatory requirements.
• Perform BMS alarms review, acknowledgement and evaluate quality impact. Escalate critical alarms to Management.
• Perform quality oversight for water system releases used in operations.
• Perform raw material Sampling and AQL inspection of finished products.
• Review equipment logbooks and executed batch records to ensure adherence to GDP, GMP, and Data Integrity standards.
• Scan reviewed batch records and upload to share point.
• Prepare batch records and perform first release of batches.
• Perform Raw material reconciliation and investigation.
• Review and approve Calibration activities in ProCal.
• Perform QA review and approval of non-routine workorders in SAP.
• Draft, revise, and review Quality Assurance SOPs and deviation reports to ensure clarity, accuracy, and regulatory alignment.
• Conduct weekly quality surveillance activities, including facility inspections, environmental monitoring checks, and audits of equipment maintenance and GMP practices to support continuous audit readiness.
• Complete all assigned training on SOPs and job-related tasks in a timely manner.
• Stay current with industry trends, updates to regulatory requirements, and emerging quality standards.
• Perform all other activities as assigned by Manager

Experience:

• 1–3+ years of experience in pharmaceutical quality assurance, regulatory affairs, or GMP auditing.
• Prior experience in providing on-the-floor quality oversight and conducting inspections or working in a regulated pharmaceutical environment preferred.

Skills:

• In-depth knowledge of GMP, GDP, GLP, and relevant international regulations (FDA, EMA).
• Strong analytical, attention to detail investigative, and problem-solving skills.
• Excellent communication (written and verbal) and interpersonal skills.
• Proficiency in MS Office and quality management systems (QMS).
• Ability to travel to facilities for inspections (as required).

**Make an Impact Where Quality Counts!**
PDS Tech Commercial is hiring a detail-oriented **QA Inspector** to join our client's manufacturing team in **Spring City, PA** . In this critical role, you'll ensure every product meets strict quality standards and specifications. This is a **temp-to-hire (3-month)** opportunity with strong potential for long-term growth and stability.
+ **Pay** = $20-25/hour
+ **Shift** = 1st shift
**What You'll Be Doing**
You'll be the frontline of quality assurance, performing key inspections and audits across the production process. Responsibilities include:
+ Conducting first-piece, in-process, and final inspections
+ Executing Layered Process Audits (LPAs)
+ Using precision tools (micrometers, calipers, thread gauges, height stands) to measure and inspect parts
+ Performing random and 100% inspections as required - recording results
+ Supporting ISO 9001 internal audits and the company's quality management system
+ Maintaining calibration schedules and quality records
**Qualifications - What You Bring to the Table**
**Required:**
+ High school diploma or GED
+ Minimum 2 years of QA experience in a manufacturing environment
+ Proficiency in reading blueprints and using inspection tools
+ Basic computer skills (Microsoft Office)
+ Strong attention to detail and communication skills
+ Ability to work in a hands-on, physical role
**Preferred:**
+ Experience with ERP systems (Oracle a plus)
+ Prior forklift operation experience
**Why Join Us?**
At PDS Tech Commercial, we connect talented professionals with leading employers who value precision, skill, and reliability. When you join us:
+ You're part of a team where **quality is not just a goal - it's the standard**
+ You'll work in an environment that encourages growth and **offers the potential for long-term employment**
+ Enjoy a consistent, daytime schedule that promotes **work-life balance**
+ Access support from a staffing partner with over **50 years of industry expertise**
**Ready to Elevate Your Career in Quality?**
Apply now to become a **QA Inspector** with PDS Tech Commercial in Spring City, PA. Take the next step toward a future built on excellence.
**Submit your application today - your next opportunity is waiting.**
**Pay Details:** $0.00 to 25.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Description We are looking for a skilled Quality Assurance Analyst to join our team in Fort Washington, Pennsylvania. In this role, you will focus on ensuring the quality and reliability of Salesforce Marketing Cloud and Data Cloud platforms, playing a key part in supporting our real estate and asset management operations. This is a long-term contract position that provides an excellent opportunity to collaborate with cross-functional teams and contribute to the success of innovative marketing and data solutions.
Responsibilities:
- Conduct thorough testing of Salesforce Marketing Cloud components, including dynamic content and various studios and builders.
- Perform validation of Salesforce Data Cloud functionalities such as identity resolution, segmentation, activations, and unified individual reconciliation.
- Identify, document, and track defects or issues discovered during testing, and collaborate with developers to resolve them efficiently.
- Ensure data quality and accuracy within Salesforce Marketing Cloud and Data Cloud platforms, including integration and management processes.
- Develop and maintain comprehensive documentation for testing processes, test cases, and resolutions to defects.
- Create detailed test plans, test cases, and scripts based on project specifications and requirements.
- Analyze testing outcomes to identify opportunities for process improvements, tools, and methodologies.
- Partner with architects, designers, and marketing teams to ensure the quality and effectiveness of marketing campaigns and data workflows. Requirements - Hands-on experience with Salesforce Marketing Cloud, including its various studios and builders.
- Familiarity with diverse testing approaches such as functional, regression, and performance testing.
- Strong understanding of data management principles and practices within Salesforce Marketing Cloud and Data Cloud.
- Proven ability to analyze complex data, identify issues, and implement effective solutions.
- Salesforce Marketing Cloud and Data Cloud certifications are highly preferred.
- Experience working within Agile environments and familiarity with tools like Jira.
- Excellent problem-solving and analytical skills.
- Strong communication skills with the ability to collaborate effectively with technical and non-technical stakeholders. Technology Doesn't Change the World, People Do.®
Robert Half is the world's first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles.
Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app ( and get 1-tap apply, notifications of AI-matched jobs, and much more.
All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information.
© 2025 Robert Half. An Equal Opportunity Employer. M/F/Disability/Veterans. By clicking "Apply Now," you're agreeing to Robert Half's Terms of Use ( .

