Quality Control Analyst Jobs in Lower Makefield, PA
- 256 Jobs
Quality Control Analyst
Title: Quality Control / LIMS Specialist$37k-62k yearly est.11d ago
Quality Assurance Associate
-Minimum of 10 years working in pharmaceutical aseptic manufacturing operations and quality assurance$47k-69k yearly est.3d ago
QC Lead Inspector
Piper Companies is looking for a QC Lead Inspector in Warminster, PA to join a leading manufacturer in the medical and aerospace industry.$25-27 hourly12d ago
Quality Control Technician
Summary
Our Client, a Fortune 500 Biomedical Company, has engaged GForce Life Sciences to provide a Quality Control Technician. This position will report to a Quality Manager within Quality. This individual will be responsible for the analysis, testing plans, and protocols of raw materials, intermediates, and finished products manufactured or received.
Duties / Expectations of Role
Responsible for the analysis of raw materials, intermediates, and finished products manufactured or received with an emphasis on standard operating procedures and good laboratory practices
Participate on special project teams designed to improve production and laboratory processes
Autonomous analysis required
Interpretation of raw data
Ability to utilize aseptic technique and other essential lab skills
Ability to troubleshoot testing issues
Receive and maintain traceability and integrity of test samples, reagents and materials used in the laboratory per approved procedures
Develop, revise and review SOPs.
Mandatory Requirements
Bachelor's degree in Biology, Chemistry, Microbiology or related discipline
1-2 years of previous lab experience
Ability to utilize aseptic technique and other essential lab skills
Ability to troubleshoot testing issues
Proven ability to follow written SOPs
Experience with Environmental Monitoring
Nice to Have
· SAP experience
· Cultures process and co-products
· Experience writing formal documents such as analytical procedures.
Term & Start
6 month+ Contract to Hire
Start ASAP
Full Time Onsite in PA
$32k-45k yearly est.11d ago
Quality Control Inspector
We are seeking an experienced Quality Control Manager$27k-44k yearly est.13d 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.24d ago
Quality Control Analyst, Microbiology
: The QC Analyst will support quality control microbiology testing operations. Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus. The quality control microbiology testing programs include in-process and final drug product microbial testing such as bioburden, endotoxin, gram stain, environmental monitoring, compressed gas monitoring, and/or sterility techniques. Perform daily cGMP quality control laboratory microbiological testing activities at the iCTC facility.$37k-60k yearly est.22d ago
Chem Tech
Our client, a leader in contract laboratory services, regulatory guidance and supply chain assurance within the pharmaceutical and biopharma industry is hiring for a Chem Tech.$36k-47k yearly est.16d ago
INT16520 Quality Control Inspector
Role: Quality Control Inspector II Location: Plainsboro, NJ - 8536$30k-49k yearly est.8d ago
Entry Level Chemist
Students should have a bachelors in chemistry/chemical engineering or any scientific field
Perform lab raw material release testing and other analyses as needed for cosmetic/ drug products and provide critical analysis of results.
Provide detailed reports of analytical results to project leadership.
The candidate should have experience in lab scale batching and formulation
, Proficient with laboratory Standard Operating Procedures, Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP).
• Proficient with the use of basic lab instrumentation skills like Viscometer, pH Meter.
• Skilled in technical documentation including writing scientific reports.
• Proficient in Microsoft Office and excellent verbal and written skills
• Preferably exposure or an internship in a personal care products company formulating Emulsions and Cleansers and at minimum, the candidate should have a Bachelor's degree in Science/Engineering.
• Ability to work cross-functionally in a team environment while being an individual contributor is required and experience managing multiple projects is required.
Chemistry background
$59k-82k yearly est.4d ago
Technology Chemist
Salvona uses microencapsulation technologies for topical cosmetic and dermatology applications. As such, the Technology Chemist will be responsible to develop product concepts, create additional technologies and interact with the customers to troubleshoot/answer any formulation based questions. Provide technical support to promote the sale of Salvona products, microencapsulation based technologies. In addition, the Technology Chemist will support Salvona's sales with technical skills and marketing tools.$42k-63k yearly est.4d ago
QC Stability Specialist
The Sr. QC Stability & Specification Specialist will be responsible for the oversight and execution of stability studies covering a growing pipeline of ground-breaking clinical and commercial programs.$37k-66k yearly est.4d ago
Chemist II (Associate)
Position: Chemist - II (Associate) Hi My name is Gaurav, and I am a recruiter with Net2Source Inc, a Global Workforce Solutions company headquartered in New Jersey.$42k-60k yearly est.11d ago
Research and Development Technologist
We are currently looking to recruit a Product Development Technologist for either our Philadelphia location or Plymouth location. At Zentis - We are Fruit Masters! The Company's North America operations are located in Philadelphia, Pennsylvania and Plymouth, Indiana, where we produce fruit and dairy preparations for a variety of customers including yogurt, ice cream and bakery manufacturers. Zentis is Europe's number one fruit processing company and one of the leading brand manufacturers of jams, sweets, and custard-based desserts.$58k-82k yearly est.10d ago
QC Analytical Chemist I
Location: On-site in Cranbury, NJ$64k-79k yearly est.25d ago
Technician - R&D Operations
Imagine
...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process.
We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture.
We are looking for an individual who enjoys working in a fast-paced, team oriented environment, likes to be challenged, and values the opportunity to make a difference.
