* Makes decisions and provides Supervisor Overrides for transactions within their supervisor authority level limits. Objective:The Universal Supervisor serves customers by being the single point of contact for walk-in customers, fulfilling sales, service and referral needs for a seamless customer experience. * Will help champion all sales, service and Firstrust strategic initiatives. * Monitors staff to ensure compliance with *Firstrust's *policies and procedures.$22k-25k yearly est.1d ago
Mavuno Harvest is a leading manufacturer of packaged organic snacks, operating a production facility in Philadelphia, PA. At Mavuno Harvest, our key values revolve around our people first. Reporting to the operations manager and CEO, the successful candidate will be responsible for managing a small team of production workers, using a multi head weigher machine and hand-packing operation. Mavuno Harvest is a performance-based culture where employees can do their best work in a rapidly growing operation.$51k-88k yearly est.1d ago
Kellogg Company is a multibillion-dollar company with over 30 thousand employees all over the globe. Having a safety first attitude is important at Kellogg Company since people safety and food safety are two of our values. to get insights into our hiring process and how to best prepare for a Kellogg interview.$40k-65k yearly est.2d ago
Gwynedd Manufacturing, a growing defense contractor located in North Wales, PA, is a state-of-the-art manufacturing facility dedicated to producing quality products for the U.S. Department of Defense and various U.S. Federal Law Enforcement Agencies. The Production Manager is responsible for a supervising the production processes and ensure they stay within budget and enhance efficiencies.$51k-88k yearly est.9d ago
Lead/Supervisor Transmission Engineer
Insight Global is looking for a Supervisor Transmission Engineer.$36k-67k yearly est.15d ago
Clinical Operations Lead
Responsible for the overall Site Management activities and therefore the overall study site relationship status for the region assigned.
An additional 2 years of on-site monitoring and clinical research experience or education; industry certification preferred.
Monitoring strategy and methods (e.g., remote, on-site, etc.)
Investigator Site File oversight
Investigational product management
Source data verification processes
Protocol deviation reporting
Actively participates in the study startup process including site identification, qualification, selection and initiation activities
Coordinate Study-Start up activities and collaborating with Global Study-Start-Up per study timelines
Lead Clinical activities through site selection, activation, maintenance and study closure
• For countries other than US and Canada, a minimum of 2 years of experience conducting and supporting RA/CA and IRB/EC submissions and regulatory document start-up activities.
• Excellent verbal and written communication, and presentation skills
• Excellent interpersonal and organizational skills with attention to detail
• Strong computer proficiency in MS Office including Outlook, Word, Excel, and PowerPoint
• Strong critical thinking, problem solving and analytical skills
• Ability to efficiently organize and prioritize tasks within a multifaceted framework and set deadlines
• Excellent documentation skills
•Ability to maintain excellent working relationships with a broad range of trial staff
• Ability to work well in a team environment but also independently without significant oversight; Flexibility in work hours and ability to travel$46k-67k yearly est.1d ago
Then this Production Operator opportunity could be the right fit for you. This exciting Production Operator opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, stock options, paid PTO, tuition reimbursement, tuition assistance etc. 1+ year of experience required as production operator pharmaceutical / manufacturing environment.$17 hourly31d ago
Quality Control Supervisor
This position is a 2nd shift position and is located in Sellersville, PA. JCW is recruiting for a Quality Control Supervisor for a globally leading Contract Development and Manufacturing Organization (CDMO) in the Pharmaceutical Industry.$55k-79k yearly est.21d ago
Location: Doylestown, PA in Doylestown, PA. FLIK Hospitality Group- a member of Compass Group USA, is now hiring a$50k-52k yearly9d ago
Chemical Production Manager
is seeking a
Chemical Production Manager
for our client's
Chemical Production Manager
will be responsible for managing and coordinating daily plastics production and ensuring safety and environmental standards, timely customer commitments, and product quality are met.