Description Primary Responsibilities:
- Develop and maintain detailed test scripts and test cases based on new and evolving website functionality.
- Execute test cases including end-to-end testing to validate functionality, usability, integration, and cross-browser compatibility.
- Log bugs and issues clearly and consistently within Jira, including steps to reproduce and indicating severity for all bug prioritization.
- Monitor Jira to track bug resolution progress and retesting activities.
- Collaborate closely with development teams to ensure timely fixes and verify issue resolution.
- Establish and document a repeatable testing workflow: test → log → resolve → retest → ready for business test → close.
- Perform smoke/sanity testing for initial build validation.
- Responsible and accountable for system and regression testing to validate system integrity after code changes.
- Serve as a consultant with Compliance Testing and Security Testing.
- Remain responsive with System testing and Regression testing updates resulting from changes with unit testing and disaster recovery testing.
- Support User Acceptance Testing (UAT) processes and coordinate with business testers as needed.
- Create and maintain test documentation and QA metrics to communicate status and risks.
- Ensure test coverage across supported browsers and devices to maintain consistent user experience.
- Coordinate and lead bug management with vendors and AD project team member with input from Product Owner and IT.
- Fulfill Quality Assurance responsibilities through Implementation including warranty.
- Participate in daily stand up and report on bug status and escalate blockers/concerns to PM and IT Manager.
Qualifications:
- Bachelor's degree in Information Systems, Computer Science, or related field, or equivalent experience.
- 3+ years of experience in website quality assurance or software testing roles.
- Strong understanding of the software development lifecycle and QA methodologies.
- Experience using Jira or similar issue tracking tools.
- Detail-oriented with strong analytical and troubleshooting skills.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively in a fast-paced project environment.
- Familiarity with content management systems such as Drupal is a plus.
- Experience in Agile/Scrum environments is preferred.
Knowledge, Skills, and Abilities:
- Strong understanding of web technologies (HTML, CSS, JavaScript) to help identify front-end issues and better communicate with developers.
- Experience with Drupal CMS or other content management systems to understand site structure and admin workflows.
- Familiarity with cross-browser and responsive design testing tools.
- Knowledge of QA tools and test case management systems.
- Understanding of software testing principles including functional, regression, smoke, and UAT testing.
- Ability to create and optimize test documentation to track cases, issues, and retesting outcomes.
- Experience in Agile development environments, including participation in sprint planning and retrospectives.
- Clear and concise communication skills to effectively report bugs and collaborate with cross-functional teams. Requirements Quality Assurance, Software Quality Assurance, JIRA, Drupal, Manual Test Scripts, Manual Testing, Automated Test Scripts Technology Doesn't Change the World, People Do.®
Robert Half is the world's first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles.
Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app ( and get 1-tap apply, notifications of AI-matched jobs, and much more.
All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information.
© 2025 Robert Half. An Equal Opportunity Employer. M/F/Disability/Veterans. By clicking "Apply Now," you're agreeing to Robert Half's Terms of Use ( .

