RWJBH is seeking a Food Service Supervisor in the Dietary-Management Department at our New Brunswick campus.$77k-128k yearly est.6d ago
Clinical Care Management Supervisor - Child Acute Services
Oversees daily operations of Clinical Care Managers and other direct reports of the Child Acute Services Team (i.e. The Clinical Care Management Supervisor is responsible for the daily supervision and oversight of clinical team members. Develops specific protocols for communication between Clinical Care Managers and other direct reports and providers. The Clinical Care Management Supervisor is responsible for ensuring that services are authorized according to medical necessity criteria and in accordance with the CBH mission and contractual obligations. Accompanies Clinical Care Managers and other direct reports into the community between 15 and 25% of work time to provide ongoing clinical supervision and feedback. Community Behavioral Health (CBH) will hold each employee accountable for the following expectations which align with our mission, vision, and corporate code of conduct. Manage day to day operations of Clinical Care Managers and other direct reports.$54k-89k yearly est.1d ago
Director, Operations Portfolio Lead
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. But working at Bristol Myers Squibb is anything but usual.$132k-165k yearly est.20h ago
Universal Supervisor
* Monitors staff to ensure compliance with *Firstrust's *policies and procedures. * Makes decisions and provides Supervisor Overrides for transactions within their supervisor authority level limits. * Will help champion all sales, service and Firstrust strategic initiatives. 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.$22k-25k yearly est.2d ago
Operations Supervisor
Kellogg Company is a multibillion-dollar company with over 30 thousand employees all over the globe. to get insights into our hiring process and how to best prepare for a Kellogg interview. Having a safety first attitude is important at Kellogg Company since people safety and food safety are two of our values.$40k-65k yearly est.3d ago
Appian Lead-Richardson,TX, 5-8 Years REMOTE
Hello All,
Good Morning!
We have an urgent need for the position of Appian Lead expecting 5-8 Years of profiles for the location Richardson, TX as a REMOTE position for the client Honeywell_Infosys
Please find the job details below and confirm. Please email me or call me if you have any questions. Thanks.
PFB JD
Job Details:
Must Have Skills
APPAIN DESIGN
APPAIN IMPLEMENTATION
APPAIN TL
Detailed Job Description
APPAIN TL with 5 years experience in requirements , design, development and leading teams in guiding in delivery should be certified TL to deliver the Appain implementation
Ability to work in PRPC UI, PM, Rules, and Integration services
Minimum years of experience
5-8 years
Top 3 responsibilities you would expect the Subcon to shoulder and execute
APPAIN DESIGN
APPAIN TL
APPAIN IMPLEMENTATION
Deepa Prasanna, US IT Recruiter
Ascii Group LLC,
www.asciigroup.com
deepa.prasanna@asciigroup.com
+1(848)-229-2222
$85k-113k yearly est.1d ago
Production Manager
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. Mavuno Harvest is a performance-based culture where employees can do their best work in a rapidly growing operation. 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.$51k-88k yearly est.2d ago
Lead/Supervisor Transmission Engineer
Insight Global is looking for a Supervisor Transmission Engineer.$36k-67k yearly est.16d ago
Production Manager
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.10d ago
Field Service Supervisor
Employment with ABARTA Coca-Cola Beverages, LLC is contingent on a pre-employment background check which may include drug screening, driving records (including minor moving violations) and will be evaluated according to ABARTA Coca-Cola Beverages, LLC guidelines to determine eligibility for this position. Accountable for delivering the Field Service vision and strategy. Supervisor, Field Service Company: ABARTA Coca-Cola Beverages Department: Field & Cooler Service Team Job Location: 4900 Lehigh Valley, PA Other Potential Locations: Lehigh Valley; Reading, PA We are actively seeking enthusiastic team players who want to work with the world's most trusted and iconic brands.$36k-54k yearly est.7d ago
Team Lead
Here are a few good reasons in addition to competitive pay to work at Conduent: Team Lead $21/Hr Full-time (ON-SITE) Do you have a great attention to detail? Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them.$21 hourly3d ago
