- Charles River Laboratories (Wilmington, MA)
- …70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, ... resume/CV must be uploaded and submitted during the application process . Please make sure work history and education are...**Job Summary** We are seeking an Instrument Field Support Specialist for our Endosafe instruments: nexgen MCS, nexgen PTS,… more
- Catalent Pharma Solutions (Greendale, IN)
- **Quality Specialist I** **Position Summary** + **Work Schedule:** Monday to Friday, 3PM - 11:30PM + 100% on-site in Greendale, IN Greendale is one of Catalent's ... gummy technology development and manufacturing facilities in North America. The site...to enhance wellness for all consumers. The **Quality Assurance Specialist I** is responsible for auditing the products and… more
- PCI Pharma Services (Rockford, IL)
- …the following but other duties may be assigned. Leads and directs cleaning specialist and process reliability expeditor on daily initiatives and activities by ... shape the future of PCI. **Job** **Title:** **Lead Cleaning Specialist ** **Department/Group:** **Maintenance** **Location:** **Assembly** **1st shift** **Summary of**… more
- Merck (West Point, PA)
- … process /equipment actions, and other related duties. This position will require development of technical expertise of process and product knowledge. Limited ... **Job Description** ** Specialist , Engineering** Our company is seeking a highly...investigation initiation and closure associated with manufacturing deviations and development of actions in response to these deviations (ie… more
- Sumitomo Pharma (Morrisville, NC)
- …to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on ... and experienced individual for the position of **Quality Assurance Specialist II** reporting to the Senior Manager Quality Assurance...includes weekends on a rotating basis, as the manufacturing process is a 7-day process . This role… more
- Bristol Myers Squibb (Summit, NJ)
- …Standard Operating Procedures (SOPs) and batch records + Executes transactions and process in all electronic systems + Demonstrate a strong practical and theoretical ... to ensure the necessary technical skills and knowledge + Proficient in process systems and supporting business systems + Provide assistance setting up manufacturing… more
- Merck (Wilson, NC)
- …writing and deviation investigation + Industrial Electrical, Utility, and HVAC system process improvement and optimization **Preferred** + cGMP in a ... control are needed + Lead in the identification and implementation of process improvement projects, productivity initiatives and corrective actions while focusing on… more
- Boehringer Ingelheim (Athens, GA)
- …to the compliance effort and is responsible for assuring compliance of validated systems, process , equipment to current cGMP , FDA, EU, USDA, BIAH and BI ... an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development , and delivery of our products to our patients and customers. Our… more
- Unither Pharmaceuticals (Rochester, NY)
- Computer Systems Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve ... If completed by an external company, the computer systems validation (CSV) specialist will be responsible for obtaining these documents prior to developing the… more
- PCI Pharma Services (Rockford, IL)
- …network to pioneer and shape the future of PCI. Position Title: Security Specialist Location: Assembly Drive, Rockford, IL 61109 Department: Security Shift: 24/7 AM ... (Staff): None **Job Summary** PCI is seeking a Security Specialist who will play a crucial role in safeguarding...designated access points per schedule. + Assist in the development and revision of security-related policies and standard operating… more