Job Summary
The R&D Technician will conduct the execution of kitchen and/or plant operations as well as demonstrate strict adherence to all safety and quality requirements for R&D Operations. They will have the ability to work independently and be self-motivated in meeting all customer service and team-oriented goals. Working in a fast-paced environment with continuously changing requirements and procedures, their ability to apprehend, adapt, and deliver results with precision will be key in successfully delivering job requirements.
Principal Accountabilities
10% - Conduct work activities in accordance with all safety and quality requirements.
15% - Execute documentation requirements accurately for all product executions per food safety and quality
programs and procedures.
50% - Operation of equipment and processes to produce safe and wholesome food.
10% - Support manual production processes of manufacturing executions.
10% - Sanitation and general cleaning in adherence to Standard Sanitation Operating Procedures.
5% - Responsibility for Health & Safety program
Job Complexity
Oversee sterilization process to ensure appropriate process occurs and is documented per regulatory requirements.
Execute critical process procedures to deliver expected production results in a timely manner
Ensure work is done in accordance with Food Safety and Health & Safety guidelines.
Maintain in-depth understanding of equipment and process operation/execution
Safely handle and utilize cleaning chemicals to administer sanitation procedures
Knowledge
and Skill Requirements
Effective communication skills
Work in a team environment and promote team values
Ability to be self-directed through time and priority management
Attention to detail
Accurate and timely completion of records
Ability to follow through on commitments
Background in food processing and quality assurance
Problem solving/analytical thinking
Education and Experience
HS Diploma or equivalent
Location:
Camden-based
Working conditions
Professional, business casual setting in fast paced food manufacturing environment. Standing environment, must be able to lift 50 pounds
Compensation and Benefits:
The base salary range for this full-time, salaried position is between
$44,000.00 - $70,400.00
Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package.
The Company is committed to providing equal opportunity for employees and applicants in all aspects of the employment relationship, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, veteran status, disability, age, religion, or any other classification protected by law.
In that regard, U.S. applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
$44k-70.4k yearly2d ago
Global Product Quality Complaints Associate
Pay Range: $23hr- $26.50hr
Support the Global Product Quality Complaint (PQC) process for the biosterile, pharmaceuticals and combination drug/device products with respect to product quality complaints.
Analyze, identify and execute continuous improvement initiatives within the process while collaborating within the PQC headquarters team as well as with key stakeholders, including internal and external sites and in-market supply chain quality.
This individual will be a valued team member of one of several cross-functional, multi-divisional teams which are responsible for developing and executing Global Quality Systems (GQS) initiatives and strategies for clients, with focus on the global PQC process.
Roles and Responsibilities:
Provide ongoing management for PQCs ensuring compliance to global framework of GMP policies and client procedures.
Support the Global Product Quality Complaint (PQC) processing activities at PQC Headquarters.
Participate in PQC HQ team meetings for the processing of, and improvements to, global client PQC processes, including but not limited to: PQC case intake, triage, due diligence activities, product replacements and patient reimbursements/refunds; metrics generation and slide presentation; PQC training delivery and management; new product launches; PQC related Quality Management System (QMS).
Support tracking, trending and other ancillary activities for controlled documents (SOPs/Job Aids/Templates); record archivals; quality deviations and CAPA involving PQC HQ and provide quality and compliance support for these processes.
Assist in implementation of Quality Risk Management principles in evaluation and investigation of PQCs. Support PQC related audits and inspections as necessary.
Participate in QMS business process requirements development and validation activities as necessary.
This opportunity is cross functional and will involve the management of mid-size projects between PQC HQ and other areas of the organization.
Qualification Requirements:
BS/BA in Sciences (i.e Chemistry, Biology, Biochemistry, Microbiology, Pharmacy), engineering, business.
Enrolled in a Bachelor's, Masters or MBA degree program.
Preferred Completion of Bachelors and enrolled in graduate studies.
Skills/Competencies:
Microsoft Office (Power point, Excel, Word, Outlook).
Project Management expertise with advanced PowerPoint preferred.
Basic statistics/analytics; clear communications.
Ability to manage deliverables within target timelines.
Must have strong analytical, interpersonal, communication, organization, and project management skills and passion to learn and grow within the biopharmaceutical industry.
$23 hourly24d ago
Quality Control Microbiologist
The successful candidate will perform all tasks and procedures related to the environmental monitoring program and microbiological testing in support of the Manufacturing areas at the company, supporting in viable and non-viable sampling, quality control testing and data analysis.$42k-67k yearly est.4d ago
Chemist - II (Associate)
Job Title: Chemist - II (Associate)$60k-77k yearly est.11d ago
Chemist I
Qualifications:
Bachelors degree with at least 2+ years of laboratory experience in industry or academia.
Candidates should have a sound basic knowledge on chromatographic techniques and the ability to apply fundamental principles and techniques to the problems assigned.
Experience with HPLC
GMP knowledge
Experience with empower systems is preferred.
Responsibilities:
Carry out routine testing on sterile pharmaceutical products
Product testing via HPLC and other analytical techniques
$47k-65k yearly est.9d ago
How much does a Quality Control Analyst earn in Lower Makefield, PA?
The average quality control analyst in Lower Makefield, PA earns between $35,000 and $90,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.
$56,000
What is the job market like for quality control analysts in Lower Makefield, PA?
You can compare the number of available jobs in Lower Makefield to the number of quality control analyst jobs in surrounding cities.
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