Team Lead Reset English Spanish
En SPAR, buscamos individuos din micos y motivados que est n apasionados por lo que hacen. You'll be responsible for providing direction to the crew and acting as the liaison between the client, crew, and SPAR management team. SPAR es una compa a l der en la industria de merchandising e instalaci n y estamos creciendo nuestro equipo! SPAR is a leading company in the merchandising and installation industry, and we're growing our team! SPAR is much more than just a retail merchandising company. At SPAR, we're looking for dynamic and driven individuals who are passionate about what they do. Follow given directions from SPAR and/or Client Management and delegate tasks to other crew members Directing the crew and being the liaison between client, crew and SPAR management team$64k-125k yearly est.3d ago
Quality Control Supervisor
JCW is recruiting for a Quality Control Supervisor for a globally leading Contract Development and Manufacturing Organization (CDMO) in the Pharmaceutical Industry. This position is a 2nd shift position and is located in Sellersville, PA.$55k-79k yearly est.22d ago
Fullstack UI Lead
React Js
Node Js
Python
AWS IOT
Kinesis
DynamoDB
Edge Framework
IOT communication Protocols
Full Stack Development
$112k-165k yearly est.19d 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.
Communication flow
Training
Monitoring strategy and methods (e.g., remote, on-site, etc.)
Site training
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
QUALIFICATIONS
• 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.2d ago
Sushi Team Leader
R0172370 As a culinary leader in our kitchen, you are a team player and positive role model that ensures the development and education of the cooks. Putting our people first and offering competitive pay and a variety of benefits & perks is just the start of what it means to work at Wegmans. At Wegmans, we've long believed we can achieve our goals only if we first fulfill the needs of our people. Location: Princeton, NJ$21-22 hourly2d ago
Quality Assurance Supervisor
Quality Assurance Supervisor
Location: New Jersey, USA
Report to: Quality Director
Key Responsibilities:
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.
Qualifications:
· 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.10d 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.
Responsibilities
:
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.22d ago
Veeva Customer Relationship Management (CRM) Team Lead
Rqmts: MS or foreign equiv deg in Computer Sci, Electronics Engg, Electrical Engg or rlt fld; 2 yrs exp as Veeva Customer Relationship Management (CRM) Team Lead or 2 yrs CRM exp in pharma industry. Veeva Customer Relationship Management (CRM) Team Lead For Conexus Solutions, Inc. - Princeton, NJ, work w/ dvlprs to plan & deliver on customer rqmts throughout dvlpmt life cycle; keep clients & serv teams informed of status, commun.$106k-153k yearly est.5d ago
Chemical Production Manager
QUAD
is seeking a
Chemical Production Manager
for our client's
Hatfield, PA
manufacturing site.
The
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.
Responsibilities:
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
Skills/ Competencies:
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
Additional Details:
Employment Type: Direct Hire
Salary: to $110k + bonus
$51k-88k yearly est.18d ago
How much does a Supervisor earn in Lower Makefield, PA?
The average supervisor in Lower Makefield, PA earns between $28,000 and $90,000 annually. This compares to the national average supervisor range of $31,000 to $92,000.
What is the job market like for supervisors in Lower Makefield, PA?
The job market is good for supervisors in Lower Makefield, PA. The number of supervisor jobs have grown by 204% in the last year. Right now there are currently 3,414 supervisor jobs available in Lower Makefield, PA.
Active Supervisors Job Openings By Month
Year
Month
Number of Supervisor Jobs
2022
May
3,414
2022
April
3,893
2022
March
3,938
2022
February
911
2022
January
2,673
2021
December
3,113
2021
November
2,711
2021
October
2,316
2021
September
1,295
2021
August
1,785
2021
July
732
2021
June
1,103
2021
May
1,123
2021
April
1,430
You can compare the number of available jobs in Lower Makefield to the number of supervisor jobs in surrounding cities.