Principal, Quality Assurance, GMP
Requisition ID:
70962
Date:
Sep 20, 2025
Location:
Exton, Pennsylvania, US
Department:
Quality
Description:
**This is a hybrid position (3 days per week) working in our office at Exton, PA. Candidates applying must be residing within a 50-mile commutable distance to the job location.**
At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
**Job Summary**
The Principal, Quality Assurance, GMP role focuses on ensuring compliance with cGMP standards within the WSS laboratories by identifying gaps, developing solutions, and overseeing their implementation. Collaborating with key stakeholders, the position ensures all improvements align with global quality and laboratory requirements. The role requires providing expert guidance on regulatory and industry standards concerning data integrity, including computer system validation, audit trails, electronic signatures, and data storage and retention.
**Essential Duties and Responsibilities**
+ Responsible to identify gaps, formulate solutions, and drive closure to achieve and maintain compliance with cGMP standards within the WSS laboratories.
+ Partner with key stakeholders to ensure that identified improvements are aligned with strategic global quality and lab requirements.
+ Provide expertise and guidance for regulatory and industry expectations in terms of data integrity requirements: computer system validation, audit trail, electronic signature, data storage and retention.
+ Perform recurring laboratory audits of quality test methods and results per established West procedures to confirm they are globally harmonized with respect to data recording and documentation.
+ Identify and implement meaningful metrics and KPI's to measure and improve WSS laboratory compliance.
+ Provide guidance to QA and WSS Lab during regulatory and client audits on issues related to Data Integrity and Computer System Validation (CSV).
+ Actively engage with the laboratory team to drive the completion of investigations and manage backlog when necessary; regularly analyze data trends to implement improvements and ensure customer expectations are met through effective reporting and communication.
+ Assist the QA Manager by ensuring WSS team members are trained in GMP-relevant topics and ensuring compliance with quality system documents, cGMPs, ISO standards, and FDA regulations.
**Education**
+ Bachelor's Degree and/or Masters in Science Technology or Engineering.
+ Master's Degree preferred
**Work Experience**
+ 8 years of quality-related experience with preferred experience in pharmaceutical and/or medical device industry
+ Expertise of cGMP requirements, ISO standards and FDA regulations
**Preferred Knowledge, Skills and Abilities**
+ Create multifaceted Laboratory procedures on GMP related topics such as data documentation, processes, documentation templates, etc., in alignment with global laboratory strategies.
+ Perform Expert-Level GMP review and approval of global laboratory documentation, i.e. check for compliance of Lab Records to cGMP requirements related to the activities of the global SME group.
+ Expertise of cGMP requirements, ISO standards, FDA regulations, and quality systems such as ISO 13485, ISO 9001, ISO 15378, 21 CFR 820, 21 CFR 11, ISO 14971
+ Working knowledge of various analytical instruments software and integration with LabVantage LIMS, Waters Nugenesis SDMS and Waters Empower desired.
+ Familiarity with MasterControl, SAP and working knowledge of statistical data analysis
+ Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description.
+ Ability to work independently, multi-task and thrive in fast-paced environment.
+ Thorough understanding of validation activities and risk management principles and techniques
+ Fluent in English
+ Excellent written and verbal communication skills
+ Strong problem-solving and critical thinking skills
+ Support and contribute to Lean Sigma programs and activities towards delivery of the set target
+ Able to comply with the company's safety policy at all times
+ Able to comply with the company's quality policy at all times. #LI-AP1 #LI-HYBRID
**Travel Requirements**
10%: Up to 26 business days per year
**Physical Requirements**
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
**Additional Requirements**
+ Adaptable to changes in the work environment, able to manage competing demands and deal with frequent change, delays, or unexpected events.
+ Must maintain the ability to work well with others in a variety of situations.
+ Maintain high attention to detail, accuracy, and overall quality of work.
+ Must be able to understand and adhere to established procedures, multi-task, work under time constraints, problem solve, and prioritize.
+ Effectively communicate and interface with various levels internally and with clients.
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.

Quality Operations Inspector -I

Position Summary

The Quality Assurance Inspector is responsible for providing on-the-floor quality oversight and support to ensure the compliance of manufacturing, packaging, labeling, and distribution operations with Piramal Standard Operating Procedures (SOPs) and applicable regulatory requirements. This includes adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity principles, and FDA regulations. The inspector plays a critical role in maintaining product quality, safety, efficacy, and regulatory compliance across operations.