Managing plant safety procedures
Documenting safety observations for improvement
Ensuring standard operating procedures are in compliance
Handling employee performance review and coaching
Holding personnel accountable for production and productivity expectations
Overseeing training processes and programs
Ensuring all quality system and control procedures are followed
Identifying continuous improvement opportunities
Collaborating with Engineering on capital project management
Ensuring all production plans and schedules are met
Ensuring effective cost controls
Bachelor's degree in Engineering, Science, or Manufacturing
Must have chemical industry experience
5-10 years plastics and/or chemical manufacturing experience
Strong organizational skills, with ability to handle multiple projects simultaneously
Strong communication skills
Ability to work effectively independently within a matrix organization
Microsoft Office proficiency
Employment Type: Direct Hire
Salary: to $110k + bonus
$51k-88k yearly est.17d ago
QUALITY ASSURANCE SUPERVISOR
IPQA Supervisor will support and assist activities related to the production of pharmaceutical products in accordance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and batch record specification. The IPQA Associate shall assure compliance with all standards and regulatory guidelines.
Supervise IPQA activities at shop floor.
Preparation and review of Annual Product Review - APR
Writes Protocols, CAPAS & Deviations as assigned and with guidance
Participate in the execution of validation and process improvement activities
Review and approvals of QRMs and Mitigation action items as part of QRM closure.
Handling of Out of specification, out of trends, and Environmental excursions.
Ensuring the implementation of CAPA and performing its effectiveness review.
Assessing the impact of the changes and ensure the closure of Change Controls as per procedure.
Responsible for review the master formulae records, manufacturing records and Batch release.
Providing training to shop floor people.
Execution of line clearances (Rooms / Equipment) and verification of start-up activities and In-Process checks.
Monitors compliance in Manufacturing, Packaging, Product Development/Technical Services (PDTS) and Warehouse areas
Performs AQL Sampling and inspection
Monitor and maintain cGMP activities at the plant.
Carrying out of Media fill validation, process validation and cleaning validations.
Preparation/review of SOPs and BMRs and BPRs.
Ensuring online documentation during manufacturing.
Involve investigations to determine root cause and corrective actions. Review of documents of respective areas and logbooks for adequacy and completeness.
Qualifications - Skills & Requirements:
Minimum of 6-8 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.
Good communication skills and capable of communicate with all levels Be able to work long hours to support production requirements Be available for overtime, including weekends, as needed for production support A familiarity with cGMPS, CFRs, OSHA and FDA regulations.$60k-85k yearly est.21d ago
URBN Production Coordinator
Location Philadelphia, PA$38k-54k yearly est.21d ago
Quality Assurance Supervisor
Quality Assurance Supervisor
Location: New Jersey, USA
Report to: Quality Director
l Responsible for establishing and maintaining the quality management system, including developing quality policies and procedures, organizing on-site inspection, conducting risk assessments, conducting internal/external audits, managing documents, managing materials and suppliers, etc.
l Responsible for Complaint, Deviation, OOS and other abnormal event handling.
l Responsible for promoting the culture of continuous improvement within the organization and encouraging employees to identify quality-related opportunities for improvement to drive process efficiency and effectiveness.
l Responsible for guiding, training, and motivating members of the quality assurance team to ensure that they possess the necessary skills and knowledge to effectively fulfill their job responsibilities.
l Participate in and contribute to other QA and cross-functional projects as required.
· BS/MS in Life Science or related field.
· 5+ years of experience in biotech industry/drug/IVD quality assurance.
· Experienced in ISO9001:2015/ISO13485/cGMP compliance requirements, clear understanding of pharma/ biotech industry compliance principles and practices.