Key Responsibilities

• Issue batch records in alignment with the production schedule to support timely manufacturing activities and Perform potency calculations as applicable.
• Conduct line clearance and batch readiness assessments, including verification of concurrent documentation, equipment status, and preventive maintenance records.
• Review and evaluate Environmental Monitoring (EM) data for compliance with internal standards and regulatory requirements.
• Perform BMS alarms review, acknowledgement and evaluate quality impact. Escalate critical alarms to Management.
• Perform quality oversight for water system releases used in operations.
• Perform raw material Sampling and AQL inspection of finished products.
• Review equipment logbooks and executed batch records to ensure adherence to GDP, GMP, and Data Integrity standards.
• Scan reviewed batch records and upload to share point.
• Prepare batch records and perform first release of batches.
• Perform Raw material reconciliation and investigation.
• Review and approve Calibration activities in ProCal.
• Perform QA review and approval of non-routine workorders in SAP.
• Draft, revise, and review Quality Assurance SOPs and deviation reports to ensure clarity, accuracy, and regulatory alignment.
• Conduct weekly quality surveillance activities, including facility inspections, environmental monitoring checks, and audits of equipment maintenance and GMP practices to support continuous audit readiness.
• Complete all assigned training on SOPs and job-related tasks in a timely manner.
• Stay current with industry trends, updates to regulatory requirements, and emerging quality standards.
• Perform all other activities as assigned by Manager

Experience:

• 13+ years of experience in pharmaceutical quality assurance, regulatory affairs, or GMP auditing.
• Prior experience in providing on-the-floor quality oversight and conducting inspections or working in a regulated pharmaceutical environment preferred.

Skills:

• In-depth knowledge of GMP, GDP, GLP, and relevant international regulations (FDA, EMA).
• Strong analytical, attention to detail investigative, and problem-solving skills.
• Excellent communication (written and verbal) and interpersonal skills.
• Proficiency in MS Office and quality management systems (QMS).
• Ability to travel to facilities for inspections (as required).

Job Overview

The Supervisor, Quality Assurance (QA) will lead and develop assigned quality personnel and provide guidance for cross-functional teams to support the quality and food safety requirements of the products produced and shipped from their location. This role also supports and enforces the certification, regulatory, customer, and brand requirements as outlined by the business and implements continuous improvement projects to meet these requirements while ensuring the safety of our people, workplace and environment and meeting all company, legal and other requirements.

Duties & Responsibilities

• Supervise, lead, and motivate a team on the manufacturing floor and QA Lab to deliver results by communicating company goals; including quality and customer satisfaction, safety practices, and deadlines.
• Direction of all QA associates.
• Engage and develop teammates through effective performance management, coaching, and training.
• Implement continuous improvement methods while maintaining customer focus, and embody company purpose and values to inspire servant leadership
• Manage and support Libertys vision that ensures company quality assurance specifications, and regulatory requirements are met; understand and support the documentation, training, and organizational requirements for maintaining a globally recognized quality and food safety certification; serve as a program owner, and perform internal audits to ensure compliance.
• Manage the processing of laboratory data, monitor the data for accuracy through exception reporting, analyze the data, recognize unfavorable trends, and make process improvement recommendations.
• Support and assist in audits from internal and external regulatory, certification, customer, and or brand owner sources.
• Any special projects relating to Quality Assurance.
• Focus on removing costs, continuous improvement, removing inefficiencies, and complexity for the supply chain.
• Ensures that all work assessments and activities are in accordance with policies of LCCB and presiding labor agreements.

Knowledge, Skills, & Abilities

• Manufacturing experience and Food Industry knowledge
• Familiarity with lab equipment and testing within a manufacturing environment
• Math and analytical skills and problem-solving ability
• Computer skills including MS Office, statistical software, SAP preferred
• Knowledge of sanitation and beverage processes
• Must be able give direction and make critical decisions
• Knowledge of microbial and aseptic techniques
• Ability to multitask in team development, time management, and effective communication skills
• Ability to work in a fast-paced food manufacturing environment with seasonal temperatures and flexible shifts based on business needs
• Ability to stand for extended periods of time; walking manufacturing floor; climbing stairs, and lift, up to 60lbs

Minimum Qualifications

• 1 -3 years Manufacturing experience and Food Industry knowledge
• Familiarity with lab equipment and testing within a manufacturing environment
• Math and analytical skills and problem-solving ability
• Computer skills including MS Office, statistical software, SAP preferred
• Knowledge of sanitation and beverage processes
• Must be able give direction and make critical decisions
• Knowledge of microbial and aseptic techniques
• Ability to multitask in team development, time management, and effective communication skills
• Ability to work in a fast-paced food manufacturing environment with seasonal temperatures and flexible shifts based on business needs
• Ability to stand for extended periods of time; walking manufacturing floor; climbing stairs, and lift, up to 60lbs

Preferred Qualifications

• Degree or experience in Biology, Chemistry, Food Science, Health Sciences.
• Previous supervisory experience in a Manufacturing environment is an asset.
• Knowledge of water treatment systems.
• Labor relations experience is an asset.

Work Environment

• Noisy, wet, and extreme temperature environment

Quality Assurance Batch Record Reviewer – Newtown, PA

Responsible for performing tasks to specifications related to oral solid and liquid dose pharmaceutical packaging. Processes include reviewing of batch records for the packaging department. Author the Quality Assurance related procedures and process them through Master Control. When required, provide assistance in deviation related activity.

• Key duties and Responsibilities Review the completed batch records for packaging.
• Serve as backup for review of packaging documents when required.
• Ensure the batch records have the proper signature, documentation and completed entries.
• Review to ensure accurate completion of equipment logs.
• Ensure all batch records are accounted for and transferred to the QA department.
• Ensure all entries are entered into the computer system.
• Identify and report quality issues to management.
• Report accidents, unsafe conditions or unusual circumstances to supervisor.
• Adhere to all relevant cGMP and FDA regulations.
• Maintaining a neat and orderly work area at all times
• Provide a support to Investigation team as and when needed.
• Other duties, which may be assigned from time to time, by management of the company
• Comply with FDA guidelines/Company Policies of Data Integrity
• Prepare, review and approve Standard Operating Procedures in Master Control.
• Education and Experience High school diploma or equivalent preferred ‘
• 1+ year of previous experience in a similar position
• Ability to read and comprehend documents such as batch records, packaging instructions, SOPs and training materials.
• Proficient communication skills, both verbal and written.
• Computer experience with basic programs preferred.

Job Description

JOB SUMMARY

Lehigh Valley Dairy has an immediate job opening for a quality assurance technician to perform microbiological and chemical testing of finished products, raw materials and associated items, while adhering to food safety and quality system requirements by committing to meet all pertinent regulatory, customer and SQF requirements. The person in this position would need to maintain all applicable standard operating procedures, while utilizing a continuous improvement mindset, and assist in identifying opportunities to improve processes.

Lehigh Valley Dairy is a farmer-owned brand of Dairy Farmers of America (DFA), a dairy marketing cooperative owned by more than 12,500 family farmers. Our mark matters and it represents the wholesomeness of dairy that we share with our communities and loved ones. DFA manufactures a variety of dairy products, including cheese, butter, fluid milk, ice cream, dairy ingredients and more, under well-known and established regional brands. Our fingerprints touch thousands of brands across the marketplace, and we’re passionate about delivering the simple pleasures of dairy to people everywhere, straight from our family farm-owners. At Lehigh Valley Dairy we are proud to provide families with fresh, delicious dairy.

By joining DFA, you can help us continue to make a difference that matters. We care deeply about the well-being of our neighbors and friends, and we celebrate the diversity of our company and our world. It takes an incredible team to deliver the goodness of dairy and enrich our communities – come join us!

OUR TECHNICIANS FOR THIS POSITION CAN MAKE UP TO:

• $27.97

SCHEDULE: 2nd Shift - Rotating four 10 hour shifts

BENEFITS:

• 401(k) or 401(k) with company contribution*

• Competitive pay

• Paid vacation and holidays*

• Career growth opportunities – we promote from within!

• Comprehensive healthcare benefits

• Service recognition and employee rewards*

• Employee referral program

• Uniforms provided

• Work for dairy farm families

• More benefits, too many to name

* varies by company and governing CBAs

Requirements

REQUIREMENTS:

• High school diploma or GED required

• Associate’s or bachelor’s degree in related field preferred

• 1–2 years related experience required

• Must be able to pass all pre-employment screenings including drug, background and criminal checks

• Able to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals

• Effective verbal and written communication skills

• Ability to flavor milk-based, sugar-based and caffeine-based products

• Must be able to stand, walk, kneel, and bend for virtually the entire shift

• Must be able to lift up to 25 pounds, occasionally including overhead

• Must be able to effectively work in a team environment

• Must be able to work in a wet environment

• May occasionally be exposed to chemicals

• Must be willing to work flexible hours including overtime as required, occasional weekends and holidays

DFA is an Equal Opportunity Employer

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EEO Statement

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Pay Range 27.97