· Excellent personal skills, the ability to lead and influence by example, strong analytical and problem-solving skills, effective communication and interpersonal skills.$71k-92k yearly est.9d ago
Finishing End Operator - Production Technician
Operator must have completed Pennsauken forklift program.$41k-50k yearly est.22d ago
Landscape Production Manager
We're looking for a Production Manager to join our team. + Coordinating materials, people, equipment and subcontractors to ensure job site quality meets BrightView standards At BrightView, we're a tight-knit crew who are as passionate about caring for our clients as we are about each other.$46k-69k yearly est.60d+ ago
Quality Control Laboratory Supervisor
12. Participates in all 005 and OOT investigations within the Quality Control Lab. Provides oversight of the Chemists within their group, the testing methods of pharmaceutical dosage forms (OTC)/Dietary Supplements and raw materials to ensure that the proper quantitative analysis is conducted upon receipt of pharmaceutical raw material and finished products within the Quality Control Laboratory. The Quality Control (QC) Supervisor position supervises a small group of laboratory chemists who are responsible for conducting analysis of pharmaceutical dosage forms (OTC)/ Dietary Supplements and raw materials utilizing HPLC, GC, dissolution testing, spectroscopic and wet chemistry techniques. 11. Performs supervisory responsibilities for the team to ensure cGMP and cGLP in Quality Control Lab. 6. Conducts routine analytical testing for the release of raw materials, in process and finished products, writes SOPs, all analytical data, reports and documents for Quality Control laboratory.$54k-83k yearly est.15d ago
is a key member of the Prestone Freehold Leadership Team and is responsibilities for overall production management of a high-volume automotive chemicals consumer products manufacturing plant. We are searching for a manufacturing leader to own the entire production process and strategize with other internal teams to ensure operational excellence and continuous improvement. Must be a demonstrated progressive leader, with track record of meeting and exceeding production goals. Is technically talented, entrepreneurial, and a self starter. Strengths will include communication, coaching and mentoring skills, and promotes enhanced employee relations.
Specific duties and responsibilities:
Achieve adherence of daily packaging line schedule, including production line standard rates, labor efficiencies, product quality, overall Good Manufacturing Practices (GMP/Housekeeping) and employee safety
Oversee activities of production lines to achieve production rates that meet or exceed standards (including efficient changeovers)
Accountable for overall preparation to run, including coordination of line mechanical set-ups, product supply and material supply from leads and warehousing that meets scheduled line start-up
Train and manage performance of team members to ensure that each line is staffed with qualified and motivated individuals
Ensure the identification of product quality problems and implementation of corrective actions
Utilize theory of constraints or lean manufacturing techniques to evaluate and manage production counts, machine speeds, scrap and downtime to drive reliability to desired levels
Record and report accurate production counts, machine speeds, scrap counts, line down time, and other data
Ensure adequate supply of materials (skid tickets, skid records, gloves) (staging and de-staging)
Ensure correct product labor/speed standard
Meet deadlines to deliver production requirements (Flexible work schedule)
Prepare and conduct new hire and annual performance reviews
Bachelor's degree in Engineering with 3+ years' experience managing a team is preferred; however 10 years of relevant manufacturing leadership experience including filling operations, lean manufacturing practices and/or 5S may be considered in lieu of degree
Liquid filling and packaging operations experience is preferred; blow molding and chemical manufacturing an added plus
SAP, JDE or relevant ERP experience required
Experience with mechanical preventative maintenance systems required, including knowledge of and/or learning equipment as needed
Must be driven with a desire to progress through promotion
Must be collaborative - a relationship and team builder
Strong Excel skills a must
KIK is an Equal Employment Opportunity / Affirmative Action employer. KIK does not discriminate against qualified applicants or employees based on race, color, age, religion, sex, pregnancy, national origin, ancestry, age, physical or mental disability, veteran status, status in uniformed services, sexual orientation, gender identity, gender expression, marital status, genetic information, or any other status protected by law.
$52k-88k yearly est.1d ago
Production Supervisor - Day Shift
Today, that discovery is Rust-Oleum Corporation. As our Production Supervisor you will be there to supervise the shift to manufacture paint and related products.$39k-49k yearly est.60d+ ago
ARC Production Supervisor
The Salvation Army ARC is seeking a Production Supervisor to supervise and coordinate the warehouse and truck operations to ensure efficiency in production. The Salvation Army's Adult Rehabilitation Centers make a difference in people's lives.$40k-58k yearly est.16d ago
Dowhas an exciting opportunity available as Production Operatorat the Croydon, PAsite. Primary location Croydon (PA, USA), Pennsylvania, United States of America Withcareers at Dow, we take time to explore questions and talk to each other. Learn more about our partnerships, collaborations and innovations on LinkedIn (@Dow) or Twitter (@DowNewsroom). At Dow, we believe in putting people first and we're passionate about delivering integrity, respect and safety to our customers, our employees and the planet.$34k-39k yearly est.60d+ ago
What is the job market like for production supervisors in Lower Makefield, PA?
The job market is good for production supervisors in Lower Makefield, PA. The number of production supervisor jobs have grown by 295% in the last year. Right now there are currently 1,193 production supervisor jobs available in Lower Makefield, PA.
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